nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
341* ‘About Me’ adolescents introduce themselves to the adult CF team at transition
|
Francis, J. |
|
2007 |
6 |
S1 |
p. S83- 1 p. |
artikel |
2 |
271* Achieving sustained compliance with nebulised therapies in a paediatric CF population
|
McCormack, P. |
|
2007 |
6 |
S1 |
p. S67- 1 p. |
artikel |
3 |
325 Acupuncture in CF: is there a point?
|
Scott, E. |
|
2007 |
6 |
S1 |
p. S79- 1 p. |
artikel |
4 |
231* Adiponectin levels and body composition of cystic fibrosis patients
|
Panagopoulou, P. |
|
2007 |
6 |
S1 |
p. S57- 1 p. |
artikel |
5 |
10 Adult and atypical cystic fibrosis In Serbia
|
Radojkovic, D. |
|
2007 |
6 |
S1 |
p. S3- 1 p. |
artikel |
6 |
123* AGE and sRAGE levels in cystic fibrosis
|
Wilson, J.W. |
|
2007 |
6 |
S1 |
p. S30- 1 p. |
artikel |
7 |
4 Analysis of CFTR gene mutations in Moscow region
|
Radionovitch, A. |
|
2007 |
6 |
S1 |
p. S1- 1 p. |
artikel |
8 |
179* Analysis of local flow and resistance in the lower airways in five children suffering from cystic fibrosis using computational fluid dynamics
|
Vos, W. |
|
2007 |
6 |
S1 |
p. S44- 1 p. |
artikel |
9 |
362 Analytical characteristics of the Dynabio® pancreatitis associated protein (PAP) enzyme linked immunosorbent assay (ELISA)
|
Wilde, H.M. |
|
2007 |
6 |
S1 |
p. S88- 1 p. |
artikel |
10 |
304 An assessment of needs towards the development of a non-malignant palliative care model
|
Braithwaite, M. |
|
2007 |
6 |
S1 |
p. S74- 1 p. |
artikel |
11 |
74 Antibiotic resistance and hypermutator P. aeruginosa
|
Waine, D.J. |
|
2007 |
6 |
S1 |
p. S18- 1 p. |
artikel |
12 |
57 Anti-IgE therapy for cystic fibrosis patients with difficulties in treating allergic bronchopulmonary aspergillosis
|
Geidel, C. |
|
2007 |
6 |
S1 |
p. S14- 1 p. |
artikel |
13 |
305 Anxiety and depression: important factors in our understanding of quality of life
|
Havermans, T. |
|
2007 |
6 |
S1 |
p. S75- 1 p. |
artikel |
14 |
245 A phase III trial of EUR-1008 in young cystic fibrosis (CF) patients with exocrine pancreatic insufficiency (EPI)
|
Wooldridge, J. |
|
2007 |
6 |
S1 |
p. S60- 1 p. |
artikel |
15 |
253* A prospective randomized trial comparing airway clearance strategies following lung transplant
|
Munro, P. |
|
2007 |
6 |
S1 |
p. S62- 1 p. |
artikel |
16 |
140 A prospective trial on the efficacy and tolerability of twice-daily dosing (TDD) versus once-daily dosing (ODD) amikacin in cystic fibrosis patients
|
Postnikov, S.S. |
|
2007 |
6 |
S1 |
p. S34- 1 p. |
artikel |
17 |
315 Are the patient-reported outcomes (PROs) of value in annual review (AR) of adult patients with CF?
|
Salek, M.S. |
|
2007 |
6 |
S1 |
p. S77- 1 p. |
artikel |
18 |
404 Are there any sex differences in lung function of CFTR – knock out mice?
|
Bolle, I. |
|
2007 |
6 |
S1 |
p. S99- 1 p. |
artikel |
19 |
254* A retrospective analysis of physiotherapy input during a standard admission compared to a terminal admission in adults with CF
|
Agent, P. |
|
2007 |
6 |
S1 |
p. S63- 1 p. |
artikel |
20 |
251 A retrospective analysis of various airways clearance techniques on FEV1 decline over one year in cystic fibrosis patients
|
Mills, R.C. |
|
2007 |
6 |
S1 |
p. S62- 1 p. |
artikel |
21 |
208 A review of itraconazole use in a regional paediatric CF centre
|
Gopal Kothandapani, J.S. |
|
2007 |
6 |
S1 |
p. S51- 1 p. |
artikel |
22 |
285 A second chronic illness: how do adults with CF experience being diagnosed with diabetes?
|
Collins, S. |
|
2007 |
6 |
S1 |
p. S70- 1 p. |
artikel |
23 |
218 A snapshot audit of the dietary fruit and vegetable consumption in adults with cystic fibrosis (CF): How many portions are consumed daily?
|
Chinuck, R.S. |
|
2007 |
6 |
S1 |
p. S54- 1 p. |
artikel |
24 |
180 Assessment of the impact of a dedicated multi disciplinary
|
Healy, F. |
|
2007 |
6 |
S1 |
p. S44- 1 p. |
artikel |
25 |
171 Association between exhaled nitric oxide and disease severity in cystic fibrosis
|
van Haren Noman, S. |
|
2007 |
6 |
S1 |
p. S42- 1 p. |
artikel |
26 |
165 Association in the mannose binding lectin (MBL) gene with severity of lung disease and survival in cystic fibrosis (CF)
|
Castanos, C.M. |
|
2007 |
6 |
S1 |
p. S40- 1 p. |
artikel |
27 |
331 A survey of transition to the adult cystic fibrosis (CF) Centre at Papworth Hospital
|
Murphy, C. |
|
2007 |
6 |
S1 |
p. S81- 1 p. |
artikel |
28 |
29 Attempts of facilitated trafficking ΔF508-CFTR to the plasma membrane
|
Shityakov, S.W. |
|
2007 |
6 |
S1 |
p. S7- 1 p. |
artikel |
29 |
81 Audit of MRSA positive cultures at a UK adult CF centre
|
Barker, H.C. |
|
2007 |
6 |
S1 |
p. S20- 1 p. |
artikel |
30 |
Author Index
|
|
|
2007 |
6 |
S1 |
p. S101-S108 8 p. |
artikel |
31 |
53 Azithromycin (AZM) decreases Glutathione-S-Transferase (GST) – T1 expression and activity in CF airway epithelial cells
|
Bergamini, G. |
|
2007 |
6 |
S1 |
p. S13- 1 p. |
artikel |
32 |
40* Aztreonam lysine for inhalation (AZLI) for CF patients with P. aeruginosa (PA) infection
|
McCoy, K. |
|
2007 |
6 |
S1 |
p. S10- 1 p. |
artikel |
33 |
79 Bacterial contamination of PEP masks
|
Jakobsson, B.M. |
|
2007 |
6 |
S1 |
p. S19- 1 p. |
artikel |
34 |
333 Basic structure of daily programme for patients with cystic fibrosis
|
Stepankova, K. |
|
2007 |
6 |
S1 |
p. S81- 1 p. |
artikel |
35 |
131 Basophil activation test for the early diagnosis of allergic bronchopulmonary aspergillosis (ABPA)
|
Katelari, A. |
|
2007 |
6 |
S1 |
p. S32- 1 p. |
artikel |
36 |
279 Benefits of aromatherapy massage for adult cystic fibrosis patients
|
Haynes, F. |
|
2007 |
6 |
S1 |
p. S69- 1 p. |
artikel |
37 |
90 Binding of A549 cells by clinical isolates of P. aeruginosa
|
Ryley, H.C. |
|
2007 |
6 |
S1 |
p. S22- 1 p. |
artikel |
38 |
60 Biocide resistance in the multidrug resistant cystic fibrosis pathogens Pseudomonas aeruginosa and Burkholderia cepacia complex
|
Rose, H. |
|
2007 |
6 |
S1 |
p. S15- 1 p. |
artikel |
39 |
89 Biofilm formation by anaerobic bacteria isolated from the sputum of patients with Cystic Fibrosis
|
Field, T.R. |
|
2007 |
6 |
S1 |
p. S22- 1 p. |
artikel |
40 |
278* BODE index and functional health status in cystic fibrosis patients
|
Savci, S. |
|
2007 |
6 |
S1 |
p. S69- 1 p. |
artikel |
41 |
202 Bone health status in children with cystic fibrosis
|
Kapustina, T. |
|
2007 |
6 |
S1 |
p. S49- 1 p. |
artikel |
42 |
189 Bowel habit audit in one regional adult CF centre
|
Sobanska, A. |
|
2007 |
6 |
S1 |
p. S46- 1 p. |
artikel |
43 |
353 Breadth of disciplines attending international CF conferences
|
Burhan, H. |
|
2007 |
6 |
S1 |
p. S86- 1 p. |
artikel |
44 |
98 Burkholderia pseudomallei in a cystic fibrosis (CF) patient in Brazil: an emerging pathogen?
|
Hoffmann, A. |
|
2007 |
6 |
S1 |
p. S24- 1 p. |
artikel |
45 |
296 Can computers improve the in-patient experience? A survey of patients' views
|
Frankcom, W. |
|
2007 |
6 |
S1 |
p. S72- 1 p. |
artikel |
46 |
313 Can patient-reported health-related quality of life predict survival in cystic fibrosis?
|
Abbott, J. |
|
2007 |
6 |
S1 |
p. S77- 1 p. |
artikel |
47 |
250* Can physiological parameters determine the optimal method of airway clearance for the individual patient with cystic fibosis?
|
McIlwaine, P.M. |
|
2007 |
6 |
S1 |
p. S62- 1 p. |
artikel |
48 |
233 Carotenoid supplementation in CF – How to find a way to do it safely?
|
Sommerburg, O. |
|
2007 |
6 |
S1 |
p. S57- 1 p. |
artikel |
49 |
147 Categorization of patients by “Leeds criteria” for Pseudomonas aeruginosa infection in cystic fibrosis center in Republic of Macedonia
|
Jakovska-Maretti, T. |
|
2007 |
6 |
S1 |
p. S36- 1 p. |
artikel |
50 |
139 Cefradine for anti-staphylococcal prophylaxis in children with cystic fibrosis
|
Upadrasta, S. |
|
2007 |
6 |
S1 |
p. S34- 1 p. |
artikel |
51 |
292 CF and Me – a colouring book for children
|
McDonald, R. |
|
2007 |
6 |
S1 |
p. S71- 1 p. |
artikel |
52 |
342 CF and sexuality fertility and reproduction: Is the nursing staff adequately educated to deal with issues of sexuality, fertility and reproduction related to CF patients
|
Hattem van, M. |
|
2007 |
6 |
S1 |
p. S83- 1 p. |
artikel |
53 |
5 CFTR mutations detection in patients with cystic fibrosis from Romania using Elucigene CF29 kit
|
Tamas, L. |
|
2007 |
6 |
S1 |
p. S2- 1 p. |
artikel |
54 |
84 Characterisation of fibrinogen degradation by the CF-related pathogens, Burkholderia cenocepacia and Pseudomonas aeruginosa
|
Einarsson, G.G. |
|
2007 |
6 |
S1 |
p. S21- 1 p. |
artikel |
55 |
162 Characteristics of the patients with cystic fibrosis
|
Uzuner, N. |
|
2007 |
6 |
S1 |
p. S39- 1 p. |
artikel |
56 |
263 Chest strength and mobility training: How do we do it?
|
Demry, A. |
|
2007 |
6 |
S1 |
p. S65- 1 p. |
artikel |
57 |
145 Clinical correlates of hypermutator P. aeruginosa in CF
|
Waine, D.J. |
|
2007 |
6 |
S1 |
p. S35- 1 p. |
artikel |
58 |
197 Clinical follow up after liver transplantation in children with cystic fibrosis
|
Junge, S. |
|
2007 |
6 |
S1 |
p. S48- 1 p. |
artikel |
59 |
380* Clinical management system for cystic fibrosis
|
Peckham, D. |
|
2007 |
6 |
S1 |
p. S93- 1 p. |
artikel |
60 |
346 Clinical manifestations of cystic fibrosis among patients diagnosed in childhood and patients diagnosed in adulthood
|
Cobanoglu, N. |
|
2007 |
6 |
S1 |
p. S84- 1 p. |
artikel |
61 |
264 Clinical outcome and social parameters impact on sport activity in children with CF: a prospective survey
|
Vital-Foucher, A. |
|
2007 |
6 |
S1 |
p. S65- 1 p. |
artikel |
62 |
97 Clostridium difficile colitis in transplanted cystic fibrosis patients.
|
Theunissen, C. |
|
2007 |
6 |
S1 |
p. S24- 1 p. |
artikel |
63 |
386 Cochleotoxicity of systemically administered tobramycin in Cystic Fibrosis patients
|
Scheenstra, R.J. |
|
2007 |
6 |
S1 |
p. S94- 1 p. |
artikel |
64 |
168* Combined lung and liver transplantation in cystic fibrosis
|
Souilamas, R. |
|
2007 |
6 |
S1 |
p. S41- 1 p. |
artikel |
65 |
107 Comparison of 6 culture media, 5 DNA-extraction methods and PCR and nested PCR for sensitive detection of P. aeruginosa from CF sputa
|
Schelstraete, P. |
|
2007 |
6 |
S1 |
p. S26- 1 p. |
artikel |
66 |
241 Comparison of inpatient blood glucose monitoring with UK Cystic Fibrosis Trust Guidelines
|
Robb, L. |
|
2007 |
6 |
S1 |
p. S59- 1 p. |
artikel |
67 |
153 Comparison of lung function tests (LFT) in infants with CF and healthy subjects (HS)
|
Tancredi, G. |
|
2007 |
6 |
S1 |
p. S37- 1 p. |
artikel |
68 |
78 Comparison of pathogen prevalence in CF patients treated at the Children's Memorial Health Institute in years 1999–2002 and 2003–2006
|
Dmenska, H. |
|
2007 |
6 |
S1 |
p. S19- 1 p. |
artikel |
69 |
308 Comparison of sleep quality, anxiety and depression between mothers of children with cystic fibrosis and with asthma
|
Yilmaz, O. |
|
2007 |
6 |
S1 |
p. S75- 1 p. |
artikel |
70 |
80 Comparison of the bacterial communities sampled from the healthy and the cystic fibrosis lung
|
Stressmann, F.A. |
|
2007 |
6 |
S1 |
p. S20- 1 p. |
artikel |
71 |
230 Comparison of three methods to measure body composition in patients with cystic fibrosis. Relation with retrotricipital skinfold thickness and brachial circumference
|
Beaumesnil, M. |
|
2007 |
6 |
S1 |
p. S57- 1 p. |
artikel |
72 |
95* Comparison of T-RFLP profiles generated directly from sputum with those generated from conventional culture plates
|
Rogers, G.B. |
|
2007 |
6 |
S1 |
p. S23- 1 p. |
artikel |
73 |
393 Complex CF facultative classes at the University of Medical Sciences, Poznan, Poland
|
Krzyzanowski, M. |
|
2007 |
6 |
S1 |
p. S96- 1 p. |
artikel |
74 |
137 Concordance between intravenous antibiotics (IV) and in vitro susceptibility of sputum bacteria does not influence the outcome of pulmonary exacerbations in adult cystic fibrosis patients
|
Jarad, N.A. |
|
2007 |
6 |
S1 |
p. S33- 1 p. |
artikel |
75 |
198 Consideration on ursodeoxicholic acid treatment
|
Popa, I. |
|
2007 |
6 |
S1 |
p. S48- 1 p. |
artikel |
76 |
125 CRITICAL role for cytosolic phospholipase A2 in bronchial mucus hyper-secretion in CFTR-/- mice
|
Dif, F. |
|
2007 |
6 |
S1 |
p. S31- 1 p. |
artikel |
77 |
396 CT scans from CF patients screened for lung transplant; the Severe Advance Lung Disease (SALD) CT scoring system
|
Loeve, M. |
|
2007 |
6 |
S1 |
p. S97- 1 p. |
artikel |
78 |
385 Cutaneous phototoxicity secondary to ciprofloxacin in adult patients with cystic fibrosis: incidence and association with genotype
|
Tolland, J.P. |
|
2007 |
6 |
S1 |
p. S94- 1 p. |
artikel |
79 |
375 Cystic fibrosis, apple peel disease and normal neonatal trypsin
|
Repetto, T. |
|
2007 |
6 |
S1 |
p. S92- 1 p. |
artikel |
80 |
350 Cystic fibrosis (CF) and the risk of pancreatic cancer (PDAC)
|
Lowenfels, A. |
|
2007 |
6 |
S1 |
p. S85- 1 p. |
artikel |
81 |
365 Cystic fibrosis newborn screening in the Czech Republic: overview of a pilot study
|
Balascakova, M. |
|
2007 |
6 |
S1 |
p. S89- 1 p. |
artikel |
82 |
370 Cystic fibrosis transmembrane conductance regulator ion channel function testing in recurrent acute pancreatitis
|
Wilschanski, M. |
|
2007 |
6 |
S1 |
p. S90- 1 p. |
artikel |
83 |
322 Danish lung transplanted CF patients connection to the labour market prior to and after the transplantation
|
Lund, L.D. |
|
2007 |
6 |
S1 |
p. S78- 1 p. |
artikel |
84 |
400 Decreased bone mineral density in adolescents and young adults with cystic fibrosis: prevalence and risk factors
|
Jourdain, A. |
|
2007 |
6 |
S1 |
p. S98- 1 p. |
artikel |
85 |
188 Delayed gastric emptying is associated with lower BMI in adults with cystic fibrosis
|
King, S.J. |
|
2007 |
6 |
S1 |
p. S45- 1 p. |
artikel |
86 |
46* Deposition and pharmacokinetic studies with inhaled P2Y2 agonists – evidence of high lung delivery and minimal systemic exposure
|
Kellerman, D. |
|
2007 |
6 |
S1 |
p. S11- 1 p. |
artikel |
87 |
88* Detection of anaerobic bacteria in high numbers in sputum from Cystic Fibrosis patients with an acute exacerbation of pulmonary infection
|
Moriarty, T.F. |
|
2007 |
6 |
S1 |
p. S22- 1 p. |
artikel |
88 |
260 Determinants of anaerobic performance in cystic fibrosis patients
|
Inal-Ince, D. |
|
2007 |
6 |
S1 |
p. S64- 1 p. |
artikel |
89 |
160 Determinants of delivered dose from the I-neb® AAD® System
|
Potter, R.W. |
|
2007 |
6 |
S1 |
p. S39- 1 p. |
artikel |
90 |
297* Developing patient information material: a collaborative effort
|
McDonald, R. |
|
2007 |
6 |
S1 |
p. S73- 1 p. |
artikel |
91 |
106 Development of a diagnostic multiplex PCR test for the identification of three CF epidemic strains of Pseudomonas aeruginosa
|
Fothergill, J.L. |
|
2007 |
6 |
S1 |
p. S26- 1 p. |
artikel |
92 |
310 Development of a unidimentional health status measure for cystic fibrosis (CF)
|
Scott, S.F. |
|
2007 |
6 |
S1 |
p. S76- 1 p. |
artikel |
93 |
8 DHPLC in Cystic Fibrosis diagnostics in the German population
|
Froster, U. |
|
2007 |
6 |
S1 |
p. S2- 1 p. |
artikel |
94 |
290 Diagnosis – how does it feel?
|
Lambert, C. |
|
2007 |
6 |
S1 |
p. S71- 1 p. |
artikel |
95 |
212 Dietary treatment in adult patients with cystic fibrosis related diabetes
|
Hollander, F.M. |
|
2007 |
6 |
S1 |
p. S52- 1 p. |
artikel |
96 |
15 Differences in lung function and physical performance in children with CF: the effect of ACE polymorphisms
|
Slieker, M.G. |
|
2007 |
6 |
S1 |
p. S4- 1 p. |
artikel |
97 |
93* Different genetic adaptation strategies of mucoid and non-mucoid Pseudomonas aeruginosa in the airway of cystic fibrosis patients
|
Lee, B. |
|
2007 |
6 |
S1 |
p. S23- 1 p. |
artikel |
98 |
35* Disruption of CFTR-dependent Lung and Intestine Organogenesis Results in Adult-Onset Diseases
|
Cohen, J.C. |
|
2007 |
6 |
S1 |
p. S8- 1 p. |
artikel |
99 |
211 Does an integrated clinical and nutritional approach prevent pre-diabetic decline?
|
White, H. |
|
2007 |
6 |
S1 |
p. S52- 1 p. |
artikel |
100 |
187 Does fundoplication reduce the decline in lung function and frequency of IV antibiotics in CF adults?
|
Page, G. |
|
2007 |
6 |
S1 |
p. S45- 1 p. |
artikel |
101 |
143 Does increased frequency of sputum sampling alter antibiotic choice during exacerbations?
|
Boyle, L.R. |
|
2007 |
6 |
S1 |
p. S35- 1 p. |
artikel |
102 |
26* Does male fertility impairment due to idiopathic semen hyperviscosity depend on CFTR gene mutations?
|
Lucarelli, M. |
|
2007 |
6 |
S1 |
p. S6- 1 p. |
artikel |
103 |
221* Do overweight and obesity improve clinical outcome in the French cystic fibrosis population?
|
Munck, A. |
|
2007 |
6 |
S1 |
p. S54- 1 p. |
artikel |
104 |
11 Do people with Cystic Fibrosis (CF) and one R117H allele have less severe phenotype compared with ΔF508 homozygotes?
|
Shimmin, D. |
|
2007 |
6 |
S1 |
p. S3- 1 p. |
artikel |
105 |
115 Dynamics of Staphylococcus aureus strains in adults with cystic fibrosis (CF)
|
Jonte, J. |
|
2007 |
6 |
S1 |
p. S28- 1 p. |
artikel |
106 |
149 Early warning signs of bacterial exacerbation in cystic fibrosis patients
|
Jimenez, H.A. |
|
2007 |
6 |
S1 |
p. S36- 1 p. |
artikel |
107 |
324* Eating disorder symptomatology in cystic fibrosis before and after transplant: A case presentation
|
Brager, N. |
|
2007 |
6 |
S1 |
p. S79- 1 p. |
artikel |
108 |
273 Educational leaflets to improve use of volume space device in children with CF
|
Sallort, M. |
|
2007 |
6 |
S1 |
p. S67- 1 p. |
artikel |
109 |
113 Effect of a segregation policy on the incidence of multi-resistant Pseudomonas aeruginosa (mrPA) in adult patients with cystic fibrosis (CF)
|
Clifton, I. |
|
2007 |
6 |
S1 |
p. S28- 1 p. |
artikel |
110 |
258* Effect of global posture reeducation (GPR) program on respiratory muscle strength
|
Buonpensiero, P. |
|
2007 |
6 |
S1 |
p. S64- 1 p. |
artikel |
111 |
130 Effect of hypertonic saline on Exhaled Breath Condensate
|
Hansen, C.R. |
|
2007 |
6 |
S1 |
p. S32- 1 p. |
artikel |
112 |
37 Effect of mist tent on ion content of nasal fluid in patients with cystic fibrosis
|
Kozlova, I. |
|
2007 |
6 |
S1 |
p. S8- 1 p. |
artikel |
113 |
307 Effects of a clinic-based intervention on caregiving stress for parents of children with CF
|
McDonald, L. |
|
2007 |
6 |
S1 |
p. S75- 1 p. |
artikel |
114 |
287 Effects of a clinic-based intervention on knowledge and treatment skills for parents and young children with CF
|
Cruz, I. |
|
2007 |
6 |
S1 |
p. S70- 1 p. |
artikel |
115 |
138 Effects of antibiotic treatment of initial Pseudomonas aeruginosa colonization on acquisition of chronic infection in cystic fibrosis
|
Fustik, S. |
|
2007 |
6 |
S1 |
p. S33- 1 p. |
artikel |
116 |
401 Effects of disease progression on peripheral muscle strength and bulk, aerobic capacity and physical activity in cystic fibrosis (CF)
|
Opdekamp, C. |
|
2007 |
6 |
S1 |
p. S98- 1 p. |
artikel |
117 |
319 Effects of maternal depression on electronically monitored enzyme adherence and changes in weight for children with CF
|
Quittner, A.L. |
|
2007 |
6 |
S1 |
p. S78- 1 p. |
artikel |
118 |
298 Efficacy of educational intervention to practice hygiene measures at routine clinic visits
|
Armoni, S. |
|
2007 |
6 |
S1 |
p. S73- 1 p. |
artikel |
119 |
389 Efficacy of home versus hospital-administered intravenous antibiotics in cystic fibrosis
|
Termoz, A. |
|
2007 |
6 |
S1 |
p. S95- 1 p. |
artikel |
120 |
83 Emergence of an epidemic clone of community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) Panton-Valentine leukocidin (PVL) negative in Cystic Fibrosis patients
|
Cocchi, P. |
|
2007 |
6 |
S1 |
p. S20- 1 p. |
artikel |
121 |
351* Employment status of cystic fibrosis adults–a10year improving picture
|
Gunn, E. |
|
2007 |
6 |
S1 |
p. S85- 1 p. |
artikel |
122 |
213* Energy and nutrient intakes of paediatric subjects with cystic fibrosis (CF)
|
Corridon, C. |
|
2007 |
6 |
S1 |
p. S52- 1 p. |
artikel |
123 |
219 Energy intake from PEG feeds and long-term anthropometric changes in children with CF
|
Hopkins, D. |
|
2007 |
6 |
S1 |
p. S54- 1 p. |
artikel |
124 |
207* Essential fatty acid (EFA) profile in CF patients with ‘severe’ and ‘mild’ mutations
|
De Boeck, K. |
|
2007 |
6 |
S1 |
p. S50- 1 p. |
artikel |
125 |
403 Estimating the age of common CFTR mutations in Brittany (western France)
|
Fichou, Y. |
|
2007 |
6 |
S1 |
p. S98- 1 p. |
artikel |
126 |
246 EUR-1008 (a new pancraetic enzyme product, PEP) was shown to be safe and effective in cystic fibrosis (CF) patients with exocrine pancreatic insufficiency (EPI)
|
Heubi, J.E. |
|
2007 |
6 |
S1 |
p. S61- 1 p. |
artikel |
127 |
224 Evaluating knowledge about nutrition in CF adult patients
|
Lahoreau, D. |
|
2007 |
6 |
S1 |
p. S55- 1 p. |
artikel |
128 |
347 Evaluation and evolution of the national Belgian CF database
|
Jansen, H. |
|
2007 |
6 |
S1 |
p. S84- 1 p. |
artikel |
129 |
111* Evaluation of anti-A-band LPS antibodies to Pseudomonas aeruginosa in serum from patients with cystic fibrosis
|
Weisner, A.M. |
|
2007 |
6 |
S1 |
p. S27- 1 p. |
artikel |
130 |
68* Evaluation of new guidelines for the eradication of Staphylococcus aureus in children with cystic fibrosis
|
Aldag, I. |
|
2007 |
6 |
S1 |
p. S17- 1 p. |
artikel |
131 |
371 Evaluation of nonclassic CF: interpretation of sweat test methods in correlation to ICM and CFTR genotype
|
Derichs, N. |
|
2007 |
6 |
S1 |
p. S91- 1 p. |
artikel |
132 |
399 Evaluation of urinary incontinence in girls and female adolescents with cystic fibrosis
|
Van Schaijk, M. |
|
2007 |
6 |
S1 |
p. S97- 1 p. |
artikel |
133 |
204 Evolution of glucose intolerance in adolescent CF patients
|
Carpenter, S. |
|
2007 |
6 |
S1 |
p. S50- 1 p. |
artikel |
134 |
256* Exercise capacity, muscle strength and quality of life in adult CF patients
|
Vrijsen, B. |
|
2007 |
6 |
S1 |
p. S63- 1 p. |
artikel |
135 |
172 Exhaled nitric oxide is not correlated with inflammation in Cystic Fibrosis
|
Hatziagorou, E. |
|
2007 |
6 |
S1 |
p. S42- 1 p. |
artikel |
136 |
124* Exhaled NO and exhaled breath condensate in patients with cystic fibrosis and healthy controls
|
Bloemen, K. |
|
2007 |
6 |
S1 |
p. S31- 1 p. |
artikel |
137 |
355 Family testing: the 17-year experience of Brittany (western France)
|
Duguépéroux, I. |
|
2007 |
6 |
S1 |
p. S87- 1 p. |
artikel |
138 |
374 18FDG-PET/CT in CF: correlation with both inflammatory markers and FEV1
|
Cohen-Cymberknoh, M. |
|
2007 |
6 |
S1 |
p. S91- 1 p. |
artikel |
139 |
337 Feasibility and tolerance of percutaneous central catheters in children with cystic fibrosis (CF)
|
Bui, S. |
|
2007 |
6 |
S1 |
p. S82- 1 p. |
artikel |
140 |
36 Feasibility of airway surface liquid (ASL) height measurement in human nasal and bronchial biopsies
|
Griesenbach, U. |
|
2007 |
6 |
S1 |
p. S8- 1 p. |
artikel |
141 |
141 FEV1% predicted may not be a simple end point for CF studies
|
Goldman, M.H. |
|
2007 |
6 |
S1 |
p. S34- 1 p. |
artikel |
142 |
49 Flavonoid-serum-levels in patients with cystic fibrosis
|
Schüler, D. |
|
2007 |
6 |
S1 |
p. S12- 1 p. |
artikel |
143 |
170 Following of lung transplantation for CF patients in Hungary
|
Kelemen, K. |
|
2007 |
6 |
S1 |
p. S41- 1 p. |
artikel |
144 |
71 Follow-up of P. aeruginosa eradication in CF patients by RAPD analysis
|
Ravenni, N. |
|
2007 |
6 |
S1 |
p. S17- 1 p. |
artikel |
145 |
Foreword
|
Göçmen, Ayhan |
|
2007 |
6 |
S1 |
p. v- 1 p. |
artikel |
146 |
142 Frequency of sputum sampling in an adult CF outpatient clinic:How much is too much?
|
Boyle, L.R. |
|
2007 |
6 |
S1 |
p. S34- 1 p. |
artikel |
147 |
159 Fundoplication for reflux induced cough in cystic fibrosis
|
Haley, N.M. |
|
2007 |
6 |
S1 |
p. S39- 1 p. |
artikel |
148 |
199 Gallbladder anomalies among children with CF
|
Ciuca Popa, I.M. |
|
2007 |
6 |
S1 |
p. S48- 1 p. |
artikel |
149 |
301 Gender differences in life satisfaction of adolescent and adult patients with cystic fibrosis
|
Besier, T. |
|
2007 |
6 |
S1 |
p. S74- 1 p. |
artikel |
150 |
19 Gene therapy for CF: a survey of patients' knowledge and opinions
|
Thomas, A. |
|
2007 |
6 |
S1 |
p. S5- 1 p. |
artikel |
151 |
110 Genetic fingerprinting of Pseudomonas aeruginosa (PA) from Italian CF patients (pts): comparison with isolates from environment and other clinical origins in Europe
|
Manno, G. |
|
2007 |
6 |
S1 |
p. S27- 1 p. |
artikel |
152 |
13 Genetic markers of musculoskeletal changes in cystic fibrosis
|
Norek, A. |
|
2007 |
6 |
S1 |
p. S3- 1 p. |
artikel |
153 |
395 Genital human papillomavirus (HPV) infection and its consequences in CF lung transplant (tx) recipients
|
Knoop, C. |
|
2007 |
6 |
S1 |
p. S96- 1 p. |
artikel |
154 |
105 Genomic fingerprinting of Pseudomonas aeruginosa isolates from all Swedish CF Centres. A Scandinavian Cystic Fibrosis Study Consortium study
|
Johansson, E. |
|
2007 |
6 |
S1 |
p. S26- 1 p. |
artikel |
155 |
103 Genotype diversity of P. aeruginosa in CF sputum samples
|
Waine, D.J. |
|
2007 |
6 |
S1 |
p. S25- 1 p. |
artikel |
156 |
109 Genotyping of P. aeruginosa, A. xylosoxidans and S. maltophilia in a CF centre
|
Van daele, S. |
|
2007 |
6 |
S1 |
p. S27- 1 p. |
artikel |
157 |
329 Gift of life: Young adult lung transplant recipients talk about their new lungs
|
Ullrich, G. |
|
2007 |
6 |
S1 |
p. S80- 1 p. |
artikel |
158 |
16* Glutathione S-transferase activity-genotype association with time and severity of Pseudomonas aeruginosa lung infection in cystic fibrosis children
|
Feuillet-Fieux, M.N. |
|
2007 |
6 |
S1 |
p. S4- 1 p. |
artikel |
159 |
289 Group work as a coping skill for children with CF, ages 9–12
|
Amitzur, M. |
|
2007 |
6 |
S1 |
p. S71- 1 p. |
artikel |
160 |
7 GT repetition on 5T allele
|
Maschio, M. |
|
2007 |
6 |
S1 |
p. S2- 1 p. |
artikel |
161 |
229 Hand grip strength values correlate with recognised outcome measures in a cohort of adult CF patients
|
Al Siaidi, J. |
|
2007 |
6 |
S1 |
p. S56- 1 p. |
artikel |
162 |
237 Hand radiograms as an alternative for dual X-ray absorptiometry in bone mass assessment in cystic fibrosis patients?
|
Tomalak, W. |
|
2007 |
6 |
S1 |
p. S58- 1 p. |
artikel |
163 |
69 Healthcare costs of infection with the major transmissible UK Pseudomonas aeruginosa strain, LES
|
Spencer-Clegg, E. |
|
2007 |
6 |
S1 |
p. S17- 1 p. |
artikel |
164 |
94 High bacterial diversity of Staphylococcus aureus populations in airway specimens of cystic fibrosis patients
|
Goerke, C. |
|
2007 |
6 |
S1 |
p. S23- 1 p. |
artikel |
165 |
252 High frequency chest wall oscillation: an adjunct to other airway clearance techniques in CF adults?
|
Gumery, L. |
|
2007 |
6 |
S1 |
p. S62- 1 p. |
artikel |
166 |
154 Home monitoring using portable spirometry and SMS reminder service in CF
|
Desager, K.N. |
|
2007 |
6 |
S1 |
p. S37- 1 p. |
artikel |
167 |
332* How to improve the daily management of implantable catheter ports (ICP)? Proposal of a practical tool for nurses and physicians
|
Dupont, C. |
|
2007 |
6 |
S1 |
p. S81- 1 p. |
artikel |
168 |
268 Hygiene of the inhalation equipment: a Belgian national survey
|
Reychler, G. |
|
2007 |
6 |
S1 |
p. S66- 1 p. |
artikel |
169 |
267 Hygiene of the inhalation equipment: what about vibrating-mesh nebulizers?
|
Lessire, F. |
|
2007 |
6 |
S1 |
p. S66- 1 p. |
artikel |
170 |
100 Identification algorithms for Burkholderia cepacia complex bacteria
|
Vanlaere, E. |
|
2007 |
6 |
S1 |
p. S25- 1 p. |
artikel |
171 |
17 Identification of a de novo mRNA molecular defect in a CF patient
|
Audrezet, M.P. |
|
2007 |
6 |
S1 |
p. S4- 1 p. |
artikel |
172 |
117 Identification of airborne fungi in an adult CF unit
|
Nagano, Y. |
|
2007 |
6 |
S1 |
p. S29- 1 p. |
artikel |
173 |
2* Identification of two Alu insertions in the CFTR gene
|
Audrezet, M.P. |
|
2007 |
6 |
S1 |
p. S1- 1 p. |
artikel |
174 |
121 Immunoglobulin levels in cystic fibrosis patients: influence of age and gender
|
Hanssens, L. |
|
2007 |
6 |
S1 |
p. S30- 1 p. |
artikel |
175 |
381 Impact of practice guidelines on the activity of cystic fibrosis centres
|
Decullier, E. |
|
2007 |
6 |
S1 |
p. S93- 1 p. |
artikel |
176 |
77* Impact of reducing routine sensitivity testing in chronic Pseudomonas aeruginosa infections in cystic fibrosis
|
Etherington, C. |
|
2007 |
6 |
S1 |
p. S19- 1 p. |
artikel |
177 |
210 Importance of CF-formula in the nutrition of children with cystic fibrosis
|
Sands, D. |
|
2007 |
6 |
S1 |
p. S52- 1 p. |
artikel |
178 |
266 Improved pulmonary function and quality of life perception after respiratory training with a specific commercial device
|
Sartori, R. |
|
2007 |
6 |
S1 |
p. S66- 1 p. |
artikel |
179 |
306 Improving the quality of life for CF patients by facilitating their creativity
|
Chladova, H. |
|
2007 |
6 |
S1 |
p. S75- 1 p. |
artikel |
180 |
177 Incidence and evolution of nasal polyposis in cystic fibrosis children and adolescents
|
Weber, S.A. |
|
2007 |
6 |
S1 |
p. S43- 1 p. |
artikel |
181 |
352 Incidence and evolution of nasal polyposis in cystic fibrosis children and adolescents
|
Weber, S.A. |
|
2007 |
6 |
S1 |
p. S85- 1 p. |
artikel |
182 |
206 Incidence of nephrocalcinosis and hypercalciuria in Turkish cystic fibrosis children
|
Pekcan, S. |
|
2007 |
6 |
S1 |
p. S50- 1 p. |
artikel |
183 |
200 Inflammatory cytokines and markers of bone metabolism during CF infective exacerbations
|
Shead, E.F. |
|
2007 |
6 |
S1 |
p. S49- 1 p. |
artikel |
184 |
240 Influence of pancreatic status on plasma and erythrocyte membrane fatty acid composition in CF
|
Coste, T.C. |
|
2007 |
6 |
S1 |
p. S59- 1 p. |
artikel |
185 |
167 Inhalation with PARI eFlow® rapid reduces treatment burden significantly in adult CF patients without altering lung function
|
Fischer, R. |
|
2007 |
6 |
S1 |
p. S41- 1 p. |
artikel |
186 |
70 Initial colonization with Pseudomonas aeruginosa in cystic fibrosis: preliminary results of an eradication protocol
|
Adde, F.V. |
|
2007 |
6 |
S1 |
p. S17- 1 p. |
artikel |
187 |
367 Intestinal current measurement as a diagnostic procedure in cystic fibrosis in infants and young children
|
Wilschanski, M. |
|
2007 |
6 |
S1 |
p. S90- 1 p. |
artikel |
188 |
135 Intravenous antibiotic treatment in children with cystic fibrosis: home versus hospital setting
|
Proesmans, M. |
|
2007 |
6 |
S1 |
p. S33- 1 p. |
artikel |
189 |
382* Introduction & evaluation of a pharmacist-run medication review for cystic fibrosis patients
|
Philpott, L. |
|
2007 |
6 |
S1 |
p. S93- 1 p. |
artikel |
190 |
178 Introduction of dual energy X-ray absorptiometry into the annual review of adult cystic fibrosis patients at All Wales Adult Regional Centre, UK
|
Palamarthy, A.B. |
|
2007 |
6 |
S1 |
p. S43- 1 p. |
artikel |
191 |
223 Inverse gender gap in nutritional status; Scandinavian CF study consortium
|
Olesen, H.V. |
|
2007 |
6 |
S1 |
p. S55- 1 p. |
artikel |
192 |
232* Is puberty delayed in cystic fibrosis?
|
Panagopoulou, P. |
|
2007 |
6 |
S1 |
p. S57- 1 p. |
artikel |
193 |
52 Joint effect of alpha-melanocyte stimulating hormone and met-enkephalin on respiratory function in guinea-pigs
|
T-Drinkovic, D. |
|
2007 |
6 |
S1 |
p. S13- 1 p. |
artikel |
194 |
300 Keeping CF kids connected – Ability Online
|
Taylor, L. |
|
2007 |
6 |
S1 |
p. S73- 1 p. |
artikel |
195 |
86* Lactate production and Pseudomonas aeruginosa metabolism in CF sputum
|
Worlitzsch, D. |
|
2007 |
6 |
S1 |
p. S21- 1 p. |
artikel |
196 |
6* Large CFTR gene rearrangements in Italian population
|
Paracchini, V. |
|
2007 |
6 |
S1 |
p. S2- 1 p. |
artikel |
197 |
44 Lentiviral vector-mediated expression of RNA interference for ENaC in cell models of airway epithelium suitable for functional evaluation of ENaC activity
|
Copreni, E. |
|
2007 |
6 |
S1 |
p. S11- 1 p. |
artikel |
198 |
43 Lentiviral vector-mediated expression of RNA interference sequences for ENaC in cell models of human airway epithelium
|
Copreni, E. |
|
2007 |
6 |
S1 |
p. S10- 1 p. |
artikel |
199 |
67 Linezolid-induced neurological adverse effects after prolonged treatment for MRSA respiratory infections in CF
|
De Wachter, E. |
|
2007 |
6 |
S1 |
p. S16- 1 p. |
artikel |
200 |
402 Lip enlargement as a clinical feature of cystic fibrosis
|
Cakic, S.S. |
|
2007 |
6 |
S1 |
p. S98- 1 p. |
artikel |
201 |
196 Liver transplantation in children with cystic fibrosis: single centre experience
|
Loganathan, S. |
|
2007 |
6 |
S1 |
p. S47- 1 p. |
artikel |
202 |
312 Living with Cystic Fibrosis Questionnaire (CFLC-Q): Development and preliminary validation of a new measure of the challenge experienced by caregivers
|
Glasscoe, C. |
|
2007 |
6 |
S1 |
p. S76- 1 p. |
artikel |
203 |
190 Long-term outcome after meconium ileus
|
Kappler, M. |
|
2007 |
6 |
S1 |
p. S46- 1 p. |
artikel |
204 |
129 Long-term treatment with glucocorticoids in low doses restores affected cytokine production in cystic fibrosis patients
|
Pukhalsky, A.L. |
|
2007 |
6 |
S1 |
p. S32- 1 p. |
artikel |
205 |
384 Long-term treatment with Pulmozyme® is associated with slower rate or improvement of lung functions decline in CF patients
|
Kayserova, H. |
|
2007 |
6 |
S1 |
p. S94- 1 p. |
artikel |
206 |
51 Lung deposition and pharmacokinetics in 12 lung transplanted patients after inhalation of a liposomal Ciclosporin A (CsA) formulation by the eFlow electronic nebuliser
|
Keller, M. |
|
2007 |
6 |
S1 |
p. S12- 1 p. |
artikel |
207 |
163* Lung disease progression in children with cystic fibrosis
|
Terheggen/Lagro, S.W. |
|
2007 |
6 |
S1 |
p. S40- 1 p. |
artikel |
208 |
156* Lung function in children with CF – from infants to seven years old
|
Geborek, A. |
|
2007 |
6 |
S1 |
p. S38- 1 p. |
artikel |
209 |
193 Major differences in pancreatic enzyme replacement in Scandinavia
|
Hjelte, L. |
|
2007 |
6 |
S1 |
p. S47- 1 p. |
artikel |
210 |
397 Malignant disease adults with cystic fibrosis: a 10 year review
|
Khan, Z. |
|
2007 |
6 |
S1 |
p. S97- 1 p. |
artikel |
211 |
388 May peripherally inserted central catheters (PICC) be an alternative for implantable catheter ports (ICP) for intravenous (IV) antibiotic therapy?
|
Dupont, C. |
|
2007 |
6 |
S1 |
p. S95- 1 p. |
artikel |
212 |
288 Mediating and negotiating and in-patient stay for families and patients with cystic fibrosis
|
Latage, K. |
|
2007 |
6 |
S1 |
p. S70- 1 p. |
artikel |
213 |
82 Methicillin-resistant Staphylococcus aureus from airway secretions from patients with cystic fibrosis
|
Alexandrou-Athanasoulis, H. |
|
2007 |
6 |
S1 |
p. S20- 1 p. |
artikel |
214 |
205 Microalbuminuria in patients with cystic fibrosis: diabetic or cystic fibrosis-related?
|
Kannekens, A.L. |
|
2007 |
6 |
S1 |
p. S50- 1 p. |
artikel |
215 |
96 Microbiological audit in Cystic Fibrosis Romanian children
|
Popa, I. |
|
2007 |
6 |
S1 |
p. S24- 1 p. |
artikel |
216 |
12* Modulatory effect of MBL2 on the onset of Pseudomonas aeruginosa infection is influenced by the TGFβ1 variants in pediatric CF patients
|
Dorfman, R. |
|
2007 |
6 |
S1 |
p. S3- 1 p. |
artikel |
217 |
104 Molecular analysis of diversity within the genus Pseudomonas in the lungs of cystic fibrosis patients
|
Spasenovski, T. |
|
2007 |
6 |
S1 |
p. S26- 1 p. |
artikel |
218 |
25* Molecular and functional characterization of CBAVD-causing mutations located in both NBDs of the CFTR protein
|
Grangeia, A. |
|
2007 |
6 |
S1 |
p. S6- 1 p. |
artikel |
219 |
157 Monitoring of Dornase alfa treatment efficacy for children with cystic fibrosis
|
Dumcius, S. |
|
2007 |
6 |
S1 |
p. S38- 1 p. |
artikel |
220 |
363 Monthly variation in newborn screening immunoreactive trypsinogen concentrations [IRT]
|
Montgomery, M.D. |
|
2007 |
6 |
S1 |
p. S89- 1 p. |
artikel |
221 |
102 Morbidity of a peadiatric population with CF, according to chronic P. aeruginosa (Pa) colonization
|
Sad, I. |
|
2007 |
6 |
S1 |
p. S25- 1 p. |
artikel |
222 |
120* Multiplex cytokine profile detection in young children with cystic fibrosis
|
Terheggen-Lagro, S. |
|
2007 |
6 |
S1 |
p. S30- 1 p. |
artikel |
223 |
146 Mycobacterium abscessus infection in lung transplant patients: Review of our series
|
Morales, P. |
|
2007 |
6 |
S1 |
p. S35- 1 p. |
artikel |
224 |
369* Nasal potential difference in hypertrypsinemic children
|
Sermet-Gaudelus, I. |
|
2007 |
6 |
S1 |
p. S90- 1 p. |
artikel |
225 |
368 Nasal potential difference testing in the diagnostic algorithm of CF
|
Middleton, P.G. |
|
2007 |
6 |
S1 |
p. S90- 1 p. |
artikel |
226 |
118 Navigating microbial space using the StrainInfo.net bioportal
|
Van Brabant, B. |
|
2007 |
6 |
S1 |
p. S29- 1 p. |
artikel |
227 |
48* Nebulized SLIT™ Amikacin in the treatment of cystic fibrosis patients with chronic Pseudomonas aeruginosa lung infection in Serbia and Hungary
|
Mackinson, C. |
|
2007 |
6 |
S1 |
p. S12- 1 p. |
artikel |
228 |
359 Negative genetic neonatal screening for cystic fibrosis caused by compound heterozygosity for two large CFTR rearrangements
|
Guittard, C. |
|
2007 |
6 |
S1 |
p. S88- 1 p. |
artikel |
229 |
366 Neonatal cystic fibrosis screening in Russian Federation
|
Tolstova, V.D. |
|
2007 |
6 |
S1 |
p. S89- 1 p. |
artikel |
230 |
364 Newborn screening in the Czech Republic: an effective tool for early detection of CF
|
Zemkova, D. |
|
2007 |
6 |
S1 |
p. S89- 1 p. |
artikel |
231 |
356 Newborn screening (NBS) facilitates diagnosis of previously unrecognised CF in older siblings
|
Skalicka, V. |
|
2007 |
6 |
S1 |
p. S87- 1 p. |
artikel |
232 |
270 New nebulisers and colistin-resistant Pseudomonas aeuginosa (crPA) in patients with cystic fibrosis (CF)
|
Hurlow, A. |
|
2007 |
6 |
S1 |
p. S67- 1 p. |
artikel |
233 |
158 Nocturnal cough frequency in children with cystic fibrosis
|
van der Giessen, L.J. |
|
2007 |
6 |
S1 |
p. S38- 1 p. |
artikel |
234 |
155* Noninvasive evaluation of pulmonary disease using volumetric capnography in adult patients with cystic fibrosis
|
Paschoal, I.A. |
|
2007 |
6 |
S1 |
p. S38- 1 p. |
artikel |
235 |
175 Noninvasive ventilation (NIV) in cystic fibrosis patients (CF) with past pneumothorax (PNX): a case report
|
Casciaro, R. |
|
2007 |
6 |
S1 |
p. S43- 1 p. |
artikel |
236 |
214 Nutritional assessment of three groups of paediatric subjects with cystic fibrosis (CF), classified according to normal glucose tolerance (NGT), impaired glucose tolerance (IGT) and cystic fibrosis related diabetes (CFRD)
|
Caffrey, J.M. |
|
2007 |
6 |
S1 |
p. S53- 1 p. |
artikel |
237 |
225 Nutritional status and dietary intake in patients with cystic fibrosis
|
Spirevska, L. |
|
2007 |
6 |
S1 |
p. S55- 1 p. |
artikel |
238 |
291* Nutrition education program in cystic fibrosis children
|
Cazenave-Givelet, A. |
|
2007 |
6 |
S1 |
p. S71- 1 p. |
artikel |
239 |
220 Obesity in childhood cystic fibrosis
|
Stack, M. |
|
2007 |
6 |
S1 |
p. S54- 1 p. |
artikel |
240 |
73* Occurrence of P. aeruginosa (PA) with hypermutable phenotype (HPM) in Italian CF patients
|
Manno, G. |
|
2007 |
6 |
S1 |
p. S18- 1 p. |
artikel |
241 |
185 Oesophagitis, gastritis, duodenitis, hiatus hernia and Barrett's oesophagus in adults with cystic fibrosis
|
Button, B.M. |
|
2007 |
6 |
S1 |
p. S45- 1 p. |
artikel |
242 |
108 Only a subset of Pseudomonas aeruginosa strains is able to colonize CF patients
|
Vaneechoutte, M. |
|
2007 |
6 |
S1 |
p. S27- 1 p. |
artikel |
243 |
244 On which foods can pancreatic enzyme preparations (PEPs) be sprinkled?
|
Shepherd, D. |
|
2007 |
6 |
S1 |
p. S60- 1 p. |
artikel |
244 |
33* Optical imaging of calcium-evoked fluid secretion by murine airway submucosal gland serous acinar cells
|
Lee, R.J. |
|
2007 |
6 |
S1 |
p. S7- 1 p. |
artikel |
245 |
372* Outcome of the pregnancies with an echogenic bowel detected by ultrasonography: the 15 year-experience of Brittany (western France)
|
Scotet, V. |
|
2007 |
6 |
S1 |
p. S91- 1 p. |
artikel |
246 |
243 Overfilling in pancreatic enzyme preparations: still an unresolved issue
|
Foresti, R. |
|
2007 |
6 |
S1 |
p. S60- 1 p. |
artikel |
247 |
127* Oxidative stress activates ERK1/2 but no NF-κB signalling in CFTR-deficient bronchial epithelial cells
|
Boncoeur, E. |
|
2007 |
6 |
S1 |
p. S31- 1 p. |
artikel |
248 |
194 Pancreatitis in cystic fibrosis patients
|
Sojo, A. |
|
2007 |
6 |
S1 |
p. S47- 1 p. |
artikel |
249 |
295 Parents' perceptions and recommendations for follow-up of newborn screening
|
Semple, L.K. |
|
2007 |
6 |
S1 |
p. S72- 1 p. |
artikel |
250 |
336 Patient assessment of a new intravenous infusion device
|
Catling, T. |
|
2007 |
6 |
S1 |
p. S82- 1 p. |
artikel |
251 |
215 Patient satisfaction and staff perceptions of food provision on an adult CF unit following segregation
|
Watson, H. |
|
2007 |
6 |
S1 |
p. S53- 1 p. |
artikel |
252 |
286 Perceptions of young people with CF on the lack of knowledge and understanding of the condition within the general public
|
Hogan, J. |
|
2007 |
6 |
S1 |
p. S70- 1 p. |
artikel |
253 |
276 Perception versus objective assessment of diseases severity in cohort adult cystic fibrosis (CF) patients
|
Douglass, H. |
|
2007 |
6 |
S1 |
p. S68- 1 p. |
artikel |
254 |
75 Persistence of metallo-β–lactamase-producing Pseudomonas aeruginosa in cystic fibrosis patients
|
Campana, S. |
|
2007 |
6 |
S1 |
p. S18- 1 p. |
artikel |
255 |
50 Pharmacokinetic comparison of inhaled tobramycin (TOBI®) via PARI eFlow® rapid or PARI LC Plus™ nebulizers in cystic fibrosis patients
|
Hubert, D. |
|
2007 |
6 |
S1 |
p. S12- 1 p. |
artikel |
256 |
65 Pharmacokinetics of Azithromycin during once weekly dosing in cystic fibrosis patients
|
Wilms, E.B. |
|
2007 |
6 |
S1 |
p. S16- 1 p. |
artikel |
257 |
61* Photodynamic therapy against antibiotic resistant Pseudomonas aeruginosa isolates from CF patients
|
Torun, O.Y. |
|
2007 |
6 |
S1 |
p. S15- 1 p. |
artikel |
258 |
262 Physiological responses of cardiovascular and muscle endurance in cystic fibrosis patients
|
Arikan, H. |
|
2007 |
6 |
S1 |
p. S65- 1 p. |
artikel |
259 |
309 Piloting the use of the cystic fibrosis questionnaire (CFQ) in CF patients changing to dry powder inhaled colistimethate
|
Conway, S.P. |
|
2007 |
6 |
S1 |
p. S76- 1 p. |
artikel |
260 |
239 Pilot study for evaluation of essential fatty acids deficiency in Slovak CF patients
|
Sabolova, G. |
|
2007 |
6 |
S1 |
p. S59- 1 p. |
artikel |
261 |
217 Placement and replacement of gastrostomies under general anaesthetic in adults with cystic fibrosis (CF)
|
Chinuck, R.S. |
|
2007 |
6 |
S1 |
p. S53- 1 p. |
artikel |
262 |
85* Plant host and sugar alcohol induced exopolysaccharide biosynthesis in the Burkholderia cepacia complex
|
Bartholdson, J. |
|
2007 |
6 |
S1 |
p. S21- 1 p. |
artikel |
263 |
64 Population pharmacokinetics (PK) of tobramycin administered thrice daily (TD) and once daily (OD) in children and adults with CF
|
Touw, D.J. |
|
2007 |
6 |
S1 |
p. S16- 1 p. |
artikel |
264 |
161 PortaNeb® or CR60®? Inhalation of tobramycin (TOBI®) with the Pari LC Plus® nebuliser: an in vivo pilot study
|
Westerman, E.M. |
|
2007 |
6 |
S1 |
p. S39- 1 p. |
artikel |
265 |
62 Potential use of photodynamic antimicrobial therapy for treatment of Pseudomonas aeruginosa Cystic Fibrosis pulmonary infection
|
Donnelly, R.F. |
|
2007 |
6 |
S1 |
p. S15- 1 p. |
artikel |
266 |
45* Preclinical evidence that sildenafil corrects cystic fibrosis defects
|
Lubamba, B. |
|
2007 |
6 |
S1 |
p. S11- 1 p. |
artikel |
267 |
303 Predicting change in depression for parents of children with CF: health and demographic factors
|
Kinnamon, C. |
|
2007 |
6 |
S1 |
p. S74- 1 p. |
artikel |
268 |
173 Predictive factors of sleep hypoxemia in children with cystic fibrosis
|
Uyan, Z.S. |
|
2007 |
6 |
S1 |
p. S42- 1 p. |
artikel |
269 |
209 Pregnancy in lung transplant recipients in France
|
Hubert, D. |
|
2007 |
6 |
S1 |
p. S51- 1 p. |
artikel |
270 |
392* Preliminary results of motivation program for CF patients “LifeClubCF”
|
Krzyzanowski, M. |
|
2007 |
6 |
S1 |
p. S96- 1 p. |
artikel |
271 |
186 Presence of weakly acidic reflux and gastric aspiration in adult patients with CF
|
Blondeau, K. |
|
2007 |
6 |
S1 |
p. S45- 1 p. |
artikel |
272 |
150 Prevalence of nontuberculous mycobacteria in a Czech Cystic Fibrosis centre
|
Holcikova, A. |
|
2007 |
6 |
S1 |
p. S36- 1 p. |
artikel |
273 |
122 Pro-inflammatory cytokines in serum, sputum and lavage fluid (BALF) in cystic fibrosis lungs
|
Bulgakova, T.V. |
|
2007 |
6 |
S1 |
p. S30- 1 p. |
artikel |
274 |
32* Pro-inflammatory effects of sodium 4-phenylbutyrate in CF lung epithelial cells containing F508del-CFTR
|
Roque, T. |
|
2007 |
6 |
S1 |
p. S7- 1 p. |
artikel |
275 |
164 Pseudomonas aeruginosa in children with cystic fibrosis
|
Laurans, M. |
|
2007 |
6 |
S1 |
p. S40- 1 p. |
artikel |
276 |
148 Pseudomonas aeruginosa infection: utility of microbiological, PCR-based and serological techniques
|
Brazova, J. |
|
2007 |
6 |
S1 |
p. S36- 1 p. |
artikel |
277 |
114 Pseudomonas aeruginosa transmission at a winter camp in spite of rigorous precautions
|
Meyer, P. |
|
2007 |
6 |
S1 |
p. S28- 1 p. |
artikel |
278 |
340 Psychopathological overview of adolescents with cystic fibrosis (CF)
|
Kirszenbaum, M. |
|
2007 |
6 |
S1 |
p. S83- 1 p. |
artikel |
279 |
328* Psychosocial case study: infant diagnosed with CF through newborn screening
|
Tluczek, A. |
|
2007 |
6 |
S1 |
p. S80- 1 p. |
artikel |
280 |
41* PTC124 activity in CF patients carrying stop mutations: results of a phase 2 study
|
Kerem, E. |
|
2007 |
6 |
S1 |
p. S10- 1 p. |
artikel |
281 |
360 Pulmonary and nutritional outcomes in children with cystic fibrosis (CF) detected through neonatal screening and by symptoms in Argentina
|
D'Alessandro, V. |
|
2007 |
6 |
S1 |
p. S88- 1 p. |
artikel |
282 |
361 Pulmonary function in infants with cystic fibrosis (CF) detected through neonatal screening and by symptoms in Argentina
|
D'Alessandro, V. |
|
2007 |
6 |
S1 |
p. S88- 1 p. |
artikel |
283 |
174 Pulmonary mechanics in cystic fibrosis (CF) patients awaiting lung transplantation. Evaluation of non invasive mechanical ventilation (NIV)
|
Tardivo, I. |
|
2007 |
6 |
S1 |
p. S42- 1 p. |
artikel |
284 |
255* Pulmonary rehabilitation following lung transplantation
|
Munro, P. |
|
2007 |
6 |
S1 |
p. S63- 1 p. |
artikel |
285 |
302 Quality of life and anxious and depressive symptoms in mothers of children with CF
|
Driscoll, K.A. |
|
2007 |
6 |
S1 |
p. S74- 1 p. |
artikel |
286 |
275 Questionnaire survey of stress urinary incontinence (UI) in 9–16 year olds with cystic fibrosis, compared to other chronic respiratory conditions and a normal group
|
Browne, W.J. |
|
2007 |
6 |
S1 |
p. S68- 1 p. |
artikel |
287 |
47 Reactive airway disease and cystic fibrosis: a retrospective analysis of the safety and tolerability with denufosol inhalation solution
|
Rossi, A. |
|
2007 |
6 |
S1 |
p. S11- 1 p. |
artikel |
288 |
38 Reduction of activity of Arylsulfatasi B in patient with Cystic Fibrosis
|
Pagliardini, S. |
|
2007 |
6 |
S1 |
p. S9- 1 p. |
artikel |
289 |
326 Referrals to a new adult CF psychology service
|
Lamb, D. |
|
2007 |
6 |
S1 |
p. S79- 1 p. |
artikel |
290 |
238 Relation between fatty acid (FA) composition and clinical status/genotype in CF?
|
Van Biervliet, S. |
|
2007 |
6 |
S1 |
p. S59- 1 p. |
artikel |
291 |
152 Relationship between HRCT score, lung function and clubbing in patients with cystic fibrosis (CF)
|
Clifton, I. |
|
2007 |
6 |
S1 |
p. S37- 1 p. |
artikel |
292 |
265 Relationship between nutritional status and muscle strength in patients with cystic fibrosis (CF)
|
Bosnak-Guclu, M. |
|
2007 |
6 |
S1 |
p. S65- 1 p. |
artikel |
293 |
257 Relationship between upper limb muscle strength and functional capacity in patients with cystic fibrosis (CF)
|
Ozturk, M. |
|
2007 |
6 |
S1 |
p. S63- 1 p. |
artikel |
294 |
398 Renal function in relation to age in cystic fibrosis
|
Giourtzis, S. |
|
2007 |
6 |
S1 |
p. S97- 1 p. |
artikel |
295 |
72 Repeated Eradications of Pseudomonas aeruginosa in Cystic Fibrosis Patients
|
Taccetti, G. |
|
2007 |
6 |
S1 |
p. S18- 1 p. |
artikel |
296 |
31 Rescue of deltaF508 CFTR in CFBE41o- cells is dependent on actin cytoskeleton interaction with ezrin and NHERF1
|
Guerra, L. |
|
2007 |
6 |
S1 |
p. S7- 1 p. |
artikel |
297 |
391 Residential deprivation has no adverse effects on clinical parameters in adult CF patients
|
Youzguin, A. |
|
2007 |
6 |
S1 |
p. S95- 1 p. |
artikel |
298 |
373* Respiratory exacerbations in childhood associated with compound heterozygote CFTR genotype ΔF508/R117H on a background of 7T polythymidine tract at intron 8
|
Lee, T.W. |
|
2007 |
6 |
S1 |
p. S91- 1 p. |
artikel |
299 |
226 Resting energy expenditure and nutritional status pre and post lung transplantation
|
Kalnins, D. |
|
2007 |
6 |
S1 |
p. S56- 1 p. |
artikel |
300 |
18* Restoration of the CFTR function by splicing modulation
|
Nissim-Rafinia, M. |
|
2007 |
6 |
S1 |
p. S5- 1 p. |
artikel |
301 |
274* RhDNase before or after going to sleep in children with cystic fibrosis?
|
van der Giessen, L.J. |
|
2007 |
6 |
S1 |
p. S68- 1 p. |
artikel |
302 |
169 Risk factors for bronchiolitis obliterans syndrome (BOS) after double lung transplantation for cystic fibrosis (CF): 10-year experience
|
Quattrucci, S. |
|
2007 |
6 |
S1 |
p. S41- 1 p. |
artikel |
303 |
66 Safety of oral choramphenicol for pseudomonas aeruginosa infections in cystic fibrosis
|
Orchard, C.D. |
|
2007 |
6 |
S1 |
p. S16- 1 p. |
artikel |
304 |
272 Satisfaction survey concerning vibrating mesh-nebulizer in CF patients
|
Reychler, G. |
|
2007 |
6 |
S1 |
p. S67- 1 p. |
artikel |
305 |
116 Scedosporium apiospermum. Environmental study in the homes of patients with cystic fibrosis
|
Sidot, C. |
|
2007 |
6 |
S1 |
p. S29- 1 p. |
artikel |
306 |
335 Segregation of children with cystic fibrosis: difference in psychosocial impact between young children and adolescents
|
Keizer, F. |
|
2007 |
6 |
S1 |
p. S82- 1 p. |
artikel |
307 |
99 Sensitivity of recA PCR for direct detection of Burkholderia cepacia complex (BCC) from sputum of CF patients
|
Ergunay, K. |
|
2007 |
6 |
S1 |
p. S24- 1 p. |
artikel |
308 |
394 Seroconversion after Hepatitis B (HB) and Hepatitis A (HA) vaccination in CF patients (pts)
|
De Schutter, I. |
|
2007 |
6 |
S1 |
p. S96- 1 p. |
artikel |
309 |
235 Serum vitamin E and IL-6 are influenced by type of physical training in patients with CF
|
Sahlberg, M. |
|
2007 |
6 |
S1 |
p. S58- 1 p. |
artikel |
310 |
236 Serum zinc concentrations of the CF population above the age of 4 years: a cross-sectional evaluation
|
Van Biervliet, S. |
|
2007 |
6 |
S1 |
p. S58- 1 p. |
artikel |
311 |
390 Socio-economic deprivation in the North West of England predicts work status in adult cystic fibrosis patients
|
Youzguin, A. |
|
2007 |
6 |
S1 |
p. S95- 1 p. |
artikel |
312 |
3* Spectrum of CFTR mutations in a group of black patients from South Africa: Identification of a novel large rearrangement
|
des Georges, M. |
|
2007 |
6 |
S1 |
p. S1- 1 p. |
artikel |
313 |
126 Sphingomyelinase and ceramidase activities in tissues of delta-F508 CFTR mice
|
Olsson, L. |
|
2007 |
6 |
S1 |
p. S31- 1 p. |
artikel |
314 |
234 Status of fat soluble vitamins in Scandinavian CF patients
|
Nilsson, K. |
|
2007 |
6 |
S1 |
p. S58- 1 p. |
artikel |
315 |
87 Strict anaerobes persist in CF sputum despite antibiotic treatment
|
Worlitzsch, D. |
|
2007 |
6 |
S1 |
p. S21- 1 p. |
artikel |
316 |
28* Study of the unfolded protein response (UPR) in cystic fibrosis (CF)
|
Kerbiriou, M. |
|
2007 |
6 |
S1 |
p. S6- 1 p. |
artikel |
317 |
128 Supplementation with n-3 PUFA in CF patients: analysis of exhaled breath condensate
|
Fila, L. |
|
2007 |
6 |
S1 |
p. S32- 1 p. |
artikel |
318 |
269 Survey of the contamination of home nebulizers of cystic fibrosis patients and assessment of the implementation of a standardised recommendation
|
Reychler, G. |
|
2007 |
6 |
S1 |
p. S66- 1 p. |
artikel |
319 |
357 Survey of the information provided for parents about newborn screening for CF in European programmes
|
Munck, A. |
|
2007 |
6 |
S1 |
p. S87- 1 p. |
artikel |
320 |
345* Survival factors in cystic fibrosis: a case-control study
|
Simmonds, N.J. |
|
2007 |
6 |
S1 |
p. S84- 1 p. |
artikel |
321 |
101* Survival of Cepacia Syndrome
|
Kassim, I. |
|
2007 |
6 |
S1 |
p. S25- 1 p. |
artikel |
322 |
376 Sweat test results on a suspected cystic fibrosis population with CF mutation analysis and the frequency of borderline results
|
Tanyalcin, T. |
|
2007 |
6 |
S1 |
p. S92- 1 p. |
artikel |
323 |
330 Telephone calls received by CF nurse specialists – best use of a scarce resource?
|
Miller, H. |
|
2007 |
6 |
S1 |
p. S80- 1 p. |
artikel |
324 |
299* Ten years' of experience in patient education of families with a child/adolescent suffering from cystic fibrosis
|
Bregnballe, V. |
|
2007 |
6 |
S1 |
p. S73- 1 p. |
artikel |
325 |
327 The adult cystic fibrosis patient: education, sports and work
|
de Vrankrijker, A. |
|
2007 |
6 |
S1 |
p. S80- 1 p. |
artikel |
326 |
76* The bacterial burden of the CF lung – Uncovering the black box
|
Bjarnsholt, T. |
|
2007 |
6 |
S1 |
p. S19- 1 p. |
artikel |
327 |
348* The Belgian CF registry (BMR-RBM)
|
Sevens, C. |
|
2007 |
6 |
S1 |
p. S84- 1 p. |
artikel |
328 |
216 The benefits to patients with cystic fibrosis of a dedicated dietician
|
Kelly, V. |
|
2007 |
6 |
S1 |
p. S53- 1 p. |
artikel |
329 |
293 The CF family/teen teaching day – do the benefits outweigh the risks?
|
Taylor, L. |
|
2007 |
6 |
S1 |
p. S72- 1 p. |
artikel |
330 |
112* The change in Pseudomonas status of CF patients in Merseyside, UK – how are we doing?
|
Miller, H. |
|
2007 |
6 |
S1 |
p. S28- 1 p. |
artikel |
331 |
136 The degree of change in FEV1 and FVC after 2 weeks of intravenous antibiotics for severe pulmonary exacerbation in adult patients with cystic fibrosis
|
Jarad, N.A. |
|
2007 |
6 |
S1 |
p. S33- 1 p. |
artikel |
332 |
259* The effect of maximal exercise on FEV1 in adult cystic fibrosis (CF)
|
Turner, S.M. |
|
2007 |
6 |
S1 |
p. S64- 1 p. |
artikel |
333 |
201 The effect of vitamin D and calcium supplementation in children and adolescents with cystic fibrosis and low bone mineral density
|
Hatziagorou, E. |
|
2007 |
6 |
S1 |
p. S49- 1 p. |
artikel |
334 |
277 The effects of musculoskeletal physiotherapy and massage on pain and ease of breathing in adults with cystic fibrosis
|
Lee, A.L. |
|
2007 |
6 |
S1 |
p. S68- 1 p. |
artikel |
335 |
242 The impact of a referral pathway on management of CFRD
|
Rezaie, M. |
|
2007 |
6 |
S1 |
p. S60- 1 p. |
artikel |
336 |
166 The impact of gender, pulmonary disease severity and presence of diabetes on azithromycin (AZ) benefit in cystic fibrosis (CF)
|
Butler, M. |
|
2007 |
6 |
S1 |
p. S40- 1 p. |
artikel |
337 |
191 The impact of meconium ileus on the liver course of children with cystic fibrosis
|
Cuny, C. |
|
2007 |
6 |
S1 |
p. S46- 1 p. |
artikel |
338 |
339 The role of acceptance in adolescents with cystic fibrosis
|
Casier, A. |
|
2007 |
6 |
S1 |
p. S83- 1 p. |
artikel |
339 |
318 The role of parental supervision on medical adherence in adolescents with Cystic Fibrosis
|
Modi, A.C. |
|
2007 |
6 |
S1 |
p. S77- 1 p. |
artikel |
340 |
144 The significance of complete pulmonary function test data in the respiratory exacerbation of cystic fibrosis
|
Shoseyov, D. |
|
2007 |
6 |
S1 |
p. S35- 1 p. |
artikel |
341 |
195 The Stewart Ultrasound Score (SUSS): a new tool for quantitative assessment of CFLD
|
Stewart, L. |
|
2007 |
6 |
S1 |
p. S47- 1 p. |
artikel |
342 |
338 The theory and practice of childhood attachment and family systems for disease outcomes and service utilisation in adult cystic fibrosis patients. Research findings from a mixed methodological study
|
Sutherland, S.M. |
|
2007 |
6 |
S1 |
p. S82- 1 p. |
artikel |
343 |
228 The value of a non-invasive method to assess fat free mass in adult CF patients – correlation with outcome measures in a cohort of adult CF patients
|
Al Siaidi, J. |
|
2007 |
6 |
S1 |
p. S56- 1 p. |
artikel |
344 |
261 The value of exercise training in severely ill adult CF patients
|
Morris, A. |
|
2007 |
6 |
S1 |
p. S64- 1 p. |
artikel |
345 |
203 Three day continuous subcutaneous glucose monitoring (CSGM) in the clinical management of adult patients with CF and diabetes (CFRD)
|
Watson, H. |
|
2007 |
6 |
S1 |
p. S49- 1 p. |
artikel |
346 |
1 Three novel CFTR mutations found in Turkish patients with cystic fibrosis
|
Ulgenalp, A. |
|
2007 |
6 |
S1 |
p. S1- 1 p. |
artikel |
347 |
222* Too short but not too light – analysis of height and weight in a Belgian CF population
|
Vermeulen, F. |
|
2007 |
6 |
S1 |
p. S55- 1 p. |
artikel |
348 |
358* Towards a consensus on the investigation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis
|
Mayell, S.J. |
|
2007 |
6 |
S1 |
p. S87- 1 p. |
artikel |
349 |
34* Tracheal structure abnormalities in Cftr-/- knockout mice
|
Bonvin, E. |
|
2007 |
6 |
S1 |
p. S8- 1 p. |
artikel |
350 |
27* Transcription factors: new therapeutic targets in cystic fibrosis lung disease?
|
Rene, C. |
|
2007 |
6 |
S1 |
p. S6- 1 p. |
artikel |
351 |
181 Transition program for cystic fibrosis adult patients
|
Lopes, C. |
|
2007 |
6 |
S1 |
p. S44- 1 p. |
artikel |
352 |
323 Transplantation and changes in importance of social support
|
Matossian, A. |
|
2007 |
6 |
S1 |
p. S79- 1 p. |
artikel |
353 |
55* Treatment of CF sinonasal disease using a combination of surgical procedure and coblation, a new therapeutic approach
|
Faict, H. |
|
2007 |
6 |
S1 |
p. S13- 1 p. |
artikel |
354 |
176 Treatment of recurrent pneumothorax in adult cystic fibrosis patients
|
Cowperthwaite, C. |
|
2007 |
6 |
S1 |
p. S43- 1 p. |
artikel |
355 |
14 Tumor necrosis factor gene polymorphisms in cystic fibrosis patients
|
Shmarina, G.V. |
|
2007 |
6 |
S1 |
p. S4- 1 p. |
artikel |
356 |
314 Turkish translation and validation of revised Cystic Fibrosis Questionnaire (CFQ-R) for children
|
Yuksel, H. |
|
2007 |
6 |
S1 |
p. S77- 1 p. |
artikel |
357 |
349* Twenty years of care for CF adults in Czech Republic
|
Fila, L. |
|
2007 |
6 |
S1 |
p. S85- 1 p. |
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358 |
334 Use of central venous catheters in people with cystic fibrosis in Italy
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Ballarin, S. |
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192 Use of fecal elastase-1 to classify pancreatic status in patients with cystic fibrosis and mutations analisis
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Ducasse, K. |
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383 Use of non-prescribed drugs in adult CF patients
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151* Use of the Northern X-Ray scoring system over time in adult CF patients
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Burhan, H. |
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63 Use of tigecycline to treat difficult respiratory pathogens in cystic fibrosis – early experiences
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92* Using insertion sequences to determine gene function in epidemic Pseudomonas aeruginosa
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42* Validating assays on invasive airway samples as end-points for gene therapy trials.
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311 Validity and responsiveness of CF-38 health status measure
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227 Validity of the Tanita TBF-300M body composition analyser in children with cystic fibrosis
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320 Variance between perception score and objective score in adult CF patients – What are the reasons for the difference?
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91 Variations in phenotype and virulence amongst isolates of a cystic fibrosis epidemic strain of Pseudomonas aeruginosa
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387 Vestibulotoxicity as a consequence of systemically administered tobramycin in Cystic Fibrosis patients
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54 Visualization of human sinus ventilation by radioactive Krypton using the PARI Sinus pulsating system
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405 Water mobility by 3D-MR imaging in normal and CFTR KO mouse trachea
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294* West Midlands cystic fibrosis (CF) newborn screening training evaluation
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321 What do professionals think about adherence in CF?
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