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                             69 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 360 A case series of thrombotic and thromboembolic complications of central venous access in cystic fibrosis patients Kandamany, N.
 2012
 11 Supplement 1 p. S149-
1 p.
 artikel
2 322 Advances in transition: multi-level factors associated with adult achievement Barto, T.L.
 2012
 11 Supplement 1 p. S139-
1 p.
 artikel
3 A fat lot of good: Balance and trends in fat intake in children with cystic fibrosis Smith, C.
 2012
 11 Supplement 1 p. 154-157
4 p.
 artikel
4 A novel neutrophil derived inflammatory biomarker of pulmonary exacerbation in cystic fibrosis Reeves, Emer P.
 2012
 11 Supplement 1 p. 100-107
8 p.
 artikel
5 6 A novel StripAssay for the detection of cystic fibrosis mutations in the Turkish population Puehringer, H.
 2012
 11 Supplement 1 p. S56-
1 p.
 artikel
6 242 Are we missing salt depletion in cystic fibrosis? Sharp, S.
 2012
 11 Supplement 1 p. S118-
1 p.
 artikel
7 Australian epidemic strain pseudomonas (AES-1) declines further in a cohort segregated cystic fibrosis clinic Griffiths, Amanda L.
 2012
 11 Supplement 1 p. 49-52
4 p.
 artikel
8 47 Bronchitol (inhaled dry powder mannitol) in adult patients with cystic fibrosis Aitken, M.
 2012
 11 Supplement 1 p. S68-
1 p.
 artikel
9 274 CF experience for respiratory trainees in the UK Nazareth, D.
 2012
 11 Supplement 1 p. S127-
1 p.
 artikel
10 288 CF patients with totally implantable venous access devices (TIVAD): prospective survey of Doppler-US (DUS) central venous thrombosis (CVT) and thrombophilia (TB) assessment Munck, A.
 2012
 11 Supplement 1 p. S130-
1 p.
 artikel
11 166 CF sputum rheology and the role of the airway mucin MUC5AC Horsley, A.
 2012
 11 Supplement 1 p. S99-
1 p.
 artikel
12 Clinical evidence that V456A is a Cystic Fibrosis causing mutation in South Asians Uppaluri, L.
 2012
 11 Supplement 1 p. 312-315
4 p.
 artikel
13 305 Comparison of contacts to adult and paediatric cystic fibrosis Clinical Nurse Specialists Butler, M.
 2012
 11 Supplement 1 p. S135-
1 p.
 artikel
14 214 Core competencies for physiotherapists working with cystic fibrosis patients in Italy Tartali, C.
 2012
 11 Supplement 1 p. S111-
1 p.
 artikel
15 20 Cystic fibrosis newborn screening in Italy: survey for assessment of technical-scientific and organizational issues Repetto, T.
 2012
 11 Supplement 1 p. S60-
1 p.
 artikel
16 Cystic fibrosis research in allied health and nursing professions Bradley, Judy M.
 2012
 11 Supplement 1 p. 387-392
6 p.
 artikel
17 Diabetes mellitus and survival in cystic fibrosis patients after lung transplantation Hofer, Markus
 2012
 11 Supplement 1 p. 131-136
6 p.
 artikel
18 319 Do symptoms of depression determine the course of lung function in patients with cystic fibrosis? Fidika, A.
 2012
 11 Supplement 1 p. S138-
1 p.
 artikel
19 111 Epidemiology and species distribution of Burkholderia cepacia complex in Ireland. A 10 year review Collins, J.
 2012
 11 Supplement 1 p. S84-
1 p.
 artikel
20 239 Establishment of an F508del pseudoislet model for the study of CF-related diabetes McClenaghan, N.H.
 2012
 11 Supplement 1 p. S117-
1 p.
 artikel
21 152 Estrogen-regulated MicroRNAs control the expression of secretory leukoprotease inhibitor in monocytes McKiernan, P.
 2012
 11 Supplement 1 p. S95-
1 p.
 artikel
22 197 Evaluation of aerobic exercise capacity and daily functioning of patients with cystic fibrosis Eisenstadt, I.
 2012
 11 Supplement 1 p. S107-
1 p.
 artikel
23 270 Factors associated with vitamin K deficiency in adults with cystic fibrosis Ochota, A.
 2012
 11 Supplement 1 p. S125-
1 p.
 artikel
24 108 First identification of non-lactose fermenting Gram negative respiratory isolates from an Irish cystic fibrosis population using matrix-assisted laser desorption ionisation-time of flight mass spectrometry (MALDI-TOF MS) Prior, A.-R.
 2012
 11 Supplement 1 p. S84-
1 p.
 artikel
25 149 Gibberellin induces the NF-úB inhibitor A20 in airway epithelial cells Schock, B.C.
 2012
 11 Supplement 1 p. S94-
1 p.
 artikel
26 33 Hypoxia reduces internalization of Pseudomonas aeruginosa in pulmonary epithelial cells Schaible, B.
 2012
 11 Supplement 1 p. S64-
1 p.
 artikel
27 IL-17A as a regulator of neutrophil survival in nasal polyp disease of patients with and without cystic fibrosis Derycke, L.
 2012
 11 Supplement 1 p. 193-200
8 p.
 artikel
28 Immunomodulatory activity of vardenafil on induced lung inflammation in cystic fibrosis mice Lubamba, Bob
 2012
 11 Supplement 1 p. 266-273
8 p.
 artikel
29 183 Impact of progression of cystic fibrosis lung disease on quality of life Tepper, L.A.
 2012
 11 Supplement 1 p. S103-
1 p.
 artikel
30 80 Investigation of the potential mechanisms of antibiotic resistance in the cystic fibrosis pathogen, Burkholderia cepacia complex Kennedy, S.
 2012
 11 Supplement 1 p. S77-
1 p.
 artikel
31 135 Is the lung of cystic fibrosis patients a reservoir of extended-spectrum beta-lactamase-producing Enterobacteriaceae? Fiscarelli, E.
 2012
 11 Supplement 1 p. S90-
1 p.
 artikel
32 200 Long inhalation time is associated with short treatment time when using the I-neb AAD System in target inhalation mode Spencer, T.
 2012
 11 Supplement 1 p. S107-
1 p.
 artikel
33 Multiple antibiotic-resistant Pseudomonas aeruginosa and lung function decline in patients with cystic fibrosis Ren, Clement L.
 2012
 11 Supplement 1 p. 293-299
7 p.
 artikel
34 58 No antibiotic cross-resistance after 1 year of continuous aztreonam for inhalation solution (AZLI) in cystic fibrosis (CF) patients (pts) with chronic Burkholderia (BURK) infection Burns, J.
 2012
 11 Supplement 1 p. S71-
1 p.
 artikel
35 PCR detection of Burkholderia cepacia complex as one of key factors to handle a long-term outbreak Dedeckova, Klara
 2012
 11 Supplement 1 p. 440-445
6 p.
 artikel
36 125 Presence of Pandoraea and Herbaspirillum species within the Irish CF population Collins, J.
 2012
 11 Supplement 1 p. S88-
1 p.
 artikel
37 229 Prucalopride: a review of the first 12 months of use Williams, K.
 2012
 11 Supplement 1 p. S115-
1 p.
 artikel
38 Qualitative analysis of parent experiences with achieving cystic fibrosis nutrition recommendations Filigno, Stephanie S.
 2012
 11 Supplement 1 p. 125-130
6 p.
 artikel
39 Reduced levels of active GLP-1 in patients with cystic fibrosis with and without diabetes mellitus Hillman, Magnus
 2012
 11 Supplement 1 p. 144-149
6 p.
 artikel
40 77 Risk factor of multi-drug resistant Pseudomonas aeruginosa (MDR-PA) emergence in cystic fibrosis patients Patout, M.
 2012
 11 Supplement 1 p. S76-
1 p.
 artikel
41 Sinonasal persistence of Pseudomonas aeruginosa after lung transplantation Mainz, J.G.
 2012
 11 Supplement 1 p. 158-161
4 p.
 artikel
42 Smoking prevention and cessation programme in cystic fibrosis: Integrating an environmental health approach Ortega-García, Juan Antonio
 2012
 11 Supplement 1 p. 34-39
6 p.
 artikel
43 94 Statins, a widely used cholesterol-lowering drug, modulate key virulence behaviour of Pseudomonas aeruginosa Hennessy, E.
 2012
 11 Supplement 1 p. S80-
1 p.
 artikel
44 23 Sweat testing in a tertiary clinic – reasons, results and methodology Mense, L.
 2012
 11 Supplement 1 p. S61-
1 p.
 artikel
45 332 The prevalence of eating disordered attitudes and behaviour in the cystic fibrosis lung transplant population Mohan, K.
 2012
 11 Supplement 1 p. S141-
1 p.
 artikel
46 346 The prevalence of F508del and its relation to clinical manifestation in CF patients from Albania Vevecka, E.
 2012
 11 Supplement 1 p. S145-
1 p.
 artikel
47 1 The role of CFTR genetic testing in diagnosis of cystic fibrosis Fustik, S.
 2012
 11 Supplement 1 p. S55-
1 p.
 artikel
48 256 The use of high energy milk formula for alimentary status correction in children with cystic fibrosis (CF) Roslavtseva, E.
 2012
 11 Supplement 1 p. S122-
1 p.
 artikel
49 63 Time to recurrence and antimicrobial susceptibility of first-time detected Achromobacter xylosoxidans in respiratory tract specimens from patients with cystic fibrosis Wang, M.
 2012
 11 Supplement 1 p. S72-
1 p.
 artikel
50 Towards an individualized protocol for workload increments in cardiopulmonary exercise testing in children and adolescents with cystic fibrosis Hulzebos, H.J.
 2012
 11 Supplement 1 p. 550-554
5 p.
 artikel
51 WS16.5 Airway clearance therapy and exercise in cystic fibrosis: patients’ perceptions versus participation Kennedy, F.
 2012
 11 Supplement 1 p. S36-
1 p.
 artikel
52 WS5.5 A randomised, open label phase 3 study to evaluate the efficacy and safety of a dry powder formulation of inhaled colistimethate sodium (Colobreathe®) versus tobramycin nebuliser solution (TNS) in cystic fibrosis subjects with chronic Pseudomonas aeruginosa lung infection Goldman, M.
 2012
 11 Supplement 1 p. S12-
1 p.
 artikel
53 WS9.5 CF epithelial cells are a source of pulmonary cathepsin S via increased IRF-1 Weldon, S.
 2012
 11 Supplement 1 p. S20-
1 p.
 artikel
54 WS8.6 Decision algorithm and scoring method for the classification of variants of unknown clinical significance in the CFTR gene Raynal, C.
 2012
 11 Supplement 1 p. S17-
1 p.
 artikel
55 WS11.6 Environmental Burkholderia cenocepacia strains can disrupt epithelial integrity in bronchial epithelial cells in vitro and have a more profound effect on ZO-1 in CF cells Bevivino, A.
 2012
 11 Supplement 1 p. S25-
1 p.
 artikel
56 WS10.1 Evaluation of musculoskeletal and postural function in cystic fibrosis using a physiotherapy screening tool Button, B.M.
 2012
 11 Supplement 1 p. S22-
1 p.
 artikel
57 WS23.4 High Rhinovirus burden in lower airways of children with cystic fibrosis Kieninger, E.
 2012
 11 Supplement 1 p. S51-
1 p.
 artikel
58 WS17.8 Inhibition of leukotriene B4 signaling by alpha-1 antitrypsin: support for the use of aerosolized alpha-1 antitrypsin therapy in cystic fibrosis O'Dwyer, C.A.
 2012
 11 Supplement 1 p. S39-
1 p.
 artikel
59 WS2.1 Investigation of MiRNA regulation of ER stress in cystic fibrosis airway epithelium Oglesby, I.K.
 2012
 11 Supplement 1 p. S3-
1 p.
 artikel
60 WS10.4 Length of hospital stay and changed weekend physiotherapy cystic fibrosis service Moran, F.C.
 2012
 11 Supplement 1 p. S22-
1 p.
 artikel
61 WS6.3 Measures of nutritional status in two Phase 3 trials of ivacaftor in subjects with cystic fibrosis who have the G551D-CFTR mutation Borowitz, D.
 2012
 11 Supplement 1 p. S13-
1 p.
 artikel
62 WS17.1 Modulation of inflammatory mediators associated with cystic fibrosis by alpha-1 antitrypsin Bergin, D.A.
 2012
 11 Supplement 1 p. S38-
1 p.
 artikel
63 WS12.2 Outcomes of patients with cystic fibrosis admitted to an intensive care unit Markewitz, B.
 2012
 11 Supplement 1 p. S27-
1 p.
 artikel
64 WS18.2 Persistent elevation of antibodies against Pseudomonas aeruginosa following successful eradication? Kappler, M.
 2012
 11 Supplement 1 p. S41-
1 p.
 artikel
65 WS23.1 Progression of lung disease within specific genotypes of patients with cystic fibrosis (CF) – Which lung function parameter differentiates best? Gallati, S.
 2012
 11 Supplement 1 p. S51-
1 p.
 artikel
66 WS20.4 Real-time PCR (RT-PCR) provides a “window of opportunity”: optimal screening of patients with cystic fibrosis (CF) through an earlier detection of Pseudomonas aeruginosa (PA) Hérv-Arnaud, G.
 2012
 11 Supplement 1 p. S45-
1 p.
 artikel
67 WS17.9 The B lymphocyte differentiation factor, BAFF, is expressed in the lung of cystic fibrosis patients and in a mouse model of Pseudomonas aeruginosa infection Saint, G.
 2012
 11 Supplement 1 p. S40-
1 p.
 artikel
68 WS3.6 The CF-ABLE score: a novel clinical prediction tool in cystic fibrosis McCarthy, C.
 2012
 11 Supplement 1 p. S7-
1 p.
 artikel
69 WS1.6 The need of an appropriate diagnosis of gastroesophageal reflux disease in cystic fibrosis patients: impact on clinical management Alghisi, F.
 2012
 11 Supplement 1 p. S2-
1 p.
 artikel
                             69 gevonden resultaten
 
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