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                             49 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Blood Pressure Ortiz, Alberto
2012
34 4S p. e12-e13
nvt p.
artikel
2 Children With Fabry Disease Ramaswami, Uma
2012
34 4S p. e18-
1 p.
artikel
3 Endocrinology Feldt-Rasmussen, Ulla
2012
34 4S p. e14-
1 p.
artikel
4 Fabry International Network De Bare, Lut
2012
34 4S p. e15-
1 p.
artikel
5 Foreword Germain, Dominique P.
2012
34 4S p. e1-
1 p.
artikel
6 How to Assess Kidney Function: Overview Froissart, Marc
2012
34 4S p. e4-e5
nvt p.
artikel
7 How to Stage and Assess the Deterioration of Kidney Function in Children? Svarstad, Einar
2012
34 4S p. e5-e7
nvt p.
artikel
8 Keynote Lecture: Fabry Disease Germain, Dominique P.
2012
34 4S p. e3-
1 p.
artikel
9 Kidney Histology Fogo, Agnes B.
2012
34 4S p. e11-
1 p.
artikel
10 Lysosomal Biology Heales, Simon
2012
34 4S p. e10-e11
nvt p.
artikel
11 Managing Cardiac Complications: Drugs and Devices Weidemann, Frank
2012
34 4S p. e15-
1 p.
artikel
12 Managing Patients With Chronic Kidney Disease Warnock, David G.
2012
34 4S p. e16-e17
nvt p.
artikel
13 Meeting the Current Clinical Management Challenges Waldek, Stephen
2012
34 4S p. e3-e4
nvt p.
artikel
14 Neuropathic Pain Sommer, Claudia
2012
34 4S p. e17-e18
nvt p.
artikel
15 New Techniques for Assessing the Heart (Cardiac Imaging) Schmitt, Matthias
2012
34 4S p. e7-e8
nvt p.
artikel
16 Overlooked Signs and Symptoms: Lung Linhart, Aleš
2012
34 4S p. e11-e12
nvt p.
artikel
17 P13—A Case of Fabry Disease With Unexplained Abdominal Pain Küçükçongar, A.
2012
34 4S p. e23-e24
nvt p.
artikel
18 P18—Agalsidase Alfa and Agalsidase Beta have Similar Effects on Outcomes in Fabry Disease: Results From the Canadian Fabry Disease Initiative West, M.
2012
34 4S p. e25-
1 p.
artikel
19 P20—Agalsidase Beta Treatment is Associated With Improvement in Quality of Life in Patients With Fabry Disease: Findings From the Fabry Registry Feldt-Rasmussen, U.
2012
34 4S p. e26-
1 p.
artikel
20 P26—Anti-CD3 Antibody Reduces AntibodY Formation and Prevents Potentially Fatal Hypersensitivity Reaction in Enzyme-Replacement Therapy for Murine Lysosomal Storage Diseases Ohashi, T.
2012
34 4S p. e28-
1 p.
artikel
21 P15—Cardiovascular Manifestations of Fabry Disease in Mexico Pazarín-Villaseñor, L.
2012
34 4S p. e24-
1 p.
artikel
22 P10—Comprehensive Assessment of Long-Term Enzyme Replacement Therapy in Fabry Disease: The 5-Year Data Baumgärtner, E.K.
2012
34 4S p. e22-
1 p.
artikel
23 P09—Early Onset of Cardiomyopathy Demonstrated by Tissue Doppler Imaging in a Child With Fabry Disease Mignani, R.
2012
34 4S p. e22-
1 p.
artikel
24 P06—Enzyme Replacement Therapy with Agalsidase Beta for Fabry Disease: Importance of the Doses—A Case Report Smelten, N.
2012
34 4S p. e20-e21
nvt p.
artikel
25 Peripheral Blood Cytopenias and Spleen Pathology Oliveira, João Paulo
2012
34 4S p. e13-e14
nvt p.
artikel
26 P03—Excessive Daytime Sleepiness is a Common Symptom in Fabry Disease Duning, T.
2012
34 4S p. e19-
1 p.
artikel
27 P12—Fabry Disease in Latin America: A Report From the Fabry Registry Martins, A.M.
2012
34 4S p. e23-
1 p.
artikel
28 P21—Fabry Disease in Women: Findings From the Fabry Registry Linthorst, G.
2012
34 4S p. e26-
1 p.
artikel
29 P02—Fabry International Network: Fabry Patient Survey Sedal, R.
2012
34 4S p. e19-
1 p.
artikel
30 P17—Importance of Family Screening in Fabry Disease: Reaching the Bottom of the iceberg Koca, S.
2012
34 4S p. e24-e25
nvt p.
artikel
31 P19—Influence of Anti-Agalsidase Antibodies on Clinical Outcomes in the Canadian Fabry Disease Initiative Study West, M.
2012
34 4S p. e25-
1 p.
artikel
32 P25—Late Diagnosis of Fabry Disease with Cardiovascular Manifestations Godenèche, G.
2012
34 4S p. e27-e28
nvt p.
artikel
33 P28—Metabolomic Studies in Fabry Disease Auray-Blais, C.
2012
34 4S p. e28-
1 p.
artikel
34 P11—Natural History of Fabry Disease: Characterization of Symptom Onset in a Turkish Family Bahçebasşi, Z. Bicik
2012
34 4S p. e22-e23
nvt p.
artikel
35 P22—Nephropathy in Fabry Disease with Proteinuria, Minterpreted as Chronic Glomerulonephritis with Subsequent Inadequate Immunosuppressive Therapy Fomin, V.V.
2012
34 4S p. e26-
1 p.
artikel
36 P04—Neurophysiologic Examinations in Patients with Fabry-Anderson Disease Hajas, A.
2012
34 4S p. e19-e20
nvt p.
artikel
37 P23—New Guidelines for the Evaluation and Management of Fabry Disease in Children Tylki-Szymanska, A.
2012
34 4S p. e27-
1 p.
artikel
38 P16—Ophthalmologic Manifestations of Fabry Disease in Mexico Pazarín-Villaseñor, L.
2012
34 4S p. e24-
1 p.
artikel
39 P05—Peripheral Vasculature Involvement in Fabry Patients: Is There any Difference Between Genders? Cabrera, G.
2012
34 4S p. e20-
1 p.
artikel
40 P24—Prognostic Indicators of Renal Disease Progression: Natural History Data From the Fabry Registry Wanner, C.
2012
34 4S p. e27-
1 p.
artikel
41 P08—Quality of Life did not Worsen for 7 Years in Enzyme-Replacement Therapy Recipients with Fabry Disease Kantola, I.
2012
34 4S p. e21-e22
nvt p.
artikel
42 P01—The Fabry International Network De Baere, L.
2012
34 4S p. e19-
1 p.
artikel
43 P27—Uptake of α-Galactosidase a in Human Glomerular Podocytes is Mediated by Various Receptors in Fabry Disease Prabakaran, T.
2012
34 4S p. e28-
1 p.
artikel
44 P07—Ventricular Arrhythmias are the Major Cause of Death in Patients With the Classical Phenotype of Fabry Disease Niemann, M.
2012
34 4S p. e21-
1 p.
artikel
45 Review of Brain-Assessment Techniques Politei, Juan
2012
34 4S p. e9-
1 p.
artikel
46 Stroke: Prevention and Management Tyrrell, Pippa
2012
34 4S p. e17-
1 p.
artikel
47 The Vessels: Focusing on the Aorta Mousseaux, Elie
2012
34 4S p. e8-e9
nvt p.
artikel
48 Title Page 2012
34 4S p. A1-
1 p.
artikel
49 White Matter Lesions and Brain Vessels Fellgiebel, Andreas
2012
34 4S p. e9-e10
nvt p.
artikel
                             49 gevonden resultaten
 
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