nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Absence of mutations in the prion-protein gene in a large cohort of HMSN patients
|
Koop, Olga |
|
2005 |
15 |
8 |
p. 549-551 3 p. |
artikel |
2 |
A novel desmin R355P mutation causes cardiac and skeletal myopathy
|
Fidziańska, Anna |
|
2005 |
15 |
8 |
p. 525-531 7 p. |
artikel |
3 |
Clinical features and neurophysiological follow-up in a case of Brown-Vialetto-Van Laere syndrome
|
De Grandis, D. |
|
2005 |
15 |
8 |
p. 565-568 4 p. |
artikel |
4 |
Complete innervation of extensor digitorum brevis by accessory peroneal nerve
|
Ubogu, Eroboghene E. |
|
2005 |
15 |
8 |
p. 562-564 3 p. |
artikel |
5 |
Corrigendum to “Dystroglycan: important player in skeletal muscle and beyond” [Neuromuscular Disorders 15 (2005) 207–217]
|
Cohn, Ronald D. |
|
2005 |
15 |
8 |
p. 573- 1 p. |
artikel |
6 |
IFC: Editorial Board
|
|
|
2005 |
15 |
8 |
p. co2- 1 p. |
artikel |
7 |
Impaired primary hemostasis with normal platelet function in Duchenne muscular dystrophy during highly-invasive spinal surgery
|
Turturro, Francesco |
|
2005 |
15 |
8 |
p. 532-540 9 p. |
artikel |
8 |
Instructions to Authors
|
|
|
2005 |
15 |
8 |
p. 574-575 2 p. |
artikel |
9 |
Localization of coxsackie virus and adenovirus receptor (CAR) in normal and regenerating human muscle
|
Sinnreich, M. |
|
2005 |
15 |
8 |
p. 541-548 8 p. |
artikel |
10 |
Postnatal changes in sarcolemmal organization in the mdx mouse
|
Reed, Patrick |
|
2005 |
15 |
8 |
p. 552-561 10 p. |
artikel |
11 |
Report of the 4th annual scientific meeting of the Asian and Oceanian myology center, Kaohsiung, Taiwan 2005
|
|
|
2005 |
15 |
8 |
p. 572- 1 p. |
artikel |
12 |
Tracheoinnominate fistula in a Duchenne muscular dystrophy patient: Successful management with an endovascular stent
|
Vianello, Andrea |
|
2005 |
15 |
8 |
p. 569-571 3 p. |
artikel |
13 |
Two patients with ‘Dropped head syndrome’ due to mutations in LMNA or SEPN1 genes
|
D'Amico, A. |
|
2005 |
15 |
8 |
p. 521-524 4 p. |
artikel |