| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A new phenotype of autosomal dominant nemaline myopathy
|
Gommans, I.M.P.
|
|
2002
|
12 |
1 |
p. 13-18
6 p.
|
artikel
|
| 2 |
A novel nonsense mutation (Q352X) in the mitochondrial cytochrome b gene associated with a combined deficiency of complexes I and III
|
Lamantea, Eleonora
|
|
2002
|
12 |
1 |
p. 49-52
4 p.
|
artikel
|
| 3 |
A point mutation of mitochondrial ATPase 6 gene in Leigh syndrome
|
Akagi, Motohiro
|
|
2002
|
12 |
1 |
p. 53-55
3 p.
|
artikel
|
| 4 |
Autosomal dominant distal spinal muscular atrophy: an Italian family not linked to 12q24 and 7p14
|
De Angelis, M.V.
|
|
2002
|
12 |
1 |
p. 26-30
5 p.
|
artikel
|
| 5 |
Autosomal dominant Emery–Dreifuss muscular dystrophy: a new family with late diagnosis
|
Colomer, J.
|
|
2002
|
12 |
1 |
p. 19-25
7 p.
|
artikel
|
| 6 |
Commentary from the Editor
|
|
|
2002
|
12 |
1 |
p. 1-3
3 p.
|
artikel
|
| 7 |
Coping with a Myositis Disease. James R. Kilpatrick (Editor and Publisher). Kilpatrick Publishing Company, 2000. 158 pp. Price £12.00 approx., ISBN 0970167105
|
Brigden, Raymond
|
|
2002
|
12 |
1 |
p. 81-
1 p.
|
artikel
|
| 8 |
Expression of dystrophin-associated proteins during neuronal differentiation of P19 embryonal carcinoma cells
|
Ceccarini, Marina
|
|
2002
|
12 |
1 |
p. 36-48
13 p.
|
artikel
|
| 9 |
Hypertrophic cardiomyopathy and mtDNA depletion. Successful treatment with heart transplantation
|
Santorelli, F.M.
|
|
2002
|
12 |
1 |
p. 56-59
4 p.
|
artikel
|
| 10 |
Instructions to authors
|
|
|
2002
|
12 |
1 |
p. 111-112
2 p.
|
artikel
|
| 11 |
Intolerance to neuroleptics and susceptibility for malignant hyperthermia in a patient with proximal myotonic myopathy (PROMM) and schizophrenia
|
Schneider, C.
|
|
2002
|
12 |
1 |
p. 31-35
5 p.
|
artikel
|
| 12 |
Merritt's Neurology. Tenth Edition. Edited by Lewis Rowland, 2000, 1024 pages, £62, Lippincott Williams and Wilkins. ISBN 0 683 30474 7
|
Ghosh, A.
|
|
2002
|
12 |
1 |
p. 80-
1 p.
|
artikel
|
| 13 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
2002
|
12 |
1 |
p. 101-110
10 p.
|
artikel
|
| 14 |
Motor DisordersDavid S Younger, Lippincott Williams, 1999, 576 pages, 219 illustrations, Hardback $129, ISBN: 0 316 97600 8
|
Busby, M.
|
|
2002
|
12 |
1 |
p. 80-81
2 p.
|
artikel
|
| 15 |
Myopathy with lobulated muscle fibers: evidence for heterogeneous etiology and clinical presentation
|
Figarella-Branger, D.
|
|
2002
|
12 |
1 |
p. 4-12
9 p.
|
artikel
|
| 16 |
Neuromuscular disorders: gene location
|
|
|
2002
|
12 |
1 |
p. 82-100
19 p.
|
artikel
|
| 17 |
Neurotoxin injection tracking and movement disorder software medsystechnologies Inc.http://www.medsystechnologies.com/piqureperfect/piqure_default.html
|
Gregory, Ralph
|
|
2002
|
12 |
1 |
p. 79-
1 p.
|
artikel
|
| 18 |
85th ENMC International Workshop on Congenital Muscular Dystrophy 6th International CMD Workshop 1st Workshop of the Myo-Cluster Project ‘GENRE’27–28th October 2000, Naarden, The Netherlands
|
Muntoni, Francesco
|
|
2002
|
12 |
1 |
p. 69-78
10 p.
|
artikel
|
| 19 |
80th ENMC International Workshop on Multi-Minicore Disease: 1st International MmD Workshop 12–13th May, 2000, Soestduinen, The Netherlands
|
Ferreiro, Ana
|
|
2002
|
12 |
1 |
p. 60-68
9 p.
|
artikel
|
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