| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Altered pathological progression of diaphragm and quadriceps muscle in TNF-deficient, dystrophin-deficient mice
|
Spencer, Melissa J
|
|
2000
|
10 |
8 |
p. 612-619
8 p.
|
artikel
|
| 2 |
Book review
|
Emery, Alan E.H
|
|
2000
|
10 |
8 |
p. 622-623
2 p.
|
artikel
|
| 3 |
Book review
|
Wills, Adrian J
|
|
2000
|
10 |
8 |
p. 620-621
2 p.
|
artikel
|
| 4 |
Book review
|
Hill, Marguerite
|
|
2000
|
10 |
8 |
p. 620-
1 p.
|
artikel
|
| 5 |
Book review
|
Németh, Andrea H
|
|
2000
|
10 |
8 |
p. 623-624
2 p.
|
artikel
|
| 6 |
Book review
|
Emery, Alan E.H
|
|
2000
|
10 |
8 |
p. 623-
1 p.
|
artikel
|
| 7 |
Book review
|
Elston, John S.
|
|
2000
|
10 |
8 |
p. 621-
1 p.
|
artikel
|
| 8 |
Book review
|
Emery, Alan E.H
|
|
2000
|
10 |
8 |
p. 621-622
2 p.
|
artikel
|
| 9 |
Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy
|
Zemmouri, R.
|
|
2000
|
10 |
8 |
p. 592-598
7 p.
|
artikel
|
| 10 |
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome
|
Villanova, Marcello
|
|
2000
|
10 |
8 |
p. 541-547
7 p.
|
artikel
|
| 11 |
Evaluation of heart involvement in gamma-sarcoglycanopathy (LGMD2C). A study of ten patients
|
Calvo, Francisco
|
|
2000
|
10 |
8 |
p. 560-566
7 p.
|
artikel
|
| 12 |
Frequent mutations in Japanese patients with acid maltase deficiency
|
Tsujino, Seiichi
|
|
2000
|
10 |
8 |
p. 599-603
5 p.
|
artikel
|
| 13 |
Hereditary Motor and Sensory Neuropathy-Lom (HMSNL) in a Spanish family: clinical, electrophysiological, pathological and genetic studies
|
Colomer, J
|
|
2000
|
10 |
8 |
p. 578-583
6 p.
|
artikel
|
| 14 |
Hereditary motor and sensory neuropathy – Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries
|
Chandler, David
|
|
2000
|
10 |
8 |
p. 584-591
8 p.
|
artikel
|
| 15 |
Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy
|
Kerst, Birgit
|
|
2000
|
10 |
8 |
p. 572-577
6 p.
|
artikel
|
| 16 |
Index
|
|
|
2000
|
10 |
8 |
p. XXVII-XXIX
nvt p.
|
artikel
|
| 17 |
Index
|
|
|
2000
|
10 |
8 |
p. XXII-XXVI
nvt p.
|
artikel
|
| 18 |
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci
|
Talim, Beril
|
|
2000
|
10 |
8 |
p. 548-552
5 p.
|
artikel
|
| 19 |
Mitochondrial DNA variants in inclusion body myositis
|
Kok, Chee Choy
|
|
2000
|
10 |
8 |
p. 604-611
8 p.
|
artikel
|
| 20 |
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)
|
Anderson, Louise V.B
|
|
2000
|
10 |
8 |
p. 553-559
7 p.
|
artikel
|
| 21 |
Unusual expression of emerin in a patient with X-linked Emery–Dreifuss muscular dystrophy
|
Di Blasi, C
|
|
2000
|
10 |
8 |
p. 567-571
5 p.
|
artikel
|
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