nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Abstract
|
|
|
1998 |
|
3-4 |
p. 234-285 52 p. |
artikel |
2 |
Charcot-Marie-Tooth disease – muscle biopsy findings in relation to neurophysiology
|
Ericson, UllaBritt |
|
1998 |
|
3-4 |
p. 175-181 7 p. |
artikel |
3 |
Commentary: extraocular muscle sparing in muscular dystrophy: a critical evaluation of potential protective mechanisms
|
Porter, John D |
|
1998 |
|
3-4 |
p. 198-203 6 p. |
artikel |
4 |
Conference
|
|
|
1998 |
|
3-4 |
p. 213-219 7 p. |
artikel |
5 |
Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndrome
|
Makino, Michiko |
|
1998 |
|
3-4 |
p. 149-151 3 p. |
artikel |
6 |
Congenital myopathies with inclusion bodies: a brief review
|
Goebel, Hans H |
|
1998 |
|
3-4 |
p. 162-168 7 p. |
artikel |
7 |
Critical illness myopathy unrelated to corticosteroids or neuromuscular blocking agents
|
Deconinck, N |
|
1998 |
|
3-4 |
p. 186-192 7 p. |
artikel |
8 |
Effect of vitamin B6 supplementation in McArdle's disease: a strategic case study
|
Phoenix, Joanne |
|
1998 |
|
3-4 |
p. 210-212 3 p. |
artikel |
9 |
Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy family
|
Merlini, L |
|
1998 |
|
3-4 |
p. 182-185 4 p. |
artikel |
10 |
Heterogeneity in chronic fatigue syndrome: evidence from magnetic resonance spectroscopy of muscle
|
Lane, Russell J.M |
|
1998 |
|
3-4 |
p. 204-209 6 p. |
artikel |
11 |
Implications of maturation for viral gene delivery to skeletal muscle
|
van Deutekom, Judith C.T |
|
1998 |
|
3-4 |
p. 135-148 14 p. |
artikel |
12 |
LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3
|
Bönnemann, C.G |
|
1998 |
|
3-4 |
p. 193-197 5 p. |
artikel |
13 |
Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings
|
Topaloğlu, Haluk |
|
1998 |
|
3-4 |
p. 169-174 6 p. |
artikel |
14 |
Myotubular myopathy: morphological, immunohistochemical and clinical variation
|
Helliwell, T.R |
|
1998 |
|
3-4 |
p. 152-161 10 p. |
artikel |