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                             14 results found
no title author magazine year volume issue page(s) type
1 Abstract 1998
8 3-4 p. 234-285
52 p.
article
2 Charcot-Marie-Tooth disease – muscle biopsy findings in relation to neurophysiology Ericson, UllaBritt
1998
8 3-4 p. 175-181
7 p.
article
3 Commentary: extraocular muscle sparing in muscular dystrophy: a critical evaluation of potential protective mechanisms Porter, John D
1998
8 3-4 p. 198-203
6 p.
article
4 Conference 1998
8 3-4 p. 213-219
7 p.
article
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
8 3-4 p. 149-151
3 p.
article
6 Congenital myopathies with inclusion bodies: a brief review Goebel, Hans H
1998
8 3-4 p. 162-168
7 p.
article
7 Critical illness myopathy unrelated to corticosteroids or neuromuscular blocking agents Deconinck, N
1998
8 3-4 p. 186-192
7 p.
article
8 Effect of vitamin B6 supplementation in McArdle's disease: a strategic case study Phoenix, Joanne
1998
8 3-4 p. 210-212
3 p.
article
9 Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy family Merlini, L
1998
8 3-4 p. 182-185
4 p.
article
10 Heterogeneity in chronic fatigue syndrome: evidence from magnetic resonance spectroscopy of muscle Lane, Russell J.M
1998
8 3-4 p. 204-209
6 p.
article
11 Implications of maturation for viral gene delivery to skeletal muscle van Deutekom, Judith C.T
1998
8 3-4 p. 135-148
14 p.
article
12 LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3 Bönnemann, C.G
1998
8 3-4 p. 193-197
5 p.
article
13 Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings Topaloğlu, Haluk
1998
8 3-4 p. 169-174
6 p.
article
14 Myotubular myopathy: morphological, immunohistochemical and clinical variation Helliwell, T.R
1998
8 3-4 p. 152-161
10 p.
article
                             14 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands