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                             15 results found
no title author magazine year volume issue page(s) type
1 Adiposity is increased among high-functioning, non-ambulatory patients with spinal muscular atrophy Sproule, Douglas M.
2010
20 7 p. 448-452
5 p.
article
2 DOK7 mutations presenting as a proximal myopathy in French Canadians Srour, Myriam
2010
20 7 p. 453-457
5 p.
article
3 Editorial Board 2010
20 7 p. IFC-
1 p.
article
4 Eduardo Bonilla MD (1937–2010) DiMauro, Salvatore
2010
20 7 p. 477-478
2 p.
article
5 Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3 Waddell, Leigh B
2010
20 7 p. 464-466
3 p.
article
6 Heritability of common neuromuscular diseases Emery, Alan E.H.
2010
20 7 p. 476-
1 p.
article
7 Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation Odgerel, Zagaa
2010
20 7 p. 438-442
5 p.
article
8 Mitochondrial DNA depletion syndromes – Many genes, common mechanisms Suomalainen, Anu
2010
20 7 p. 429-437
9 p.
article
9 Myopathies in the elderly: A hospital-based study Echaniz-Laguna, Andoni
2010
20 7 p. 443-447
5 p.
article
10 Pseudomyotonia, a muscle function disorder associated with an inherited ATP2A1 (SERCA1) defect in a Dutch Improved Red and White cross-breed calf Grünberg, Walter
2010
20 7 p. 467-470
4 p.
article
11 Sleep and well-being in young men with neuromuscular disorders receiving non-invasive ventilation and their carers Read, Joy
2010
20 7 p. 458-463
6 p.
article
12 171st ENMC International Workshop: Standards of care and management of facioscapulohumeral muscular dystrophy Tawil, Rabi
2010
20 7 p. 471-475
5 p.
article
13 WMS 2010 2010
20 7 p. I-
1 p.
article
14 WMS News 2010
20 7 p. III-IV
nvt p.
article
15 WMS online application form 2010
20 7 p. II-
1 p.
article
                             15 results found
 
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