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Neurology
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Muscle disease

Citations 181-190 of 283 total displayed.

Past content (since Jan 2001):

ARTICLES
Muscle weakness in critically ill children
B. L. Banwell, R. J. Mildner, A. C. Hassall, L. E. Becker, J. Vajsar, and S. D. Shemie
Neurology 2003; 61: 1779-1782. [Abstract] [Full text] [PDF]  

ARTICLES
A CAV3 microdeletion differentially affects skeletal muscle and myocardium
R. Cagliani, N. Bresolin, A. Prelle, A. Gallanti, F. Fortunato, M. Sironi, P. Ciscato, G. Fagiolari, S. Bonato, S. Galbiati, S. Corti, C. Lamperti, M. Moggio, and G. P. Comi
Neurology 2003; 61: 1513-1519. [Abstract] [Full text] [PDF]  

ARTICLES
Autosomal dominant hyaline body myopathy: Clinical variability and pathologic findings
S. Bohlega, B. Lach, B. F. Meyer, Y. Al Said, M. Kambouris, M. Al Homsi, and E. J. Cupler
Neurology 2003; 61: 1519-1523. [Abstract] [Full text] [PDF]  

EDITORIALS
Echo of silence: Silent mutations, RNA splicing, and neuromuscular diseases
Ami Mankodi and Tetsuo Ashizawa
Neurology 2003; 61: 1330-1331. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Splicing mosaic of the myophosphorylase gene due to a silent mutation in McArdle disease
I. Fernandez-Cadenas, A.L. Andreu, J. Gamez, R. Gonzalo, M.A. Martín, J.C. Rubio, and J. Arenas
Neurology 2003; 61: 1432-1434. [Abstract] [Full text] [PDF]  

ARTICLES
Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 alleles
M. Wohlgemuth, R. J. Lemmers, E. L. van der Kooi, M. J. van der Wielen, P. G. van Overveld, H. Dauwerse, E. Bakker, R. R. Frants, G. W. Padberg, and S. M. van der Maarel
Neurology 2003; 61: 909-913. [Abstract] [Full text] [PDF]  

ARTICLES
Cold induces shifts of voltage dependence in mutant SCN4A, causing hypokalemic periodic paralysis
Y. Sugiura, N. Makita, L. Li, P. J. Noble, J. Kimura, Y. Kumagai, T. Soeda, and T. Yamamoto
Neurology 2003; 61: 914-918. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Patients with severe muscle wasting are prone to develop hypoglycemia during fasting
M. C. Ørngreen, M. Zacho, A. Hebert, M. Laub, and J. Vissing
Neurology 2003; 61: 997-1000. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Lack of association of the potassium channel–associated peptide MiRP2-R83H variant with periodic paralysis
D. Sternberg, N. Tabti, E. Fournier, B. Hainque, and B. Fontaine
Neurology 2003; 61: 857-859. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Reversible upper limb muscle weakness with selective loss of thick filaments
G. Vattemi, P. Tonin, M. Filosto, C. Savio, N. Rizzuto, and G. Tomelleri
Neurology 2003; 61: 863-864. [Full text] [PDF]  

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* Collected Resources Home

* Related collections:
 Neuromuscular disease
 All Neuromuscular Disease
 Anterior nerve cell disease
 Amyotrophic lateral sclerosis
 Myasthenia
 Lambert-Eaton syndrome
 Peripheral neuropathy
 Carpal tunnel syndrome
 Cranial neuropathy
 Guillain-Barre syndrome
 Chronic inflammatory demyelinating polyneuropathy
 Transverse myelitis
 Muscle disease


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