Muscle disease

Citations 151-160 of 283 total displayed.

Past content (since Jan 2001):

ARTICLES
Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV)

C. Bruno, O. P. van Diggelen, D. Cassandrini, M. Gimpelev, B. Giuffrè, M. A. Donati, P. Introvini, A. Alegria, S. Assereto, L. Morandi, M. Mora, E. Tonoli, S. Mascelli, M. Traverso, E. Pasquini, M. Bado, L. Vilarinho, G. van Noort, F. Mosca, S. DiMauro, F. Zara, and C. Minetti
Neurology 2004; 63: 1053-1058. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Familial myopathy with tubular aggregates associated with abnormal pupils

Nortina Shahrizaila, James Lowe, and Adrian Wills
Neurology 2004; 63: 1111-1113. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Mutant ubiquitin UBB⁺¹ is accumulated in sporadic inclusion-body myositis muscle fibers

P. Fratta, W. K. Engel, F. W. Van Leeuwen, E. M. Hol, G. Vattemi, and V. Askanas
Neurology 2004; 63: 1114-1117. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy

P. Prandini, A. Berardinelli, M. Fanin, F. Morello, E. Zardini, A. Pichiecchio, C. Uggetti, G. Lanzi, C. Angelini, and E. Pegoraro
Neurology 2004; 63: 1118-1121. [Abstract] [Full text] [PDF]  

ARTICLES
Strength training and albuterol in facioscapulohumeral muscular dystrophy

E.L. van der Kooi, O.J.M. Vogels, R.J.G.P. van Asseldonk, E. Lindeman, J.C.M. Hendriks, M. Wohlgemuth, S.M. van der Maarel, and G.W. Padberg
Neurology 2004; 63: 702-708. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Progression despite replacement of a myopathic form of coenzyme Q₁₀ defect

K. Auré, J. F. Benoist, H. Ogier de Baulny, N. B. Romero, O. Rigal, and A. Lombès
Neurology 2004; 63: 727-729. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Bilateral extraocular muscle atrophy in myotonic dystrophy type 1

T. Yamashita, E. Matsubara, I. Nagano, M. Shoji, and K. Abe
Neurology 2004; 63: 759-760. [Full text] [PDF]  

BRIEF COMMUNICATIONS
FSHD in Chinese population: Characteristics of translocation and genotype-phenotype correlation

Zhi-Ying Wu, Zhi-Qiang Wang, Shen-Xing Murong, and Ning Wang
Neurology 2004; 63: 581-583. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Interferon ß-responsive inclusion body myositis in a hepatitis C virus carrier

Y. Yakushiji, J. Satoh, M. Yukitake, K. Yamaguchi, I. Nakamura, I. Nishino, and Y. Kuroda
Neurology 2004; 63: 587-588. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Ventilatory support in facioscapulohumeral muscular dystrophy

M. Wohlgemuth, E. L. van der Kooi, R. G. van Kesteren, S. M. van der Maarel, and G. W. Padberg
Neurology 2004; 63: 176-178. [Abstract] [Full text] [PDF]  

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