Advertisement
Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
 QUICK SEARCH:   [advanced]


     


Muscle disease

Citations 151-160 of 281 total displayed.

Past content (since Jan 2001):

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]  

ARTICLES
Creatine monohydrate enhances strength and body composition in Duchenne muscular dystrophy
M. A. Tarnopolsky, D. J. Mahoney, J. Vajsar, C. Rodriguez, T. J. Doherty, B. D. Roy, and D. Biggar
Neurology 2004; 62: 1771-1777. [Abstract] [Full text] [PDF]  

ARTICLES
Expression of protein kinase C isoforms and interleukin-1ß in myofibrillar myopathy
G. Vattemi, P. Tonin, M. Mora, M. Filosto, L. Morandi, C. Savio, I. Dal Pra, N. Rizzuto, and G. Tomelleri
Neurology 2004; 62: 1778-1782. [Abstract] [Full text] [PDF]  

[First page]   [Previous page]   [Next page]
Pages: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29

* 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


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
Copyright © 2009 by AAN Enterprises, Inc.
Advertisement