All Neuromuscular Disease

Citations 1-10 of 136 total displayed.

Most recent content (6 Jan 2009):

ARTICLES
A novel ALS2 splice-site mutation in a Cypriot juvenile-onset primary lateral sclerosis family

Nikolay Mintchev, Eleni Zamba-Papanicolaou, Kleopas A. Kleopa, and Kyproula Christodoulou
Neurology 2009; 72: 28-32. [Abstract] [Full text] [PDF]  

Past content (since Jan 2000):

RESIDENT AND FELLOW SECTION
Teaching Video NeuroImage: Chvostek sign with Fahr syndrome in a patient with hypoparathyroidism

Sunil K. Narayan, P. Sivaprasad, Ram Niranjan Sahoo, and V. Bhuvaneswari
Neurology 2008; 71: e79. [Full text] [PDF]  

ARTICLES
Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2

H. Houlden, M. Laura, F. Wavrant–De Vrièze, J. Blake, N. Wood, and M. M. Reilly
Neurology 2008; 71: 1660-1668. [Abstract] [Full text] [PDF]  

ARTICLES
A novel dominant mutation of the Na_v1.4 -subunit domain I leading to sodium channel myotonia

S. Petitprez, L. Tiab, L. Chen, L. Kappeler, K. M. Rösler, D. Schorderet, H. Abriel, and J-M Burgunder
Neurology 2008; 71: 1669-1675. [Abstract] [Full text] [PDF]  

EDITORIALS
Sporadically occurring neurologic disease: HSP genes and apparently sporadic spastic paraplegia

John K. Fink
Neurology 2008; 71: 1468-1469. [Full text] [PDF]  

ARTICLES
Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes

F. Brugman, H. Scheffer, J.H.J. Wokke, W. M. Nillesen, M. de Visser, E. Aronica, J. H. Veldink, and L. H. van den Berg
Neurology 2008; 71: 1500-1505. [Abstract] [Full text] [PDF]  

ARTICLES
Distinct muscle imaging patterns in myofibrillar myopathies

D. Fischer, R. A. Kley, K. Strach, C. Meyer, T. Sommer, K. Eger, A. Rolfs, W. Meyer, A. Pou, J. Pradas, C. M. Heyer, A. Grossmann, A. Huebner, W. Kress, J. Reimann, R. Schröder, B. Eymard, M. Fardeau, B. Udd, L. Goldfarb, M. Vorgerd, and M. Olivé
Neurology 2008; 71: 758-765. [Abstract] [Full text] [PDF]  

ARTICLES
Natural history of SMA IIIb: Muscle strength decreases in a predictable sequence and magnitude

Feza Deymeer, Piraye Serdaroglu, Yesim Parman, and Mehves Poda
Neurology 2008; 71: 644-649. [Abstract] [Full text] [PDF]  

EDITORIALS
A "nema" of hope in the treatment of late-onset nemaline myopathy

Marinos C. Dalakas and Stephen A. Smith
Neurology 2008; 71: 472-473. [Full text] [PDF]  

ARTICLES
Dehydroepiandrosterone for myotonic dystrophy type 1

I. Pénisson-Besnier, M. Devillers, R. Porcher, D. Orlikowski, V. Doppler, C. Desnuelle, X. Ferrer, M. -C.A. Bes, F. Bouhour, C. Tranchant, E. Lagrange, A. Vershueren, D. Uzenot, P. Cintas, G. Solé, J. -Y. Hogrel, P. Laforêt, C. Vial, A. L. Vila, S. Sacconi, J. Pouget, B. Eymard, S. Chevret, and D. Annane
Neurology 2008; 71: 407-412. [Abstract] [Full text] [PDF]  

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