Neuromuscular diseases

Contributing journals to this collection:
JAMA & Archives Journals

Citations 231-240 of 399 total displayed.

Past content

Correspondence
Disease Course of Charcot-Marie-Tooth Disease Type 2 and Comorbidity

Franco Gemignani; Adriana Marbini
Arch Neurol 2004; 61: 1470. [Extract] [Full text] [PDF]  

History of Neurology: Seminal Citations
Bulbospinal Muscular Atrophy: Kennedy’s Disease

Michael Sinnreich; Christopher Jon Klein
Arch Neurol 2004; 61: 1324-1326. [Extract] [Full text] [PDF]  

Neurological Reviews
Anti-GQ1b Ganglioside Antibody in Peripheral Nervous System Disorders: Pathophysiologic Role and Clinical Relevance

Konstantinos Paparounas
Arch Neurol 2004; 61: 1013-1016. [Abstract] [Full text] [PDF]  

Original Contributions
Immunolocalization and Activation of Transcription Factor Nuclear Factor B in Dysimmune Neuropathies and Familial Amyloidotic Polyneuropathy

Anna Mazzeo; Mohammed Aguennouz; Corrado Messina; Giuseppe Vita
Arch Neurol 2004; 61: 1097-1102. [Abstract] [Full text] [PDF]  

History of Neurology
Alfred Hauptmann, Siegfried Thannhauser, and an Endangered Muscular Disorder

Michael Krasnianski; Uwe Ehrt; Stephan Neudecker; Stephan Zierz
Arch Neurol 2004; 61: 1139-1141. [Extract] [Full text] [PDF]  

History of Neurology: Seminal Citations
Postpolio Syndrome

Frans Nollet; Marianne de Visser
Arch Neurol 2004; 61: 1142-1144. [Extract] [Full text] [PDF]  

The World in Medicine
Gene Therapy and ALS

Joan Stephenson
JAMA 2004; 291: 2809-c. [Extract] [Full text] [PDF]  

Original Contributions
Hereditary Spastic Paraplegia: Clinical Genetic Study of 15 Families

Antonio Orlacchio; Toshitaka Kawarai; Antonio Totaro; Alessia Errico; Peter H. St George-Hyslop; Elena I. Rugarli; Giorgio Bernardi
Arch Neurol 2004; 61: 849-855. [Abstract] [Full text] [PDF]  

Original Contributions
Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders

Corrine O. Smith; Hillary P. Lipe; Thomas D. Bird
Arch Neurol 2004; 61: 875-880. [Abstract] [Full text] [PDF]  

Original Contributions
CTG Repeat Number at the Myotonic Dystrophy Locus in Healthy Kuwaiti Individuals: Possible Explanation of Why Myotonic Dystrophy Is Rare in Kuwait

Suad Alfadhli; Alaa E. Elshafey; Lailá Bastaki; Sadeqa Al-Awadi
Arch Neurol 2004; 61: 895-898. [Abstract] [Full text] [PDF]  

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