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Neuromuscular diseases

Citations 161-170 of 238 total displayed.

Past content (since Jan 1998):

Observations
Polymyositis Masquerading as Motor Neuron Disease
Aisling Ryan; Azli M. Nor; Donal Costigan; Daragh Foley-Nolan; Ahmed El-Rafie; Michael A. Farrell; Orla Hardiman
Arch Neurol 2003; 60: 1001-1003. [Abstract] [Full text] [PDF]  

Original Contributions
Disease Course of Charcot-Marie-Tooth Disease Type 2: A 5-Year Follow-up Study
Laurien L. Teunissen; Nicolette C. Notermans; Hessel Franssen; Baziel G. M. van Engelen; Frank Baas; John H. J. Wokke
Arch Neurol 2003; 60: 823-828. [Abstract] [Full text] [PDF]  

Images in Neurology
Kennedy Disease: Avoiding Misdiagnosis
Konstantinos Paparounas; Anna Gotsi; Maria Syrrou; Nikolaos Akritidis
Arch Neurol 2003; 60: 893-894. [Extract] [Full text] [PDF]  

Observations
Congenital Myasthenic Syndrome With Episodic Apnea in Patients Homozygous for a CHAT Missense Mutation
Simone Kraner; Iris Laufenberg; Hans M. Straßburg; Joern P. Sieb; Ortrud K. Steinlein
Arch Neurol 2003; 60: 761-763. [Abstract] [Full text] [PDF]  

Editorials
Genetics of Charcot-Marie-Tooth Disease
David E. Pleasure
Arch Neurol 2003; 60: 481-482. [Extract] [Full text] [PDF]  

Original Contributions
A Clustering of Conjugal Amyotrophic Lateral Sclerosis in Southeastern France
Philippe Corcia; Helene-Farnase Jafari-Schluep; Dominique Lardillier; Hassan Mazyad; Pieric Giraud; Pierre Clavelou; Jean Pouget; William Camu
Arch Neurol 2003; 60: 553-557. [Abstract] [Full text] [PDF]  

Observations
Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene
Nazha Birouk; Hamid Azzedine; Odile Dubourg; Marie-Paule Muriel; Ali Benomar; Tarik Hamadouche; Thierry Maisonobe; Reda Ouazzani; Alexis Brice; Mohamed Yahyaoui; Taïb Chkili; Eric Le Guern
Arch Neurol 2003; 60: 598-604. [Abstract] [Full text] [PDF]  

Observations
Transient, Recurrent, White Matter Lesions in X-linked Charcot-Marie-Tooth Disease With Novel Connexin 32 Mutation
C. Oliver Hanemann; Carsten Bergmann; Jan Senderek; Klaus Zerres; Ann-Dorte Sperfeld
Arch Neurol 2003; 60: 605-609. [Abstract] [Full text] [PDF]  

Neurological Reviews
Autosomal Dominant Inherited Neuropathies With Prominent Sensory Loss and Mutilations: A Review
Michaela Auer-Grumbach; Peter De Jonghe; Kristien Verhoeven; Vincent Timmerman; Klaus Wagner; Hans-Peter Hartung; Garth A. Nicholson
Arch Neurol 2003; 60: 329-334. [Abstract] [Full text] [PDF]  

Original Contributions
Development of Generalized Disease at 2 Years in Patients With Ocular Myasthenia Gravis
Mark J. Kupersmith; Robert Latkany; Peter Homel
Arch Neurol 2003; 60: 243-248. [Abstract] [Full text] [PDF]  

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