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Neuromuscular diseases
Citations 51-60 of 238 total displayed.
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Past content
(since Jan 1998):
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- Observations
Congenital Myopathy With Nemaline Rods and Cap Structures Caused by a Mutation in the  -Tropomyosin Gene (TPM2)
- Homa Tajsharghi; Monica Ohlsson; Christopher Lindberg; Anders Oldfors
Arch Neurol 2007; 64: 1334-1338.
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- Observations
Two Novel Mitochondrial DNA Mutations in Muscle Tissue of a Patient With Limb-Girdle Myopathy
- Ann Meulemans; Boel De Paepe; Jan De Bleecker; Joél Smet; Willy Lissens; Rudy Van Coster; Linda De Meirleir; Sara Seneca
Arch Neurol 2007; 64: 1339-1343.
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- Original Contributions
Classification of Myasthenia Gravis Based on Autoantibody Status
- Shigeaki Suzuki; Kimiaki Utsugisawa; Yuriko Nagane; Takashi Satoh; Yasuo Terayama; Norihiro Suzuki; Masataka Kuwana
Arch Neurol 2007; 64: 1121-1124.
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- Original Contributions
Phenotypic Study in 40 Patients With Dysferlin Gene Mutations: High Frequency of Atypical Phenotypes
- Karine Nguyen; Guillaume Bassez; Martin Krahn; Rafaelle Bernard; Pascal Laforêt; Véronique Labelle; Jon Andoni Urtizberea; Dominique Figarella-Branger; Norma Romero; Shahram Attarian; France Leturcq; Jean Pouget; Nicolas Lévy; Bruno Eymard
Arch Neurol 2007; 64: 1176-1182.
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- Images in Neurology
Magnetic Resonance Imaging of Biceps Femoris Muscles in Benign Acute Childhood Myositis
- Toshitaka Kawarai; Hirotake Nishimura; Koichiro Taniguchi; Naoki Saji; Hirotaka Shimizu; Makoto Tadano; Teruo Shirabe; Yasushi Kita
Arch Neurol 2007; 64: 1200-1201.
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- Editorials
Dwindling Indications for Sural Nerve Biopsy
- David E. Pleasure
Arch Neurol 2007; 64: 935-936.
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- Original Contributions
Clinical and Electrophysiological Features in Charcot-Marie-Tooth Disease With Mutations in the NEFL Gene
- Gabriel Miltenberger-Miltenyi; Andreas R. Janecke; Julia V. Wanschitz; Vincent Timmerman; Christian Windpassinger; Michaela Auer-Grumbach; Wolfgang N. Löscher
Arch Neurol 2007; 64: 966-970.
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- Observations
Limb-Girdle Muscular Dystrophy Due to Emerin Gene Mutations
- Shigehisa Ura; Yukiko K. Hayashi; Kanako Goto; Mina Nolasco Astejada; Terumi Murakami; Masako Nagato; Shigeru Ohta; Yasuhisa Daimon; Hidehiro Takekawa; Koichi Hirata; Ikuya Nonaka; Satoru Noguchi; Ichizo Nishino
Arch Neurol 2007; 64: 1038-1041.
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- Observations
A MELAS-Associated ND1 Mutation Causing Leber Hereditary Optic Neuropathy and Spastic Dystonia
- Liesbeth Spruijt; Hubert J. Smeets; Alexandra Hendrickx; Marijke Wefers Bettink-Remeijer; A. Maat-Kievit; Kees C. Schoonderwoerd; Wim Sluiter; Ireneaus F. de Coo; Rogier Q. Hintzen
Arch Neurol 2007; 64: 890-893.
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- Correspondence
Cardiac Involvement in Bethlem Myopathy—Reply
- Anneke J. van der Kooi; Willem G. de Voogt; Marianne de Visser
Arch Neurol 2007; 64: 915-a-916-a.
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