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Neuromuscular diseases
Citations 111-120 of 238 total displayed.
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Past content
(since Jan 1998):
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- Observations
Postinfectious Myeloradiculoneuropathy With Cranial Nerve Involvements Associated With Human Herpesvirus 7 Infection
- Takateru Mihara; Tatsuro Mutoh; Tetsusi Yoshikawa; Shigeaki Yano; Yoshizo Asano; Hiroko Yamamoto
Arch Neurol 2005; 62: 1755-1757.
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- Original Contributions
LAMA2 Gene Analysis in Congenital Muscular Dystrophy: New Mutations, Prenatal Diagnosis, and Founder Effect
- Claudia Di Blasi; Daniela Piga; Paolo Brioschi; Isabella Moroni; Antonella Pini; Alessandra Ruggieri; Simona Zanotti; Graziella Uziel; Laura Jarre; Elvio Della Giustina; Carmela Scuderi; Christoffer Jonsrud; Renato Mantegazza; Lucia Morandi; Marina Mora
Arch Neurol 2005; 62: 1582-1586.
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- Observations
Effect of Fuels on Exercise Capacity in Muscle Phosphoglycerate Mutase Deficiency
- John Vissing; Bjørn Quistorff; Ronald G. Haller
Arch Neurol 2005; 62: 1440-1443.
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- Editorials
Chaperoning Motor Neurons
- David Pleasure
Arch Neurol 2005; 62: 1193.
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- Neurological Reviews
Supportive Care for Patients With Guillain-Barré Syndrome
- Richard A. C. Hughes; Eelco F. M. Wijdicks; Estelle Benson; David R. Cornblath; Angelika F. Hahn; Jay M. Meythaler; John T. Sladky; Richard J. Barohn; James C. Stevens
Arch Neurol 2005; 62: 1194-1198.
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- Original Contributions
Mutation Analysis of the Small Heat Shock Protein 27 Gene in Chinese Patients With Charcot-Marie-Tooth Disease
- Beisha Tang; Xiaomin Liu; Guohua Zhao; Wei Luo; Kun Xia; Qian Pan; Fang Cai; Zhengmao Hu; Cheng Zhang; Biao Chen; Fufeng Zhang; Lu Shen; Ruxu Zhang; Hong Jiang
Arch Neurol 2005; 62: 1201-1207.
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- Original Contributions
Identification of a Novel Founder Mutation in the DYSF Gene Causing Clinical Variability in the Spanish Population
- Juan J. Vilchez; Pia Gallano; Eduard Gallardo; Adriana Lasa; Ricardo Rojas-García; Alba Freixas; Noemí De Luna; Francesc Calafell; Teresa Sevilla; Fernando Mayordomo; Montserrat Baiget; Isabel Illa
Arch Neurol 2005; 62: 1256-1259.
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- History of Neurology: Seminal Citations
Myotonic Dystrophy
- Jeffrey J. Tramonte; Ted M. Burns
Arch Neurol 2005; 62: 1316-1319.
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- Original Contributions
Mutation Analysis of SPG4 and SPG3A Genes and Its Implication in Molecular Diagnosis of Korean Patients With Hereditary Spastic Paraplegia
- Su-Yon Park; Chang-Seok Ki; Hee-Jin Kim; Jong-Won Kim; Duk Hyun Sung; Byoung Joon Kim; Won Yong Lee
Arch Neurol 2005; 62: 1118-1121.
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- Book Reviews
Myology, 3rd ed
- Lewis P. Rowland
Arch Neurol 2005; 62: 1171-a-1172-a.
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