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Neurology, Other
Citations 261-270 of 1002 total displayed.
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Past content
(since Jan 1998):
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- Correspondence
Babinski, Pseudo-Babinski, and Dystonia—Reply
- Dominick J. H. McCabe; Elijah C. Chaila; Norman Delanty; Danny Costello; Raymond P. Murphy
Arch Neurol 2007; 64: 1209.
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- Correspondence
Progression to Dementia in Probable and Possible Mild Cognitive Impairment—Reply
- Oscar L. Lopez; Lewis H. Kuller; James T. Becker
Arch Neurol 2007; 64: 1210-1211.
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- Editorials
New Initiatives: Clinical Trials and Videos
- Roger N. Rosenberg
Arch Neurol 2007; 64: 934.
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- Editorials
Dwindling Indications for Sural Nerve Biopsy
- David E. Pleasure
Arch Neurol 2007; 64: 935-936.
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- Clinical Trials
Randomized, Double-blind, Placebo-Controlled Trial on Symptomatic Effects of Coenzyme Q10 in Parkinson Disease
- Alexander Storch; Wolfgang H. Jost; Peter Vieregge; Jörg Spiegel; Wolfgang Greulich; Joachim Durner; Thomas Müller; Andreas Kupsch; Henning Henningsen; Wolfgang H. Oertel; Gerd Fuchs; Wilfried Kuhn; Petra Niklowitz; Rainer Koch; Birgit Herting; Heinz Reichmann; for the German Coenzyme Q10 Study Group
Arch Neurol 2007; 64: 938-944.
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- Neurological Reviews
The New Neurobiology of Autism: Cortex, Connectivity, and Neuronal Organization
- Nancy J. Minshew; Diane L. Williams
Arch Neurol 2007; 64: 945-950.
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- Neurological Reviews
Damage to Lipids, Proteins, DNA, and RNA in Mild Cognitive Impairment
- William R. Markesbery; Mark A. Lovell
Arch Neurol 2007; 64: 954-956.
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- Original Contributions
Skin Denervation and Cutaneous Vasculitis in Eosinophilia-Associated Neuropathy
- Chi-Chao Chao; Sung-Tsang Hsieh; Chia-Tung Shun; Song-Chou Hsieh
Arch Neurol 2007; 64: 959-965.
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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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- Original Contributions
Stoichiometric Alteration of PMP22 Protein Determines the Phenotype of Hereditary Neuropathy With Liability to Pressure Palsies
- Jun Li; Khaled Ghandour; Danijela Radovanovic; Rosemary R. Shy; Karen M. Krajewski; Michael E. Shy; Garth A. Nicholson
Arch Neurol 2007; 64: 974-978.
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