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Neurogenetics
Citations 161-170 of 574 total displayed.
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Past content
(since May 1998):
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- Observations
Dissociation of Neuropathologic Findings and Cognition: Case Report of an Apolipoprotein E  2/2 Genotype
- Daniel J. Berlau; Kristin Kahle-Wrobleski; Elizabeth Head; Matthew Goodus; Ronald Kim; Claudia Kawas
Arch Neurol 2007; 64: 1193-1196.
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- Editorials
Dwindling Indications for Sural Nerve Biopsy
- David E. Pleasure
Arch Neurol 2007; 64: 935-936.
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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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- 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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- Original Contributions
Familial Parkinsonism and Ophthalmoplegia From a Mutation in the Mitochondrial DNA Helicase Twinkle
- Robert H. Baloh; Ezequiel Salavaggione; Jeffrey Milbrandt; Alan Pestronk
Arch Neurol 2007; 64: 998-1000.
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- Original Contributions
Screen for Excess FMR1 Premutation Alleles Among Males With Parkinsonism
- Jeremy Kraff; Hiu-Tung Tang; Roberto Cilia; Margherita Canesi; Gianni Pezzoli; Stefano Goldwurm; Paul J. Hagerman; Flora Tassone
Arch Neurol 2007; 64: 1002-1006.
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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
Mitochondrial Complex I Gene Variant Associated With Early Age at Onset in Spinocerebellar Ataxia Type 2
- David K. Simon; Kangni Zheng; Luis Velázquez; Nieves Santos; Luis Almaguer; K. Pattie Figueroa; Stefan-M. Pulst
Arch Neurol 2007; 64: 1042-1044.
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- Research Letters
Glucocerebrosidase Mutations and Risk of Parkinson Disease in Chinese Patients
- Eng-King Tan; Justina Tong; Stephanie Fook-Chong; Yuen Yih; Meng-Cheong Wong; Ratnagopal Pavanni; Yi Zhao
Arch Neurol 2007; 64: 1056-1058.
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