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Neurogenetics
Citations 291-300 of 574 total displayed.
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Past content
(since May 1998):
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- Original Contributions
Sex, Apolipoprotein E  4 Status, and Hippocampal Volume in Mild Cognitive Impairment
- Adam Fleisher; Michael Grundman; Clifford R. Jack Jr; Ronald C. Petersen; Curtis Taylor; Hyun T. Kim; Denise H. B. Schiller; Victor Bagwell; Drahomira Sencakova; Myron F. Weiner; Charles DeCarli; Steven T. DeKosky; Christopher H. van Dyck; Leon J. Thal; for the Alzheimer’s Disease Cooperative Study
Arch Neurol 2005; 62: 953-957.
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- Original Contributions
FMR1 Premutations Associated With Fragile X–Associated Tremor/Ataxia Syndrome in Multiple System Atrophy
- Valérie Biancalana; Mathias Toft; Isabelle Le Ber; François Tison; Elisabeth Scherrer; Stephen Thibodeau; Jean Louis Mandel; Alexis Brice; Matthew J. Farrer; Alexandra Dürr
Arch Neurol 2005; 62: 962-966.
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- Original Contributions
Predictive Utility of Apolipoprotein E Genotype for Alzheimer Disease in Outpatients With Mild Cognitive Impairment
- D. P. Devanand; Gregory H. Pelton; Diana Zamora; Xinhua Liu; Matthias H. Tabert; Madeleine Goodkind; Nikolaos Scarmeas; Ilana Braun; Yaakov Stern; Richard Mayeux
Arch Neurol 2005; 62: 975-980.
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- Observations
Monozygotic Twins Discordant for Huntington Disease After 7 Years
- Joseph H. Friedman; Martha E. Trieschmann; Richard H. Myers; Hubert H. Fernandez
Arch Neurol 2005; 62: 995-997.
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- Editorials
Leber Hereditary Optic Neuropathy: Biochemical Lights in a Blurry Scenario
- Michio Hirano; Salvatore DiMauro
Arch Neurol 2005; 62: 711-712.
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- Original Contributions
Severe Impairment of Complex I–Driven Adenosine Triphosphate Synthesis in Leber Hereditary Optic Neuropathy Cybrids
- Alessandra Baracca; Giancarlo Solaini; Gianluca Sgarbi; Giorgio Lenaz; Agostino Baruzzi; Anthony H. V. Schapira; Andrea Martinuzzi; Valerio Carelli
Arch Neurol 2005; 62: 730-736.
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- Original Contributions
New DGK Gene Mutations in the Hepatocerebral Form of Mitochondrial DNA Depletion Syndrome
- Michelangelo Mancuso; Silvio Ferraris; Jacklyn Pancrudo; Annette Feigenbaum; Julian Raiman; John Christodoulou; David R. Thorburn; Salvatore DiMauro
Arch Neurol 2005; 62: 745-747.
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- Original Contributions
Restless Legs Syndrome: Confirmation of Linkage to Chromosome 12q, Genetic Heterogeneity, and Evidence of Complexity
- Alex Desautels; Gustavo Turecki; Jacques Montplaisir; Lan Xiong; Arthur S. Walters; Bruce L. Ehrenberg; Kateri Brisebois; Amelie K. Desautels; Yves Gingras; William G. Johnson; Elio Lugaresi; Giorgio Coccagna; Daniel L. Picchietti; Alice Lazzarini; Guy A. Rouleau
Arch Neurol 2005; 62: 591-596.
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- Original Contributions
Early Clinical Heterogeneity in Choreoacanthocytosis
- Alexander Lossos; Carol Dobson-Stone; Anthony P. Monaco; Dov Soffer; Ezra Rahamim; J. P. Newman; Saidi Mohiddin; Lameh Fananapazir; Israela Lerer; Eduard Linetsky; Avinoam Reches; Zohar Argov; Oded Abramsky; Natan Gadoth; Menachem Sadeh; John M. Gomori; Moshe Boher; Vardiella Meiner
Arch Neurol 2005; 62: 611-614.
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- Original Contributions
Founder Haplotype for Machado-Joseph Disease in the Indian Population: Novel Insights From History and Polymorphism Studies
- Uma Mittal; Achal K. Srivastava; Satish Jain; Sanjeev Jain; Mitali Mukerji
Arch Neurol 2005; 62: 637-640.
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