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Neurogenetics
Citations 241-250 of 574 total displayed.
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Past content
(since May 1998):
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- Basic Science Seminars in Neurology
Mitochondria in Parkinson Disease: Back in Fashion With a Little Help From Genetics
- Miratul M. K. Muqit; Sonia Gandhi; Nicholas W. Wood
Arch Neurol 2006; 63: 649-654.
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- Original Contributions
Nerve Conduction Abnormalities in Patients With MELAS and the A3243G Mutation
- Petra Kaufmann; Juan M. Pascual; Yaacov Anziska; Clifton L. Gooch; Kristin Engelstad; Sarah Jhung; Salvatore DiMauro; Darryl C. De Vivo
Arch Neurol 2006; 63: 746-748.
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- Original Contributions
Eight Novel Mutations in SPG4 in a Large Sample of Patients With Hereditary Spastic Paraplegia
- Francesca Crippa; Chris Panzeri; Andrea Martinuzzi; Alessia Arnoldi; Francesca Redaelli; Alessandra Tonelli; Cinzia Baschirotto; Giovanni Vazza; Maria Luisa Mostacciuolo; Andrea Daga; Genny Orso; Paolo Profice; Antonio Trabacca; Maria Grazia D’Angelo; Giacomo Pietro Comi; Sara Galbiati; Costanza Lamperti; Sara Bonato; Massimo Pandolfo; Giovanni Meola; Olimpia Musumeci; Antonio Toscano; Carlo Pietro Trevisan; Nereo Bresolin; Maria Teresa Bassi
Arch Neurol 2006; 63: 750-755.
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- Original Contributions
Hereditary Spastic Paraplegia With Thin Corpus Callosum: Reduction of the SPG11 Interval and Evidence for Further Genetic Heterogeneity
- Alexander Lossos; Giovanni Stevanin; Vardiella Meiner; Zohar Argov; Naima Bouslam; J. P. Newman; John M. Gomori; Stephan Klebe; Israela Lerer; Nizar Elleuch; Shira Silverstein; Alexandra Durr; Oded Abramsky; Ziva Ben-Nariah; Alexis Brice
Arch Neurol 2006; 63: 756-760.
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- Original Contributions
Case-Control Study of the Parkin Gene in Early-Onset Parkinson Disease
- Lorraine N. Clark; Shehla Afridi; Eric Karlins; Yuanjia Wang; Helen Mejia-Santana; Juliette Harris; Elan D. Louis; Lucien J. Cote; Howard Andrews; Stanley Fahn; Cheryl Waters; Blair Ford; Steven Frucht; Ruth Ottman; Karen Marder
Arch Neurol 2006; 63: 548-552.
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- Neurological Reviews
Implications of Genetics on the Diagnosis and Care of Patients With Parkinson Disease
- Christine Klein
Arch Neurol 2006; 63: 328-334.
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- Original Contributions
Lewy Body Pathology in Familial Alzheimer Disease: Evidence for Disease- and Mutation-Specific Pathologic Phenotype
- James B. Leverenz; Mark A. Fishel; Elaine R. Peskind; Thomas J. Montine; David Nochlin; Ellen Steinbart; Murray A. Raskind; Gerard D. Schellenberg; Thomas D. Bird; Debby Tsuang
Arch Neurol 2006; 63: 370-376.
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- Original Contributions
LRRK2 Mutations in Spanish Patients With Parkinson Disease: Frequency, Clinical Features, and Incomplete Penetrance
- Carles Gaig; Mario Ezquerra; Maria Jose Marti; Esteban Muñoz; Francesc Valldeoriola; Eduardo Tolosa
Arch Neurol 2006; 63: 377-382.
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- Original Contributions
Association of Apolipoprotein E Genotype and Alzheimer Disease in African Americans
- Jill R. Murrell; Brandon Price; Kathleen A. Lane; Olusegun Baiyewu; Oye Gureje; Adesola Ogunniyi; Frederick W. Unverzagt; Valerie Smith-Gamble; Sujuan Gao; Hugh C. Hendrie; Kathleen S. Hall
Arch Neurol 2006; 63: 431-434.
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- Original Contributions
Depression, Apolipoprotein E Genotype, and the Incidence of Mild Cognitive Impairment: A Prospective Cohort Study
- Yonas E. Geda; David S. Knopman; David A. Mrazek; Gregory A. Jicha; Glenn E. Smith; Selamawit Negash; Bradley F. Boeve; Robert J. Ivnik; Ronald C. Petersen; V. Shane Pankratz; Walter A. Rocca
Arch Neurol 2006; 63: 435-440.
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