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Neurogenetics
Contributing journals to this collection:
JAMA & Archives Journals
Citations 231-240 of 623 total displayed.
- Observations
Reduced Penetrance in a Brazilian Family With Spinocerebellar Ataxia Type 10
- Salmo Raskin; Tetsuo Ashizawa; Hélio A. G. Teive; Walter O. Arruda; Ping Fang; Rui Gao; Misti C. White; Lineu C. Werneck; Benjamin Roa
Arch Neurol 2007; 64: 591-594.
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- Original Contributions
Genotype and Protein Expression After Bone Marrow Transplantation for Adrenoleukodystrophy
- Stefan Schönberger; Peter Roerig; Dominik T. Schneider; Guido Reifenberger; Ulrich Göbel; Jutta Gärtner
Arch Neurol 64.5.noc60105.
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- Clinical Trials
Effects of Methylphenidate on Response to Oral Levodopa: A Double-blind Clinical Trial
- John G. Nutt; Julie H. Carter; Nichole E. Carlson
Arch Neurol 2007; 64: 319-323.
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- Neurological Reviews
New Ideas in Epilepsy Genetics: Novel Epilepsy Genes, Copy Number Alterations, and Gene Regulation
- Christina A. Gurnett; Peter Hedera
Arch Neurol 2007; 64: 324-328.
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- Original Articles
Serotonin Receptor 2A Gene and the Influence of Childhood Maternal Nurturance on Adulthood Depressive Symptoms
- Markus Jokela; Liisa Keltikangas-Järvinen; Mika Kivimäki; Sampsa Puttonen; Marko Elovainio; Riikka Rontu; Terho Lehtimäki
Arch Gen Psychiatry 2007; 64: 356-360.
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- Original Articles
Association of a Functional Polymorphism in the µ-Opioid Receptor Gene With Alcohol Response and Consumption in Male Rhesus Macaques
- Christina S. Barr; Melanie Schwandt; Stephen G. Lindell; Scott A. Chen; David Goldman; Stephen J. Suomi; J. Dee Higley; Markus Heilig
Arch Gen Psychiatry 2007; 64: 369-376.
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- Original Contributions
Voxel-Based Morphometry in Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions With and Without Progranulin Mutations
- Jennifer L. Whitwell; Clifford R. Jack Jr; Matthew Baker; Rosa Rademakers; Jennifer Adamson; Bradley F. Boeve; David S. Knopman; Joseph F. Parisi; Ronald C. Petersen; Dennis W. Dickson; Michael L. Hutton; Keith A. Josephs
Arch Neurol 2007; 64: 371-376.
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- Original Contributions
A Family With Parkinson Disease, Essential Tremor, Bell Palsy, and Parkin Mutations
- Hao Deng; Wei-Dong Le; Christine B. Hunter; Nicte Mejia; Wen-Jie Xie; Joseph Jankovic
Arch Neurol 2007; 64: 421-424.
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- Original Contributions
LRRK2 Exon 41 Mutations in Sporadic Parkinson Disease in Europeans
- Suzanne Lesage; Sabine Janin; Ebba Lohmann; Anne-Louise Leutenegger; Laurence Leclere; François Viallet; Pierre Pollak; Franck Durif; Stéphane Thobois; Valérie Layet; Marie Vidailhet; Yves Agid; Alexandra Dürr; Alexis Brice; for the French Parkinson's Disease Genetics Study Group
Arch Neurol 2007; 64: 425-430.
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- Original Contributions
Two Novel Epilepsy-Linked Mutations Leading to a Loss of Function of LGI1
- Elodie Chabrol; Cyprian Popescu; Isabelle Gourfinkel-An; Oriane Trouillard; Christel Depienne; Kristen Senechal; Michel Baulac; Eric LeGuern; Stéphanie Baulac
Arch Neurol 2007; 64: 217-222.
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