|
Neurogenetics
Citations 401-410 of 574 total displayed.
|
Past content
(since May 1998):
|
- Basic Science Seminars in Neurology
Functional Genomics, Fragile X Syndrome, and RNA Interference
- Savitha Kalidas; Dean P. Smith
Arch Neurol 2003; 60: 1197-1200.
[Extract]
[Full text]
[PDF]
- Original Contributions
Total tau and Phosphorylated tau 181 Levels in the Cerebrospinal Fluid of Patients With Frontotemporal Dementia Due to P301L and G272V tau Mutations
- Sonia M. Rosso; Esther van Herpen; Yolande A. L. Pijnenburg; Niki S. M. Schoonenboom; Philip Scheltens; Peter Heutink; John C. van Swieten
Arch Neurol 2003; 60: 1209-1213.
[Abstract]
[Full text]
[PDF]
- Original Contributions
Coding Polymorphisms in the Parkin Gene and Susceptibility to Parkinson Disease
- Christoph-Burkhard Lücking; Véronique Chesneau; Ebba Lohmann; Patrice Verpillat; Cyprien Dulac; Anne-Marie Bonnet; Francesca Gasparini; Yves Agid; Alexandra Dürr; Alexis Brice
Arch Neurol 2003; 60: 1253-1256.
[Abstract]
[Full text]
[PDF]
- Corrections
Frequency Analysis and Clinical Characterization of Spinocerebellar Ataxia Types 1, 2, 3, 6, and 7 in Korean PatientsCorrection
-
Arch Neurol 2003; 60: 1256.
[Full text]
[PDF]
- Original Contributions
Frequency and Phenotypic Variability of the GAG Deletion of the DYT1 Gene in an Unselected Group of Patients With Dystonia
- Kathrin Grundmann; Ulrike Laubis-Herrmann; Ingrid Bauer; Dirk Dressler; Juliane Vollmer-Haase; Peter Bauer; Manfred Stuhrmann; Thorsten Schulte; Ludger Schöls; Helge Topka; Olaf Riess
Arch Neurol 2003; 60: 1266-1270.
[Abstract]
[Full text]
[PDF]
- Original Contributions
Clinical and Genetic Heterogeneity in Progressive External Ophthalmoplegia Due to Mutations in Polymerase
- Massimiliano Filosto; Michelangelo Mancuso; Yutaka Nishigaki; Jacklyn Pancrudo; Yadollah Harati; Clifton Gooch; Ami Mankodi; Lydia Bayne; Eduardo Bonilla; Sara Shanske; Michio Hirano; Salvatore DiMauro
Arch Neurol 2003; 60: 1279-1284.
[Abstract]
[Full text]
[PDF]
- Observations
Adult Alexander Disease With Autosomal Dominant Transmission: A Distinct Entity Caused by Mutation in the Glial Fibrillary Acid Protein Gene
- Erika Stumpf; Hélène Masson; Antoine Duquette; France Berthelet; Julia McNabb; Anne Lortie; Jacques Lesage; Jacques Montplaisir; Bernard Brais; Patrick Cossette
Arch Neurol 2003; 60: 1307-1312.
[Abstract]
[Full text]
[PDF]
- Observations
Somatic Instability of the NF2 Gene in Schwannomatosis
- David L. Kaufman; Bianca S. Heinrich; Christine Willett; Arie Perry; Frederick Finseth; Raymond A. Sobel; Mia MacCollin
Arch Neurol 2003; 60: 1317-1320.
[Abstract]
[Full text]
[PDF]
- Observations
The Second Kindred With Autosomal Dominant Distal Myopathy Linked to Chromosome 14q: Genetic and Clinical Analysis
- Peter Hedera; Elizabeth M. Petty; Melanie R. Bui; Mila Blaivas; John K. Fink
Arch Neurol 2003; 60: 1321-1325.
[Abstract]
[Full text]
[PDF]
- Neurological Reviews
The Hereditary Spastic Paraplegias: Nine Genes and Counting
- John K. Fink
Arch Neurol 2003; 60: 1045-1049.
[Abstract]
[Full text]
[PDF]
|
|