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Genetic Disorders
Citations 231-240 of 396 total displayed.
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Past content
(since Jan 1998):
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- Original Contributions
Diffusion-Weighted Magnetic Resonance Imaging and Identification of the Epileptogenic Tuber in Patients With Tuberous Sclerosis
- Floor E. Jansen; Kees P. J. Braun; Onno van Nieuwenhuizen; Geertjan Huiskamp; Koen L. Vincken; Alexander C. van Huffelen; Jeroen van der Grond
Arch Neurol 2003; 60: 1580-1584.
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- Original Contributions
Migraine Headache in Patients With Tourette Syndrome
- Carolyn Kwak; Kevin Dat Vuong; Joseph Jankovic
Arch Neurol 2003; 60: 1595-1598.
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- Observations
A Korean Kindred With Autosomal Dominant Nocturnal Frontal Lobe Epilepsy and Mental Retardation
- Yong-Won Cho; Gholam K. Motamedi; Iris Laufenberg; Sung-Il Sohn; Jeong-Geun Lim; Hyung Lee; Sang-Doe Yi; Ju-Hwa Lee; Dae-Kwang Kim; Richard Reba; William D. Gaillard; William H. Theodore; Ronald P. Lesser; Ortrud K. Steinlein
Arch Neurol 2003; 60: 1625-1632.
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- Original Contributions
Risk Factors for Mild Cognitive Impairment in the Cardiovascular Health Study Cognition Study: Part 2
- Oscar L. Lopez; William J. Jagust; Corinne Dulberg; James T. Becker; Steven T. DeKosky; Annette Fitzpatrick; John Breitner; Constantine Lyketsos; Beverly Jones; Claudia Kawas; Michelle Carlson; Lewis H. Kuller
Arch Neurol 2003; 60: 1394-1399.
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- Original Contributions
Atypical Phenotypes in Patients With Facioscapulohumeral Muscular Dystrophy 4q35 Deletion
- Michael Krasnianski; Katharina Eger; Stephan Neudecker; Sibylle Jakubiczka; Stephan Zierz
Arch Neurol 2003; 60: 1421-1425.
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- Observations
Muscle Glycogenosis and Mitochondrial Hepatopathy in an Infant With Mutations in Both the Myophosphorylase and Deoxyguanosine Kinase Genes
- Michelangelo Mancuso; Massimiliano Filosto; Seiichi Tsujino; Costanza Lamperti; Sara Shanske; Michéle Coquet; Claude Desnuelle; Salvatore DiMauro
Arch Neurol 2003; 60: 1445-1447.
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- Basic Science Seminars in Neurology
Functional Genomics, Fragile X Syndrome, and RNA Interference
- Savitha Kalidas; Dean P. Smith
Arch Neurol 2003; 60: 1197-1200.
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- 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.
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- Original Contributions
Seizure Remission and Antiepileptic Drug Discontinuation in Children With Tuberous Sclerosis Complex
- Steven P. Sparagana; Mauricio R. Delgado; Lori L. Batchelor; E. Steve Roach
Arch Neurol 2003; 60: 1286-1289.
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- 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.
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