Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 561-570 of 623 total displayed.

Past content

Original Contributions
Hereditary Neuropathy With Liability to Pressure Palsies Is Not a Major Cause of Idiopathic Carpal Tunnel Syndrome

David W. Stockton; Ricardo A. Meade; David T. Netscher; Michael J. Epstein; Saleh M. Shenaq; Lisa G. Shaffer; James R. Lupski
Arch Neurol 2001; 58: 1635-1637. [Abstract] [Full text] [PDF]  

Original Contributions
Association of Moderate Polyglutamine Tract Expansions in the Slow Calcium-Activated Potassium Channel Type 3 With Ataxia

Karla Patricia Figueroa; Piu Chan; Ludger Schöls; Carline Tanner; Olaff Riess; Susan L. Perlman; Daniel H. Geschwind; Stefan M. Pulst
Arch Neurol 2001; 58: 1649-1653. [Abstract] [Full text] [PDF]  

Original Contributions
A Novel Mutation in the Notch3 Gene in an Italian Family With Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Genetic and Magnetic Resonance Spectroscopic Findings

Rosario L. Oliveri; Maria Muglia; Nicole De Stefano; Rosalucia Mazzei; Angelo Labate; Francesca L. Conforti; Allessandra Patitucci; Anna L. Gabriele; Giuseppe Tagarelli; Angela Magariello; Mario Zappia; Antonio Gambardella; Antonio Federico; Aldo Quattrone
Arch Neurol 2001; 58: 1418-1422. [Abstract] [Full text] [PDF]  

Original Contributions
The 5-HTTPR*S/*L Polymorphism and Aggressive Behavior in Alzheimer Disease

Danielle L. Sukonick; Bruce G. Pollock; Robert A. Sweet; Benoit H. Mulsant; Jules Rosen; William E. Klunk; Kari B. Kastango; Steven T. DeKosky; Robert E. Ferrell
Arch Neurol 2001; 58: 1425-1428. [Abstract] [Full text] [PDF]  

Original Contributions
Cognitive Deficits Associated With a Recently Reported Familial Neurodegenerative Disease: Familial Encephalopathy With Neuroserpin Inclusion Bodies

Charles B. Bradshaw; Richard L. Davis; Antony E. Shrimpton; Peter D. Holohan; Cornelia B. Rea; David Fieglin; Paul Kent; George H. Collins
Arch Neurol 2001; 58: 1429-1434. [Abstract] [Full text] [PDF]  

Editorials
What Is Kearns-Sayre Syndrome After All?

Tetsuo Ashizawa; S. H. Subramony
Arch Neurol 2001; 58: 1053-1054. [Extract] [Full text] [PDF]  

Original Contributions
Familial Advanced Sleep Phase Syndrome

Kathryn J. Reid; Anne-Marie Chang; Margarita L. Dubocovich; Fred W. Turek; Joseph S. Takahashi; Phyllis C. Zee
Arch Neurol 2001; 58: 1089-1094. [Abstract] [Full text] [PDF]  

Original Contributions
Frequency Analysis of Autosomal Dominant Cerebellar Ataxias in Taiwanese Patients and Clinical and Molecular Characterization of Spinocerebellar Ataxia Type 6

Bing-wen Soong; Yi-chun Lu; Kong-bung Choo; Hsiang-ying Lee
Arch Neurol 2001; 58: 1105-1109. [Abstract] [Full text] [PDF]  

Observations
A New Mitochondrial Point Mutation in the Transfer RNA^Leu Gene in a Patient With a Clinical Phenotype Resembling Kearns-Sayre Syndrome

Sara Seneca; Helene Verhelst; Linda De Meirleir; Françoise Meire; Chantal Ceuterick-De Groote; Willy Lissens; Rudy Van Coster
Arch Neurol 2001; 58: 1113-1118. [Abstract] [Full text] [PDF]  

Original Contributions
Autopsy-Confirmed Familial Early-Onset Alzheimer Disease Caused by the L153V Presenilin 1 Mutation

John C. Janssen; Peter L. Lantos; Nicholas C. Fox; Richard J. Harvey; Jonathan Beck; Andrew Dickinson; Tracey A. Campbell; John Collinge; Diane P. Hanger; Lisa Cipolotti; John M. Stevens; Martin N. Rossor
Arch Neurol 2001; 58: 953-958. [Abstract] [Full text] [PDF]  

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