Genetics, Other

Contributing journals to this collection:
JAMA & Archives Journals

Citations 341-350 of 396 total displayed.

Past content

Editorials
Thoughts on the Relationship of the Human Genome Project to Neurology

Thomas D. Bird
Arch Neurol 2001; 58: 1764-1765. [Extract] [Full text] [PDF]  

Editorials
2025: The Practice of Neurology: Back From the Future

Allen D. Roses
Arch Neurol 2001; 58: 1766-1767. [Extract] [Full text] [PDF]  

Basic Science Seminars in Neurology
Sequence Analysis of the Human Genome: Implications for the Understanding of Nervous System Function and Disease

Anibal Cravchik; G. Subramanian; Samuel Broder; J. Craig Venter
Arch Neurol 2001; 58: 1772-1778. [Abstract] [Full text] [PDF]  

Special Topics
Genetics, the Facial Plastic and Reconstructive Surgeon, and the Future

Michael D. Seidman
Arch Facial Plast Surg 2001; 3: 227-229. [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
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]  

Contempo Updates
Influential Ideas and Experimental Progress in Schizophrenia Genetics Research

Alan R. Sanders; Pablo V. Gejman
JAMA 2001; 285: 2831-2833. [Extract] [Full text] [PDF]  

Original Contributions
Mutation Analysis and the Correlation Between Genotype and Phenotype of Arg778Leu Mutation in Chinese Patients With Wilson Disease

Zhi-Ying Wu; Ning Wang; Min-Ting Lin; Ling Fang; Shen-Xing Murong; Long Yu
Arch Neurol 2001; 58: 971-976. [Abstract] [Full text] [PDF]  

Original Contributions
Prevalence of C282Y and H63D Mutations in the Hemochromatosis (HFE) Gene in the United States

Karen K. Steinberg; Mary E. Cogswell; Joy C. Chang; Samuel P. Caudill; Geraldine M. McQuillan; Barbara A. Bowman; Laurence M. Grummer-Strawn; Eric J. Sampson; Muin J. Khoury; Margaret L. Gallagher
JAMA 2001; 285: 2216-2222. [Abstract] [Full text] [PDF]  

Original Contributions
Neurologic and Psychiatric Manifestations in a Family With a Mutation in Exon 2 of the Guanosine Triphosphate–Cyclohydrolase Gene

Heidi Hahn; Melissa R. Trant; Michael J. Brownstein; R. Andrew Harper; Sheldon Milstien; Ian J. Butler
Arch Neurol 2001; 58: 749-755. [Abstract] [Full text] [PDF]  

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