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Genetic Disorders
Citations 151-160 of 396 total displayed.
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Past content
(since Jan 1998):
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- Original Contributions
Clinical Heterogeneity of the LRRK2 G2019S Mutation
- Spiridon Papapetropoulos; Carlos Singer; Owen A. Ross; Mathias Toft; Joseph L. Johnson; Matthew J. Farrer; Deborah C. Mash
Arch Neurol 2006; 63: 1242-1246.
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- Original Contributions
Clinical Features of Parkinson Disease Patients With Homozygous Leucine-Rich Repeat Kinase 2 G2019S Mutations
- Lianna Ishihara; Liling Warren; Rachel Gibson; Rim Amouri; Suzanne Lesage; Alexandra Dürr; Meriem Tazir; Zbigniew K. Wszolek; Ryan J. Uitti; William C. Nichols; Alida Griffith; Nobutaka Hattori; David Leppert; Ray Watts; Cyrus P. Zabetian; Tatiana M. Foroud; Matthew J. Farrer; Alexis Brice; Lefkos Middleton; Faycal Hentati
Arch Neurol 2006; 63: 1250-1254.
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- Original Contributions
Juvenile-Onset Parkinsonism as a Result of the First Mutation in the Adenosine Triphosphate Orientation Domain of PINK1
- Anne-Louise Leutenegger; Mustafa A. M. Salih; Pablo Ibáñez; Maowia M. Mukhtar; Suzanne Lesage; Ali Arabi; Ebba Lohmann; Alexandra Dürr; Ammar E. M. Ahmed; Alexis Brice
Arch Neurol 2006; 63: 1257-1261.
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- Original Contributions
Early-Onset Alzheimer Disease in Families With Late-Onset Alzheimer Disease: A Potential Important Subtype of Familial Alzheimer Disease
- Kiri L. Brickell; Ellen J. Steinbart; Malia Rumbaugh; Haydeh Payami; Gerard D. Schellenberg; Vivianna Van Deerlin; Wuxing Yuan; Thomas D. Bird
Arch Neurol 2006; 63: 1307-1311.
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- Correspondence
LRRK2 Gene and Tremor-Dominant Parkinsonism
- Kristoffer Haugarvoll; Ryan J. Uitti; Matthew J. Farrer; Zbigniew K. Wszolek
Arch Neurol 2006; 63: 1346-a-1347-a.
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- Original Contributions
Fragile X Premutation With Atypical Symptoms at Onset
- Elena Cellini; Paolo Forleo; Andrea Ginestroni; Benedetta Nacmias; Andrea Tedde; Silvia Bagnoli; Mario Mascalchi; Sandro Sorbi; Silvia Piacentini
Arch Neurol 2006; 63: 1135-1138.
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- Original Contributions
Age and Apolipoprotein E*4 Allele Effects on Cerebrospinal Fluid  -Amyloid 42 in Adults With Normal Cognition
- Elaine R. Peskind; Ge Li; Jane Shofer; Joseph F. Quinn; Jeffrey A. Kaye; Chris M. Clark; Martin R. Farlow; Charles DeCarli; Murray A. Raskind; Gerard D. Schellenberg; Virginia M.-Y. Lee; Douglas R. Galasko
Arch Neurol 2006; 63: 936-939.
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- Original Contributions
At Risk for Huntington Disease: The PHAROS (Prospective Huntington At Risk Observational Study) Cohort Enrolled
- The Huntington Study Group PHAROS Investigators
Arch Neurol 2006; 63: 991-996.
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- Original Contributions
Type 1 Diabetes and Multiple Sclerosis: A Danish Population-Based Cohort Study
- Nete M. Nielsen; Tine Westergaard; Morten Frisch; Klaus Rostgaard; Jan Wohlfahrt; Nils Koch-Henriksen; Mads Melbye; Henrik Hjalgrim
Arch Neurol 2006; 63: 1001-1004.
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- Observations
Childhood Onset in Familial Prion Disease With a Novel Mutation in the PRNP Gene
- Ekaterina Rogaeva; Cindy Zadikoff; Jonathan Ponesse; Gerold Schmitt-Ulms; Toshitaka Kawarai; Christine Sato; Shabnam Salehi-Rad; Peter St. George-Hyslop; Anthony E. Lang
Arch Neurol 2006; 63: 1016-1021.
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