Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 261-270 of 623 total displayed.

Past content

Observations
T313M PINK1 Mutation in an Extended Highly Consanguineous Saudi Family With Early-Onset Parkinson Disease

Muhammad A. Chishti; Saeed Bohlega; Maqbool Ahmed; Arslan Loualich; Pamela Carroll; Christine Sato; Peter St George-Hyslop; David Westaway; Ekaterina Rogaeva
Arch Neurol 2006; 63: 1483-1485. [Abstract] [Full text] [PDF]  

Observations
POMGnT1 Mutations in Congenital Muscular Dystrophy: Genotype-Phenotype Correlation and Expanded Clinical Spectrum

Roberta Biancheri; Enrico Bertini; Antonio Falace; Marina Pedemonte; Andrea Rossi; Adele D’Amico; Sara Scapolan; Laura Bergamino; Stefania Petrini; Denise Cassandrini; Paolo Broda; Mario Manfredi; Federico Zara; Filippo M. Santorelli; Carlo Minetti; Claudio Bruno
Arch Neurol 2006; 63: 1491-1495. [Abstract] [Full text] [PDF]  

Editorials
The Importance of LRRK2 Mutations in Parkinson Disease

Anthony H. V. Schapira
Arch Neurol 2006; 63: 1225-1228. [Extract] [Full text] [PDF]  

Neurological Reviews
Genetic Testing in Parkinson Disease: Promises and Pitfalls

Eng-King Tan; Joseph Jankovic
Arch Neurol 2006; 63: 1232-1237. [Extract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Extract] [Full text] [PDF]  

Original Contributions
Clinical Spectrum of Mitochondrial DNA Depletion Due to Mutations in the Thymidine Kinase 2 Gene

Maryam Oskoui; Guido Davidzon; Juan Pascual; Ricardo Erazo; Juliana Gurgel-Giannetti; Sindu Krishna; Eduardo Bonilla; Darryl C. De Vivo; Sara Shanske; Salvatore DiMauro
Arch Neurol 2006; 63: 1122-1126. [Abstract] [Full text] [PDF]  

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