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Parkinson Disease/ Parkinsonian Disorders

Contributing journals to this collection:
JAMA & Archives Journals

Citations 121-130 of 407 total displayed.

Past content

Arch Neurol
Original Contributions
Factors Associated With the Development of Motor Fluctuations and Dyskinesias in Parkinson Disease
Robert A. Hauser; Michael P. McDermott; Susan Messing; for the Parkinson Study Group
Arch Neurol 2006; 63: 1756-1760. [Abstract] [Full text] [PDF]  

JAMA
Medical News & Perspectives
Researchers Tap Into the Male Brain
Tracy Hampton
JAMA 2006; 296: 2301-2302. [Extract] [Full text] [PDF]  

Arch Neurol
Original Contributions
Visual Hallucinations in Posterior Cortical Atrophy
Keith A. Josephs; Jennifer L. Whitwell; Bradley F. Boeve; David S. Knopman; David F. Tang-Wai; Daniel A. Drubach; Clifford R. Jack Jr; Ronald C. Petersen
Arch Neurol 2006; 63: 1427-1432. [Abstract] [Full text] [PDF]  

Arch Neurol
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]  

Arch Neurol
Correspondence
Benign Tremulous Parkinsonism?
Gage Van Horn; Mya C. Schiess
Arch Neurol 2006; 63: 1507. [Extract] [Full text] [PDF]  

Arch Neurol
Editorials
The Importance of LRRK2 Mutations in Parkinson Disease
Anthony H. V. Schapira
Arch Neurol 2006; 63: 1225-1228. [Extract] [Full text] [PDF]  

Arch Neurol
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]  

Arch Neurol
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]  

Arch Neurol
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]  

Arch Neurol
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]  

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