Parkinson Disease/ Parkinsonian Disorders

Contributing journals to this collection:
JAMA & Archives Journals

Citations 1-10 of 350 total displayed.

Most recent content

Clinical Trials
Tesofensine (NS 2330), a Monoamine Reuptake Inhibitor, in Patients With Advanced Parkinson Disease and Motor Fluctuations: The ADVANS Study

Olivier Rascol; Werner Poewe; Andrew Lees; Marina Aristin; Laurence Salin; Nolwenn Juhel; Lisa Waldhauser; Thomas Schindler; for the ADVANS Study Group
Arch Neurol 2008; 65: 577-583. [Abstract] [Full text] [PDF]  

Original Contributions
Improvement in Parkinson Disease by Subthalamic Nucleus Stimulation Based on Electrode Placement: Effects of Reimplantation

Mathieu Anheim; Alina Batir; Valérie Fraix; Madjid Silem; Stéphan Chabardès; Eric Seigneuret; Paul Krack; Alim-Louis Benabid; Pierre Pollak
Arch Neurol 2008; 65: 612-616. [Abstract] [Full text] [PDF]  

Past content

Clinical Trials
Serum Urate as a Predictor of Clinical and Radiographic Progression in Parkinson Disease

Michael A. Schwarzschild; Steven R. Schwid; Kenneth Marek; Arthur Watts; Anthony E. Lang; David Oakes; Ira Shoulson; Alberto Ascherio; and the Parkinson Study Group PRECEPT Investigators
Arch Neurol 2008.65.6.nct70003. [Abstract] [Full text] [PDF]  

Editorials
How to Predict the Risk of Parkinson Disease in Relatives of Parkin Mutation Carriers: A Complex Puzzle of Age, Penetrance, and Number of Mutated Alleles

Christine Klein; Andreas Ziegler
Arch Neurol 2008; 65: 443-444. [Extract] [Full text] [PDF]  

Neurological Reviews
The Changing Face of Neural Stem Cell Therapy in Neurologic Diseases

Ofira Einstein; Tamir Ben-Hur
Arch Neurol 2008; 65: 452-456. [Abstract] [Full text] [PDF]  

Neurological Reviews
Refining Frontotemporal Dementia With Parkinsonism Linked to Chromosome 17: Introducing FTDP-17 (MAPT) and FTDP-17 (PGRN)

Bradley F. Boeve; Mike Hutton
Arch Neurol 2008; 65: 460-464. [Abstract] [Full text] [PDF]  

Original Contributions
Risk of Parkinson Disease in Carriers of Parkin Mutations: Estimation Using the Kin-Cohort Method

Yuanjia Wang; Lorraine N. Clark; Elan D. Louis; Helen Mejia-Santana; Juliette Harris; Lucien J. Cote; Cheryl Waters; Howard Andrews; Blair Ford; Steven Frucht; Stanley Fahn; Ruth Ottman; Daniel Rabinowitz; Karen Marder
Arch Neurol 2008; 65: 467-474. [Abstract] [Full text] [PDF]  

Original Contributions
Patients Homozygous and Heterozygous for SNCA Duplication in a Family With Parkinsonism and Dementia

Takeshi Ikeuchi; Akiyoshi Kakita; Atsushi Shiga; Kensaku Kasuga; Hiryoyuki Kaneko; Chun-Feng Tan; Jiro Idezuka; Koichi Wakabayashi; Osamu Onodera; Takeshi Iwatsubo; Masatoyo Nishizawa; Hitoshi Takahashi; Atsushi Ishikawa
Arch Neurol 2008; 65: 514-519. [Abstract] [Full text] [PDF]  

Original Contributions
Glucocerebrosidase Gene Mutations: A Risk Factor for Lewy Body Disorders

Ignacio F. Mata; Ali Samii; Seth H. Schneer; John W. Roberts; Alida Griffith; Berta C. Leis; Gerard D. Schellenberg; Ellen Sidransky; Thomas D. Bird; James B. Leverenz; Debby Tsuang; Cyrus P. Zabetian
Arch Neurol 2008; 65: 379-382. [Abstract] [Full text] [PDF]  

Neurological Reviews
Protein Misfolding and Neurodegeneration

Claudio Soto; Lisbell D. Estrada
Arch Neurol 2008; 65: 184-189. [Abstract] [Full text] [PDF]  

[Next page] Pages: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35