Movement Disorders

Contributing journals to this collection:
JAMA & Archives Journals

Citations 91-100 of 535 total displayed.

Past content

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
Glucose Homeostasis in Huntington Disease: Abnormalities in Insulin Sensitivity and Early-Phase Insulin Secretion

Nebojsa M. Lalic; Jelena Maric; Marina Svetel; Aleksandra Jotic; Elka Stefanova; Katarina Lalic; Natasa Dragasevic; Tanja Milicic; Ljiljana Lukic; Vladimir S. Kostic
Arch Neurol 2008; 65: 476-480. [Abstract] [Full text] [PDF]  

Original Contributions
Rapid Eye Movement Sleep Disturbances in Huntington Disease

Isabelle Arnulf; Jørgen Nielsen; Ebba Lohmann; Johannes Schieffer; Edward Wild; Poul Jennum; Eric Konofal; Matthew Walker; Delphine Oudiette; Sarah Tabrizi; Alexandra Durr
Arch Neurol 2008; 65: 482-488. [Abstract] [Full text] [PDF] [ VIDEO SUPPLEMENT ]  

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]  

Original Contributions
Hereditary Spastic Paraplegia With Mental Impairment and Thin Corpus Callosum in Tunisia: SPG11, SPG15, and Further Genetic Heterogeneity

Amir Boukhris; Giovanni Stevanin; Imed Feki; Elodie Denis; Nizar Elleuch; Mohamed Imed Miladi; Jérémy Truchetto; Paola Denora; Samir Belal; Chokri Mhiri; Alexis Brice
Arch Neurol 2008; 65: 393-402. [Abstract] [Full text] [PDF]  

Original Articles
Longitudinal Progression of Movement Abnormalities in Relation to Psychotic Symptoms in Adolescents at High Risk of Schizophrenia

Vijay A. Mittal; Craig Neumann; Mary Saczawa; Elaine F. Walker
Arch Gen Psychiatry 2008; 65: 165-171. [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]  

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