✦ LIBER ✦

Sydenham's chorea: Clinical observations from a Brazilian movement disorder clinic

✍ Scribed by Vitor Tumas; Carla Tanuri Caldas; Antonio Carlos Santos; Auro Nobre; Regina Maria França Fernandes

Book ID: 116820294
Publisher: Elsevier Science
Year: 2007
Tongue: English
Weight: 477 KB
Volume: 13
Category: Article
ISSN: 1353-8020
DOI: 10.1016/j.parkreldis.2006.11.010

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

[Handbook of Clinical Neurology] Hyperki

[Handbook of Clinical Neurology] Hyperkinetic Movement Disorders Volume 100 || Sydenham's chorea

✍ Cardoso, Francisco 📂 Article 📅 2011 🏛 Elsevier 🌐 English ⚖ 524 KB

Poster 396 Sydenham Chorea in a Teenage

Poster 396 Sydenham Chorea in a Teenage Boy With a Debilitating and Complicated Clinical Course Due to Underlying Seizure Disorder: A Case Report

✍ Bradley Benson; Jane A. Emerson 📂 Article 📅 2011 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 54 KB

Neuroimaging in the Clinical Diagnosis o

Neuroimaging in the Clinical Diagnosis of Dementia: Observations from a Memory Disorders Clinic

✍ Paul R. Borghesani; Shaune M. DeMers; Vivek Manchanda; Sumit Pruthi; David H. Le 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 93 KB

1.309 Clinical and molecular studies of

1.309 Clinical and molecular studies of patients screened for Huntington's disease in a movement disorders clinic from Brazil

✍ G. Riccioppo; V. Tumas; W. Marques Jr.; B. Bader; A. Danek; C. Cazeneuve; A. Bri 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 171 KB

A 9-year review of dystonia from a movem

A 9-year review of dystonia from a movement disorders clinic in Singapore

✍ R. D. G. Jamora; A. K. Y. Tan; L. C. S. Tan 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 80 KB

Parkinson's disease and LRRK2: Frequency

Parkinson's disease and LRRK2: Frequency of a common mutation in U.S. movement disorder clinics

✍ Denise M. Kay; Cyrus P. Zabetian; Stewart A. Factor; John G. Nutt; Ali Samii; Al 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 67 KB 👁 1 views

## Abstract The G2019S mutation in the __LRRK2__ gene is reportedly a common cause of familial Parkinson's disease (PD) and may also have a significant role in nonfamilial PD. The objective of this study was to assess mutation carrier frequency in PD patients from movement disorder clinics in the U