Huntington disease

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Hunt·ing·ton dis·ease

n. corea; enfermedad de Huntington, padecimiento nervioso que se manifiesta en movimientos abruptos coordinados aunque involuntarios de las extremidades y los músculos faciales;

pop. baile se San Vito.

English-Spanish Medical Dictionary © Farlex 2012

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References in periodicals archive ?

In a 2009 study, Subramaniam found that Rhes also alters the Huntington disease protein's structure making it more toxic to brain cells.

Here's why Huntington's disease attacks brain cells in human

Acute psychosis in a verified Huntington disease gene carrier with subtle motor signs: psychiatric criteria should be considered for the diagnosis.

The angry disciple

Reportedly, the results will be presented at an oral session on 16 September 2018 and as a poster titled 'LEGATO-HD Study: A phase 2 study assessing the efficacy and safety of laquinimod as a treatment for Huntington disease'.

Active Biotech to present data from the phase 2 LEGATO-HD study of laquinimod in Huntington's disease at EHDN plenary meeting 2018 in Vienna

Huntington disease (HD) is a progressive neurodegenerative disease that belongs to a unique group of autosomal-dominant disorders.

Evaluating the current state of the art of Huntington disease research: a scientometric analysis

"That's when the Huntington disease was suspected and the genetic testing was ordered," said Al Madani.

Dubai doctors diagnose rare brain disease

Global Markets Direct's, 'Huntington Disease - Pipeline Review, H1 2016', provides an overview of the Huntington Disease pipeline landscape.

Huntington Disease - Pipeline Review, H1 2016 - New Study Released

In conjunction with the Huntington Disease Society of America (HDSA) Los Angeles Chapter, they've chartered a boat to go whale watching, an uplifting and life affirming experience.

Whale Watching Gives Hope to Families Affected by Huntington's Disease

M2 PHARMA-August 13, 2015-Teva's NDA for SD-809 accepted by the US FDA for treating Huntington Disease

Teva's NDA for SD-809 accepted by the US FDA for treating Huntington Disease

Objective: The objective was to review the major differences of Huntington disease (HD) in Asian population from those in the Caucasian population.

Huntington Disease in Asia

Shirley's children wish to thank the Lowell Health Care Center in Lowell, MA for their dedicated long term care of Shirley and for their commitment to HD patients.The family asks that memorial contributions be made to the Huntington Disease Society of America (HDSA) through their secure web site or by mailing to: HDSA, 505 Eighth Avenue, Suite 902, NY, NY 10018.Relatives and friends are invited to visit with Shirley's family on Thursday, February 19, 2015 from 10:00-11:00 AM in the Britton-Wallace Funeral Home, 91 Central Street, Auburn.

Shirley Bohanan

A trial conducted at Massachusetts General Hospital has uncovered a benefit for creatine in delaying the symptoms of the inherited neurodegenerative disorder known as Huntington disease in asymptomatic adults.*