International audienceThe European Huntington's Disease Network (EHDN) commissioned an international task force to provide global evidence-based recommendations for everyday clinical practice for treatment of Huntington's disease (HD). The objectives of such guidelines are to standardize pharmacological, surgical and non-pharmacological treatment regimen and improve care and quality of life of patients. A formalized consensus method, adapted from the French Health Authority recommendations was used. First, national committees (French and English Experts) reviewed all studies published between 1965 and 2015 included dealing with HD symptoms classified in motor, cognitive, psychiatric, and somatic categories. Quality grades were attributed to...
Huntington's disease (HD) is an inherited neurodegenerative disease characterised by neuropsychiatri...
International audienceThe Unified Huntington's Disease Rating Scale (UHDRS) adequately measures decl...
Huntington’s Disease (HD) is an autosomal dominant condition that typically presents in midlife with...
International audienceThe European Huntington's Disease Network (EHDN) commissioned an international...
The European Huntington's Disease Network (EHDN) commissioned an international task force to provide...
International audienceOBJECTIVE: Evidence-based medicine is a difficult goal to achieve in rare dise...
The European Huntington's Disease Network (EHDN) commissioned an international task force to provide...
The European Huntington's Disease Network (EHDN) commissioned an international task force to provide...
OBJECTIVE: Evidence-based medicine is a difficult goal to achieve in rare diseases where randomized ...
Background: Physiotherapy may provide a means of delaying onset or progression of Huntington’s disea...
© 2021 International Parkinson and Movement Disorder SocietyBackground: Huntington's disease (HD) is...
BACKGROUND: Huntington's disease (HD) is a rare triplet repeat (CAG) disorder. Advanced, multi-c...
Background: Huntington?s disease is a complex neurodegenerative hereditary disease with symptoms in ...
Huntington's disease [HD] is a progressive neurodegenerative condition characterized by movement dis...
BACKGROUND Huntington's disease (HD) is a rare neurodegenerative disorder with protean clinical m...
Huntington's disease (HD) is an inherited neurodegenerative disease characterised by neuropsychiatri...
International audienceThe Unified Huntington's Disease Rating Scale (UHDRS) adequately measures decl...
Huntington’s Disease (HD) is an autosomal dominant condition that typically presents in midlife with...
International audienceThe European Huntington's Disease Network (EHDN) commissioned an international...
The European Huntington's Disease Network (EHDN) commissioned an international task force to provide...
International audienceOBJECTIVE: Evidence-based medicine is a difficult goal to achieve in rare dise...
The European Huntington's Disease Network (EHDN) commissioned an international task force to provide...
The European Huntington's Disease Network (EHDN) commissioned an international task force to provide...
OBJECTIVE: Evidence-based medicine is a difficult goal to achieve in rare diseases where randomized ...
Background: Physiotherapy may provide a means of delaying onset or progression of Huntington’s disea...
© 2021 International Parkinson and Movement Disorder SocietyBackground: Huntington's disease (HD) is...
BACKGROUND: Huntington's disease (HD) is a rare triplet repeat (CAG) disorder. Advanced, multi-c...
Background: Huntington?s disease is a complex neurodegenerative hereditary disease with symptoms in ...
Huntington's disease [HD] is a progressive neurodegenerative condition characterized by movement dis...
BACKGROUND Huntington's disease (HD) is a rare neurodegenerative disorder with protean clinical m...
Huntington's disease (HD) is an inherited neurodegenerative disease characterised by neuropsychiatri...
International audienceThe Unified Huntington's Disease Rating Scale (UHDRS) adequately measures decl...
Huntington’s Disease (HD) is an autosomal dominant condition that typically presents in midlife with...