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Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype
(Assoc Arquivos Neuro- PsiquiatriaSao Paulo SpBrasil, 2011)
Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype
(Academia Brasileira de Neurologia - ABNEURO, 2011)
Huntington's disease (HD) is a neurodegenerative disorder characterized by chorea, behavioral disturbances and dementia, caused by a pathological expansion of the CAG trinucleotide in the HTT gene. Several patients have ...
Huntington`s Disease-Like 2 in Brazil-Report of 4 Patients
(WILEY-BLACKWELL, 2008)
Huntington`s disease-like 2 (HDL2) is a neurodegenerative disorder found in people of African ancestry with clinical, radiological, and neuropathological manifestations similar to Huntington`s disease (HD). HDL2 is caused ...
Swallowing endoscopy findings in Huntington's disease: A case report
(2016-01-01)
Huntington's disease (HD) is a degenerative genetic disorder with autosomal-dominant transmission. The triad of symptoms of this disease consists of psychiatric disorders, jerky movements, and dementia. Oropharyngeal ...
Inhibition of TRPC1-dependent store-operated calcium entry improves synaptic stability and motor performance in a mouse model of huntington's disease
(IOS Press, 2018)
Abstract: Huntington disease (HD) is a dominantly inherited neurodegenerative disorder caused by a CAG repeat expansion in the huntingtin gene. We previously discovered that mutant Huntingtin sensitizes type 1 inositol ...
Características clínicas y genético-moleculares de la enfermedad de Huntington en pacientes costarricenses: experiencia de 14 años de diagnóstico molecular
(2018-11-13)
Introducción: La enfermedad de Huntington (HD) es un trastorno neurodegenerativo hereditario, caracterizado por signos y síntomas motores, cognitivos y neuropsiquiátricos, causado por una expansión del trinucleótido ...
Neuromuscular synapse degeneration without muscle function loss in the diaphragm of a murine model for Huntington's Disease
(2018-06-01)
Huntington's disease (HD) is an autosomal dominant neurodegenerative disease characterized by chorea, incoordination and psychiatric and behavioral symptoms. The leading cause of death in HD patients is aspiration pneumonia, ...
Brain SPECT imaging in Huntington's disease before and after therapy with olanzapine - Case report
(Assoc Arquivos De Neuro- PsiquiatriaSao Paulo SpBrasil, 1999)
Beneficios de la terapia física en la enfermedad de Huntington
(2015)
La enfermedad de Huntington (EH) es
una patología neurodegenerativa progresiva,
que se manifesta en una triada de síntomas
de tipo motor, cognitivo y psiquiátrico,
para la cual no hay cura en la actualidad.
Se hereda ...