Melatonin for huntington disease (HD) gene carriers with HD-related sleep disturbance – a pilot study
Objective: To evaluate the efficacy of exogenous melatonin in improving sleep quality in Huntington disease (HD) gene carriers. Background: Various sleep disorders have been identified…The Quebec Parkinson Network (QPN): Interdisciplinary Collaboration in Parkinson’s Disease and Related Disorders Research.
Objective: By creating a participant registry, gathering information on participants, and ensuring appropriate data exchange with research groups, the QPN's primary goal is to increase…Improvements in Parkinson’s disease motor complications after treatment with opicapone: results from the OPTI-ON study
Objective: To describe motor complications as measured by the Movement Disorder Society-Unified Parkinson’s Disease Rating Scale (MDS-UPDRS) Part IV in participants from the Opicapone Treatment…Rapidly progressive dementia – catatonia – myoclonus in 80 years old patient: An unusual case
Objective: Objective:Sporadic Creutzfeldt-Jakob Disease (sCJD) will be challenging to differentiate from other diseases, like NMDA autoimmune encephalitis (AE). The classic rapidly progressive dementia phenotype that…A forgotten cause of ocular motor apraxia
Objective: To report an example of the rare association between acquired hepatocerebral degeneration (AHD) and ocular motor apraxia (OA), and discuss its relevance for topical…Implementation and effects of telehealth exercise therapy on satisfaction and Mobility In persons with Parkinson’s.
Objective: To improve PD care and motor performance using telehealth exercise therapy in individuals with PD. Background: Parkinson’s disease (PD) is a chronic disease with…Quantitative investigation of the pathway between dopamine receptors and Ca2+ channels in layer II stellate cells towards Parkinson’s disease
Objective: Recent experimental data suggest a putative coupling between dopamine D2 receptors (D2R) and T-type Ca2+ channels as another biophysical explanation for the firing pattern…dystonia caused by a rare variant of TUBB4A gene: a case report in a non-asian population
Objective: To describe the first case of a rare variant of the TUBB4A gene in a Brazilian individual Background: TUBB4A-related leukodystrophy presents with various clinical…Opsoclonus Myoclonus Syndrome due to subdural hematoma: an uncommon etiology
Objective: . Background: Introduction:Opsoclonus myoclonus syndrome is characterized by myoclonic jerks and ocular opsoclonus (spontaneous, arrhythmic, and conjugate ocular saccades that occur in all directions…Clinical correlates of olfactory dysfunction in Huntington’s disease
Objective: To assess olfactory dysfunction in patients with HD and correlate the degree of olfactory dysfunction with symptomatic domains of HD. Background: Olfactory dysfunction is…
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