Huntington disease in a Patient with Extensive Psychiatric History
Objective: Huntington's Disease (HD) is an autosomal dominant neurodegenerative disorder resulting from an expansion of CAG trinucleotide repeats in the gene encoding the huntingtin protein.…Global Genetic Ataxia Resource: An MDSGene Online Platform
Objective: To create a comprehensive global resource integrating epidemiological, phenotypic, and diagnostic data on genetic ataxias through an online platform. Background: Genetic ataxias exhibit variable…Breaking Away From the Ivory Tower
Objective: We describe the evolution of the Geriatric Flying Squad (GFS), a rapid response outreach team for residential aged care facilities (RACFs) in the local…A VUS and the Value of a Biomarker in Ataxia with Oculomotor Apraxia Type 2
Objective: Objective: To demonstrate the importance of serum biomarkers, such as alpha-fetoprotein (AFP), in the diagnostic evaluation of Ataxia with Oculomotor Apraxia Type 2 (AOA2).…Hyperemesis Gravidarum Induced Wernicke’s Encephalopathy: A Case Report
Objective: This report aims to bring awareness of Hyperemesis Gravidarum induced Wernicke’s Encephalopathy as a rare cause of ataxia. Background: Wernicke’s Encephalopathy is a neuropsychiatric…Specialized palliative care for advanced Parkinsonian syndromes: bridging the gap
Objective: The Advanced Care Team for Parkinson’s (ACT-PD) pilot program at the Calgary Movement Disorders Clinic aimed to bridge gaps in specialized palliative care for…Analysis of Emergency Department Encounters and Hospital Admissions of People with Huntington’s Disease
Objective: Define characteristics of emergency department encounters and hospital admissions of people with Huntington’s disease and identify opportunities for intervention to reduce hospitalizations. Background: Huntington’s…Peripheral neuropathy in Autosomal Recessive Spinocerebellar Ataxia due to ANO10 mutation – Expanding the phenotypic spectrum
Objective: SCAR10/ Adult-onset autosomal recessive cerebellar ataxia is an exceptionally rare form of ataxia, caused by mutations in the ANO10 gene and the specific genotype–phenotypecorrelation…Effectiveness, Safety, and Quality of Life Outcomes of Neurotoxin Injections in the Treatment of Essential Tremors: A Systematic Review
Objective: This systematic review aims to evaluate the outcomes of neurotoxins such as botulinum neurotoxin (BoNT) injections as a therapeutic intervention for essential tremors with…Hyperkinetic Movement Disorder associated with Papillary Thyroid Carcinoma
Objective: To describe a case of hyperkinetic movement disorder associated with papillary thyroid carcinoma, highlighting the diagnostic workup and therapeutic interventions. Background: Paraneoplastic neurological syndromes…
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