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…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…Tremor in Multifocal Motor Neuropathy
Objective: Study of the effect of tremor on the quality of life of patients with multifocal motor neuropathy and its dynamics in response to therapy…Limb Myorhythmia in a Patient With Anti-LGI-1 Encephalitis
Objective: N/a Background: Myorhythmia is a hyperkinetic involuntary movement disorder characterized by slow rhythmic movements (1-4 Hz), typically affecting cranial and/or limb muscles. Recognizing the…Systemic Lupus Erythematosus presenting as Chorea
Objective: To study the clinical course, imaging, diagnosis and management of acute onset of generalized chorea with suspected Systemic lupus Erythematosus (SLE). Background: Neuropsychiatric symptoms…Chorea as the initial presentation of Erdheim-Chester disease
Objective: to describe clinical and radiological findings, and disease progression in a patient with Erdheim-Chester disease (ECD) initially presenting with chorea. Background: ECD is a…Retrospective series of adult-onset myoclonus presenting to an outpatient movement disorders clinic
Objective: To describe the phenomenology, etiology and treatment response in adults presenting to our clinic with myoclonus. Background: Myoclonus in the inpatient setting range often…A novel homozygous mutation in PANK2 gene mutation in a South- Asian male with typical PKAN
Objective: To study the clinical course, imaging and genetics in a case of early onset generalized dystonia with suspected Neurodegeneration with Brain Iron Accumulation (NBIA).…Biallelic Variants in ACER3 Encoding Alkaline Ceramidase 3 Cause Infantile- and Early-Childhood-Onset Neurodegeneration with Progressive Leukodystrophy
Objective: To delineate the clinical phenotype and molecular spectrum of alkaline ceramidase 3 -related disease (ACER3-RD) by characterizing 60 patients from 55 independent families. Background:…Atypical Onset and Presentation of Rare DYT30-VPS16 Dystonia
Objective: To provide a description of a young patient with atypical onset and presentation of rare DYT30-VPS16 dystonia. Background: To date, 44 patients from 31…
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