Uremic Striatopallidal Syndrome Manifesting As Acute Onset Chorea
Objective: The relationship between movement disorders and renal diseases is complex and multifaceted. Movement disorders can occur as manifestations of azotemia (uremic encephalopathy, uremic striatopallidal…A Dance with Sydenham, it’s Never Too Late to Tango
Objective: Sydenham’s Chorea (SC) is a predominantly female childhood disorder characterized by irregular, fluid-like, involuntary movements. Here we present a case of isolated Sydenham’s chorea…Huntington-like disease type 2 caused by a JPH3 repeat expansion in a patient from Iraq
Objective: To report the case of a patient from Iraq with a Huntington disease-like phenotype who was found to have a heterozygous trinucleotide repeat expansion…Amyloid Pathology and its association with Cognitive Status in Huntington’s Disease
Objective: To investigate the presence of beta-amyloid pathology in Huntington's disease (HD) and its potential impact on patients' cognitive status. Background: Recent evidence indicates that…Machine Learning-Driven Exploration of Epigenetic Patterns in Huntington’s Disease: Understanding Histone Modification Dynamics
Objective: This study explores histone modifications, an underexplored aspect of HD's epigenetics, aiming to uncover markers influencing disease severity and onset for potential therapeutic targets.…Modifiable factors associated with Huntington’s disease progression in presymptomatic participants: explained longitudinal machine learning modelling
Objective: We aimed to identify, as early as the presymptomatic phase, the modifiable factors likely to influence the progression of Huntington's disease (HD), while identifying…Serum urea and clinical outcomes in Huntington’s disease
Objective: To investigate the relationship between serum urea levels and clinical outcomes in people with Huntington’s disease. Background: Several studies in people with Huntington’s disease…Muscle mass, body fat mass, and nutrition in patients with Huntington´s Disease
Objective: To assess skeletal muscle and fat mass, sarcopenia, and nutritional status in Huntington ́s Disease (HD) patients in different disease stages. Background: HD is…Asymmetric Symptomatic Huntington’s Disease in a Patient with Intermediate Range Trinucleotide Repeats
Objective: We report a case of probable symptomatic Huntington’s Disease (HD) in a patient with intermediate range trinucleotide repeats. Background: Huntington’s Disease is an autosomal…Post-stroke Movement Disorders: A Systematic Review of the Clinical Spectrum, Neuroanatomy, and Demographic Characteristics of 577 Published cases
Objective: To comprehensively examine the spectrum of post-stroke movement disorders (PSMDs), with a focus on understanding their prevalence, clinical characteristics, neuroanatomical correlates, and demographic profiles…
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