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…Correlation of the FXTAS Staging System and the FXTAS Rating Scale
Objective: To determine correlation between the Fragile X-associated tremor ataxia syndrome (FXTAS) staging system and the FXTAS rating scale Background: FXTAS is an X-linked, neurodegenerative…Community Awareness of Parkinson’s Disease as a Driver of Stigma in Kilifi, Kenya
Objective: To gain a holistic understanding of stigma surrounding Parkinson’s disease in Kenya from the perspective of those who are stigmatised, and those who might…Spinocerebellar Ataxia Type 7: First Report of Clinical and Molecular Findings of Two Family in Senegal – West Africa (Video Cases)
Objective: Describe the clinical and molecular findings in two families originating from Senegal. Background: Spinocerebellar ataxia type 7 is an inherited neurodegenerative disease caused by…AOA1 Versus AOA2 : A Comparative Study Of A Tunisian Cohort
Objective: The aim of our study is to compare the epidemiological, clinical, paraclinical and follow-up features of AOA1 and AOA2 in order to identify distinctive…Oculomotor Abnormalities in Spinocerebellar Ataxia Type-12: A Functional Neuroimaging Study
Objective: This study aimed to investigate eye movements, specifically dysmetric saccades and cerebellar nystagmus, in Spinocerebellar Ataxia Type-12 (SCA12) using functional magnetic resonance imaging (fMRI)…Physiotherapy for Dystonia in the UK: Current Practice, Patient Perspectives, and Future Directions
Objective: To determine the proportion of patients with dystonia accessing physiotherapy services in the United Kingdom, identify potential barriers to access, and gather patient perspectives…A Case Report of Two Affected Siblings with Spinocerebellar Ataxia Type 1
Objective: To present a case of two affected siblings with Spinocerebellar ataxia type 1 Background: Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant neurodegenerative…Developing an Electronic Medical Record-Based Dystonia Tracking Tool for use in a Pediatric Hospital Setting
Objective: To develop an electronic medical record (EMR) tool for documenting and tracking dystonia severity in pediatric inpatients. Our goal was to enable easy input…Progressive Ataxia in a Young Patient: Atypical Presentation of a Probable Creutzfeldt-Jakob Disease Variant VV1
Objective: To report an unusual presentation of probable Creutzfeldt-Jakob disease (CJD) subtype VV1 in a 27-year-old man. Background: CJD is a rare prion neurodegenerative disorder…
- « Previous Page
- 1
- …
- 117
- 118
- 119
- 120
- 121
- …
- 1734
- Next Page »