Related Experiment Videos
[Case of probable spino-pontine degeneration]
Neurologia I Neurochirurgia Polska
|September 1, 1984
Abstract:
The reported case illustrated the nosological difficulties in diseases grouped under the term hereditary ataxia.
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients.
Neurologia i neurochirurgia polska·2013
Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options.
European journal of neurology·2009
Charcot-Marie-Tooth disease type 4C4 caused by a novel Pro153Leu substitution in the GDAP1 gene.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology·2008
Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 gene.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology·2006
The triglyceride-glucose index in parkinsonian syndromes: a clinical dead end or a hint at central dysregulation?
Neurologia i neurochirurgia polska·2026
Montreal Cognitive Assessment performance in older adults with post-stroke delirium: global and subscale analysis.
Neurologia i neurochirurgia polska·2026
The significance of inflammation and biomarkers of neurodegeneration in essential tremor: a systematic review.
Neurologia i neurochirurgia polska·2026
Endovascular embolization of carotid-cavernous fistulas: a single-center analysis of safety, technical success, and long-term outcomes.
Neurologia i neurochirurgia polska·2026
Evaluation of the humoral response during ocrelizumab therapy in multiple sclerosis - an observational study.
Neurologia i neurochirurgia polska·2026