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Pontocerebellar atrophy is the hallmark neuroradiological finding in late-onset Tay-Sachs disease.
Májovská, Jitka; Hennig, Anita; Nestrasil, Igor; Schneider, Susanne A; Jahnová, Helena; Vanecková, Manuela; Magner, Martin; Dusek, Petr.
  • Májovská J; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
  • Hennig A; Department of Neurology, Ludwig-Maximilians University, Munich, Germany.
  • Nestrasil I; Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
  • Schneider SA; Department of Neurology, Ludwig-Maximilians University, Munich, Germany.
  • Jahnová H; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
  • Vanecková M; Department of Radiology, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
  • Magner M; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
  • Dusek P; Department of Pediatrics, University Thomayer Hospital and First Faculty of Medicine, Charles University, Prague, Czech Republic.
Neurol Sci ; 43(5): 3273-3281, 2022 May.
Article en En | MEDLINE | ID: mdl-34800199

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Tay-Sachs / Enfermedades Cerebelosas / Enfermedad de la Neurona Motora / Gangliosidosis GM2 Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Tay-Sachs / Enfermedades Cerebelosas / Enfermedad de la Neurona Motora / Gangliosidosis GM2 Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Humans Idioma: En Año: 2022 Tipo del documento: Article