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A diagnosis of progressive myoclonic ataxia guided by blood biomarkers.
Dubot, Patricia; Rafiq, Marie; Curot, Jonathan; Simonetta-Moreau, Marion; Sabourdy, Frédérique; Pettazzoni, Magali; Froissart, Roseline; Levade, Thierry; Ory-Magne, Fabienne.
Afiliación
  • Dubot P; Metabolic Biochemistry Laboratory, Reference Center for Hereditary Metabolic Disorders, Biology Institute, Toulouse University Hospital, Toulouse, France; Toulouse Cancer Research Center, INSERM-University of Toulouse Paul Sabatier, Toulouse, France.
  • Rafiq M; Neuroscience Center, Toulouse University Hospital, Toulouse, France.
  • Curot J; Neuroscience Center, Toulouse University Hospital, Toulouse, France; Brain and Cognition Research Center (CerCo), CNRS-University of Toulouse Paul Sabatier, Toulouse, France.
  • Simonetta-Moreau M; Neuroscience Center, Toulouse University Hospital, Toulouse, France; Toulouse NeuroImaging Center (ToNIC), INSERM-University of Toulouse Paul Sabatier, Toulouse, France.
  • Sabourdy F; Metabolic Biochemistry Laboratory, Reference Center for Hereditary Metabolic Disorders, Biology Institute, Toulouse University Hospital, Toulouse, France; Toulouse Cancer Research Center, INSERM-University of Toulouse Paul Sabatier, Toulouse, France.
  • Pettazzoni M; Biochemistry Laboratory, Lyon Hospitals, Bron, France.
  • Froissart R; Biochemistry Laboratory, Lyon Hospitals, Bron, France.
  • Levade T; Metabolic Biochemistry Laboratory, Reference Center for Hereditary Metabolic Disorders, Biology Institute, Toulouse University Hospital, Toulouse, France; Toulouse Cancer Research Center, INSERM-University of Toulouse Paul Sabatier, Toulouse, France. Electronic address: thierry.levade@inserm.fr.
  • Ory-Magne F; Neuroscience Center, Toulouse University Hospital, Toulouse, France; Toulouse NeuroImaging Center (ToNIC), INSERM-University of Toulouse Paul Sabatier, Toulouse, France. Electronic address: ory.f@chu-toulouse.fr.
Parkinsonism Relat Disord ; 94: 124-126, 2022 01.
Article en En | MEDLINE | ID: mdl-34275752
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Degeneraciones Espinocerebelosas / Epilepsias Mioclónicas / Epilepsias Mioclónicas Progresivas Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Francia
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Degeneraciones Espinocerebelosas / Epilepsias Mioclónicas / Epilepsias Mioclónicas Progresivas Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Francia