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3-Methylglutaconic Aciduria Type I: A Rare Cause of Late-Onset Leukoencephalopathy.
Benzoni, Chiara; Magri, Stefania; Moscatelli, Marco; Fenu, Silvia; Caccia, Claudio; Taroni, Franco; Salsano, Ettore; Di Bella, Daniela.
Afiliação
  • Benzoni C; Unit of Rare Neurodegenerative and Neurometabolic Diseases (C.B., S.F., E.S.), Fondazione IRCCS Istituto Neurologico Carlo Besta; Unit of Medical Genetics and Neurogenetics (S.M., C.C., F.T., D.D.B.), Fondazione IRCCS Istituto Neurologico Carlo Besta; and Unit of Neuroradiology (M.M.), Fondazione IR
  • Magri S; Unit of Rare Neurodegenerative and Neurometabolic Diseases (C.B., S.F., E.S.), Fondazione IRCCS Istituto Neurologico Carlo Besta; Unit of Medical Genetics and Neurogenetics (S.M., C.C., F.T., D.D.B.), Fondazione IRCCS Istituto Neurologico Carlo Besta; and Unit of Neuroradiology (M.M.), Fondazione IR
  • Moscatelli M; Unit of Rare Neurodegenerative and Neurometabolic Diseases (C.B., S.F., E.S.), Fondazione IRCCS Istituto Neurologico Carlo Besta; Unit of Medical Genetics and Neurogenetics (S.M., C.C., F.T., D.D.B.), Fondazione IRCCS Istituto Neurologico Carlo Besta; and Unit of Neuroradiology (M.M.), Fondazione IR
  • Fenu S; Unit of Rare Neurodegenerative and Neurometabolic Diseases (C.B., S.F., E.S.), Fondazione IRCCS Istituto Neurologico Carlo Besta; Unit of Medical Genetics and Neurogenetics (S.M., C.C., F.T., D.D.B.), Fondazione IRCCS Istituto Neurologico Carlo Besta; and Unit of Neuroradiology (M.M.), Fondazione IR
  • Caccia C; Unit of Rare Neurodegenerative and Neurometabolic Diseases (C.B., S.F., E.S.), Fondazione IRCCS Istituto Neurologico Carlo Besta; Unit of Medical Genetics and Neurogenetics (S.M., C.C., F.T., D.D.B.), Fondazione IRCCS Istituto Neurologico Carlo Besta; and Unit of Neuroradiology (M.M.), Fondazione IR
  • Taroni F; Unit of Rare Neurodegenerative and Neurometabolic Diseases (C.B., S.F., E.S.), Fondazione IRCCS Istituto Neurologico Carlo Besta; Unit of Medical Genetics and Neurogenetics (S.M., C.C., F.T., D.D.B.), Fondazione IRCCS Istituto Neurologico Carlo Besta; and Unit of Neuroradiology (M.M.), Fondazione IR
  • Salsano E; Unit of Rare Neurodegenerative and Neurometabolic Diseases (C.B., S.F., E.S.), Fondazione IRCCS Istituto Neurologico Carlo Besta; Unit of Medical Genetics and Neurogenetics (S.M., C.C., F.T., D.D.B.), Fondazione IRCCS Istituto Neurologico Carlo Besta; and Unit of Neuroradiology (M.M.), Fondazione IR
  • Di Bella D; Unit of Rare Neurodegenerative and Neurometabolic Diseases (C.B., S.F., E.S.), Fondazione IRCCS Istituto Neurologico Carlo Besta; Unit of Medical Genetics and Neurogenetics (S.M., C.C., F.T., D.D.B.), Fondazione IRCCS Istituto Neurologico Carlo Besta; and Unit of Neuroradiology (M.M.), Fondazione IR
Neurol Genet ; 8(5): e200023, 2022 Oct.
Article em En | MEDLINE | ID: mdl-36092981
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article