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Hereditary defect of cobalamin metabolism with adolescence onset resembling multiple sclerosis: 41-year follow up in two cases.
Motte, Jeremias; Kneiphof, Janina; Straßburger-Krogias, Katrin; Pitarokoili, Kalliopi; Fisse, Anna Lena; Kappos, Ludwig; Gold, Ralf.
Afiliação
  • Motte J; Department of Neurology, Ruhr-University Bochum, St Josef- Hospital, Gudrunstrasse 56, Bochum 44791, Germany.
  • Kneiphof J; Department of Neurology, Ruhr-University Bochum, Bochum, Germany.
  • Straßburger-Krogias K; Department of Neurology, Ruhr-University Bochum, Bochum, Germany.
  • Pitarokoili K; Department of Neurology, Ruhr-University Bochum, Bochum, Germany.
  • Fisse AL; Department of Neurology, Ruhr-University Bochum, Bochum, Germany.
  • Kappos L; Neurologic Clinic and Policlinic, University Hospital Basel, Basel, Switzerland.
  • Gold R; Department of Neurology, Ruhr-University Bochum, Bochum, Germany.
Ther Adv Neurol Disord ; 12: 1756286419872115, 2019.
Article em En | MEDLINE | ID: mdl-31489032
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article