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Early onset hereditary neuronopathies: an update on non-5q motor neuron diseases.
Zambon, Alberto A; Pini, Veronica; Bosco, Luca; Falzone, Yuri M; Munot, Pinki; Muntoni, Francesco; Previtali, Stefano C.
Afiliação
  • Zambon AA; Neuromuscular Repair Unit, Institute of Experimental Neurology (InSpe), Division of Neuroscience, IRCCS Ospedale San Raffaele, 20132 Milan, Italy.
  • Pini V; Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health and Great Ormond Street Hospital, London, WC1N 1EH, UK.
  • Bosco L; Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health and Great Ormond Street Hospital, London, WC1N 1EH, UK.
  • Falzone YM; Neuromuscular Repair Unit, Institute of Experimental Neurology (InSpe), Division of Neuroscience, IRCCS Ospedale San Raffaele, 20132 Milan, Italy.
  • Munot P; Neuromuscular Repair Unit, Institute of Experimental Neurology (InSpe), Division of Neuroscience, IRCCS Ospedale San Raffaele, 20132 Milan, Italy.
  • Muntoni F; NIHR Great Ormond Street Hospital Biomedical Research Centre, London, WC1N 1EH, UK.
  • Previtali SC; Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health and Great Ormond Street Hospital, London, WC1N 1EH, UK.
Brain ; 146(3): 806-822, 2023 03 01.
Article em En | MEDLINE | ID: mdl-36445400
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Doença de Charcot-Marie-Tooth Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Brain Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Doença de Charcot-Marie-Tooth Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Brain Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália