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Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature review.
Mari, Francesco; Berti, Beatrice; Romano, Alessandro; Baldacci, Jacopo; Rizzi, Riccardo; Grazia Alessandrì, M; Tessa, Alessandra; Procopio, Elena; Rubegni, Anna; Lourenco, Charles Marques; Simonati, Alessandro; Guerrini, Renzo; Santorelli, Filippo Maria.
Afiliação
  • Mari F; Pediatric Neurology Unit, Children's Hospital A. Meyer, University of Firenze, Viale Pieraccini 24, 50139, Florence, Italy.
  • Berti B; Pediatric Neurology Unit, Children's Hospital A. Meyer, University of Firenze, Viale Pieraccini 24, 50139, Florence, Italy.
  • Romano A; Neuropathology Unit, Institute of Experimental Neurology and Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Baldacci J; IRCCS Stella Maris, via dei Giacinti 2, 56128, Pisa, Calambrone, Italy.
  • Rizzi R; Pediatric Neurology Unit, Children's Hospital A. Meyer, University of Firenze, Viale Pieraccini 24, 50139, Florence, Italy.
  • Grazia Alessandrì M; IRCCS Stella Maris, via dei Giacinti 2, 56128, Pisa, Calambrone, Italy.
  • Tessa A; IRCCS Stella Maris, via dei Giacinti 2, 56128, Pisa, Calambrone, Italy.
  • Procopio E; Pediatric Neurology Unit, Children's Hospital A. Meyer, University of Firenze, Viale Pieraccini 24, 50139, Florence, Italy.
  • Rubegni A; IRCCS Stella Maris, via dei Giacinti 2, 56128, Pisa, Calambrone, Italy.
  • Lourenco CM; Neurogenetics Division, Clinics Hospital of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
  • Simonati A; Department of Neuroscience, Biomedicine and Movement, University of Verona, Verona, Italy.
  • Guerrini R; Pediatric Neurology Unit, Children's Hospital A. Meyer, University of Firenze, Viale Pieraccini 24, 50139, Florence, Italy. renzo.guerrini@unifi.it.
  • Santorelli FM; IRCCS Stella Maris, via dei Giacinti 2, 56128, Pisa, Calambrone, Italy. renzo.guerrini@unifi.it.
Neurogenetics ; 19(2): 123-130, 2018 05.
Article em En | MEDLINE | ID: mdl-29423566
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Oxigenases de Função Mista Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Oxigenases de Função Mista Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article