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Correspondence on "Expanded phenotype of AARS1-related white matter disease" by Helman et al.
Leidi, Alessia; Previtali, Roberto; Parazzini, Cecilia; Raviglione, Federico; Carelli, Stephana; Mendes, Marisa I; Salomons, Gajja S; Iascone, Maria; Tonduti, Davide.
Afiliação
  • Leidi A; Department of Biomedical and Clinical Sciences "L. Sacco", University of Milan, Milan, Italy.
  • Previtali R; Department of Biomedical and Clinical Sciences "L. Sacco", University of Milan, Milan, Italy.
  • Parazzini C; Pediatric Radiology and Neuroradiology Department, Vittore Buzzi Children's Hospital, Milan, Italy; COALA (Center for diagnosis and treatment of leukodystrophies), Vittore Buzzi Children's Hospital, Milan, Italy.
  • Raviglione F; Child Neuropsychiatry Unit, UONPIA ASST Rhodense, Milan, Italy.
  • Carelli S; Department of Biomedical and Clinical Sciences "L. Sacco", University of Milan, Milan, Italy; Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, University of Milan, Milan, Italy.
  • Mendes MI; Laboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Vrije Universiteit Amsterdam, University of Amsterdam, Amsterdam, The Netherlands.
  • Salomons GS; Laboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Vrije Universiteit Amsterdam, University of Amsterdam, Amsterdam, The Netherlands.
  • Iascone M; Molecular Genetics Section, Medical Genetics Laboratory, Papa Giovanni XXIII Hospital, Bergamo, Italy.
  • Tonduti D; COALA (Center for diagnosis and treatment of leukodystrophies), Vittore Buzzi Children's Hospital, Milan, Italy; Child Neurology Unit, Vittore Buzzi Children's Hospital, Milan, Italy. Electronic address: davide.tonduti@asst-fbf-sacco.it.
Genet Med ; 24(5): 1152-1153, 2022 05.
Article em En | MEDLINE | ID: mdl-35168888
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucoencefalopatias Limite: Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucoencefalopatias Limite: Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália