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Early-onset pathologically proven multiple system atrophy with LRRK2 G2019S mutation.
Riboldi, Giulietta Maria; Palma, Jose-Alberto; Cortes, Etty; Iida, Megan A; Sikder, Tamjeed; Henderson, Brooklyn; Raj, Towfique; Walker, Ruth H; Crary, John F; Kaufmann, Horacio; Frucht, Steven.
Afiliação
  • Riboldi GM; Fresco Institute for Parkinson's and Movement Disorders, Department of Neurology, New York University School of Medicine, New York, New York, USA.
  • Palma JA; Department of Neurology, Dysautonomia Center, New York University School of Medicine, New York, New York, USA.
  • Cortes E; Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Iida MA; Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Sikder T; Fishberg Department of Neuroscience, Friedman Brain Institute, Ronald M. Loeb Center for Alzheimer's Disease, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Henderson B; Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Raj T; Fishberg Department of Neuroscience, Friedman Brain Institute, Ronald M. Loeb Center for Alzheimer's Disease, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Walker RH; Fresco Institute for Parkinson's and Movement Disorders, Department of Neurology, New York University School of Medicine, New York, New York, USA.
  • Crary JF; Fishberg Department of Neuroscience, Friedman Brain Institute, Ronald M. Loeb Center for Alzheimer's Disease, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Kaufmann H; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Frucht S; James J. Peters Veterans Affairs Medical Center, Bronx, New York, USA.
Mov Disord ; 34(7): 1080-1082, 2019 07.
Article em En | MEDLINE | ID: mdl-31077434
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Idade de Início / Atrofia de Múltiplos Sistemas / Serina-Treonina Proteína Quinase-2 com Repetições Ricas em Leucina / Mutação Tipo de estudo: Diagnostic_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Idade de Início / Atrofia de Múltiplos Sistemas / Serina-Treonina Proteína Quinase-2 com Repetições Ricas em Leucina / Mutação Tipo de estudo: Diagnostic_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article