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Immune-mediated myositis following gene therapy for Duchenne muscular dystrophy: a case report.
Iannaccone, Susan T; Cai, Chunyu; Rhem, Brittney; Batley, Kaitlin; Rajaram, Veena; Greenberg, Benjamin M; Dharia, Sachi; Zaidman, Craig M.
Afiliação
  • Iannaccone ST; Departments of Pediatrics and Neurology, University of Texas Southwestern Medical Center and Children's Health, Dallas, TX, USA. Susan.Iannaccone@UTSouthwestern.edu.
  • Cai C; Department of Pathology, University of Texas Southwestern Medical Center and Children's Health, Dallas, TX, USA. Chunyu.Cai@UTSouthwestern.edu.
  • Rhem B; Departments of Pediatrics and Neurology, University of Texas Southwestern Medical Center and Children's Health, Dallas, TX, USA.
  • Batley K; Departments of Pediatrics and Neurology, University of Texas Southwestern Medical Center and Children's Health, Dallas, TX, USA.
  • Rajaram V; Department of Pathology, University of Texas Southwestern Medical Center and Children's Health, Dallas, TX, USA.
  • Greenberg BM; Department of Neurology, University of Texas Southwestern Medical Center and Children's Health, Dallas, TX, USA.
  • Dharia S; Sarepta Therapeutics, Inc., Cambridge, MA, USA.
  • Zaidman CM; Department of Neurology, Washington University, St. Louis, MO, USA.
J Neurol ; 271(8): 5659-5664, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38907024
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terapia Genética / Distrofia Muscular de Duchenne / Miosite Idioma: En Ano de publicação: 2024 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terapia Genética / Distrofia Muscular de Duchenne / Miosite Idioma: En Ano de publicação: 2024 Tipo de documento: Article