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A cross-sectional analysis of clinical evaluation in 35 individuals with mutations of the valosin-containing protein gene.
Plewa, Jake; Surampalli, Abhilasha; Wencel, Marie; Milad, Merit; Donkervoort, Sandra; Caiozzo, Vincent J; Goyal, Namita; Mozaffar, Tahseen; Kimonis, Virginia.
Afiliação
  • Plewa J; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine Medical Center, 101 The City Drive South, ZC4482, Orange, CA 92868, United States.
  • Surampalli A; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine Medical Center, 101 The City Drive South, ZC4482, Orange, CA 92868, United States.
  • Wencel M; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine Medical Center, 101 The City Drive South, ZC4482, Orange, CA 92868, United States.
  • Milad M; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine Medical Center, 101 The City Drive South, ZC4482, Orange, CA 92868, United States.
  • Donkervoort S; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine Medical Center, 101 The City Drive South, ZC4482, Orange, CA 92868, United States; National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, United States
  • Caiozzo VJ; Department of Orthopedics and Physiology & Biophysics, University of California, Irvine, CA, United States.
  • Goyal N; ALS and Neuromuscular Center, Department of Neurology, University of California, Irvine, CA, United States.
  • Mozaffar T; ALS and Neuromuscular Center, Department of Neurology, University of California, Irvine, CA, United States.
  • Kimonis V; Division of Genetics and Genomic Medicine, Department of Pediatrics, University of California, Irvine Medical Center, 101 The City Drive South, ZC4482, Orange, CA 92868, United States. Electronic address: vkimonis@uci.edu.
Neuromuscul Disord ; 28(9): 778-786, 2018 09.
Article em En | MEDLINE | ID: mdl-30097247
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteíte Deformante / Miosite de Corpos de Inclusão / Distrofia Muscular do Cíngulo dos Membros / Demência Frontotemporal / Proteína com Valosina Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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XML
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Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteíte Deformante / Miosite de Corpos de Inclusão / Distrofia Muscular do Cíngulo dos Membros / Demência Frontotemporal / Proteína com Valosina Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos