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Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHAD.
Barclay, Sarah F; Rand, Casey M; Gray, Paul A; Gibson, William T; Wilson, Richard J A; Berry-Kravis, Elizabeth M; Ize-Ludlow, Diego; Bech-Hansen, N Torben; Weese-Mayer, Debra E.
Afiliação
  • Barclay SF; Department of Medical Genetics, Cumming School of Medicine, Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada. Electronic address: sarah.barclay@ucalgary.ca.
  • Rand CM; Center for Autonomic Medicine in Pediatrics (CAMP) in Stanley Manne Children's Research Institute and in Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA. Electronic address: CRand@luriechildrens.org.
  • Gray PA; Department of Anatomy and Neurobiology, Washington University of Medicine, St. Louis, MO, USA. Electronic address: pgray@pcg.wustl.edu.
  • Gibson WT; Department of Medical Genetics, University of British Columbia and Child & Family Research Institute, Vancouver, BC, Canada. Electronic address: wtgibson@cfri.ubc.ca.
  • Wilson RJ; Department of Physiology and Pharmacology, Alberta Children's Hospital Research Institute and Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada. Electronic address: wilsonr@ucalgary.ca.
  • Berry-Kravis EM; Departments of Pediatrics, Neurological Sciences, and Biochemistry, Rush University Medical Center, Chicago, IL, USA. Electronic address: Elizabeth_Berry-Kravis@rush.edu.
  • Ize-Ludlow D; Department of Pediatrics, Division of Pediatric Endocrinology at University of Illinois at Chicago, Chicago, IL, USA. Electronic address: diegoize@uic.edu.
  • Bech-Hansen NT; Department of Medical Genetics, Cumming School of Medicine, Alberta Children's Hospital Research Institute, University of Calgary, Calgary, AB, Canada. Electronic address: ntbech@ucalgary.ca.
  • Weese-Mayer DE; Center for Autonomic Medicine in Pediatrics (CAMP) in Stanley Manne Children's Research Institute and in Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA; Northwestern University Feinberg School of Medicine, Chicago, IL, USA. Electronic address: D-
Respir Physiol Neurobiol ; 221: 59-63, 2016 Jan 15.
Article em En | MEDLINE | ID: mdl-26555080
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Hipoventilação por Obesidade / Doenças do Sistema Nervoso Autônomo / Receptores de Orexina / Orexinas / Doenças Hipotalâmicas / Mutação Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Hipoventilação por Obesidade / Doenças do Sistema Nervoso Autônomo / Receptores de Orexina / Orexinas / Doenças Hipotalâmicas / Mutação Idioma: En Ano de publicação: 2016 Tipo de documento: Article