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A single nucleotide polymorphism in the corticotropin receptor gene is associated with a blunted cortisol response during pediatric critical illness.
Jardine, David; Emond, Mary; Meert, Kathleen L; Harrison, Rick; Carcillo, Joseph A; Anand, Kanwaljeet J S; Berger, John; Newth, Christopher J L; Willson, Douglas F; Nicholson, Carol; Dean, J Michael; Zimmerman, Jerry J.
Afiliação
  • Jardine D; 1Department of Anesthesiology, University of Washington School of Medicine, Seattle, WA. 2Department of Biostatistics, University of Washington School of Medicine, Seattle, WA. 3Department of Pediatrics, Children's Hospital of Michigan, Detroit, MI. 4Department of Pediatrics, University of California at Los Angeles, Los Angeles, CA. 5Department of Critical Care Medicine, Children's Hospital of Pittsburgh, Pittsburgh, PA. 6Department of Pediatrics, Le Bonheur Children's Hospital and University of
Pediatr Crit Care Med ; 15(8): 698-705, 2014 Oct.
Article em En | MEDLINE | ID: mdl-25055195
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hidrocortisona / Estado Terminal / Polimorfismo de Nucleotídeo Único / Receptor Tipo 2 de Melanocortina Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2014 Tipo de documento: Article
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hidrocortisona / Estado Terminal / Polimorfismo de Nucleotídeo Único / Receptor Tipo 2 de Melanocortina Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2014 Tipo de documento: Article