Your browser doesn't support javascript.
loading
Comprehensive Genetic Results for Primary Immunodeficiency Disorders in a Highly Consanguineous Population.
Al-Herz, Waleed; Chou, Janet; Delmonte, Ottavia Maria; Massaad, Michel J; Bainter, Wayne; Castagnoli, Riccardo; Klein, Christoph; Bryceson, Yenan T; Geha, Raif S; Notarangelo, Luigi D.
Afiliação
  • Al-Herz W; Department of Pediatrics, Faculty of Medicine, Kuwait University, Kuwait City, Kuwait.
  • Chou J; Allergy and Clinical Immunology Unit, Pediatric Department, Al-Sabah Hospital, Kuwait City, Kuwait.
  • Delmonte OM; Division of Immunology, Department of Pediatrics, Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Massaad MJ; Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
  • Bainter W; Department of Experimental Pathology, Immunology, and Microbiology, Pediatrics and Adolescent Medicine, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.
  • Castagnoli R; Division of Immunology, Department of Pediatrics, Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Klein C; Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
  • Bryceson YT; Department of Pediatrics, University of Pavia, Foundation IRCCS Policlinico San Matteo, Pavia, Italy.
  • Geha RS; Department of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, LMU, Munich, Germany.
  • Notarangelo LD; Department of Medicine, Centre for Hematology and Regenerative Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Front Immunol ; 9: 3146, 2018.
Article em En | MEDLINE | ID: mdl-30697212
Assuntos
Palavras-chave
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Consanguinidade / Predisposição Genética para Doença / Estudos de Associação Genética / Síndromes de Imunodeficiência Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Front Immunol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Kuait País de publicação: Suíça
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Consanguinidade / Predisposição Genética para Doença / Estudos de Associação Genética / Síndromes de Imunodeficiência Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Front Immunol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Kuait País de publicação: Suíça