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Preference of Genetic Diagnosis of CXCR4 Mutation Compared with Clinical Diagnosis of WHIM Syndrome.
Aghamohammadi, Asghar; Abolhassani, Hassan; Puchalka, Jacek; Greif-Kohistani, Naschla; Zoghi, Samaneh; Klein, Christoph; Rezaei, Nima.
Afiliação
  • Aghamohammadi A; Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Science, 62 Qarib St., Keshavarz Blvd., Tehran, 14194, Iran.
  • Abolhassani H; Primary Immunodeficiency Diseases Network (PIDNet), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
  • Puchalka J; Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Science, 62 Qarib St., Keshavarz Blvd., Tehran, 14194, Iran.
  • Greif-Kohistani N; Division of Clinical Immunology, Department of Laboratory Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden.
  • Zoghi S; Primary Immunodeficiency Diseases Network (PIDNet), Universal Scientific Education and Research Network (USERN), Stockholm, Sweden.
  • Klein C; Department of Pediatrics, Dr. von Hauner Children's Hospital, Ludwig Maximilians University, Munich, Germany.
  • Rezaei N; Department of Pediatrics, Dr. von Hauner Children's Hospital, Ludwig Maximilians University, Munich, Germany.
J Clin Immunol ; 37(3): 282-286, 2017 04.
Article em En | MEDLINE | ID: mdl-28353164
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Verrugas / Receptores CXCR4 / Agamaglobulinemia / Patologia Molecular / Síndromes de Imunodeficiência / Mutação Tipo de estudo: Diagnostic_studies Aspecto: Patient_preference Limite: Child, preschool / Female / Humans / Male Idioma: En Revista: J Clin Immunol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Irã País de publicação: Holanda
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: Verrugas / Receptores CXCR4 / Agamaglobulinemia / Patologia Molecular / Síndromes de Imunodeficiência / Mutação Tipo de estudo: Diagnostic_studies Aspecto: Patient_preference Limite: Child, preschool / Female / Humans / Male Idioma: En Revista: J Clin Immunol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Irã País de publicação: Holanda