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B cell repertoire in patients with a novel BTK mutation: expanding the spectrum of atypical X-linked agammaglobulinemia.
Toker, Ori; Broides, Arnon; Lev, Atar; Simon, Amos J; Megged, Orli; Shamriz, Oded; Tal, Yuval; Somech, Raz; Lee, Yu Nee; Nahum, Amit.
  • Toker O; Faculty of Medicine, The Allergy and Immunology Unit, Hebrew University of Jerusalem, Shaare Zedek Medical Center, 12 Bayit Street, 91031, Jerusalem, Israel. oritoker@gmail.com.
  • Broides A; Immunology Clinic, Soroka University Medical Center, Beer-Sheva, Israel.
  • Lev A; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
  • Simon AJ; Pediatric Department A and the Immunology Service, Sackler" Faculty of Medicine, Jeffrey Modell Foundation Center; "Edmond and Lily Safra" Children's Hospital, Sheba Medical Center, Tel Aviv University, Tel-Aviv, Israel.
  • Megged O; Pediatric Department A and the Immunology Service, Sackler" Faculty of Medicine, Jeffrey Modell Foundation Center; "Edmond and Lily Safra" Children's Hospital, Sheba Medical Center, Tel Aviv University, Tel-Aviv, Israel.
  • Shamriz O; Faculty of Medicine, The Pediatric Infectious Diseases Unit, Hebrew University of Jerusalem, Shaare Zedek Medical Center, Jerusalem, Israel.
  • Tal Y; The Lautenberg Center for Immunology and Cancer Research, Faculty of Medicine, Institute of Medical Research Israel-Canada, Hebrew University of Jerusalem, Jerusalem, Israel.
  • Somech R; Allergy and Clinical Immunology Unit, Department of Medicine, Faculty of Medicine, Hadassah Medical Organization, Hebrew University of Jerusalem, Jerusalem, Israel.
  • Lee YN; Allergy and Clinical Immunology Unit, Department of Medicine, Faculty of Medicine, Hadassah Medical Organization, Hebrew University of Jerusalem, Jerusalem, Israel.
  • Nahum A; Pediatric Department A and the Immunology Service, Sackler" Faculty of Medicine, Jeffrey Modell Foundation Center; "Edmond and Lily Safra" Children's Hospital, Sheba Medical Center, Tel Aviv University, Tel-Aviv, Israel.
Immunol Res ; 70(2): 216-223, 2022 04.
Article en En | MEDLINE | ID: mdl-35001352

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Agammaglobulinemia / Enfermedades Genéticas Ligadas al Cromosoma X Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Agammaglobulinemia / Enfermedades Genéticas Ligadas al Cromosoma X Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article