Works matching IS 02719142 AND DT 2013 AND VI 33 AND IP 7


Results: 15
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    Comparative Study of Subcutaneous Versus Intravenous IgG Replacement Therapy in Pediatric Patients with Primary Immunodeficiency Diseases: A Multicenter Study in Argentina.

    Published in:
    Journal of Clinical Immunology, 2013, v. 33, n. 7, p. 1216, doi. 10.1007/s10875-013-9916-z
    By:
    • Bezrodnik, Liliana;
    • Gómez Raccio, Andrea;
    • Belardinelli, Gabriela;
    • Regairaz, Lorena;
    • Díaz Ballve, Damacia;
    • Seminario, Gisela;
    • Moreira, Ileana;
    • Riganti, Carlos;
    • Cantisano, Claudio;
    • Díaz, Héctor;
    • Giovanni, Daniela
    Publication type:
    Article
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    The Natural History of Children with Severe Combined Immunodeficiency: Baseline Features of the First Fifty Patients of the Primary Immune Deficiency Treatment Consortium Prospective Study 6901.

    Published in:
    Journal of Clinical Immunology, 2013, v. 33, n. 7, p. 1156, doi. 10.1007/s10875-013-9917-y
    By:
    • Dvorak, Christopher;
    • Cowan, Morton;
    • Logan, Brent;
    • Notarangelo, Luigi;
    • Griffith, Linda;
    • Puck, Jennifer;
    • Kohn, Donald;
    • Shearer, William;
    • O'Reilly, Richard;
    • Fleisher, Thomas;
    • Pai, Sung-Yun;
    • Hanson, I.;
    • Pulsipher, Michael;
    • Fuleihan, Ramsay;
    • Filipovich, Alexandra;
    • Goldman, Frederick;
    • Kapoor, Neena;
    • Small, Trudy;
    • Smith, Angela;
    • Chan, Ka-Wah
    Publication type:
    Article
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    Erratum to: Molecular Diagnosis of Severe Combined Immunodeficiency-Identification of IL2RG, JAK3, IL7R, DCLRE1C, RAG1, and RAG2 Mutations in a Cohort of Chinese and Southeast Asian Children.

    Published in:
    2013
    By:
    • Lee, Pamela;
    • Chan, Koon-Wing;
    • Chen, Tong-Xin;
    • Jiang, Li-Ping;
    • Wang, Xiao-Chuan;
    • Zeng, Hua-Song;
    • Chen, Xiang-Yuan;
    • Liew, Woei-Kang;
    • Chen, Jing;
    • Chu, Kit-Man;
    • Chan, Lee-Lee;
    • Shek, Lynette;
    • Lee, Anselm;
    • Yu, Hsin-Hui;
    • Li, Qiang;
    • Xu, Chen-Guang;
    • Sultan-Ugdoracion, Geraldine;
    • Latiff, Zarina;
    • Latiff, Amir;
    • Jirapongsananuruk, Orathai
    Publication type:
    Correction Notice
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    Autosomal Dominant Anhidrotic Ectodermal Dysplasia with Immunodeficiency Caused by a Novel NFKBIA Mutation, p.Ser36Tyr, Presents with Mild Ectodermal Dysplasia and Non-Infectious Systemic Inflammation.

    Published in:
    Journal of Clinical Immunology, 2013, v. 33, n. 7, p. 1165, doi. 10.1007/s10875-013-9924-z
    By:
    • Yoshioka, Takakazu;
    • Nishikomori, Ryuta;
    • Hara, Junichi;
    • Okada, Keiko;
    • Hashii, Yoshiko;
    • Okafuji, Ikuo;
    • Nodomi, Seishiro;
    • Kawai, Tomoki;
    • Izawa, Kazushi;
    • Ohnishi, Hidenori;
    • Yasumi, Takahiro;
    • Nakahata, Tatsutoshi;
    • Heike, Toshio
    Publication type:
    Article
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    Combined De-Novo Mutation and Non-Random X-Chromosome Inactivation Causing Wiskott-Aldrich Syndrome in a Female with Thrombocytopenia.

    Published in:
    Journal of Clinical Immunology, 2013, v. 33, n. 7, p. 1150, doi. 10.1007/s10875-013-9927-9
    By:
    • Boonyawat, Boonchai;
    • Dhanraj, Santhosh;
    • Abbas, Fahad;
    • Zlateska, Bozana;
    • Grunenbaum, Eyal;
    • Roifman, Chaim;
    • Steele, Leslie;
    • Meyn, Stephen;
    • Blanchette, Victor;
    • Scherer, Stephen;
    • Swierczek, Sabina;
    • Prchal, Josef;
    • Zhu, Qili;
    • Torgerson, Troy;
    • Ochs, Hans;
    • Dror, Yigal
    Publication type:
    Article