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Journal Abstract Search

161 related items for PubMed ID: 35470097

  • 1. A Sherlock Approach to a Kindred With a Variable Immunohematologic Phenotype.
    Walkovich K, Grunebaum E.
    J Allergy Clin Immunol Pract; 2022 Jul; 10(7):1714-1722. PubMed ID: 35470097
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  • 3. Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome.
    Dotta L, Tassone L, Badolato R.
    Curr Mol Med; 2011 Jun; 11(4):317-25. PubMed ID: 21506920
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  • 7. Recurrent CXCR4 sequence variation in a girl with WHIM syndrome.
    Alapi K, Erdos M, Kovács G, Maródi L.
    Eur J Haematol; 2007 Jan; 78(1):86-8. PubMed ID: 17087743
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  • 8. Tetralogy of fallot is an uncommon manifestation of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome.
    Badolato R, Dotta L, Tassone L, Amendola G, Porta F, Locatelli F, Notarangelo LD, Bertrand Y, Bachelerie F, Donadieu J.
    J Pediatr; 2012 Oct; 161(4):763-5. PubMed ID: 22748845
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  • 16. WHIM syndrome myelokathexis reproduced in the NOD/SCID mouse xenotransplant model engrafted with healthy human stem cells transduced with C-terminus-truncated CXCR4.
    Kawai T, Choi U, Cardwell L, DeRavin SS, Naumann N, Whiting-Theobald NL, Linton GF, Moon J, Murphy PM, Malech HL.
    Blood; 2007 Jan 01; 109(1):78-84. PubMed ID: 16946301
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  • 17. Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry.
    Beaussant Cohen S, Fenneteau O, Plouvier E, Rohrlich PS, Daltroff G, Plantier I, Dupuy A, Kerob D, Beaupain B, Bordigoni P, Fouyssac F, Delezoide AL, Devouassoux G, Nicolas JF, Bensaid P, Bertrand Y, Balabanian K, Chantelot CB, Bachelerie F, Donadieu J.
    Orphanet J Rare Dis; 2012 Sep 25; 7():71. PubMed ID: 23009155
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  • 18. WHIM syndrome: Immunopathogenesis, treatment and cure strategies.
    McDermott DH, Murphy PM.
    Immunol Rev; 2019 Jan 25; 287(1):91-102. PubMed ID: 30565238
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  • 20. Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease.
    Hernandez PA, Gorlin RJ, Lukens JN, Taniuchi S, Bohinjec J, Francois F, Klotman ME, Diaz GA.
    Nat Genet; 2003 May 25; 34(1):70-4. PubMed ID: 12692554
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