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Journal Abstract Search

556 related items for PubMed ID: 12692554

  • 21. WHIM syndrome: congenital immune deficiency disease.
    Kawai T, Malech HL.
    Curr Opin Hematol; 2009 Jan; 16(1):20-6. PubMed ID: 19057201
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  • 23. Stromal-derived factor-1 abolishes constitutive apoptosis of WHIM syndrome neutrophils harbouring a truncating CXCR4 mutation.
    Sanmun D, Garwicz D, Smith CI, Palmblad J, Fadeel B.
    Br J Haematol; 2006 Sep; 134(6):640-4. PubMed ID: 16899028
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  • 28. Live imaging of neutrophil motility in a zebrafish model of WHIM syndrome.
    Walters KB, Green JM, Surfus JC, Yoo SK, Huttenlocher A.
    Blood; 2010 Oct 14; 116(15):2803-11. PubMed ID: 20592249
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  • 29. The CXCR4 mutations in WHIM syndrome impair the stability of the T-cell immunologic synapse.
    Kallikourdis M, Trovato AE, Anselmi F, Sarukhan A, Roselli G, Tassone L, Badolato R, Viola A.
    Blood; 2013 Aug 01; 122(5):666-73. PubMed ID: 23794067
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  • 30. Genotype-phenotype correlations in WHIM syndrome: a systematic characterization of CXCR4WHIM variants.
    Zmajkovicova K, Pawar S, Maier-Munsa S, Maierhofer B, Wiest I, Skerlj R, Taveras AG, Badarau A.
    Genes Immun; 2022 Sep 01; 23(6):196-204. PubMed ID: 36089616
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  • 35. Successful umbilical cord blood stem cell transplantation in a child with WHIM syndrome.
    Kriván G, Erdos M, Kállay K, Benyó G, Tóth A, Sinkó J, Goda V, Tóth B, Maródi L.
    Eur J Haematol; 2010 Mar 01; 84(3):274-5. PubMed ID: 19878273
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  • 39. 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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