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Journal Abstract Search

238 related items for PubMed ID: 35947323

  • 1. Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients.
    Geier CB, Ellison M, Cruz R, Pawar S, Leiss-Piller A, Zmajkovicova K, McNulty SM, Yilmaz M, Evans MO, Gordon S, Ujhazi B, Wiest I, Abolhassani H, Aghamohammadi A, Barmettler S, Bhar S, Bondarenko A, Bolyard AA, Buchbinder D, Cada M, Cavieres M, Connelly JA, Dale DC, Deordieva E, Dorsey MJ, Drysdale SB, Ehl S, Elfeky R, Fioredda F, Firkin F, Förster-Waldl E, Geng B, Goda V, Gonzalez-Granado L, Grunebaum E, Grzesk E, Henrickson SE, Hilfanova A, Hiwatari M, Imai C, Ip W, Jyonouchi S, Kanegane H, Kawahara Y, Khojah AM, Kim VH, Kojić M, Kołtan S, Krivan G, Langguth D, Lau YL, Leung D, Miano M, Mersyanova I, Mousallem T, Muskat M, Naoum FA, Noronha SA, Ouederni M, Ozono S, Richmond GW, Sakovich I, Salzer U, Schuetz C, Seeborg FO, Sharapova SO, Sockel K, Volokha A, von Bonin M, Warnatz K, Wegehaupt O, Weinberg GA, Wong KJ, Worth A, Yu H, Zharankova Y, Zhao X, Devlin L, Badarau A, Csomos K, Keszei M, Pereira J, Taveras AG, Beaussant-Cohen SL, Ong MS, Shcherbina A, Walter JE.
    J Clin Immunol; 2022 Nov; 42(8):1748-1765. PubMed ID: 35947323
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  • 4. Long-Term Outcome of WHIM Syndrome in 18 Patients: High Risk of Lung Disease and HPV-Related Malignancies.
    Dotta L, Notarangelo LD, Moratto D, Kumar R, Porta F, Soresina A, Lougaris V, Plebani A, Smith CIE, Norlin AC, Gòmez Raccio AC, Bubanska E, Bertolini P, Amendola G, Visentini M, Fiorilli M, Venuti A, Badolato R.
    J Allergy Clin Immunol Pract; 2019 Nov; 7(5):1568-1577. PubMed ID: 30716504
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  • 5. Severe CD8+ T Lymphopenia in WHIM Syndrome Caused by Selective Sequestration in Primary Immune Organs.
    Majumdar S, Pontejo SM, Jaiswal H, Gao JL, Salancy A, Stassenko E, Yamane H, McDermott DH, Balabanian K, Bachelerie F, Murphy PM.
    J Immunol; 2023 Jun 15; 210(12):1913-1924. PubMed ID: 37133343
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  • 6. 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 15; 23(6):196-204. PubMed ID: 36089616
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  • 8. Familial occurrence of warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome.
    Siedlar M, Rudzki Z, Strach M, Trzyna E, Pituch-Noworolska A, Błaut-Szlósarczyk A, Bukowska-Strakova K, Lenart M, Grodzicki T, Zembala M.
    Arch Immunol Ther Exp (Warsz); 2008 Sep 15; 56(6):419-25. PubMed ID: 19043667
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  • 9. Recurrent CXCR4 sequence variation in a girl with WHIM syndrome.
    Alapi K, Erdos M, Kovács G, Maródi L.
    Eur J Haematol; 2007 Jan 15; 78(1):86-8. PubMed ID: 17087743
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  • 10. WHIM syndrome: congenital immune deficiency disease.
    Kawai T, Malech HL.
    Curr Opin Hematol; 2009 Jan 15; 16(1):20-6. PubMed ID: 19057201
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  • 11. Clinical and Hematologic Effects of Endotoxin in Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome Model Mice.
    Majumdar S, Gao JL, Pontejo SM, Balabanian K, Bachelerie F, Murphy PM.
    Immunohorizons; 2022 Jul 26; 6(7):543-558. PubMed ID: 35882421
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  • 12. Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: neuroimaging and clinical findings.
    Galli J, Pinelli L, Micheletti S, Palumbo G, Notarangelo LD, Lougaris V, Dotta L, Fazzi E, Badolato R.
    Orphanet J Rare Dis; 2019 Feb 28; 14(1):61. PubMed ID: 30819232
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  • 13. Multicenter Experience of Hematopoietic Stem Cell Transplantation in WHIM Syndrome.
    Laberko A, Deordieva E, Krivan G, Goda V, Bhar S, Kawahara Y, Rao K, Worth A, McDermott DH, Balashov D, Maschan A, Shcherbina A.
    J Clin Immunol; 2022 Jan 28; 42(1):171-182. PubMed ID: 34697698
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  • 14. 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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  • 16. How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome.
    Badolato R, Donadieu J, WHIM Research Group.
    Blood; 2017 Dec 07; 130(23):2491-2498. PubMed ID: 29066537
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  • 18. Genetics on a WHIM.
    Al Ustwani O, Kurzrock R, Wetzler M.
    Br J Haematol; 2014 Jan 07; 164(1):15-23. PubMed ID: 24111611
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  • 19. Periodontal disease in patients with WHIM syndrome.
    Brenchley L, McDermott DH, Gardner PJ, Silva LM, Gao JL, Cho E, Velez D, Moutsopoulos NM, Murphy PM, Fraser D.
    J Clin Periodontol; 2024 Apr 07; 51(4):464-473. PubMed ID: 38185798
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  • 20. 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 07; 161(4):763-5. PubMed ID: 22748845
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