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PUBMED FOR HANDHELDS

Journal Abstract Search


161 related items for PubMed ID: 35470097

  • 21. 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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  • 24. Family studies of warts, hypogammaglobulinemia, immunodeficiency, myelokathexis syndrome.
    Dale DC, Dick E, Kelley M, Makaryan V, Connelly J, Bolyard AA.
    Curr Opin Hematol; 2020 Jan 28; 27(1):11-17. PubMed ID: 31652152
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  • 25. Sporadic case of warts, hypogammaglobulinemia, immunodeficiency, and myelokathexis syndrome.
    Tarzi MD, Jenner M, Hattotuwa K, Faruqi AZ, Diaz GA, Longhurst HJ.
    J Allergy Clin Immunol; 2005 Nov 28; 116(5):1101-5. PubMed ID: 16275383
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  • 28. Preference of Genetic Diagnosis of CXCR4 Mutation Compared with Clinical Diagnosis of WHIM Syndrome.
    Aghamohammadi A, Abolhassani H, Puchalka J, Greif-Kohistani N, Zoghi S, Klein C, Rezaei N.
    J Clin Immunol; 2017 Apr 28; 37(3):282-286. PubMed ID: 28353164
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  • 31. Plerixafor on a WHIM - Promise or Fantasy of a New CXCR4 Inhibitor for This Rare, but Important Syndrome?
    Merati N, Sivachandran S, Jfri A, Ben-Shoshan M, Vinh DC, Popradi G, Litvinov IV.
    Skin Therapy Lett; 2022 Mar 28; 27(2):1-5. PubMed ID: 35385630
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  • 33. Defect of plasmacytoid dendritic cells in warts, hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome patients.
    Tassone L, Moratto D, Vermi W, De Francesco M, Notarangelo LD, Porta F, Lougaris V, Facchetti F, Plebani A, Badolato R.
    Blood; 2010 Dec 02; 116(23):4870-3. PubMed ID: 20736454
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  • 35. Plerixafor for the Treatment of WHIM Syndrome.
    McDermott DH, Pastrana DV, Calvo KR, Pittaluga S, Velez D, Cho E, Liu Q, Trout HH, Neves JF, Gardner PJ, Bianchi DA, Blair EA, Landon EM, Silva SL, Buck CB, Murphy PM.
    N Engl J Med; 2019 Jan 10; 380(2):163-170. PubMed ID: 30625055
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  • 37. 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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  • 40. WHIM Syndrome With a Novel CXCR4 Variant in a Korean Child.
    Shin DW, Park SN, Kim SM, Im K, Kim JA, Hong KT, Choi JY, Hong CR, Park KD, Shin HY, Kang HJ, Kim HK, Lee DS.
    Ann Lab Med; 2017 Sep 01; 37(5):446-449. PubMed ID: 28643496
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