These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 11148489)

  • 1. B-cell lymphoma in a patient with WHIM syndrome.
    Chae KM; Ertle JO; Tharp MD
    J Am Acad Dermatol; 2001 Jan; 44(1):124-8. PubMed ID: 11148489
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epstein-Barr virus-associated T-lymphoproliferative disease with hemophagocytic syndrome, followed by fatal intestinal B lymphoma in a young adult female with WHIM syndrome. Warts, hypogammaglobulinemia, infections, and myelokathexis.
    Imashuku S; Miyagawa A; Chiyonobu T; Ishida H; Yoshihara T; Teramura T; Kuriyama K; Imamura T; Hibi S; Morimoto A; Todo S
    Ann Hematol; 2002 Aug; 81(8):470-3. PubMed ID: 12224006
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 116(5):1101-5. PubMed ID: 16275383
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human papillomavirus typing of verrucae in a patient with WHIM syndrome.
    Palm MD; Tyring SK; Rady PL; Tharp MD
    Arch Dermatol; 2010 Aug; 146(8):931-2. PubMed ID: 20713842
    [No Abstract]   [Full Text] [Related]  

  • 5. Cutaneous B-cell lymphoma associated with hypogammaglobulinemia.
    Hisler BM
    Cutis; 1993 Apr; 51(4):273-5. PubMed ID: 8477609
    [TBL] [Abstract][Full Text] [Related]  

  • 6. WHIM syndrome, an autosomal dominant disorder: clinical, hematological, and molecular studies.
    Gorlin RJ; Gelb B; Diaz GA; Lofsness KG; Pittelkow MR; Fenyk JR
    Am J Med Genet; 2000 Apr; 91(5):368-76. PubMed ID: 10767001
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enhanced function with decreased internalization of carboxy-terminus truncated CXCR4 responsible for WHIM syndrome.
    Kawai T; Choi U; Whiting-Theobald NL; Linton GF; Brenner S; Sechler JM; Murphy PM; Malech HL
    Exp Hematol; 2005 Apr; 33(4):460-8. PubMed ID: 15781337
    [TBL] [Abstract][Full Text] [Related]  

  • 9. WHIM syndrome and oral squamous cell carcinoma.
    Cipriani NA; Blair E; Taxy JB
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2010 Jan; 109(1):105-8. PubMed ID: 19926501
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 34(1):70-4. PubMed ID: 12692554
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Primary cutaneous follicle center lymphoma in a patient with WHIM syndrome.
    Yoshii Y; Kato T; Ono K; Takahashi E; Fujimoto N; Kobayashi S; Kimura F; Nonoyama S; Satoh T
    J Eur Acad Dermatol Venereol; 2016 Mar; 30(3):529-30. PubMed ID: 25571909
    [No Abstract]   [Full Text] [Related]  

  • 12. 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; 56(6):419-25. PubMed ID: 19043667
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Picture in clinical hematology no. 40: Infant case of neutropenia due to WHIM syndrome(myelokathexis)].
    Ueda K; Nakagawa S; Osono S; Inada H
    Rinsho Ketsueki; 2009 Aug; 50(8):591. PubMed ID: 19915371
    [No Abstract]   [Full Text] [Related]  

  • 14. [WHIM syndrome: presumptive diagnosis based on myelokathexis on bone marrow smear].
    Bock I; Dugué F; Loppinet E; Bellanné-Chantelot C; Bénet B
    Ann Biol Clin (Paris); 2014; 72(1):111-9. PubMed ID: 24492099
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pancoast's syndrome in a patient with B-cell lymphoma diagnosed and confirmed with immunoglobulin gene rearrangement.
    Takahashi F; Ohwada A; Higashihara Y; Yoshioka Y; Uekusa T; Takahashi K; Dambara T; Fukuchi Y
    Respirology; 2004 Mar; 9(1):137-40. PubMed ID: 14982617
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Two cases of B cell lymphoma associated with hemophagocytic syndrome].
    Abe Y; Hara K; Shiratsuchi M; Choi I; Matsushima T; Minami R; Kihara T; Nishimura J; Nawata H; Muta K
    Rinsho Ketsueki; 2001 Jan; 42(1):35-40. PubMed ID: 11235132
    [TBL] [Abstract][Full Text] [Related]  

  • 17. How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome.
    Badolato R; Donadieu J;
    Blood; 2017 Dec; 130(23):2491-2498. PubMed ID: 29066537
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Primary cutaneous B-cell lymphoma, leg type restricted to the subcutaneous fat arising in a patient with dermatomyositis.
    Levy A; Randall MB; Henson T
    Am J Dermatopathol; 2008 Dec; 30(6):578-81. PubMed ID: 19033933
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Oligoclonality, impaired class switch and B-cell memory responses in WHIM syndrome.
    Mc Guire PJ; Cunningham-Rundles C; Ochs H; Diaz GA
    Clin Immunol; 2010 Jun; 135(3):412-21. PubMed ID: 20226738
    [TBL] [Abstract][Full Text] [Related]  

  • 20. WHIM syndrome: congenital immune deficiency disease.
    Kawai T; Malech HL
    Curr Opin Hematol; 2009 Jan; 16(1):20-6. PubMed ID: 19057201
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.