BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 19878273)

  • 1. 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; 84(3):274-5. PubMed ID: 19878273
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. CXCR4 mutations in WHIM syndrome: a misguided immune system?
    Diaz GA
    Immunol Rev; 2005 Feb; 203():235-43. PubMed ID: 15661033
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. The role of a mutation of the CXCR4 gene in WHIM syndrome.
    Taniuchi S; Masuda M; Fujii Y; Izawa K; Kanegane H; Kobayashi Y
    Haematologica; 2005 Sep; 90(9):1271-2. PubMed ID: 16154852
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Purine nucleoside phosphorylase deficiency (PNP-def) presenting with lymphopenia and developmental delay: successful correction with umbilical cord blood transplantation.
    Myers LA; Hershfield MS; Neale WT; Escolar M; Kurtzberg J
    J Pediatr; 2004 Nov; 145(5):710-2. PubMed ID: 15520787
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [WHIM syndrome].
    Erdos M; Maródi L
    Orv Hetil; 2007 Jun; 148(25):1173-9. PubMed ID: 17573253
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 37(3):282-286. PubMed ID: 28353164
    [No Abstract]   [Full Text] [Related]  

  • 11. 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; 37(5):446-449. PubMed ID: 28643496
    [No Abstract]   [Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. WHIM syndromes with different genetic anomalies are accounted for by impaired CXCR4 desensitization to CXCL12.
    Balabanian K; Lagane B; Pablos JL; Laurent L; Planchenault T; Verola O; Lebbe C; Kerob D; Dupuy A; Hermine O; Nicolas JF; Latger-Cannard V; Bensoussan D; Bordigoni P; Baleux F; Le Deist F; Virelizier JL; Arenzana-Seisdedos F; Bachelerie F
    Blood; 2005 Mar; 105(6):2449-57. PubMed ID: 15536153
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Combination of umbilical cord blood with BM from a 2-month-old sibling as lifesaving BMT for very severe aplastic anemia.
    Stepensky P; Revel-Vilk S; Weintraub M; Waldman E; Harit M; Averbuch D; Weinberger J; Or R; Resnick I
    Bone Marrow Transplant; 2008 Oct; 42(8):563-4. PubMed ID: 18660843
    [No Abstract]   [Full Text] [Related]  

  • 16. WHIM syndrome: Immunopathogenesis, treatment and cure strategies.
    McDermott DH; Murphy PM
    Immunol Rev; 2019 Jan; 287(1):91-102. PubMed ID: 30565238
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Successful umbilical cord blood stem cell transplantation in a patient with Rothmund-Thomson syndrome and combined immunodeficiency.
    Broom MA; Wang LL; Otta SK; Knutsen AP; Siegfried E; Batanian JR; Kelly ME; Shah M
    Clin Genet; 2006 Apr; 69(4):337-43. PubMed ID: 16630167
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Successful unrelated cord blood transplantation for a patient with CD40 ligand deficiency.
    Tsuji Y; Imai K; Morinishi Y; Kogawa K; Morino M; Nonoyama S
    Haematologica; 2007 Dec; 92(12):1727-8. PubMed ID: 18056008
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Enhancement of stem cell engraftment on a WHIM.
    Broxmeyer HE
    J Clin Invest; 2018 Aug; 128(8):3240-3242. PubMed ID: 29939159
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.