BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

82 related articles for article (PubMed ID: 22679904)

  • 1. Molecular basis of Wiskott-Aldrich syndrome in patients from India.
    David S; Jayandharan GR; Abraham A; Jacob RR; Devi GS; Patkar N; Shaji RV; Nair SC; Viswabandya A; Ahmed R; George B; Mathews V; Chandy M; Srivastava A
    Eur J Haematol; 2012 Oct; 89(4):356-60. PubMed ID: 22679904
    [No Abstract]   [Full Text] [Related]  

  • 2. Wiskott-Aldrich syndrome.
    Notarangelo LD; Miao CH; Ochs HD
    Curr Opin Hematol; 2008 Jan; 15(1):30-6. PubMed ID: 18043243
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Wiskott-Aldrich syndrome. 2 familial cases].
    Guignard J
    Maroc Med; 1971 Nov; 51(551):646-50. PubMed ID: 5142396
    [No Abstract]   [Full Text] [Related]  

  • 4. The genotype of the original Wiskott phenotype.
    Binder V; Albert MH; Kabus M; Bertone M; Meindl A; Belohradsky BH
    N Engl J Med; 2006 Oct; 355(17):1790-3. PubMed ID: 17065640
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Second-site mutation in the Wiskott-Aldrich syndrome (WAS) protein gene causes somatic mosaicism in two WAS siblings.
    Wada T; Konno A; Schurman SH; Garabedian EK; Anderson SM; Kirby M; Nelson DL; Candotti F
    J Clin Invest; 2003 May; 111(9):1389-97. PubMed ID: 12727931
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recurrent V75M mutation within the Wiskott-Aldrich syndrome protein: description of a homozygous female patient.
    Proust A; Guillet B; Pellier I; Rachieru P; Hoarau C; Claeyssens S; Léonard C; Charrier S; Vainchenker W; Tchernia G; Delaunay J
    Eur J Haematol; 2005 Jul; 75(1):54-9. PubMed ID: 15946311
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Abnormalities of chemotactic lymphokine synthesis and mononuclear leukocyte chemotaxis in Wiskott-Aldrich syndrome.
    Altman LC; Snyderman R; Blaese RM
    J Clin Invest; 1974 Aug; 54(2):486-93. PubMed ID: 4136226
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Familial case of Wiskott-Aldrich syndrome].
    Ozhegov AM; Miakisheva LS
    Pediatriia; 1979 Aug; (8):66-8. PubMed ID: 482005
    [No Abstract]   [Full Text] [Related]  

  • 9. [Wiskott-Aldrich syndrome. Three cases in one family].
    Javier G; Tusell J; Compte J; Saenz A; Ortega JJ
    Nouv Rev Fr Hematol Blood Cells; 1977; 18(1):182-4. PubMed ID: 896438
    [No Abstract]   [Full Text] [Related]  

  • 10. Wiskott Aldrich syndrome in an Israeli family: identification of a novel G40V mutation.
    Rottem M; Alon-Shalev S; Shneor Y; Hujeirat Y
    Hum Mutat; 2000 Nov; 16(5):448. PubMed ID: 11058913
    [No Abstract]   [Full Text] [Related]  

  • 11. Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndrome.
    Gulácsy V; Freiberger T; Shcherbina A; Pac M; Chernyshova L; Avcin T; Kondratenko I; Kostyuchenko L; Prokofjeva T; Pasic S; Bernatowska E; Kutukculer N; Rascon J; Iagaru N; Mazza C; Tóth B; Erdos M; van der Burg M; Maródi L;
    Mol Immunol; 2011 Feb; 48(5):788-92. PubMed ID: 21185603
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia.
    Andreu N; Matamoros N; Escudero A; Fillat C
    Int J Mol Med; 2007 May; 19(5):777-82. PubMed ID: 17390083
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4.
    Doğu F; Ariga T; Ikincioğullari A; Bozdoğan G; Aytekin C; Metin A; Babacan E
    Turk J Pediatr; 2006; 48(1):66-8. PubMed ID: 16562789
    [TBL] [Abstract][Full Text] [Related]  

  • 14. IgA glomerulonephritis in Wiskott-Aldrich syndrome.
    DeSanto NG; Sessa A; Capodicasa G; Meroni M; Capasso G; Esposito L; Ferrara M; Torri Tarelli L; Annunziata S; Giordano C
    Child Nephrol Urol; 1988-1989; 9(1-2):118-20. PubMed ID: 3251617
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of WASP mutations in 10 Australian families with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
    Bourne HC; Weston S; Prasad M; Edkins E; Benson EM
    Pathology; 2004 Jun; 36(3):262-4. PubMed ID: 15203732
    [TBL] [Abstract][Full Text] [Related]  

  • 16. IVS6+5G>A found in Wiskott-Aldrich syndrome and X-linked thrombocytopenia in a Korean family.
    Yoon SH; Cho T; Kim HJ; Kim SY; Ko JH; Baek HS; Lee HJ; Lee CH
    Pediatr Blood Cancer; 2012 Feb; 58(2):297-9. PubMed ID: 22038941
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [The Wiskott-Aldrich syndrome].
    Belohradsky BH; Griscelli C; Fundenberg HH; Marget W
    Ergeb Inn Med Kinderheilkd; 1978; 41():85-184. PubMed ID: 361383
    [No Abstract]   [Full Text] [Related]  

  • 18. X-linked Wiskott-Aldrich syndrome in a girl.
    Parolini O; Ressmann G; Haas OA; Pawlowsky J; Gadner H; Knapp W; Holter W
    N Engl J Med; 1998 Jan; 338(5):291-5. PubMed ID: 9445409
    [No Abstract]   [Full Text] [Related]  

  • 19. [Analysis of clinical features and gene mutations in 6 patients with Wiskott-Aldrich syndrome].
    Jiang MH; Wang ZY; Su J; Cao LJ; Li JQ; Sun XH; Bai X; Wang GF; Ruan CG
    Zhonghua Xue Ye Xue Za Zhi; 2011 Sep; 32(9):577-82. PubMed ID: 22338148
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.
    Proust A; Guillet B; Picard C; de Saint Basile G; Pondarré C; Tamary H; Dreyfus M; Tchernia G; Fischer A; Delaunay J
    Blood Cells Mol Dis; 2007; 39(1):102-6. PubMed ID: 17400488
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.