BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

235 related articles for article (PubMed ID: 19398129)

  • 1. Acute lymphoblastic leukemia following severe congenital neutropenia or de novo ALL?
    Valera ET; Brassesco MS; Germeshausen M; Silveira Vda S; Queiroz RG; Roxo P; Scrideli CA; de Menezes UP; Ferriani V; Tone LG
    Leuk Res; 2009 Sep; 33(9):e139-42. PubMed ID: 19398129
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemia evolution in severe congenital neutropenia patients belonging to the original Kostmann family in northern Sweden.
    Carlsson G; Aprikyan AA; Ericson KG; Stein S; Makaryan V; Dale DC; Nordenskjöld M; Fadeel B; Palmblad J; Hentera JI
    Haematologica; 2006 May; 91(5):589-95. PubMed ID: 16670064
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Frequency of point mutations in the gene for the G-CSF receptor in patients with chronic neutropenia undergoing G-CSF therapy.
    Tidow N; Pilz C; Kasper B; Welte K
    Stem Cells; 1997; 15 Suppl 1():113-9; discussion 120. PubMed ID: 9368331
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Acute lymphoblastic leukemia in a patient with congenital neutropenia without G-CSF-R and ELA2 mutations.
    Yetgin S; Germeshausen M; Touw I; Koç A; Olcay L
    Leukemia; 2005 Sep; 19(9):1710-1. PubMed ID: 15973448
    [No Abstract]   [Full Text] [Related]  

  • 5. G-CSF receptor mutations in patients with congenital neutropenia.
    Germeshausen M; Skokowa J; Ballmaier M; Zeidler C; Welte K
    Curr Opin Hematol; 2008 Jul; 15(4):332-7. PubMed ID: 18536571
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of risk factors for myelodysplasias, leukemias and death from infection among patients with congenital neutropenia. Experience of the French Severe Chronic Neutropenia Study Group.
    Donadieu J; Leblanc T; Bader Meunier B; Barkaoui M; Fenneteau O; Bertrand Y; Maier-Redelsperger M; Micheau M; Stephan JL; Phillipe N; Bordigoni P; Babin-Boilletot A; Bensaid P; Manel AM; Vilmer E; Thuret I; Blanche S; Gluckman E; Fischer A; Mechinaud F; Joly B; Lamy T; Hermine O; Cassinat B; Bellanné-Chantelot C; Chomienne C;
    Haematologica; 2005 Jan; 90(1):45-53. PubMed ID: 15642668
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Severe congenital neutropenia: analysis of clinical features, diagnostic methods, treatment and long-term outcome].
    Milá M; Rufach A; Dapena JL; Arostegui JI; Elorza I; Llort A; Sánchez de Toledo J; Díaz de Heredia C
    An Pediatr (Barc); 2011 Dec; 75(6):396-400. PubMed ID: 21757412
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Functional interaction between mutations in the granulocyte colony-stimulating factor receptor in severe congenital neutropenia.
    Ward AC; Gits J; Majeed F; Aprikyan AA; Lewis RS; O'Sullivan LA; Freedman M; Shigdar S; Touw IP; Dale DC; Dror Y
    Br J Haematol; 2008 Aug; 142(4):653-6. PubMed ID: 18513286
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical implications of ELA2-, HAX1-, and G-CSF-receptor (CSF3R) mutations in severe congenital neutropenia.
    Zeidler C; Germeshausen M; Klein C; Welte K
    Br J Haematol; 2009 Feb; 144(4):459-67. PubMed ID: 19120359
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Acute lymphocytic leukemia after fulminant varicella associated with severe neutropenia.
    Helft DA; Correa H; Rojas P; Warrier RP
    South Med J; 2002 Sep; 95(9):1074-5. PubMed ID: 12356115
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel genetic etiologies of severe congenital neutropenia.
    Boztug K; Klein C
    Curr Opin Immunol; 2009 Oct; 21(5):472-80. PubMed ID: 19782549
    [TBL] [Abstract][Full Text] [Related]  

  • 12. HAX1 mutation in an infant with severe congenital neutropenia.
    Eghbali A; Eshghi P; Malek F; Abdollahpour H; Rezaei N
    Turk J Pediatr; 2010; 52(1):81-4. PubMed ID: 20402072
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hepatic hemangioendothelioma in an infant with severe congenital neutropenia.
    Dinand V; Yadav SP; Bellanné-Chantelot C; Jain S; Bhargava M; Sachdeva A
    J Pediatr Hematol Oncol; 2012 May; 34(4):298-300. PubMed ID: 22510773
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic analysis and clinical picture of severe congenital neutropenia in Israel.
    Lebel A; Yacobovich J; Krasnov T; Koren A; Levin C; Kaplinsky C; Ravel-Vilk S; Laor R; Attias D; Ben Barak A; Shtager D; Stein J; Kuperman A; Miskin H; Dgany O; Giri N; Alter BP; Tamary H
    Pediatr Blood Cancer; 2015 Jan; 62(1):103-8. PubMed ID: 25284454
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital neutropenia in a newborn.
    Walkovich K; Boxer LA
    J Perinatol; 2011 Apr; 31 Suppl 1():S22-3. PubMed ID: 21448199
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heterozygous M1V variant of ELA-2 gene mutation associated with G-CSF refractory severe congenital neutropenia.
    Setty BA; Yeager ND; Bajwa RP
    Pediatr Blood Cancer; 2011 Sep; 57(3):514-5. PubMed ID: 21618407
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Severe congenital neutropenia.
    Welte K; Zeidler C; Dale DC
    Semin Hematol; 2006 Jul; 43(3):189-95. PubMed ID: 16822461
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Severe chronic neutropenia--a case report.
    Bahl S; Vurgese T; Parappil A
    Indian J Pathol Microbiol; 2004 Oct; 47(4):523-5. PubMed ID: 16295383
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Screening for G-CSF receptor mutations in patients with secondary myeloid or lymphoid transformation of severe congenital neutropenia. A report from the French neutropenia register.
    Cassinat B; Bellanné-Chantelot C; Notz-Carrère A; Menot ML; Vaury C; Micheau M; Bader-Meunier B; Perel Y; Leblanc T; Donadieu J; Chomienne C
    Leukemia; 2004 Sep; 18(9):1553-5. PubMed ID: 15284863
    [No Abstract]   [Full Text] [Related]  

  • 20. [Gene Mutation and Acute Leukemia Transformation of Severe Congenital Neutropenia- Review].
    Chi ZH; Zhu P
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Oct; 25(5):1580-1584. PubMed ID: 29070147
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.