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661 related items for PubMed ID: 16670064

  • 1. 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
    [Abstract] [Full Text] [Related]

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  • 3. Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds.
    Smith BN, Ancliff PJ, Pizzey A, Khwaja A, Linch DC, Gale RE.
    Br J Haematol; 2009 Mar; 144(5):762-70. PubMed ID: 19036076
    [Abstract] [Full Text] [Related]

  • 4. Mutations in the gene for the granulocyte colony-stimulating-factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia.
    Dong F, Brynes RK, Tidow N, Welte K, Löwenberg B, Touw IP.
    N Engl J Med; 1995 Aug 24; 333(8):487-93. PubMed ID: 7542747
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  • 5. 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 24; 142(4):653-6. PubMed ID: 18513286
    [Abstract] [Full Text] [Related]

  • 6. Kostmann syndrome or infantile genetic agranulocytosis, part two: Understanding the underlying genetic defects in severe congenital neutropenia.
    Carlsson G, Melin M, Dahl N, Ramme KG, Nordenskjöld M, Palmblad J, Henter JI, Fadeel B.
    Acta Paediatr; 2007 Jun 24; 96(6):813-9. PubMed ID: 17537008
    [Abstract] [Full Text] [Related]

  • 7. Novel genetic etiologies of severe congenital neutropenia.
    Boztug K, Klein C.
    Curr Opin Immunol; 2009 Oct 24; 21(5):472-80. PubMed ID: 19782549
    [Abstract] [Full Text] [Related]

  • 8. 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 Oct 24; 15 Suppl 1():113-9; discussion 120. PubMed ID: 9368331
    [Abstract] [Full Text] [Related]

  • 9. Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutations.
    Carlsson G, van't Hooft I, Melin M, Entesarian M, Laurencikas E, Nennesmo I, Trebińska A, Grzybowska E, Palmblad J, Dahl N, Nordenskjöld M, Fadeel B, Henter JI.
    J Intern Med; 2008 Oct 24; 264(4):388-400. PubMed ID: 18513342
    [Abstract] [Full Text] [Related]

  • 10. G-CSF receptor mutations in patients with congenital neutropenia.
    Germeshausen M, Skokowa J, Ballmaier M, Zeidler C, Welte K.
    Curr Opin Hematol; 2008 Jul 24; 15(4):332-7. PubMed ID: 18536571
    [Abstract] [Full Text] [Related]

  • 11. A comparison of the defective granulopoiesis in childhood cyclic neutropenia and in severe congenital neutropenia.
    Sera Y, Kawaguchi H, Nakamura K, Sato T, Habara M, Okada S, Ishikawa N, Kojima S, Katoh O, Kobayashi M.
    Haematologica; 2005 Aug 24; 90(8):1032-41. PubMed ID: 16079102
    [Abstract] [Full Text] [Related]

  • 12. Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene.
    Ishikawa N, Okada S, Miki M, Shirao K, Kihara H, Tsumura M, Nakamura K, Kawaguchi H, Ohtsubo M, Yasunaga S, Matsubara K, Sako M, Hara J, Shiohara M, Kojima S, Sato T, Takihara Y, Kobayashi M.
    J Med Genet; 2008 Dec 24; 45(12):802-7. PubMed ID: 18611981
    [Abstract] [Full Text] [Related]

  • 13. Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities.
    Carlsson G, Elinder G, Malmgren H, Trebinska A, Grzybowska E, Dahl N, Nordenskjöld M, Fadeel B.
    Pediatr Blood Cancer; 2009 Dec 24; 53(6):1143-6. PubMed ID: 19499579
    [Abstract] [Full Text] [Related]

  • 14. 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 24; 144(4):459-67. PubMed ID: 19120359
    [Abstract] [Full Text] [Related]

  • 15. Defects of granulopoiesis in patients with severe congenital neutropenia.
    Nakamura K, Kobayashi M, Konishi N, Kawaguchi H, Miyagawa S, Sato T, Katoh O, Ueda K.
    Hiroshima J Med Sci; 2002 Sep 24; 51(3):63-74. PubMed ID: 12422946
    [Abstract] [Full Text] [Related]

  • 16. 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 24; 33(9):e139-42. PubMed ID: 19398129
    [Abstract] [Full Text] [Related]

  • 17. [Granulopoeisis and leukemogenesis: lessons from congenital neutropenia].
    Donadieu J, Beaupain B, Bellanné-Chantelot C.
    Med Sci (Paris); 2008 Mar 24; 24(3):284-9. PubMed ID: 18334177
    [Abstract] [Full Text] [Related]

  • 18. Congenital neutropenias.
    Zeidler C, Schwinzer B, Welte K.
    Rev Clin Exp Hematol; 2003 Mar 24; 7(1):72-83. PubMed ID: 14692235
    [Abstract] [Full Text] [Related]

  • 19. Neurological findings and genetic alterations in patients with Kostmann syndrome and HAX1 mutations.
    Roques G, Munzer M, Barthez MA, Beaufils S, Beaupain B, Flood T, Keren B, Bellanné-Chantelot C, Donadieu J.
    Pediatr Blood Cancer; 2014 Jun 24; 61(6):1041-8. PubMed ID: 24482108
    [Abstract] [Full Text] [Related]

  • 20. Novel variant isoform of G-CSF receptor involved in induction of proliferation of FDCP-2 cells: relevance to the pathogenesis of myelodysplastic syndrome.
    Awaya N, Uchida H, Miyakawa Y, Kinjo K, Matsushita H, Nakajima H, Ikeda Y, Kizaki M.
    J Cell Physiol; 2002 Jun 24; 191(3):327-35. PubMed ID: 12012328
    [Abstract] [Full Text] [Related]

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