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Journal Abstract Search

400 related items for PubMed ID: 19120359

  • 21. Kostmann syndrome and severe congenital neutropenia.
    Zeidler C, Welte K.
    Semin Hematol; 2002 Apr; 39(2):82-8. PubMed ID: 11957189
    [Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. Role of CSF3R mutations in the pathomechanism of congenital neutropenia and secondary acute myeloid leukemia.
    Klimiankou M, Mellor-Heineke S, Zeidler C, Welte K, Skokowa J.
    Ann N Y Acad Sci; 2016 Apr; 1370(1):119-25. PubMed ID: 27270496
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  • 24. Digenic mutations in severe congenital neutropenia.
    Germeshausen M, Zeidler C, Stuhrmann M, Lanciotti M, Ballmaier M, Welte K.
    Haematologica; 2010 Jul; 95(7):1207-10. PubMed ID: 20220065
    [Abstract] [Full Text] [Related]

  • 25. Transformation of severe congenital neutropenia to early acute lymphoblastic leukemia in a patient with HAX1 mutation and without G-CSF administration or receptor mutation.
    Yetgin S, Olcay L, Koç A, Germeshausen M.
    Leukemia; 2008 Sep; 22(9):1797. PubMed ID: 18354489
    [No Abstract] [Full Text] [Related]

  • 26. [Molecular analysis of two cases of severe congenital neutropenia].
    Park J, Kim M, Lim J, Kim Y, Cho B, Park YJ, Han K.
    Korean J Lab Med; 2010 Apr; 30(2):111-6. PubMed ID: 20445326
    [Abstract] [Full Text] [Related]

  • 27. 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; 264(4):388-400. PubMed ID: 18513342
    [Abstract] [Full Text] [Related]

  • 28. Malignant myeloid transformation in congenital forms of neutropenia.
    Freedman MH, Alter BP.
    Isr Med Assoc J; 2002 Nov; 4(11):1011-4. PubMed ID: 12489493
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  • 30. [Diagnosis and treatment procedures of congenital neutropenia].
    Qiao M, Xue SL, Zou JY, Dai L, Liu HW, Chen Y, Sun AN, Wu DP.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2012 Oct; 20(5):1221-4. PubMed ID: 23114152
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  • 31. Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis.
    Skokowa J, Steinemann D, Katsman-Kuipers JE, Zeidler C, Klimenkova O, Klimiankou M, Unalan M, Kandabarau S, Makaryan V, Beekman R, Behrens K, Stocking C, Obenauer J, Schnittger S, Kohlmann A, Valkhof MG, Hoogenboezem R, Göhring G, Reinhardt D, Schlegelberger B, Stanulla M, Vandenberghe P, Donadieu J, Zwaan CM, Touw IP, van den Heuvel-Eibrink MM, Dale DC, Welte K.
    Blood; 2014 Apr 03; 123(14):2229-37. PubMed ID: 24523240
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  • 34. Acute myeloid/NK precursor cell leukemia with trisomy 4 and a novel point mutation in the extracellular domain of the G-CSF receptor in a patient with chronic idiopathic neutropenia.
    Papadaki HA, Kosteas T, Gemetzi C, Damianaki A, Anagnou NP, Eliopoulos GD.
    Ann Hematol; 2004 Jun 03; 83(6):345-8. PubMed ID: 15014900
    [Abstract] [Full Text] [Related]

  • 35. Ultra-Sensitive CSF3R Deep Sequencing in Patients With Severe Congenital Neutropenia.
    Klimiankou M, Uenalan M, Kandabarau S, Nustede R, Steiert I, Mellor-Heineke S, Zeidler C, Skokowa J, Welte K.
    Front Immunol; 2019 Jun 03; 10():116. PubMed ID: 30891028
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  • 40. G-CSF receptor (CSF3R) mutations in X-linked neutropenia evolving to acute myeloid leukemia or myelodysplasia.
    Beel K, Vandenberghe P.
    Haematologica; 2009 Oct 03; 94(10):1449-52. PubMed ID: 19794089
    [Abstract] [Full Text] [Related]

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