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Volumn 31, Issue , 2011, Pages S22-S23

Congenital neutropenia in a newborn

Author keywords

Elane; Neutropenia; Newborn

Indexed keywords

RECOMBINANT GRANULOCYTE COLONY STIMULATING FACTOR;

EID: 79953331661     PISSN: 07438346     EISSN: 14765543     Source Type: Journal    
DOI: 10.1038/jp.2010.166     Document Type: Article
Times cited : (3)

References (19)
  • 1
    • 0242354775 scopus 로고    scopus 로고
    • Congenital neutropenia
    • Ancliff PJ. Congenital neutropenia. Blood Rev 2003; 17: 209-216.
    • (2003) Blood Rev , vol.17 , pp. 209-216
    • Ancliff, P.J.1
  • 2
    • 0030814335 scopus 로고    scopus 로고
    • Severe chronic neutropenia: Pathophysiology and therapy. Semin
    • Welte K, Boxer LA. Severe chronic neutropenia: pathophysiology and therapy. Semin. Hematol 1997; 34: 267-278.
    • (1997) Hematol , vol.34 , pp. 267-278
    • Welte, K.1    Boxer, L.A.2
  • 3
    • 77954324689 scopus 로고    scopus 로고
    • Stable long-term risk of leukemia in patients with severe congenital neutropenia maintained on g-csf therapy
    • Rosenberg P, Zeidler C, Bolyard AA, Alter BP, Bonilla MA, Dror Y et al. Stable long-term risk of leukemia in patients with severe congenital neutropenia maintained on G-CSF therapy. Brit J Haematol 2010; 150: 196-199.
    • (2010) Brit J Haematol , vol.150 , pp. 196-199
    • Rosenberg, P.1    Zeidler, C.2    Bolyard, A.A.3    Alter, B.P.4    Bonilla, M.A.5    Dror, Y.6
  • 4
    • 77049235105 scopus 로고
    • Infantile genetic agranulocytosis infantilis hereditaria
    • Kostmann R. Infantile genetic agranulocytosis infantilis hereditaria. Acta Paediatric Supple 1956; 45: 1-78.
    • (1956) Acta Paediatric Supple , vol.45 , pp. 1-78
    • Kostmann, R.1
  • 5
    • 58549087140 scopus 로고    scopus 로고
    • Clinical implications of ela2-, hax1-, and g-csf-receptor (Gsf3r) mutations in severe congenital neutropenia
    • Zeidler C, Germeshausen M, Klein C, Welte K. Clinical implications of ELA2-, HAX1-, and G-CSF-receptor (GSF3R) mutations in severe congenital neutropenia. Brit J Haematol 2009; 144: 459-467.
    • (2009) Brit J Haematol , vol.144 , pp. 459-467
    • Zeidler, C.1    Germeshausen, M.2    Klein, C.3    Welte, K.4
  • 6
    • 35148829886 scopus 로고    scopus 로고
    • A molecular classification of congenital neutropenia syndromes
    • Newburger P, Boxer LA. A molecular classification of congenital neutropenia syndromes. Pediatr Blood Cancer 2007; 49: 609-614.
    • (2007) Pediatr Blood Cancer , vol.49 , pp. 609-614
    • Newburger, P.1    Boxer, L.A.2
  • 8
    • 0016612028 scopus 로고
    • Infantile genetic agranulocytosis acta paediatric
    • Kostmann R. Infantile genetic agranulocytosis Acta Paediatric. Scand 1975; 64: 362-368.
    • (1975) Scand , vol.64 , pp. 362-368
    • Kostmann, R.1
  • 9
    • 0019798737 scopus 로고
    • Immune neutropenia: Clinical and biological implications
    • Boxer L. Immune neutropenia: clinical and biological implications. Amer J Pediatr Hemat/Oncol 1981; 3: 89-96.
    • (1981) Amer J Pediatr Hemat/Oncol , vol.3 , pp. 89-96
    • Boxer, L.1
  • 10
    • 0034307655 scopus 로고    scopus 로고
    • Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia
    • Dale DC, Person R, Bolyard AA, Aprikyan AG, Bos C, Bonilla MA et al. Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood 2000; 96: 2317-2322.
    • (2000) Blood , vol.96 , pp. 2317-2322
    • Dale, D.C.1    Person, R.2    Bolyard, A.A.3    Aprikyan, A.G.4    Bos, C.5    Bonilla, M.A.6
  • 11
    • 2542434031 scopus 로고    scopus 로고
    • Mutations in the elagene correlate with more severe expression of neutropenia: A study of patients from the french neutropenia register
    • Bellanné-Chantelot C, Clauin S, Leblanc T, Cassinat B, Rodrigues-Lima F, Beaufils S et al Mutations in the ELAgene correlate with more severe expression of neutropenia: a study of patients from the French Neutropenia Register. Blood 2004; 103: 4119-4125.
    • (2004) Blood , vol.103 , pp. 4119-4125
    • Bellanné-Chantelot, C.1    Clauin, S.2    Leblanc, T.3    Cassinat, B.4    Rodrigues-Lima, F.5    Beaufils, S.6
  • 13
    • 70350435426 scopus 로고    scopus 로고
    • Prevalence of mutations in elane, gfi1, hax1, sbds, was and g5pcin patients with severe congenital neutropenia
    • Xia J, Bolyard AA, Rodger E, Stein S, Aprikyan AA, Dale DC et al. Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G5PCin patients with severe congenital neutropenia. Brit J Haematol 2009; 147: 535-542.
    • (2009) Brit J Haematol , vol.147 , pp. 535-542
    • Xia, J.1    Bolyard, A.A.2    Rodger, E.3    Stein, S.4    Aprikyan, A.A.5    Dale, D.C.6
  • 14
    • 0024317186 scopus 로고
    • Effects of recombinant human granulocyte colony-stimulating factor on neutropenia in patients with congenital agranulocytosis
    • Bonilla MA, Gillio AP, Ruggeiro M, Kernan NA, Brochstein JA, Abboud M et al. Effects of recombinant human granulocyte colony-stimulating factor on neutropenia in patients with congenital agranulocytosis. N Engl J Med 1989; 320: 1574-1580.
    • (1989) N Engl J Med , vol.320 , pp. 1574-1580
    • Bonilla, M.A.1    Gillio, A.P.2    Ruggeiro, M.3    Kernan, N.A.4    Brochstein, J.A.5    Abboud, M.6
  • 15
    • 0027269718 scopus 로고
    • A randomized controlled phase iii trial of recombinant human g-csf for treatment of severe chronic neutropenia
    • Dale DC, Bonilla MA, Davis MW, Nakaniski A, Hammond WP, Kurtzberg J et al. A randomized controlled phase III trial of recombinant human G-CSF for treatment of severe chronic neutropenia. Blood 1993; 81: 2496-2502.
    • (1993) Blood , vol.81 , pp. 2496-2502
    • Dale, D.C.1    Bonilla, M.A.2    Davis, M.W.3    Nakaniski, A.4    Hammond, W.P.5    Kurtzberg, J.6
  • 16
    • 0034651925 scopus 로고    scopus 로고
    • Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation
    • Zeidler C, Welte K, Barak Y, Barriga F, Bolyard AA, Boxer LA et al. Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation. Blood 2000; 95: 1195-1198.
    • (2000) Blood , vol.95 , pp. 1195-1198
    • Zeidler, C.1    Welte, K.2    Barak, Y.3    Barriga, F.4    Bolyard, A.A.5    Boxer, L.A.6
  • 17
    • 15544363068 scopus 로고    scopus 로고
    • Stem cell transplantation in patients with severe congenital neutropenia with evidence of leukemic transformation
    • Choi SW, Boxer LA, Pulsipher MA, Roulston D, Hutchinson RJ, Yanik GA et al. Stem cell transplantation in patients with severe congenital neutropenia with evidence of leukemic transformation. Bone Marrow Transpl 2005; 35: 475-477.
    • (2005) Bone Marrow Transpl , vol.35 , pp. 475-477
    • Choi, S.W.1    Boxer, L.A.2    Pulsipher, M.A.3    Roulston, D.4    Hutchinson, R.J.5    Yanik, G.A.6
  • 18
    • 33845904894 scopus 로고    scopus 로고
    • Haxdeficiency causes autosomal recessive severe congenital neutropenia (kostmann disease)
    • Klein C, Grudzien M, Appaswamy G, Germeshausen M, Sandrock I, Scha¨ ffer AA et al. HAXdeficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Nat Genet 2007; 39(1): 86-92.
    • (2007) Nat Genet , vol.39 , Issue.1 , pp. 86-92
    • Klein, C.1    Grudzien, M.2    Appaswamy, G.3    Germeshausen, M.4    Sandrock, I.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.