메뉴 건너뛰기




Volumn 60, Issue 10, 2013, Pages

Association between baseline fetal hemoglobin levels and incidence of severe vaso-occlusive pain episodes in children with sickle cell anemia

Author keywords

Fetal hemoglobin; Sickle cell anemia; Vaso occlusive pain

Indexed keywords

HEMOGLOBIN F;

EID: 84881491135     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.24588     Document Type: Article
Times cited : (9)

References (14)
  • 1
    • 74049123836 scopus 로고    scopus 로고
    • Definitions of the phenotypic manifestations of sickle cell disease
    • Ballas SK, Lieff S, Benjamin LJ, et al. Definitions of the phenotypic manifestations of sickle cell disease. Am J Hematol 2010; 85:6-13.
    • (2010) Am J Hematol , vol.85 , pp. 6-13
    • Ballas, S.K.1    Lieff, S.2    Benjamin, L.J.3
  • 2
    • 0019365327 scopus 로고
    • Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood
    • Stevens MC, Hayes RJ, Vaidya S, et al. Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood. J Pediatr 1981; 98:37-41.
    • (1981) J Pediatr , vol.98 , pp. 37-41
    • Stevens, M.C.1    Hayes, R.J.2    Vaidya, S.3
  • 3
    • 0025770390 scopus 로고
    • Pain in sickle cell disease. Rates and risk factors
    • Platt OS, Thorington BD, Brambilla DJ, et al. Pain in sickle cell disease. Rates and risk factors. N Engl J Med 1991; 325:11-16.
    • (1991) N Engl J Med , vol.325 , pp. 11-16
    • Platt, O.S.1    Thorington, B.D.2    Brambilla, D.J.3
  • 4
    • 45549105597 scopus 로고    scopus 로고
    • Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease
    • Lanzkron S, Strouse JJ, Wilson R, et al. Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease. Ann Intern Med 2008; 148:939-955.
    • (2008) Ann Intern Med , vol.148 , pp. 939-955
    • Lanzkron, S.1    Strouse, J.J.2    Wilson, R.3
  • 5
    • 0029025475 scopus 로고
    • Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the multicenter study of hydroxyurea in sickle cell anemia
    • Charache S, Terrin ML, Moore RD, et al. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the multicenter study of hydroxyurea in sickle cell anemia. N Engl J Med 1995; 332:1317-1322.
    • (1995) N Engl J Med , vol.332 , pp. 1317-1322
    • Charache, S.1    Terrin, M.L.2    Moore, R.D.3
  • 6
    • 79955909191 scopus 로고    scopus 로고
    • Hydroxycarbamide in very young children with sickle-cell anaemia: A multicentre, randomised, controlled trial (BABY HUG)
    • Wang WC, Ware RE, Miller ST, et al. Hydroxycarbamide in very young children with sickle-cell anaemia: A multicentre, randomised, controlled trial (BABY HUG). Lancet 2011; 377:1663-1672.
    • (2011) Lancet , vol.377 , pp. 1663-1672
    • Wang, W.C.1    Ware, R.E.2    Miller, S.T.3
  • 7
    • 0028234283 scopus 로고
    • The acute chest syndrome in sickle cell disease: Incidence and risk factors. The cooperative study of sickle cell disease
    • Castro O, Brambilla DJ, Thorington B, et al. The acute chest syndrome in sickle cell disease: Incidence and risk factors. The cooperative study of sickle cell disease. Blood 1994; 84:643-649.
    • (1994) Blood , vol.84 , pp. 643-649
    • Castro, O.1    Brambilla, D.J.2    Thorington, B.3
  • 8
    • 0028291736 scopus 로고
    • Mortality in sickle cell disease. Life expectancy and risk factors for early death
    • Platt OS, Brambilla DJ, Rosse WF, et al. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med 1994; 330:1639-1644.
    • (1994) N Engl J Med , vol.330 , pp. 1639-1644
    • Platt, O.S.1    Brambilla, D.J.2    Rosse, W.F.3
  • 9
    • 84857912002 scopus 로고    scopus 로고
    • Sickle cell disease subphenotypes in patients from Southwestern Province of Saudi Arabia
    • Alsultan A, Aleem A, Ghabbour H, et al. Sickle cell disease subphenotypes in patients from Southwestern Province of Saudi Arabia. J Pediatr Hematol Oncol 2012; 34:79-84.
    • (2012) J Pediatr Hematol Oncol , vol.34 , pp. 79-84
    • Alsultan, A.1    Aleem, A.2    Ghabbour, H.3
  • 10
    • 38749109710 scopus 로고    scopus 로고
    • Daily assessment of pain in adults with sickle cell disease
    • Smith WR, Penberthy LT, Bovbjerg VE, et al. Daily assessment of pain in adults with sickle cell disease. Ann Intern Med 2008; 148:94-101.
    • (2008) Ann Intern Med , vol.148 , pp. 94-101
    • Smith, W.R.1    Penberthy, L.T.2    Bovbjerg, V.E.3
  • 11
    • 77749243156 scopus 로고    scopus 로고
    • Design of the silent cerebral infarct transfusion (SIT) trial
    • Casella JF, King AA, Barton B, et al. Design of the silent cerebral infarct transfusion (SIT) trial. Pediatr Hematol Oncol 2010; 27:69-89.
    • (2010) Pediatr Hematol Oncol , vol.27 , pp. 69-89
    • Casella, J.F.1    King, A.A.2    Barton, B.3
  • 12
    • 0020323557 scopus 로고
    • The cooperative study of sickle cell disease: Review of study design and objectives
    • Gaston M, Rosse WF. The cooperative study of sickle cell disease: Review of study design and objectives. Am J Pediatr Hematol Oncol 1982; 4:197-201.
    • (1982) Am J Pediatr Hematol Oncol , vol.4 , pp. 197-201
    • Gaston, M.1    Rosse, W.F.2
  • 13
    • 79957852121 scopus 로고    scopus 로고
    • Elevation of IgE in children with sickle cell disease is associated with doctor diagnosis of asthma and increased morbidity
    • An P, Barron-Casella EA, Strunk RC, et al. Elevation of IgE in children with sickle cell disease is associated with doctor diagnosis of asthma and increased morbidity. J Allergy Clin Immunol 2011; 127:1440-1446.
    • (2011) J Allergy Clin Immunol , vol.127 , pp. 1440-1446
    • An, P.1    Barron-Casella, E.A.2    Strunk, R.C.3
  • 14
    • 84855643775 scopus 로고    scopus 로고
    • Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia
    • Darbari DS, Onyekwere O, Nouraie M, et al. Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia. J Pediatr 2012; 160:286-290.
    • (2012) J Pediatr , vol.160 , pp. 286-290
    • Darbari, D.S.1    Onyekwere, O.2    Nouraie, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.