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Volumn 336, Issue 3, 2013, Pages 177-182

Hydroxycarbamide: Clinical aspects

Author keywords

Children; Hydroxyurea; Sickle cell anemia

Indexed keywords

HEMOGLOBIN F; HYDROXYUREA;

EID: 84877578186     PISSN: 16310691     EISSN: 17683238     Source Type: Journal    
DOI: 10.1016/j.crvi.2012.09.006     Document Type: Short Survey
Times cited : (15)

References (21)
  • 1
    • 0033505007 scopus 로고    scopus 로고
    • Physiologic decline in fetal hemoglobin parameters in infants with sickle cell disease: Implications for pharmacological intervention
    • S.J. Marcus, and R.E. Ware Physiologic decline in fetal hemoglobin parameters in infants with sickle cell disease: implications for pharmacological intervention J. Pediatr. Hematol./Oncol. 21 5 1999 407 411
    • (1999) J. Pediatr. Hematol./Oncol. , vol.21 , Issue.5 , pp. 407-411
    • Marcus, S.J.1    Ware, R.E.2
  • 2
    • 0027981469 scopus 로고
    • Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative Study of Sickle Cell Disease
    • A.K. Brown, L.A. Sleeper, S.T. Miller, C.H. Pegelow, F.M. Gill, and M.A. Waclawiw Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative Study of Sickle Cell Disease Arch. Pediatr. Adolesc. Med 148 8 1994 796 804
    • (1994) Arch. Pediatr. Adolesc. Med , vol.148 , Issue.8 , pp. 796-804
    • Brown, A.K.1    Sleeper, L.A.2    Miller, S.T.3    Pegelow, C.H.4    Gill, F.M.5    Waclawiw, M.A.6
  • 3
    • 0027452375 scopus 로고
    • Sickle cell anemia. Beta-S gene cluster haplotypes as genetic markers for severe disease expression
    • D. Powars, and A. Hiti Sickle cell anemia. Beta-S gene cluster haplotypes as genetic markers for severe disease expression Am. J. Dis. Child. 147 11 1993 1197 1202
    • (1993) Am. J. Dis. Child. , vol.147 , Issue.11 , pp. 1197-1202
    • Powars, D.1    Hiti, A.2
  • 4
    • 50149117726 scopus 로고    scopus 로고
    • DNA polymorphism at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease
    • G. Lettre, V.G. Sankaran, and M.A. Bezerra DNA polymorphism at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease Proc. Natl Acad. Sci. USA 105 33 2008 11869 11874
    • (2008) Proc. Natl Acad. Sci. USA , vol.105 , Issue.33 , pp. 11869-11874
    • Lettre, G.1    Sankaran, V.G.2    Bezerra, M.A.3
  • 6
    • 77955905049 scopus 로고    scopus 로고
    • How i use hydroxyurea to treat young patients with sickle cell anemia
    • R.E. Ware How I use hydroxyurea to treat young patients with sickle cell anemia Blood 115 26 2010 5300 5311
    • (2010) Blood , vol.115 , Issue.26 , pp. 5300-5311
    • Ware, R.E.1
  • 7
    • 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
    • S. Charache, M.L. Terrin, and R.D. Moore 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. 332 20 1995 1317 1322
    • (1995) N. Engl. J. Med. , vol.332 , Issue.20 , pp. 1317-1322
    • Charache, S.1    Terrin, M.L.2    Moore, R.D.3
  • 8
    • 13044277572 scopus 로고    scopus 로고
    • Safety of hydroxyurea in children with sickle cell anemia: Results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group
    • T.R. Kinney, R.W. Helms, and E.E. O'Branski Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group Blood 94 5 1999 1550 1554
    • (1999) Blood , vol.94 , Issue.5 , pp. 1550-1554
    • Kinney, T.R.1    Helms, R.W.2    O'Branski, E.E.3
  • 9
    • 79955909191 scopus 로고    scopus 로고
    • Hydroxycarbamide in very young children with sickle-cell anaemia: A multicenter, randomized, controlled trial (BABY HUG)
    • W.C. Wang, R.E. Ware, and S.T. Miller Hydroxycarbamide in very young children with sickle-cell anaemia: a multicenter, randomized, controlled trial (BABY HUG) Lancet 377 9778 2011 1663 1672
    • (2011) Lancet , vol.377 , Issue.9778 , pp. 1663-1672
    • Wang, W.C.1    Ware, R.E.2    Miller, S.T.3
  • 10
    • 0035666461 scopus 로고    scopus 로고
    • A two-year pilot trial of hydroxyurea in very young children with sickle-cell anemia
    • W.C. Wang, L.W. Wynn, Z.R. Rogers, J.P. Scott, P.A. Lane, and R.E. Ware A two-year pilot trial of hydroxyurea in very young children with sickle-cell anemia J. Pediatr. 139 6 2001 790 796
    • (2001) J. Pediatr. , vol.139 , Issue.6 , pp. 790-796
    • Wang, W.C.1    Wynn, L.W.2    Rogers, Z.R.3    Scott, J.P.4    Lane, P.A.5    Ware, R.E.6
  • 11
    • 41349090417 scopus 로고    scopus 로고
    • Hydroxyurea for children with sickle cell disease
    • M.M. Heeney, and R.E. Ware Hydroxyurea for children with sickle cell disease Pediatr. Clin. North Am. 55 2 2008 483 501
    • (2008) Pediatr. Clin. North Am. , vol.55 , Issue.2 , pp. 483-501
    • Heeney, M.M.1    Ware, R.E.2
  • 13
    • 0026631318 scopus 로고
    • Hydroxyurea: Effects on hemoglobin F production in patients with sickle cell anemia
    • S. Charache, G.J. Dover, and R.D. Moore Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia Blood 79 10 1992 2555 2565
    • (1992) Blood , vol.79 , Issue.10 , pp. 2555-2565
    • Charache, S.1    Dover, G.J.2    Moore, R.D.3
  • 14
    • 84860348352 scopus 로고    scopus 로고
    • For the SWiTCH Investigators. Stroke with transfusions changing to hydroxyurea (SWiTCH)
    • R.E. Ware, and R.W. Helms For the SWiTCH Investigators. Stroke with transfusions changing to hydroxyurea (SWiTCH) Blood 119 17 2012 3925 3932
    • (2012) Blood , vol.119 , Issue.17 , pp. 3925-3932
    • Ware, R.E.1    Helms, R.W.2
  • 15
    • 0344443803 scopus 로고    scopus 로고
    • Malignancy in sickle cell disease
    • W.H. Schultz, and R.E. Ware Malignancy in sickle cell disease Am. J. Hematol. 74 4 2003 249 253
    • (2003) Am. J. Hematol. , vol.74 , Issue.4 , pp. 249-253
    • Schultz, W.H.1    Ware, R.E.2
  • 16
    • 70350637293 scopus 로고    scopus 로고
    • Exposure to hydroxyurea and pregnancy outcomes in patients with sickle cell anemia
    • S.K. Ballas, W.F. McCarthy, and N. Guo Exposure to hydroxyurea and pregnancy outcomes in patients with sickle cell anemia J. Natl Med. Assoc. 101 10 2009 1046 1051
    • (2009) J. Natl Med. Assoc. , vol.101 , Issue.10 , pp. 1046-1051
    • Ballas, S.K.1    McCarthy, W.F.2    Guo, N.3
  • 17
    • 77953057530 scopus 로고    scopus 로고
    • The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5-year follow-up
    • M.H. Steinberg, W.F. McCarthy, and O. Castro The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: a 17.5-year follow-up Am. J. Hematol. 85 6 2010 403 408
    • (2010) Am. J. Hematol. , vol.85 , Issue.6 , pp. 403-408
    • Steinberg, M.H.1    McCarthy, W.F.2    Castro, O.3
  • 18
    • 77950622293 scopus 로고    scopus 로고
    • The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: Results of a 17-year, single-center trial (LaSHS)
    • E. Voskaridou, D. Christoulas, and A. Bilalis The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: results of a 17-year, single-center trial (LaSHS) Blood 115 12 2010 2354 2363
    • (2010) Blood , vol.115 , Issue.12 , pp. 2354-2363
    • Voskaridou, E.1    Christoulas, D.2    Bilalis, A.3
  • 19
    • 77953952024 scopus 로고    scopus 로고
    • The inherited diseases of hemoglobin are an emerging global health burden
    • D.J. Weatherall The inherited diseases of hemoglobin are an emerging global health burden Blood 115 22 2010 4331 4336
    • (2010) Blood , vol.115 , Issue.22 , pp. 4331-4336
    • Weatherall, D.J.1
  • 20
    • 80855133522 scopus 로고    scopus 로고
    • Pharmacokinetics, pharmacodynamics, and pharmacogenetics of hydroxyurea treatment for children with sickle cell anemia
    • R.E. Ware, J.M. Despotovic, and N.A. Mortier Pharmacokinetics, pharmacodynamics, and pharmacogenetics of hydroxyurea treatment for children with sickle cell anemia Blood 118 18 2011 4985 4991
    • (2011) Blood , vol.118 , Issue.18 , pp. 4985-4991
    • Ware, R.E.1    Despotovic, J.M.2    Mortier, N.A.3
  • 21
    • 79955011693 scopus 로고    scopus 로고
    • Hydroxyurea for sickle cell anemia: What have we learned and what questions still remain?
    • P.T. McGann, and R.E. Ware Hydroxyurea for sickle cell anemia: what have we learned and what questions still remain? Curr. Opin. Hematol. 18 3 2011 158 165
    • (2011) Curr. Opin. Hematol. , vol.18 , Issue.3 , pp. 158-165
    • McGann, P.T.1    Ware, R.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.