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Volumn 850, Issue , 1998, Pages 251-269

Global epidemiology of hemoglobin disorders

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN; HEMOGLOBIN C; HEMOGLOBIN E; HEMOGLOBIN S;

EID: 0031855380     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1998.tb10482.x     Document Type: Conference Paper
Times cited : (274)

References (21)
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    • Unpublished report of the WHO: HMG/WG/85.8. May be obtained free of charge from: The Hereditary Diseases Program, WHO, Geneva, Switzerland
    • WHO 1985. Update of the Progress of Hemoglobinopathies Control. Report of the Third and Fourth Annual Meetings of the WHO Working Group for the Community Control of Hereditary Anaemias. Unpublished report of the WHO: HMG/WG/85.8. May be obtained free of charge from: The Hereditary Diseases Program, WHO, Geneva, Switzerland.
    • (1985) Report of the Third and Fourth Annual Meetings of the WHO Working Group for the Community Control of Hereditary Anaemias
  • 4
    • 33646304420 scopus 로고
    • WHO Regional Office for Europe, unpublished document IPC/MCH 110. (May be obtained from: WHO Regional Office for Europe, 8 Scherfigsvej, DK-2100, Copenhagen, Denmark)
    • WHO 1987. The Hemoglobinopathies in Europe. WHO Regional Office for Europe, unpublished document IPC/MCH 110. (May be obtained from: WHO Regional Office for Europe, 8 Scherfigsvej, DK-2100, Copenhagen, Denmark).
    • (1987) The Hemoglobinopathies in Europe
  • 6
    • 0003393882 scopus 로고
    • Unpublished document of the WHO. WHO/HDP/HB/GL/94.1. Obtainable free of charge from the Hereditary Diseases Program, WHO, Geneva, Switzerland
    • WHO 1994. Guidelines for control of hemoglobin disorders. Unpublished document of the WHO. WHO/HDP/HB/GL/94.1. Obtainable free of charge from the Hereditary Diseases Program, WHO, Geneva, Switzerland.
    • (1994) Guidelines for Control of Hemoglobin Disorders
  • 7
    • 0027231519 scopus 로고
    • Frequency and clinical significance of erythrocyte genetic abnormalities in Oman
    • WHITE, J. M. et al. 1993. Frequency and clinical significance of erythrocyte genetic abnormalities in Oman. J. Med. Genet. 30: 396-400.
    • (1993) J. Med. Genet. , vol.30 , pp. 396-400
    • White, J.M.1
  • 9
    • 0022826099 scopus 로고
    • Thalassemia can be prevented
    • KULIEV, A. 1986. Thalassemia can be prevented. World Health Forum 7: 286-90.
    • (1986) World Health Forum , vol.7 , pp. 286-290
    • Kuliev, A.1
  • 10
    • 0023502358 scopus 로고
    • Results of programs for antenatal detection of thalassemia in reducing the incidence of the disorder
    • CAO, A. 1987. Results of programs for antenatal detection of thalassemia in reducing the incidence of the disorder. Blood Rev. 1: 169-76.
    • (1987) Blood Rev. , vol.1 , pp. 169-176
    • Cao, A.1
  • 12
    • 0023796168 scopus 로고
    • Counseling for prenatal diagnosis of sickle cell disease and β-Thalassemia major: A four year experience
    • ANIONWU, E. N., N. PATEL, G. KANJI, H. RENGES & M. BROSOVIC. 1987. Counseling for prenatal diagnosis of sickle cell disease and β-Thalassemia major: A four year experience. J. Med. Genet. 25: 769.
    • (1987) J. Med. Genet. , vol.25 , pp. 769
    • Anionwu, E.N.1    Patel, N.2    Kanji, G.3    Renges, H.4    Brosovic, M.5
  • 13
    • 0026484251 scopus 로고
    • Factors affecting the uptake of prenatal diagnosis for sickle cell disease
    • PETROU, M., M. BRUGIATELLI, R. H. T. WARD & B. MODELL. 1992. Factors affecting the uptake of prenatal diagnosis for sickle cell disease. J. Med. Genet. 29: 820-23.
    • (1992) J. Med. Genet. , vol.29 , pp. 820-823
    • Petrou, M.1    Brugiatelli, M.2    Ward, R.H.T.3    Modell, B.4
  • 21
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    • Alpha Thalassemia hydrops fetalis in the UK: The importance of screening pregnant women of Chinese, other South East Asian and Mediterranean extraction for alpha Thalassemia trait
    • PETROU, M., M. BRUGIATELLI, J. OLD, P. HURLEY, R. H. T. WARD, K. P. WONG et al. 1992. Alpha Thalassemia hydrops fetalis in the UK: The importance of screening pregnant women of Chinese, other South East Asian and Mediterranean extraction for alpha Thalassemia trait. Br. J. Obstet. Gynaecol. 99: 985-89.
    • (1992) Br. J. Obstet. Gynaecol. , vol.99 , pp. 985-989
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.