SICKLE-CELL-THALASSAEMIA DISEASE IN SOUTH TURKEY

被引:33
|
作者
AKSOY, M
LEHMANN, H
机构
来源
BRITISH MEDICAL JOURNAL | 1957年 / 1卷 / MAR30期
关键词
D O I
10.1136/bmj.1.5021.734
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:734 / 738
页数:5
相关论文
共 50 条
  • [21] Fertility and pregnancy in thalassaemia and sickle cell disease. The UK guidelines
    Davis, Bernard
    THALASSEMIA REPORTS, 2014, 4 (03) : 63 - 67
  • [22] The politics of sickle cell and thalassaemia.
    Haarhoff, G
    SOCIOLOGY OF HEALTH & ILLNESS, 2003, 25 (04) : 380 - 381
  • [23] The politics of sickle cell and thalassaemia.
    Walters, J
    JOURNAL OF BIOSOCIAL SCIENCE, 2004, 36 (05) : 627 - 628
  • [24] Arterial elastorrhexis in β-thalassaemia intermedia, sickle cell thalassaemia and hereditary spherocytosis
    Tsomi, K
    Karagiorga-Lagana, M
    Karabatsos, F
    Fragodimitri, C
    van Vliet-Konstantinidou, C
    Premetis, E
    Stamoulakatou, A
    EUROPEAN JOURNAL OF HAEMATOLOGY, 2001, 67 (03) : 135 - 141
  • [25] Re: Sickle cell disease and beta-thalassaemia major in pregnancy reply
    Eissa, Asma
    Tuck, Susan
    OBSTETRICIAN & GYNAECOLOGIST, 2014, 16 (02): : 144 - 144
  • [26] The influence of α-thalassaemia on the haematological & clinical expression of sickle cell disease in western India
    Mukherjee, MB
    Surve, R
    Tamankar, A
    Gangakhedkar, RR
    Ghosh, K
    Lu, CY
    Krishnamoorthy, R
    Colah, R
    Mohanty, D
    INDIAN JOURNAL OF MEDICAL RESEARCH, 1998, 107 : 178 - 181
  • [27] Re: Sickle cell disease and beta-thalassaemia major in pregnancy Reply
    Tuck, Susan M.
    Eissa, Asma A.
    OBSTETRICIAN & GYNAECOLOGIST, 2013, 15 (04): : 279 - 279
  • [28] The presence of α-thalassaemia trait blunts the response to hydroxycarbamide in patients with sickle cell disease
    Vasavda, Nisha
    Badiger, Sheela
    Rees, David
    Height, Sue
    Howard, Jo
    Thein, Swee Lay
    BRITISH JOURNAL OF HAEMATOLOGY, 2008, 143 (04) : 589 - 592
  • [29] Compound heterozygous sickle cell disease and beta(0)-thalassaemia: An interesting case
    von Fintel, R.
    Schwyzer, R.
    Poole, J.
    Alli, N. A.
    SOUTH AFRICAN JOURNAL OF CHILD HEALTH, 2013, 7 (02) : 70 - 73
  • [30] The haemoglobinopathy survey: The reality of transfusion practice in sickle cell disease and thalassaemia in England
    Trompeter, Sara
    Estcourt, Lise
    Mora, Ana
    Wong, Esther
    Collett, David
    Bolton-Maggs, Paula
    Poles, Debbi
    Deary, Alison
    Watt, Alison
    TRANSFUSION MEDICINE, 2020, 30 (06) : 456 - 466