The politics of sickle cell and thalassaemia.

被引：0
|
作者：
Haarhoff, G [1 ]
机构：
[1] Univ Cambridge, Ctr Family Res, Cambridge CB2 1TN, England
来源：
SOCIOLOGY OF HEALTH & ILLNESS | 2003年 / 25卷 / 04期
关键词：
D O I：
暂无
中图分类号：
R1 [预防医学、卫生学];
学科分类号：
1004 ; 120402 ;
摘要：
引用
收藏
页码：380 / 381
页数：2
相关论文
共 50 条
  • [31] Screening for silent globin gene mutations in areas with high prevalence of thalassaemia.
    Chan, LC
    Ma, SK
    Chan, YYA
    Ha, SY
    Waye, JS
    Lau, YL
    Chui, DHK
    BLOOD, 1999, 94 (10) : 23B - 23B
  • [32] Splenectomy in transfusion dependent thalassaemia. A follow-up study.
    Ferrara, M
    Matarese, SMR
    Borrelli, B
    Coppola, A
    Coppola, L
    Chiariello, S
    Esposito, L
    BLOOD, 1999, 94 (10) : 31B - 31B
  • [33] Cardiac iron deposition is not predicted by conventional markers of iron overload in homozygous β-thalassaemia.
    Anderson, L
    Porter, JB
    Wonke, B
    Walker, JM
    Holden, S
    Davis, BA
    Prescott, E
    Charrier, C
    Firmin, DN
    Pennell, DJ
    BLOOD, 2000, 96 (11) : 606A - +
  • [34] The use of hydroxycarbamide in sickle cell patients across the South Thames Sickle and Thalassaemia Network
    McVinnie, Kathryn
    Stuart-Smith, Sara
    BRITISH JOURNAL OF HAEMATOLOGY, 2021, 193 : 202 - 203
  • [35] Increased CA-15.3 levels in the serum of patients with homozygous β-thalassaemia and sickle cell/β-thalassaemia
    Symeonidis, A
    Kouraklis-Symeonidis, A
    Constandinidou, I
    Solomou, E
    Kougelou, S
    Vassilakos, P
    Zoumbos, N
    BRITISH JOURNAL OF HAEMATOLOGY, 2006, 133 (06) : 692 - 694
  • [36] ASSESSMENT OF BONE BIOCHEMICAL INDICATORS IN THALASSAEMIA AND SICKLE CELL ANEMIA
    Thisiadou, K.
    Karamouzis, I.
    Arampatzi, S.
    Karamouzis, M.
    OSTEOPOROSIS INTERNATIONAL, 2010, 21 : 237 - 238
  • [37] Protector effect of α-thalassaemia on cholecystitis and cholecystectomy in sickle cell disease
    Pontes, Roberia M.
    Costa, Elaine S.
    Siqueira, Patricia F. R.
    Medeiros, Jussara F. F.
    Soares, Andrea
    de Mello, Fabiana V.
    Maioli, Maria C.
    Filho, Isaac L. S.
    Alves, Liliane R.
    Land, Marcelo G. P.
    Fleury, Marcos K.
    HEMATOLOGY, 2017, 22 (07) : 444 - 449
  • [38] SICKLE CELL HAEMOGLOBIN AND 2 TYPES OF THALASSAEMIA IN SAME FAMILY
    RUSSO, G
    MOLLICA, F
    ACTA HAEMATOLOGICA, 1962, 28 (06) : 329 - &
  • [39] My working day - In a sickle-cell and thalassaemia centre
    Anie, K
    PSYCHOLOGIST, 2003, 16 (02) : 70 - 71
  • [40] Overwhelming septicaemia in a patient with sickle cell/β○ thalassaemia and partial splenectomy
    Svarch, E
    Nordet, I
    González, A
    BRITISH JOURNAL OF HAEMATOLOGY, 1999, 104 (04) : 930 - 930
12345