BETA-THALASSAEMIA, HEMOGLOBIN S AND HEREDITARY ELLIPTOCYTOSIS IN A ZAIRIAN FAMILY - ISCHEMIC COSTAL NECROSES IN A CHILD WITH SICKLE-CELL BETA-THALASSAEMIA

被引:0
作者
VANROS, G
SEYNHAEVE, V
FIASSE, L
机构
[1] INST TROP MED,DEPT HAEMATOL,B-2000 ANTWERP,BELGIUM
[2] NATL UNIV ZAIRE HOSP,DEPT PAEDIAT,KINSHASA,ZAIRE
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:241 / 252
页数:12
相关论文
共 50 条
  • [21] Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome
    Galanello, R
    Perseu, L
    Melis, MA
    Cipollina, L
    Barella, S
    Giagu, N
    Turco, MP
    Maccioni, O
    Cao, A
    BRITISH JOURNAL OF HAEMATOLOGY, 1997, 99 (02) : 433 - 436
  • [22] What are Pakistani women's experiences of prenatal carrier screening for beta-thalassaemia in the UK?
    Ahmed, S
    Green, J
    Hewison, J
    JOURNAL OF REPRODUCTIVE AND INFANT PSYCHOLOGY, 2000, 18 (03) : 253 - 253
  • [23] Adhesion molecules and high-sensitivity C-reactive protein levels in patients with sickle cell beta-thalassaemia
    Kanavaki, Ino
    Makrythanasis, Periklis
    Lazaropoulou, Christina
    Kattamis, Antonis
    Tzanetea, Revekka
    Kalotychou, Vassiliki
    Rombos, Ioannis
    Papassotiriou, Ioannis
    EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2012, 42 (01) : 27 - 33
  • [24] NON-TRANSFERRIN PLASMA IRON IN BETA-THALASSAEMIA/HB-E AND HEMOGLOBIN H DISEASES
    ANUWATANAKULCHAI, M
    POOTRAKUL, P
    THUVASETHAKUL, P
    WASI, P
    SCANDINAVIAN JOURNAL OF HAEMATOLOGY, 1984, 32 (02): : 153 - 158
  • [25] Clinical application of a protocol based on universal next-generation sequencing for the diagnosis of beta-thalassaemia and sickle cell anaemia in preimplantation embryos
    Kubikova, Nada
    Babariya, Dhruti
    Sarasa, Jonas
    Spath, Katharina
    Alfarawati, Samer
    Wells, Dagan
    REPRODUCTIVE BIOMEDICINE ONLINE, 2018, 37 (02) : 136 - 144
  • [26] Progressive splenomegaly and mild thrombocytosis in beta-thalassaemia trait and coexisting hereditary hemochromatosis: possible confounders for a subsequent hematological diagnosis
    Pelusi, Serena
    Iuculano, Federica
    Lombardi, Rosa
    Francione, Paolo
    Gianelli, Umberto
    Fracanzani, Anna Ludovica
    Fargion, Silvia
    INTERNAL AND EMERGENCY MEDICINE, 2019, 14 (05) : 763 - 766
  • [27] Progressive splenomegaly and mild thrombocytosis in beta-thalassaemia trait and coexisting hereditary hemochromatosis: possible confounders for a subsequent hematological diagnosis
    Serena Pelusi
    Federica Iuculano
    Rosa Lombardi
    Paolo Francione
    Umberto Gianelli
    Anna Ludovica Fracanzani
    Silvia Fargion
    Internal and Emergency Medicine, 2019, 14 : 763 - 766
  • [28] CORRELATION BETWEEN RED-CELL SURVIVAL AND ECXESS OF ALPHA-GLOBIN SYNTHESIS IN BETA-THALASSAEMIA
    VIGI, V
    VOLPATO, S
    GABURRO, D
    CONCONI, F
    BARGELLESI, A
    PONTREMOLI, S
    BRITISH JOURNAL OF HAEMATOLOGY, 1969, 16 (1-2) : 25 - +
  • [29] Hepatocytes of donor origin in recipient liver after haematopoietic stem cell transplantation in beta-thalassaemia major patients
    Ghavamzadeh, A.
    Mirzania, M.
    Sedighi, N.
    Yaghmaie, M.
    Kamalian, N.
    Alimoghaddam, K.
    Ghaffari, S. H.
    Azimi, P.
    BONE MARROW TRANSPLANTATION, 2008, 41 : S132 - S132
  • [30] Effectiveness of red cell osmotic fragility test with varying degrees of saline concentration in detecting beta-thalassaemia trait
    Singh, S. P.
    Gupta, S. C.
    SINGAPORE MEDICAL JOURNAL, 2008, 49 (10) : 823 - 826