CLINICAL AND HEMATOLOGICAL RESPONSE OF SICKLE-CELL CHILDREN TO TREATMENT WITH HYDROXYUREA

被引：0
|
作者：
DEMONTALEMBERT, M
BELLOY, M
BERNAUDIN, F
DUCROCQ, R
MAIERREDELSPERGER, M
PHILIPPE, N
SCHECHTER, A
GIROT, R
机构：
[1] HOP ROBERT DEBRE,SERV HEMATOL,PARIS,FRANCE
[2] NIDDKD,BETHESDA,MD
[3] HOP NECKER ENFANTS MALAD,CTR TRANSFUS SANGUINE,F-75730 PARIS 15,FRANCE
[4] CTR HOSP INTERCOMMUNAL CRETEIL,F-94010 CRETEIL,FRANCE
[5] HOP TENON,HEMATOL LAB,F-75970 PARIS 20,FRANCE
[6] HOP DEBROUSSE,SERV HEMATOL,F-69005 LYON,FRANCE
来源：
BLOOD | 1994年 / 84卷 / 10期
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：A219 / A219
页数：1
相关论文
共 50 条
  • [31] Sustained long-term hematological efficacy of hydroxyurea for children with sickle cell disease
    Zimmerman, SA
    Schultz, WH
    Pickens, CV
    Davis, JS
    MacKeigan, SF
    Howard, TA
    Ware, RE
    PEDIATRIC RESEARCH, 2002, 51 (04) : 239A - 239A
  • [32] RED-CELL SIZE AND THE CLINICAL AND HEMATOLOGICAL FEATURES OF HOMOZYGOUS SICKLE-CELL DISEASE
    SERJEANT, GR
    FOSTER, K
    SERJEANT, BE
    BRITISH JOURNAL OF HAEMATOLOGY, 1981, 48 (03) : 445 - 449
  • [33] Is Hydroxyurea Treatment Changing the Life of Children with Sickle Cell Disease?
    Al Sabbah, Mohammed Ali
    Radaideh, Mahmoud
    Saleh, Shafeeka Mohammed
    Al-Doory, Sura Ahmed
    Abdalqader, Amal Mahmoud
    Mir, Fatima Farid
    Mohammed, Aya
    DUBAI MEDICAL JOURNAL, 2023, 6 (04): : 301 - 305
  • [34] CLINICAL, HEMATOLOGICAL AND GENETIC FEATURES OF SICKLE-CELL-ANEMIA AND SICKLE-CELL BETA THALASSEMIA IN A BRAZILIAN POPULATION
    ZAGO, MA
    COSTA, FF
    FREITAS, TC
    BOTTURA, C
    CLINICAL GENETICS, 1980, 18 (01) : 58 - 64
  • [35] SICKLE-CELL BETA+-THALASSEMIA - A HEMATOLOGICAL AND CLINICAL-STUDY IN LIBERIA
    BIENZLE, U
    KAPPES, R
    REIMER, A
    FELDHEIM, M
    TISCHENDORF, FW
    KOHNE, E
    BLUT, 1983, 47 (05): : 279 - 285
  • [36] INFLUENCE OF HBS LEVELS UPON THE HEMATOLOGICAL AND CLINICAL CHARACTERISTICS OF SICKLE-CELL TRAIT
    KENNEDY, A
    WALSH, D
    NICHOLSON, R
    ADAMS, JG
    STEINBERG, MH
    CLINICAL RESEARCH, 1984, 32 (05): : A843 - A843
  • [37] OUTPATIENT TREATMENT OF FEBRILE CHILDREN WITH SICKLE-CELL DISEASE
    ROS, SP
    NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (03): : 219 - 219
  • [38] Sickle-cell disease in Brazzaville, Congo:: Genetical, hematological, biochemical and clinical aspects
    Mouélé, R
    Boukila, V
    Fourcade, V
    Feingold, J
    Galactéros, F
    ACTA HAEMATOLOGICA, 1999, 101 (04) : 178 - 184
  • [39] INFLUENCE OF HBS LEVELS UPON THE HEMATOLOGICAL AND CLINICAL CHARACTERISTICS OF SICKLE-CELL TRAIT
    KENNEDY, AP
    WALSH, DA
    NICHOLSON, R
    ADAMS, JG
    STEINBERG, MH
    AMERICAN JOURNAL OF HEMATOLOGY, 1986, 22 (01) : 51 - 54
  • [40] STUDIES IN SICKLE-CELL ANEMIA .8. FURTHER OBSERVATIONS ON THE CLINICAL MANIFESTATIONS OF SICKLE-CELL ANEMIA IN CHILDREN
    SCOTT, RB
    FERGUSON, AD
    JENKINS, ME
    CLARK, HM
    AMA AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1955, 90 (06): : 682 - 691
12345