The clinical features of haemoglobin SC disease in Jamaica.

Suppr

超能文献

作者信息

Serjeant G R, Ashcroft M T, Serjeant B E

出版信息

Br J Haematol. 1973 Apr;24(4):491-501. doi: 10.1111/j.1365-2141.1973.tb01675.x.

DOI:10.1111/j.1365-2141.1973.tb01675.x

PMID:4715144

Abstract

摘要

相似文献

The clinical features of haemoglobin SC disease in Jamaica.

Br J Haematol. 1973 Apr;24(4):491-501. doi: 10.1111/j.1365-2141.1973.tb01675.x.

Clinical features of homozygous SS disease in Jamaican children.

West Indian Med J. 1971 Mar;20(1):60-8.

The clinical features of sickle-cell- thalassaemia in Jamaica.

Br J Haematol. 1973 Jan;24(1):19-30. doi: 10.1111/j.1365-2141.1973.tb05723.x.

Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative Study of Sickle Cell Disease.

Arch Pediatr Adolesc Med. 1994 Aug;148(8):796-804. doi: 10.1001/archpedi.1994.02170080026005.

Ocular findings in hemoglobin SC disease in Jamaica.

Am J Ophthalmol. 1972 Nov;74(5):921-31. doi: 10.1016/0002-9394(72)91213-5.

A comparison of erythrocyte characteristics in sickle cell syndromes in Jamaica.

Br J Haematol. 1972 Aug;23(2):205-13. doi: 10.1111/j.1365-2141.1972.tb03473.x.

Ocular findings in children with sickle cell haemoglobin C disease in Jamaica.

Br J Ophthalmol. 1974 Jul;58(7):644-9. doi: 10.1136/bjo.58.7.644.

Haemoglobin SC disease in Jamaica.

Br J Radiol. 1973 Nov;46(551):935-42. doi: 10.1259/0007-1285-46-551-935.

Haematological factors associated with proliferative retinopathy in sickle cell-haemoglobin C disease.

Br J Ophthalmol. 1981 Oct;65(10):712-7. doi: 10.1136/bjo.65.10.712.

Homozygous sickle cell disease in Uganda and Jamaica a comparison of Bantu and Benin haplotypes.

West Indian Med J. 2012 Oct;61(7):684-91.

引用本文的文献

[>Femoral bone infarction revealing compound heterozygous SC sickle cell disease in a Moroccan patient].

Pan Afr Med J. 2020 Aug 28;36:361. doi: 10.11604/pamj.2020.36.361.22688. eCollection 2020.

Hydroxyurea decreases hospitalizations in pediatric patients with Hb SC and Hb SB+ thalassemia.

J Blood Med. 2015 Dec 15;6:285-90. doi: 10.2147/JBM.S97405. eCollection 2015.

Sickle cell haemoglobinopathies in England.

Arch Dis Child. 1981 Sep;56(9):676-83. doi: 10.1136/adc.56.9.676.

Exchange transfusion in life-threatening sickling crises.

J R Soc Med. 1982 Oct;75(10):777-80. doi: 10.1177/014107688207501006.

Sickle-cell disease in a British urban community.

Br Med J (Clin Res Ed). 1981 Jan 24;282(6260):283-6. doi: 10.1136/bmj.282.6260.283.

Sickle cell disease in Britain.

J Clin Pathol. 1984 Dec;37(12):1321-6. doi: 10.1136/jcp.37.12.1321.

Studies of the human factor VIII/von Willebrand factor protein. III. Qualitative defects in von Willebrand's disease.

J Clin Invest. 1975 Oct;56(4):814-27. doi: 10.1172/JCI108160.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

相似文献

The clinical features of haemoglobin SC disease in Jamaica.

Br J Haematol. 1973 Apr;24(4):491-501. doi: 10.1111/j.1365-2141.1973.tb01675.x.

Clinical features of homozygous SS disease in Jamaican children.

West Indian Med J. 1971 Mar;20(1):60-8.

The clinical features of sickle-cell- thalassaemia in Jamaica.

Br J Haematol. 1973 Jan;24(1):19-30. doi: 10.1111/j.1365-2141.1973.tb05723.x.

Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative Study of Sickle Cell Disease.

Arch Pediatr Adolesc Med. 1994 Aug;148(8):796-804. doi: 10.1001/archpedi.1994.02170080026005.

Ocular findings in hemoglobin SC disease in Jamaica.

Am J Ophthalmol. 1972 Nov;74(5):921-31. doi: 10.1016/0002-9394(72)91213-5.

A comparison of erythrocyte characteristics in sickle cell syndromes in Jamaica.

Br J Haematol. 1972 Aug;23(2):205-13. doi: 10.1111/j.1365-2141.1972.tb03473.x.

Ocular findings in children with sickle cell haemoglobin C disease in Jamaica.

Br J Ophthalmol. 1974 Jul;58(7):644-9. doi: 10.1136/bjo.58.7.644.

Haemoglobin SC disease in Jamaica.

Br J Radiol. 1973 Nov;46(551):935-42. doi: 10.1259/0007-1285-46-551-935.

Haematological factors associated with proliferative retinopathy in sickle cell-haemoglobin C disease.

Br J Ophthalmol. 1981 Oct;65(10):712-7. doi: 10.1136/bjo.65.10.712.

Homozygous sickle cell disease in Uganda and Jamaica a comparison of Bantu and Benin haplotypes.

West Indian Med J. 2012 Oct;61(7):684-91.

引用本文的文献

[>Femoral bone infarction revealing compound heterozygous SC sickle cell disease in a Moroccan patient].

Pan Afr Med J. 2020 Aug 28;36:361. doi: 10.11604/pamj.2020.36.361.22688. eCollection 2020.

Hydroxyurea decreases hospitalizations in pediatric patients with Hb SC and Hb SB+ thalassemia.

J Blood Med. 2015 Dec 15;6:285-90. doi: 10.2147/JBM.S97405. eCollection 2015.

Sickle cell haemoglobinopathies in England.

Arch Dis Child. 1981 Sep;56(9):676-83. doi: 10.1136/adc.56.9.676.

Exchange transfusion in life-threatening sickling crises.

J R Soc Med. 1982 Oct;75(10):777-80. doi: 10.1177/014107688207501006.

Sickle-cell disease in a British urban community.

Br Med J (Clin Res Ed). 1981 Jan 24;282(6260):283-6. doi: 10.1136/bmj.282.6260.283.

Sickle cell disease in Britain.

J Clin Pathol. 1984 Dec;37(12):1321-6. doi: 10.1136/jcp.37.12.1321.

Studies of the human factor VIII/von Willebrand factor protein. III. Qualitative defects in von Willebrand's disease.

J Clin Invest. 1975 Oct;56(4):814-27. doi: 10.1172/JCI108160.