Cholelithiasis in sickle cell anemia in a caucasian population-Reference-Cited by-同舟云学术

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Cholelithiasis in sickle cell anemia in a caucasian population

Published:1973-03 Issue:3 Volume:54 Page:327-332
ISSN:0002-9343
Container-title:The American Journal of Medicine
language:en
Short-container-title:The American Journal of Medicine

Author:

Perrine Richard P.

Publisher

Elsevier BV

Subject

General Medicine

Reference26 articles.

1. Sickle cell anemia: the known and the unknown (Editorial);Charche;Ann Intern Med,1972

2. Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin;Ali;Brit J Haemat,1970

3. Studies on abnormal hemoglobin. I. Alkali denaturation;Singer;Blood,1951

4. A new sickling disorder resulting from interaction of the genes for haemoglobin S and alpha-thalassemia;Weatherall;Brit J Haemat,1969

5. Family studies of thalassemia in Arabia;McNeil;Amer J Hum Genet,1967

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prevalence of β-S Globin Haplotypes in Jazan Region of Saudi Arabia;Clinical Laboratory;2021

2. Cholelithiasis in patients with paediatric sickle cell anaemia in a Saudi hospital;Journal of Taibah University Medical Sciences;2019-04

3. Outcome of cholelithiasis in Sudanese children with Sickle Cell Anaemia (SCA) after 13 years follow-up;African Health Sciences;2013-04-12

4. Sonographic Findings in Sudanese Children With Sickle Cell Anemia;Journal of Diagnostic Medical Sonography;2010-11

5. Sickle Cell Disease in Saudi Arabia: The Asian Haplotype;Annals of Saudi Medicine;2004-05

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