Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Anemia and HBA[original query] |
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| [Clinical phenotype genotype correlation in children with hemoglobin H disease in Zhuhai area of China]. Zhonghua er ke za zhi. Chinese journal of pediatrics 2004 Sep 42 (9): 693-6. Zhou Yu-qiu, Xiao Qi-zhi, Huang Li-juan, Xiao Ge-fei, Li Wen-dian, Zhu Lan-fang, Chen Zi-xia, Zhang Yu-m |
| Association of alpha-thalassemia, TNF-alpha (-308G>A) and VCAM-1 (c.1238G>C) gene polymorphisms with cerebrovascular disease in a newborn cohort of 411 children with sickle cell anemia. Blood cells, molecules & diseases 2015 Jan 54 (1): 44-50. Belisário André Rolim, Nogueira Frederico Lisboa, Rodrigues Rahyssa Sales, Toledo Nayara Evelin, Cattabriga Ana Luiza Moreira, Velloso-Rodrigues Cibele, Duarte Filipe Otávio Chaves, Silva Célia Maria, Viana Marcos Bora |
| Influence of alpha thalassemia on clinical and laboratory parameters among nigerian children with sickle cell anemia. Journal of clinical laboratory analysis 2018 8 33 (2): e22656. Olatunya Oladele S, Albuquerque Dulcineia M, Adekile Adekunle, Costa Fernando |
| Hemoglobin A clearance in children with sickle cell anemia on chronic transfusion therapy. Transfusion 2018 4 58 (6): 1363-1371. Yee Marianne E M, Josephson Cassandra D, Winkler Anne M, Webb Jennifer, Luban Naomi L C, Leong Traci, Stowell Sean R, Roback John D, Fasano Ross |
| Reference intervals for HbA and HbF and cut-off value of HbA for ?-thalassemia carrier screening in a Guizhou population of reproductive age. Clinical biochemistry 2018 12 65 24-28. Han Wen-Ping, Huang Ling, Li Yuan-Yuan, Han Yuan-Yuan, Li Di, An Bang-Quan, Huang Sheng-W |
| Hemoglobin variants in southern China: results obtained during the measurement of glycated hemoglobin in a large population. Clinical chemistry and laboratory medicine 2020 Jul . Xu Anping, Chen Weidong, Xie Weijie, Wang Yajun, Ji Li |
| Hematological Parameters in Individuals with Beta Thalassemia Trait in South Sumatra, Indonesia. Anemia 2022 5 2022 3572986. Sari Dian Puspita, Wahidiyat Pustika Amalia, Setianingsih Iswari, Timan Ina S, Gatot Djajadiman, Kekalih Ar |
| Significance of borderline HbA levels in ? thalassemia carrier screening. Scientific reports 2022 3 12 (1): 5414. Colaco Stacy, Colah Roshan, Nadkarni Ani |
| In vivo evaluation of the effect of sickle cell hemoglobin S, C and therapeutic transfusion on erythrocyte metabolism and cardiorenal dysfunction. American journal of hematology 2023 3 . D'Alessandro Angelo, Nouraie S Mehdi, Zhang Yingze, Cendali Francesca, Gamboni Fabia, Reisz Julie A, Zhang Xu, Bartsch Kyle W, Galbraith Matthew D, Gordeuk Victor R, Gladwin Mark |
| In vivo evaluation of the effect of sickle cell hemoglobin S, C and therapeutic transfusion on erythrocyte metabolism and cardiorenal dysfunction. bioRxiv : the preprint server for biology 2023 2 . D'Alessandro Angelo, Nouraie S Mehdi, Zhang Yingze, Cendali Francesca, Gamboni Fabia, Reisz Julie A, Zhang Xu, Bartsch Kyle W, Galbraith Matthew D, Gordeuk Victor R, Gladwin Mark |
| Case report: Whole-exome sequencing for a hereditary elliptocytosis case with an unexpectedly low HbA. Frontiers in medicine 2023 12 10 1301760. Lu Pang, Ziyi Zeng, Yadi Ding, Haiming Huang, Haixia |
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