Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 17 (of 17 Records) |
Query Trace: Hemoglobin E Disease[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 |
The clinical impact of MTHFR polymorphism on the vascular complications of sickle cell disease. Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2006 Oct 39 (10): 1291-5. Moreira Neto F, Lourenço D M, Noguti M A E, Morelli V M, Gil I C P, Beltrão A C S, Figueiredo M |
Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysis. Blood cells, molecules & diseases 0 53 (1-2): 11-5. Pakdee Naruwat, Yamsri Supawadee, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Pissard Serge, Fucharoen Sup |
Analysis of the genetic variants associated with recurrent thromboembolism in a patient with hemoglobin H disease following splenectomy: A case report. Biomedical reports 2016 Jul 5 (1): 23-26. Sun N A, Cheng Peng, Deng Dong-Hong, Liu Rong-Rong, Lai Yong-Ro |
Proliferative retinopathy and maculopathy are two independent conditions in sickle cell disease: Is there a role of blood rheology?1. Clinical hemorheology and microcirculation 2018 6 71 (3): 337-345. Beral Laurence, Lemonne Nathalie, Romana Marc, Charlot Keyne, Billaud Marie, Acomat Malik, Zorobabel Coralie, Nader Elie, Etienne-Julan Maryse, David Thierry, Connes Philip |
Progressive Decline in Estimated GFR in Patients With Sickle Cell Disease: An Observational Cohort Study. American journal of kidney diseases : the official journal of the National Kidney Foundation 2019 2 74 (1): 47-55. Derebail Vimal K, Ciccone Emily J, Zhou Qingning, Kilgore R Rosina, Cai Jianwen, Ataga Kenneth |
Polymorphisms in genes that affect the variation of lipid levels in a Brazilian pediatric population with sickle cell disease: rs662799 APOA5 and rs964184 ZPR1. Blood cells, molecules & diseases 2019 Oct 80 102376. Valente-Frossard Thaisa Netto Souza, Cruz Nilcemar Rodrigues Carvalho, Ferreira Fernanda Oliveira, Belisario Andre Rolim, Pereira Brisa Machado, Gomides Antônio Frederico de Freitas, Resende Glaucia Aparecida Domingos, Carlos Aline Menezes, Moraes-Souza Helio, Velloso-Rodrigues Cibe |
Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province. Frontiers in pediatrics 2020 5 8 159. Huang Ti-Long, Zhang Tian-Yao, Song Chun-Yan, Lin Yun-Bi, Sang Bao-Hua, Lei Qing-Ling, Lv Yu, Yang Chun-Hui, Li Na, Tian Xin, Yang Yue-Huang, Zhang Xian-W |
[Study of the genotypic and hematological feature of hemoglobin H disease in West Guangxi area]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 Dec 37 (12): 1326-1330. Nong Xuejuan, Xu Guidan, Li Jia, Liang Juhua, Zhong Shimao, Liu Chunhong, Wang Chunfa |
Telomere shortening correlates with disease severity in hemoglobin H disease patients. Blood cells, molecules & diseases 2021 4 89 102563. Panjawatanan Panadeekarn, Charoenkwan Pimlak, Tantiworawit Adisak, Strogatz David, Perry Kelly E, Tuntiwechapikul Wiro |
Prevalence and Genetic Analysis of ?-Thalassemia in the Dali Bai Autonomous Prefecture of the Yunnan Province, China. Genetic testing and molecular biomarkers 2022 3 26 (3): 152-156. Wang Xiao-Xuan, Ma Yu-Yuan, Zhang Wei, Liu Jia-Yao, Su Lan-Ying, Su Hui, Lin Xiao-Yan, Yuan Jin-Ying, Wang Yan, Liu Yun-Chun, Lai Ming-Mi |
Detecting rare thalassemia in children with anemia using third-generation sequencing. Hematology (Amsterdam, Netherlands) 2023 8 28 (1): 2241226. Zhen-Min Ren, Wu-Jiao Li, Zhi-Hao Xing, Xiao-Ying Fu, Ju-Yan Zhang, Yun-Sheng Chen, De-Fa |
Clinical significance of mutational variants in beta and alpha genes in patients with hemoglobinopathies from two large Greek centers: a complex interplay between genotype and phenotype. Journal of molecular medicine (Berlin, Germany) 2023 7 . Michael D Diamantidis, Rebecca-Anastasia Karanikola, Chrysoula Polyzoudi, Sophia Delicou, Achilles Manafas, Helen Savera, Aikaterini Xydaki, Angeliki Kotsiafti, Evangelos Tsangalas, Georgia Ikonomou, Eirini Mani, Konstantinos Ntoulas, Evangelos Alexiou, Ioanna Argyrakouli, John Koskinas, Paraskevi Foti |
Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare ?-Globin Mutations. Hemoglobin 2023 6 1-4. Yuling Qiu, Shilu Wei, Wei Hou, Ketong Lai, Hengying Zhu, Wenwei Li, Qi Li, Zheng Yang, Qisheng Shu, Ping Chen, Wuning |
[Characteristics of Silent Alpha Thalassemia Gene in Child-Bearing Adults in Guangdong]. Zhongguo shi yan xue ye xue za zhi 2023 12 31 (6): 1811-1814. Ge Huang, You-Wei Zheng, Ji Wu, Sheng-Nan L |
Alpha-Hemoglobin Stabilizing Protein Gene Polymorphism (rs4499252 A/G) and its Association with Beta-Thalassemia Major in Iraqi Patients. Archives of Razi Institute 2023 1 77 (3): 1033-1039. Adnan Khalaf M, Hasan Al-Saadi B Q, Qassim Mohammed H, Hussein Ewaid |
CETP gene polymorphisms and haplotypes are explanatory variables for HDL cholesterol level in sickle cell disease. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2024 1 57 e12879. N R C Cruz, T N S Valente, F O Ferreira, L R Macedo, A R Belisário, C M da Silva, N S Oliveira, A F F Gomides, C Velloso-Rodrigu |
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- Page last updated:Apr 16, 2024
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