HuGE Literature Finder
Records 1-18
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Varied Age of First Presentation of Sickle Cell Disease: Case Presentations and Review.
Case reports in medicine 2021 2 2021 8895020. Claeys Alexis, Van Steijn Susanne, Van Kesteren Lydia, Damen Elizabet, Van Den Akker Machi |
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Influence of Oxidative Stress Biomarkers and Genetic Polymorphisms on the Clinical Severity of Hydroxyurea-Free Senegalese Children with Sickle Cell Anemia.
Antioxidants (Basel, Switzerland) 2020 Sep 9 (9): . Gueye Tall Fatou, Martin Cyril, Ndour El Hadji Malick, Faes Camille, Déme Ly Indou, Pialoux Vincent, Connes Philippe, Gueye Papa Madieye, Ndiaye Diallo Rokhaya, Renoux Céline, Diagne Ibrahima, Diop Pape Amadou, Cissé Aynina, Sall Philomène Lopez, Joly Philip |
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Analysis of genotype distribution of thalassemia and G6PD deficiency among Hakka population in Meizhou city of Guangdong Province.
Journal of clinical laboratory analysis 2019 Dec e23140. Wu Heming, Zhu Qiuyan, Zhong Hua, Yu Zhikang, Zhang Qunji, Huang Qingy |
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Associations between erythrocyte polymorphisms and risks of uncomplicated and severe malaria in Ugandan children: A case control study.
PloS one 2018 13 (9): e0203229. Mpimbaza Arthur, Walakira Andrew, Ndeezi Grace, Katahoire Anne, Karamagi Charles, Nsobya Samuel L, Tukwasibwe Stephen, Asua Victor, Rosenthal Philip |
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Marked variation in prevalence of malaria-protective human genetic polymorphisms across Uganda.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2017 Sep . Walakira Andrew, Tukwasibwe Stephen, Kiggundu Moses, Verra Federica, Kakeeto Patrick, Ruhamyankaka Emmanuel, Drakeley Chris, Dorsey Grant, Kamya Moses R, Nsobya Samuel L, Rosenthal Philip |
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Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift ?-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2].
Hemoglobin 2017 Jul 1-7. Gueye Tall Fatou, Martin Cyril, Malick Ndour El Hadji, Déme Ly Indou, Renoux Céline, Chillotti Louis, Veyrenche Nicolas, Connes Philippe, Madieye Gueye Papa, Ndiaye Diallo Rokhaya, Lacan Philippe, Diagne Ibrahima, Amadou Diop Pape, Cissé Aynina, Lopez Sall Philomène, Joly Philip |
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Molecular Epidemiological Survey of Glucose-6-Phosphate Dehydrogenase Deficiency and Thalassemia in Uygur and Kazak Ethnic Groups in Xinjiang, Northwest China.
Hemoglobin 2016 Mar 1-8. Han Luhao, Su Hai, Wu Hao, Jiang Weiying, Chen Suq |
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Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan.
BMC pediatrics 2016 16 (1): 144. Weng Yi-Hao, Chiu Ya-Wen, Cheng Shao-Wen, Yang Chun-Y |
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Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia.
Pediatrics and neonatology 2015 Dec . Yang Hui, Wang Qian, Zheng Lei, Zheng Xiang-Bin, Lin Min, Zhan Xiao-Fen, Yang Li- |
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Influence of the ?s haplotype and ?-thalassemia on stroke development in a Brazilian population with sickle cell anaemia.
Annals of hematology 2014 Jul 93 (7): 1123-9. Domingos Igor F, Falcão Diego A, Hatzlhofer Betania L, Cunha Anderson F, Santos Magnun N, Albuquerque Dulcinéia M, Fertrin Kleber Y, Costa Fernando F, Azevedo Renata C, Machado Cíntia G, Araújo Aderson S, Lucena-Araujo Antonio R, Bezerra Marcos |
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Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes.
American journal of hematology 2013 Jul 88 (7): 571-6. Sheehan Vivien A, Luo Zhaoyu, Flanagan Jonathan M, Howard Thad A, Thompson Bruce W, Wang Winfred C, Kutlar Abdullah, Ware Russell E, |
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High prevalence of hemoglobin disorders and glucose-6-phosphate dehydrogenase (G6PD) deficiency in the Republic of Guinea (West Africa).
Hemoglobin 2012 36 (1): 25-37. Millimono Tamba S, Loua Kovana M, Rath Silvia L, Relvas Luis, Bento Celeste, Diakite Mandiou, Jarvis Martin, Daries Nathalie, Ribeiro Leticia M, Manco Licínio, Kaeda Jaspal |
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Genetic predictors for stroke in children with sickle cell anemia.
Blood 2011 Jun 117 (24): 6681-4. Flanagan Jonathan M, Frohlich Denise M, Howard Thad A, Schultz William H, Driscoll Catherine, Nagasubramanian Ramamoorthy, Mortier Nicole A, Kimble Amy C, Aygun Banu, Adams Robert J, Helms Ronald W, Ware Russell |
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G6PD deficiency, absence of alpha-thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia.
Blood 2008 Nov 112 (10): 4314-7. Bernaudin Françoise, Verlhac Suzanne, Chevret Sylvie, Torres Martine, Coic Lena, Arnaud Cécile, Kamdem Annie, Hau Isabelle, Grazia Neonato Maria, Delacourt Christop |
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Prevalence of beta-thalassemia trait and glucose-6-phosphate dehydrogenase deficiency in Iranian Jews.
Archives of medical research 2008 Feb 39 (2): 212-4. Karimi Mehran, Yavarian Majid, Afrasiabi Abdolreza, Dehbozorgian Javad, Rachmilewitz Eliez |
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Red blood cell polymorphisms in relation to Plasmodium falciparum asymptomatic parasite densities and morbidity in Senegal.
Microbes and infection / Institut Pasteur 2006 Aug 8 (9-10): 2352-8. Migot-Nabias Florence, Pelleau Stéphane, Watier Laurence, Guitard Juliette, Toly Cécile, De Araujo Carla, Ngom Mamadou I, Chevillard Christophe, Gaye Oumar, Garcia And |
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Effects of variant UDP-glucuronosyltransferase 1A1 gene, glucose-6-phosphate dehydrogenase deficiency and thalassemia on cholelithiasis.
World journal of gastroenterology : WJG 2005 Sep 11 (36): 5710-3. Huang Yang-Yang, Huang Ching-Shui, Yang Sien-Sing, Lin Min-Shung, Huang May-Jen, Huang Ching-Sh |
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UGT1A1 promoter polymorphism associated with serum bilirubin level in Saudi patients with sickle cell disease.
Annals of Saudi medicine 0 33 (4): 372-6. Hamad Zainab, Aljedai Abdullah, Halwani Rabih, AlSultan Abdulrahm |
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- Page last updated:Mar 05, 2021
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