Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: Thalassemia and G6PD[original query] |
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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 |
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 |
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 |
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 |
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 |
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 |
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 |
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, |
Influence of the ßs haplotype and a-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 |
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 |
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 |
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- |
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 |
Serum Soluble Transferrin Receptor Concentrations Are Elevated in Congolese Children with Glucose-6-Phosphate Dehydrogenase Variants, but Not Sickle Cell Variants or ?-Thalassemia. The Journal of nutrition 2017 8 147 (9): 1785-1794. Barker Mikaela K, Henderson Amanda M, Naguib Karimah, Vercauteren Suzanne M, Devlin Angela M, Albert Arianne Y, Bahizire Esto, Tugirimana Pierrot L, Akilimali Pierre Z, Boy Erick, Green Tim J, Karakochuk Crystal |
Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift ß-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 |
Prevalence of Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency in Newborns and Adults at the Ramathibodi Hospital, Bangkok, Thailand. Hemoglobin 2017 12 41 (4-6): 260-266. Banyatsuppasin Wansa, Jindadamrongwech Sumalee, Limrungsikul Anchalee, Butthep Punn |
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 |
Newborn Screening for Hemoglobinopathies and Red Cell Enzymopathies in Tripura State: A Malaria-Endemic State in Northeast India. Hemoglobin 2018 2 42 (1): 43-46. Upadhye Dipti, Das Rajat S, Ray Jayanta, Acharjee Shukdeb, Ghosh Kanjaksha, Colah Roshan B, Mukherjee Malay |
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 |
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 |
Fasting glucose-to-HbA1c ratio is a good indicator of G6PD deficiency, but not thalassemia, in patients with type 2 diabetes mellitus. Clinica chimica acta; international journal of clinical chemistry 2020 3 506 9-15. Chang Ya-Sian, Hsiao Li-Yun, Lin Chien-Yu, Shih Mu-Chin, Hsieh Ming-Chia, Chang Jan-Gow |
Association of alpha-thalassemia and Glucose-6-Phosphate Dehydrogenase deficiency with transcranial Doppler ultrasonography in Nigerian children with sickle cell anemia. Journal of clinical laboratory analysis 2021 5 35 (6): e23802. Ojewunmi Oyesola Oyewole, Adeyemo Titilope Adenike, Oyetunji Ajoke Idayat, Benn Yewande, Ekpo Mfoniso Godwin, Iwalokun Bamidele Abiod |
A case of G6PD Utrecht associated with ?-thalassemia responding to splenectomy. Pediatric blood & cancer 2022 6 69 (9): e29837. Yang Kun, Liu Xiaodong, Chen Kai, Luo Shan, Kong Wenqiang, Huang Wenying, Xiao Ji |
Hemoglobinopathies, merozoite surface protein-2 gene polymorphisms, and acquisition of Epstein Barr virus among infants in Western Kenya. BMC cancer 2023 6 23 (1): 566. Perez K Olewe, Shehu Shagari Awandu, Elly O Munde, Samuel B Anyona, Evans Raballah, Asito S Amolo, Sidney Ogola, Erick Ndenga, Clinton O Onyango, Rosemary Rochford, Douglas J Perkins, Collins Ou |
Exploring Appropriate Reference Intervals and Clinical Decision Limits for Glucose-6-Phosphate Dehydrogenase Activity in Individuals From Guangzhou, China. Annals of laboratory medicine 2024 5 . Zhenyi Huang, Ziyan Li, Yating Li, Yunshan Cao, Suping Zhong, Jinlu Liu, Zhiqian Lin, Lijuan Lin, Yanping Fang, Jing Zeng, Zhaoying Su, Huibin Li, Jianfen Liang, Biqing Zhu, Zipei Lin, Yongxin Huang, Xuexi Yang, Lingxiao Jia |
Carrier frequency estimation of pathogenic variants of autosomal recessive and X-linked recessive mendelian disorders using exome sequencing data in 1,642 Thais. BMC medical genomics 2024 1 17 (1): 9. Wanna Chetruengchai, Prasit Phowthongkum, Vorasuk Shotelers |
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