Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: Jaundice and G6PD[original query] |
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Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency. Haematologica 2001 1 86 (1): 30-5. Pietrapertosa A, Palma A, Campanale D, Delios G, Vitucci A, Tannoia |
Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays. Human mutation 2003 Jan 21 (1): 101. Ainoon O, Yu Y H, Amir Muhriz A L, Boo N Y, Cheong S K, Hamidah N |
[Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome]. Acta médica portuguesa 0 15 (6): 409-12. Costa Elísio, Vieira Emilia, Cleto Esmeralda, Cabeda José M, Pinho Luciana, Coimbra Eduarda, Dos Santos Rosário, Barbot Jo |
Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind). Blood cells, molecules & diseases 0 34 (2): 191-6. Laosombat Vichai, Sattayasevana Benjamas, Janejindamai Waricha, Viprakasit Vip, Shirakawa Taku, Nishiyama Kaoru, Matsuo Masafu |
Prevalence of G6PD deficiency in newborns in the south of Brazil. Journal of medical screening 2006 13 (2): 85-6. Castro Simone, Weber Raquel, Dadalt Vivian, Tavares Volnei, Giugliani Rober |
Three mutations analysis of glucose-6-phosphate dehydrogenase deficiency in neonates in South-west China. Pediatrics international : official journal of the Japan Pediatric Society 2007 Aug 49 (4): 463-7. Deng C, Guo CB, Xu YH, Deng B, Yu JL |
UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia. Pediatric research 2009 Jun 65 (6): 675-80. Agrawal Sunil K, Kumar Praveen, Rathi Ritu, Sharma Neeraj, DAS Reena, Prasad Rajendra, Narang An |
Prevalence of uridine glucuronosyl transferase 1A1 (UGT1A1) mutations in Malay neonates with severe jaundice. The Malaysian journal of pathology 2011 Dec 33 (2): 95-100. Azlin I, Wong F L, Ezham M, Hafiza A, Ainoon |
Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association. Molecular biology reports 2012 Oct . Laouini N, Bibi A, Ammar H, Kazdaghli K, Ouali F, Othmani R, Amdouni S, Haloui S, Sahli CA, Jouini L, Hadj Fredj S, Siala H, Ben Romdhane N, Toumi NE, Fattoum S, Messsaoud T |
Relation between Neonatal Icter and Gilbert Syndrome in Gloucose-6-Phosphate Dehydrogenase Deficient Subjects. Journal of clinical and diagnostic research : JCDR 2014 Mar 8 (3): 63-5. Zahedpasha Yadollah, Ahmadpour Mousa, Niaki Haleh Akhavan, Alaee Ehs |
Comparison of molecular mutations of G6PD deficiency gene between icteric and nonicteric neonates. International journal of molecular and cellular medicine 2013 2 (1): 14-20. Zahedpasha Yadollah, Ahmadpour Kachouri Mousa, Akhavan Niaki Haleh, Farhadi Ro |
Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency in Greek newborns: the Mediterranean C563T mutation screening. Scandinavian journal of clinical and laboratory investigation 2014 Apr 74 (3): 259-63. Molou Elina, Schulpis Kleopatra H, Thodi Georgia, Georgiou Vassiliki, Dotsikas Yannis, Papadopoulos Konstantinos, Biti Sofia, Loukas Yannis |
Molecular Characterization of Glucose-6-phosphate Dehydrogenase Deficiency in Families from the Republic of Macedonia and Genotype-phenotype Correlation. Medical archives (Sarajevo, Bosnia and Herzegovina) 2015 Oct 69 (5): 284-8. Cherepnalkovski Anet Papazovska, Zemunik Tatijana, Glamocanin Sofijanka, Piperkova Katica, Gunjaca Ivana, Kocheva Svetlana, Jovanova Biljana Coneska, Krzelj Vjekosl |
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 |
Evaluating the performance of automated UV enzymatic assay for screening of glucose 6-phosphate dehydrogenase deficiency. International journal of laboratory hematology 2018 11 41 (2): 192-199. Anantasomboon Pornchai, Chanda Makamas, Jugnam-Ang Watcharapong, Witoonpanich Pirada, Cheepsunthorn Poonlarp, Nuchprayoon Issarang, Fucharoen Suthat, Cheepsunthorn Chalisa |
Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study. BioMed research international 2018 2018 7803175. Zhou Jinfu, Yang Changyi, Zhu Wenbin, Chen Shuwei, Zeng Yinglin, Wang Jing, Zhao Hong, Chen Yao, Lin Fe |
G6PD genetic variations in neonatal Hyperbilirubinemia in Indonesian Deutromalay population. BMC pediatrics 2019 Dec 19 (1): 506. Wisnumurti Dewi A, Sribudiani Yunia, Porsch Robert M, Maskoen Ani M, Rahayuningsih Sri E, Asni Eni K, Sleutels Frank, van Ijcken Wilfred F J, Sukadi Abdurachman, Achmad Tri |
Glucose-6-phosphate dehydrogenase deficiency and susceptibility to childhood diseases in Kilifi, Kenya. Blood advances 2020 Dec 4 (23): 5942-5950. Uyoga Sophie, Macharia Alex W, Ndila Carolyne M, Nyutu Gideon, Shebe Mohammed, Awuondo Kennedy O, Mturi Neema, Peshu Norbert, Tsofa Benjamin, Scott J Anthony G, Maitland Kathryn, Williams Thomas |
[Correlation analysis of genotypes and the enzymatic activities of glucose-6-phosphate dehydrogenase in neonates in Guangzhou]. Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] 2020 11 54 (11): 1275-1282. Tang F, Tang C F, Jiang X, Jia X F, Liu S C, Chen Q Y, Huang Y |
Prevalence of UGT1A1 (TA)n promoter polymorphism in Panamanians neonates with G6PD deficiency. Journal of genetics 2021 2 99 . Chávez-Peña Teresa, Martínez-Camberos Alejandra, Cossio-Gurrola Gladys, Arámbula-Meraz Eliakym, Herrera-Rodríguez Indira, Romo-Martínez Enrique, García-Magallanes Noe |
Mutation spectrum and enzyme profiling of G6PD deficiency in neonates of north India: a prospective study. Journal of genetics 2023 9 102 . Upasana Bhattacharyya, Preeti Deswal, Sunil Kumar Polipalli, Diksha Sharma, Manpreet Kaur, , Seema Kapoor, B K Thel |
UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice. Frontiers in pediatrics 2023 1 10 1080212. Yang Zhe, Lin Fen, Xu Jia-Xin, Yang Hui, Wu Yong-Hao, Chen Zi-Kai, Xie He, Huang Bin, Lin Wei-Hao, Wu Jian-Peng, Ma Yu-Bin, Li Jian-Dong, Yang Li- |
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