Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: Hypoglycemia and ABCC8[original query] |
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Mutation spectra of ABCC8 gene in Spanish patients with Hyperinsulinism of Infancy (HI). Human mutation 2006 1 27 (2): 214. Fernández-Marmiesse Ana, Salas Antonio, Vega Ana, Fernández-Lorenzo José Ramón, Barreiro Jesús, Carracedo Ang |
Genotype-phenotype associations in patients with severe hyperinsulinism of infancy. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 0 10 (1): 25-34. Greer Ristan M, Shah Janaki, Jeske Yvette W, Brown David, Walker Rosslyn M, Cowley David, Bowling Francis G, Liaskou Daphne, Harris Mark, Thomsett Michael J, Choong Catherine, Bell John R, Jack Michelle M, Cotterill Andrew |
Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations. European journal of endocrinology / European Federation of Endocrine Societies 2010 May 162 (5): 987-92. Flanagan S E, Kapoor R R, Mali G, Cody D, Murphy N, Schwahn B, Siahanidou T, Banerjee I, Akcay T, Rubio-Cabezas O, Shield J P H, Hussain K, Ellard |
KATP channel mutations in congenital hyperinsulinism. Seminars in pediatric surgery 2010 12 20 (1): 18-22. Saint-Martin Cécile, Arnoux Jean-Baptiste, de Lonlay Pascale, Bellanné-Chantelot Christi |
ABCC8 polymorphism (Ser1369Ala): influence on severe hypoglycemia due to sulfonylureas. Pharmacogenomics 2010 Dec 11 (12): 1743-50. Sato Ryosuke, Watanabe Hiroshi, Genma Rieko, Takeuchi Masahiro, Maekawa Masato, Nakamura Hirotos |
ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia. Genetics in medicine : official journal of the American College of Medical Genetics 2011 Oct 13 (10): 891-4. Glaser Benjamin, Blech Ilana, Krakinovsky Yocheved, Ekstein Josef, Gillis David, Mazor-Aronovitch Kineret, Landau Heddy, Abeliovich Dvor |
Genotype and phenotype correlations in 417 children with congenital hyperinsulinism. The Journal of clinical endocrinology and metabolism 2012 Dec . Snider KE, Becker S, Boyajian L, Shyng SL, Macmullen C, Hughes N, Ganapathy K, Bhatti T, Stanley CA, Ganguly A |
Novel ABCC8 (SUR1) gene mutations in Asian Indian children with congenital hyperinsulinemic hypoglycemia. Annals of human genetics 2014 Sep 78 (5): 311-9. Jahnavi Suresh, Poovazhagi Varadarajan, Kanthimathi Sekar, Balamurugan Kandasamy, Bodhini Dhanasekaran, Yadav Jaivinder, Jain Vandana, Khadgawat Rajesh, Sikdar Mahuya, Bhavatharini Ayurchelvan, Das Ashok Kumar, Kaur Tanvir, Mohan Viswanathan, Radha Venkates |
CYP2C9, KCNJ11 and ABCC8 polymorphisms and the response to sulphonylurea treatment in type 2 diabetes patients. European journal of clinical pharmacology 2014 Apr 70 (4): 421-8. Klen Jasna, Dolžan Vita, Janež Andr |
ABCC8 R1420H Loss-of-Function Variant in a Southwest American Indian Community: Association With Increased Birth Weight and Doubled Risk of Type 2 Diabetes. Diabetes 2015 Aug . Baier Leslie J, Muller Yunhua Li, Remedi Maria Sara, Traurig Michael, Piaggi Paolo, Wiessner Gregory, Huang Ke, Stacy Alyssa, Kobes Sayuko, Krakoff Jonathan, Bennett Peter H, Nelson Robert G, Knowler William C, Hanson Robert L, Nichols Colin G, Bogardus Clift |
Screening for Mutations in ABCC8 and KCNJ11 Genes in Saudi Persistent Hyperinsulinemic Hypoglycemia of Infancy (PHHI) Patients. Genes 2015 6 (2): 206-15. Adi Ahmad, Abbas Bassam Bin, Hamed Mohamed Al, Tassan Nada Al, Bakheet Da |
Congenital hyperinsulinism in Chinese patients: 5-yr treatment outcome of 95 clinical cases with genetic analysis of 55 cases. Pediatric diabetes 2015 Feb . Gong Chunxiu, Huang Shuyue, Su Chang, Qi Zhan, Liu Fang, Wu Di, Cao Bingyan, Gu Yi, Li Wenjin, Liang Xuejun, Liu M |
High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism. The Journal of clinical endocrinology and metabolism 2015 Oct jc20152763. Rozenkova Klara, Malikova Jana, Nessa Azizun, Dusatkova Lenka, Bjørkhaug Lise, Obermannova Barbora, Dusatkova Petra, Kytnarova Jitka, Aukrust Ingvild, Najmi Laeya, Rypackova Blanka, Sumnik Zdenek, Lebl Jan, Njølstad Pål R, Hussain Khalid, Pruhova Stepan |
Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism. Journal of clinical research in pediatric endocrinology 2015 Dec . Güven Ayla, Cebeci Ay?e Nurcan, Ellard Sian, Flanagan Sarah |
Search for Pharmacoepigenetic Correlations in Type 2 Diabetes Under Sulfonylurea Treatment. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2018 2 127 (4): 226-233. Karaglani Makrina, Ragia Georgia, Panagopoulou Maria, Balgkouranidou Ioanna, Nena Evangelia, Kolios George, Papanas Nikolaos, Manolopoulos Vangelis G, Chatzaki Ekateri |
Analysis on the pathogenic genes of 60 Chinese children with congenital hyperinsulinemia. Endocrine connections 2018 11 7 (12): 1251-1261. Xu Zi-Di, Zhang Wei, Liu Min, Wang Huan-Min, Hui Pei-Pei, Liang Xue-Jun, Yan Jie, Wu Yu-Jun, Sang Yan-Mei, Zhu Cheng, Ni Gui-Ch |
Clinical and genetic predictors of secondary sulfonylurea failure in Type 2 diabetes patients: the SUCLINGEN study. Pharmacogenomics 2020 5 21 (9): 587-600. Loganadan Navin Kumar, Huri Hasniza Zaman, Vethakkan Shireene Ratna, Hussein Zanari |
Genetic variants of ABCC8 and phenotypic features in Chinese early onset diabetes. Journal of diabetes 2020 Dec . Li Meng, Gong Siqian, Han Xueyao, Zhang Simin, Ren Qian, Cai Xiaoling, Luo Yingying, Zhou Lingli, Zhang Rui, Liu Wei, Zhu Yu, Zhou Xianghai, Sun Yanfang, Li Yufeng, Ma Yumin, Ji Lino |
Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes. Diabetes care 2020 11 44 (1): 35-42. Bowman Pamela, Mathews Frances, Barbetti Fabrizio, Shepherd Maggie H, Sanchez Janine, Piccini Barbara, Beltrand Jacques, Letourneau-Freiberg Lisa R, Polak Michel, Greeley Siri Atma W, Rawlins Eamon, Babiker Tarig, Thomas Nicholas J, De Franco Elisa, Ellard Sian, Flanagan Sarah E, Hattersley Andrew T, |
The Genetics of Adverse Drug Outcomes in Type 2 Diabetes: A Systematic Review. Frontiers in genetics 2021 7 12 675053. Baye Assefa M, Fanta Teferi G, Siddiqui Moneeza K, Dawed Adem |
Pharmacogenetics of sulfonylurea-induced hypoglycemia in Type 2 diabetes patients: the SUCLINGEN study. Pharmacogenomics 2021 10 22 (16): 1057-1068. Loganadan Navin Kumar, Huri Hasniza Zaman, Vethakkan Shireene Ratna, Hussein Zanari |
Genetic variants of ABCC8 and clinical manifestations in eight Chinese children with hyperinsulinemic hypoglycemia. BMC endocrine disorders 2024 1 24 (1): 8. Guoying Chang, Lingwen Ying, Qianwen Zhang, Biyun Feng, Ruen Yao, Yu Ding, Juan Li, Xiaodong Huang, Yongnian Shen, Tingting Yu, Jian Wang, Xiumin Wa |
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- Page last updated:Apr 22, 2024
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