Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 1, 2023. (Total: 217488Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 8 (of 8 Records)

Query Trace: Hypoglycemia and GCK[original query]
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
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
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
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
Potential impact of GCK, MIR-196A-2 and MIR-423 gene abnormalities on the development and progression of type 2 diabetes mellitus in Asir and Tabuk regions of Saudi Arabia.
Molecular medicine reports 2022 3 25 (5): .
Mir Mohammad Muzaffar, Mir Rashid, Alghamdi Mushabab Ayed Abdullah, Wani Javed Iqbal, Elfaki Imadeldin, Sabah Zia Ul, Alhujaily Muhanad, Jeelani Mohammed, Marakala Vijaya, Alharthi Muffarah Hamid, Al-Shahrani Abdullah
Identification and management of GCK-MODY complicating pregnancy in Chinese patients with gestational diabetes.
Molecular and cellular biochemistry 2022 3 477 (5): 1629-1643.
Jiang Yanyan, Jiang Fusong, Li Ming, Wu Qingkai, Xu Chenming, Zhang Rong, Song Mingqiang, Wang Yanzhong, Wang Ying, Chen Yating, Zhang Juan, Ge Xiaoxu, Zhu Qihan, Zhuang Langen, Yang Di, Lu Ming, Wang Feng, Jiang Meisheng, Liu Xipeng, Liu Yanjun, Liu Lim
The maternal and infant outcomes in GCK-MODY complicated with pregnancy: Systemic review and meta-analysis.
The Journal of clinical endocrinology and metabolism 2023 4 .
Ren Qian, Wang Zhihui, Yang Wenjia, Han Xueyao, Ji Lino
TOP