28 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 33502730 | Analysis of clinical and genetic characteristics of Chinese children with congenital hyperinsulinemia that is spontaneously relieved. | 2021 Apr | 1 |
2 | 33770274 | Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia. | 2021 Sep | 1 |
3 | 34633981 | Birth weight and diazoxide unresponsiveness strongly predict the likelihood of congenital hyperinsulinism due to a mutation in ABCC8 or KCNJ11. | 2021 Oct 30 | 1 |
4 | 30114684 | The Use of a Long-Acting Somatostatin Analogue (Lanreotide) in Three Children with Focal Forms of Congenital Hyperinsulinaemic Hypoglycaemia. | 2019 | 1 |
5 | 31464105 | Novel dominant KATP channel mutations in infants with congenital hyperinsulinism: Validation by in vitro expression studies and in vivo carrier phenotyping. | 2019 Nov | 1 |
6 | 28270372 | Congenital Hyperinsulinism in China: A Review of Chinese Literature Over the Past 15 Years. | 2017 Sep 1 | 3 |
7 | 27181099 | A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with Sirolimus. | 2016 Dec 1 | 2 |
8 | 27646472 | Activation of ATP-sensitive potassium channels enhances DMT1-mediated iron uptake in SK-N-SH cells in vitro. | 2016 Sep 20 | 1 |
9 | 27693800 | Effects of ZD0947, a novel and potent ATP-sensitive K+ channel opener, on smooth muscle-type ATP-sensitive K+ channels. | 2016 Nov 15 | 1 |
10 | 26316440 | Nifedipine in Congenital Hyperinsulinism - A Case Report. | 2015 Jun | 1 |
11 | 26392140 | Topical sulfonylurea as a novel therapy for hypertrichosis secondary to diazoxide, and potentially for other conditions with excess hair growth. | 2015 Dec | 2 |
12 | 24686051 | Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations. | 2014 Jun | 1 |
13 | 23345197 | Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism. | 2013 Apr | 2 |
14 | 20573158 | Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemia. | 2011 Jun | 1 |
15 | 21145327 | Functional role of the activity of ATP-sensitive potassium channels in electrical behavior of hippocampal neurons: experimental and theoretical studies. | 2011 Mar 7 | 2 |
16 | 21185999 | KATP channel mutations in congenital hyperinsulinism. | 2011 Feb | 1 |
17 | 21967988 | Congenital hyperinsulinism: current trends in diagnosis and therapy. | 2011 Oct 3 | 2 |
18 | 20589481 | Persistent hyperinsulinemic hypoglycemia of infancy due to homozygous KCNJ11 (T294M) mutation. | 2010 Jul | 1 |
19 | 20685672 | ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism. | 2010 Nov | 2 |
20 | 17301957 | ATP-sensitive potassium channel: a novel target for protection against UV-induced human skin cell damage. | 2007 Jul | 1 |
21 | 16475928 | Towards selective Kir6.2/SUR1 potassium channel openers, medicinal chemistry and therapeutic perspectives. | 2006 | 1 |
22 | 16837559 | Iptakalim modulates ATP-sensitive K(+) channels in dopamine neurons from rat substantia nigra pars compacta. | 2006 Oct | 1 |
23 | 12639916 | Hypothalamic proopiomelanocortin neurons are glucose responsive and express K(ATP) channels. | 2003 Apr | 2 |
24 | 12961066 | Potent and selective activation of the pancreatic beta-cell type K(ATP) channel by two novel diazoxide analogues. | 2003 Oct | 1 |
25 | 11808879 | Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases. | 2002 Jan | 1 |
26 | 12031979 | The novel diazoxide analog 3-isopropylamino-7-methoxy-4H-1,2,4-benzothiadiazine 1,1-dioxide is a selective Kir6.2/SUR1 channel opener. | 2002 Jun | 1 |
27 | 10518593 | Pharmacological plasticity of cardiac ATP-sensitive potassium channels toward diazoxide revealed by ADP. | 1999 Oct 12 | 2 |
28 | 20301549 | Familial Hyperinsulinism | 1993 | 1 |