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Year | Number of Results |
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2014 | 1 |
2015 | 3 |
2024 | 0 |
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Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism.
Clin Genet. 2015 May;87(5):448-54. doi: 10.1111/cge.12428. Epub 2014 Jun 6.
Clin Genet. 2015.
PMID: 24814349
Free PMC article.
Alternating hypoglycemia and hyperglycemia in a toddler with a homozygous p.R1419H ABCC8 mutation: an unusual clinical picture.
Harel S, Cohen AS, Hussain K, Flanagan SE, Schlade-Bartusiak K, Patel M, Courtade J, Li JB, Van Karnebeek C, Kurata H, Ellard S, Chanoine JP, Gibson WT.
Harel S, et al.
J Pediatr Endocrinol Metab. 2015 Mar;28(3-4):345-51. doi: 10.1515/jpem-2014-0265.
J Pediatr Endocrinol Metab. 2015.
PMID: 25720052
Free article.
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Molecular determinants of ATP-sensitive potassium channel MgATPase activity: diabetes risk variants and diazoxide sensitivity.
Fatehi M, Carter CR, Youssef N, Hunter BE, Holt A, Light PE.
Fatehi M, et al.
Biosci Rep. 2015 Jul 7;35(4):e00238. doi: 10.1042/BSR20150143.
Biosci Rep. 2015.
PMID: 26181369
Free PMC article.
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