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名词信息
中 文 名:
解偶联蛋白2(UCP2)突变所致的高胰岛素血症
英 文 名:
hyperinsulinism caused by UCP2 mutation
中文又称:
中文曾称:
名词来源:
所属专业:
内分泌科
所属类别:
疾病诊断名词
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Pubmed相关的文献
hyperinsulinism caused by UCP2 mutation
相关文献:
Genotype and phenotype correlations in 417 children with congenital hyperinsulinism.
Snider KE, Becker S, Boyajian L, Shyng SL, MacMullen C, Hughes N, Ganapathy K, Bhatti T, Stanley CA, Ganguly A.
J Clin Endocrinol Metab. 2013 Feb;98(2):E355-63. doi: 10.1210/jc.2012-2169. Epub 2012 Dec 28.
PMID:23275527
Rare forms of congenital hyperinsulinism.
Marquard J, Palladino AA, Stanley CA, Mayatepek E, Meissner T.
Semin Pediatr Surg. 2011 Feb;20(1):38-44. doi: 10.1053/j.sempedsurg.2010.10.006.
PMID:21186003
Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism Disorders.
Stanley CA.
J Clin Endocrinol Metab. 2016 Mar;101(3):815-26. doi: 10.1210/jc.2015-3651. Epub 2016 Feb 23.
PMID:26908106
Clinical and genetic characterization of congenital hyperinsulinism in Spain.
Martínez R, Fernández-Ramos C, Vela A, Velayos T, Aguayo A, Urrutia I, Rica I, Castaño L; Spanish Congenital Hyperinsulinism Group.
Eur J Endocrinol. 2016 Jun;174(6):717-26. doi: 10.1530/EJE-16-0027.
PMID:27188453
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