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Can network biology unravel the aetiology of congenital hyperinsulinism?
Orphanet J Rare Dis. 2013 Feb 8;8:21. doi: 10.1186/1750-1172-8-21.
Orphanet J Rare Dis. 2013.
PMID: 23394473
Free PMC article.
Is current management of neonatal jaundice evidence based?
Skae MS, Moise J, Clarke P.
Skae MS, et al.
Arch Dis Child Fetal Neonatal Ed. 2005 Nov;90(6):F540. doi: 10.1136/adc.2004.070060.
Arch Dis Child Fetal Neonatal Ed. 2005.
PMID: 16244219
Free PMC article.
No abstract available.
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Increased plasma incretin concentrations identifies a subset of patients with persistent congenital hyperinsulinism without KATP channel gene defects.
Shi Y, Avatapalle HB, Skae MS, Padidela R, Newbould M, Rigby L, Flanagan SE, Ellard S, Rahier J, Clayton PE, Dunne MJ, Banerjee I, Cosgrove KE.
Shi Y, et al. Among authors: skae ms.
J Pediatr. 2015 Jan;166(1):191-4. doi: 10.1016/j.jpeds.2014.09.019. Epub 2014 Oct 23.
J Pediatr. 2015.
PMID: 25444530
Free article.
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A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency.
Parsons SJH, Wright NB, Burkitt-Wright E, Skae MS, Murray PG.
Parsons SJH, et al. Among authors: skae ms.
Am J Med Genet A. 2017 Aug;173(8):2261-2267. doi: 10.1002/ajmg.a.38306. Epub 2017 Jun 6.
Am J Med Genet A. 2017.
PMID: 28586151
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