Found: 13
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Treatment of congenital hyperinsulinism with lanreotide acetate (Somatuline Autogel).
- Published in:
- 2011
- By:
- Publication type:
- journal article
Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.
- Published in:
- 2004
- By:
- Publication type:
- journal article
Age as a determinant of the impact of growth hormone therapy on predicted adult height.
- Published in:
- Clinical Endocrinology, 1994, v. 41, n. 3, p. 331, doi. 10.1111/j.1365-2265.1994.tb02553.x
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- Publication type:
- Article
PERSISTENT HYPERINSULINAEMIC HYPOGLYCAEMIA OF INFANCY: LONG-TERM TREATMENT WITH THE SOMATOSTATIN ANALOGUE SANDOSTATIN.
- Published in:
- Clinical Endocrinology, 1989, v. 31, n. 1, p. 71, doi. 10.1111/j.1365-2265.1989.tb00455.x
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- Publication type:
- Article
Cognitive and developmental outcome of conservatively treated children with congenital hyperinsulinism.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 3/4, p. 301, doi. 10.1515/jpem-2012-0289
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- Publication type:
- Article
Celiac Disease and Short Stature - Not Always Cause and Effect.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2001, v. 14, n. 1, p. 71, doi. 10.1515/jpem.2001.14.1.71
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- Publication type:
- Article
Who Will Benefit From Growth Hormone Therapy? Growth Hormone Therapy in Short Children.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 1992, v. 5, n. 1/2, p. 113, doi. 10.1515/jpem.1992.5.1-2.113
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- Publication type:
- Article
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.
- Published in:
- 1999
- By:
- Publication type:
- journal article
A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism.
- Published in:
- 1997
- By:
- Publication type:
- journal article
Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism.
- Published in:
- Human Mutation, 1999, v. 14, n. 1, p. 23, doi. 10.1002/(SICI)1098-1004(1999)14:1<23::AID-HUMU3>3.0.CO;2-#
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- Publication type:
- Article
Mutations in the Sulfonylurea Receptor Gene Are Associated with Familial Hyperinsulinism in Ashkenazi Jews.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 11, p. 1813, doi. 10.1093/hmg/5.11.1813
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- Publication type:
- Article
Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews.
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 11, p. 2187
- By:
- Publication type:
- Article
Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews.
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 5, p. 879
- By:
- Publication type:
- Article