Landau H - Search Results

1

ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia.

Glaser B, Blech I, Krakinovsky Y, Ekstein J, Gillis D, Mazor-Aronovitch K, Landau H, Abeliovich D. Glaser B, et al. Among authors: landau h. Genet Med. 2011 Oct;13(10):891-4. doi: 10.1097/GIM.0b013e31821fea33. Genet Med. 2011. PMID: 21716120 Free article.

2

Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.

Tornovsky S, Crane A, Cosgrove KE, Hussain K, Lavie J, Heyman M, Nesher Y, Kuchinski N, Ben-Shushan E, Shatz O, Nahari E, Potikha T, Zangen D, Tenenbaum-Rakover Y, de Vries L, Argente J, Gracia R, Landau H, Eliakim A, Lindley K, Dunne MJ, Aguilar-Bryan L, Glaser B. Tornovsky S, et al. Among authors: landau h. J Clin Endocrinol Metab. 2004 Dec;89(12):6224-34. doi: 10.1210/jc.2004-1233. J Clin Endocrinol Metab. 2004. PMID: 15579781

3

Surgical versus non-surgical treatment of congenital hyperinsulinism.

Mazor-Aronovitch K, Landau H, Gillis D. Mazor-Aronovitch K, et al. Among authors: landau h. Pediatr Endocrinol Rev. 2009 Mar;6(3):424-30. Pediatr Endocrinol Rev. 2009. PMID: 19396028 Review.

4

Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.

Nestorowicz A, Wilson BA, Schoor KP, Inoue H, Glaser B, Landau H, Stanley CA, Thornton PS, Clement JP 4th, Bryan J, Aguilar-Bryan L, Permutt MA. Nestorowicz A, et al. Among authors: landau h. Hum Mol Genet. 1996 Nov;5(11):1813-22. doi: 10.1093/hmg/5.11.1813. Hum Mol Genet. 1996. PMID: 8923011

5

Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism.

Glaser B, Furth J, Stanley CA, Baker L, Thornton PS, Landau H, Permutt MA. Glaser B, et al. Among authors: landau h. Hum Mutat. 1999;14(1):23-9. doi: 10.1002/(SICI)1098-1004(1999)14:1<23::AID-HUMU3>3.0.CO;2-#. Hum Mutat. 1999. PMID: 10447255

6

Persistent hyperinsulinemic hypoglycemia of infancy ("nesidioblastosis"): autosomal recessive inheritance in 7 pedigrees.

Glaser B, Phillip M, Carmi R, Lieberman E, Landau H. Glaser B, et al. Among authors: landau h. Am J Med Genet. 1990 Dec;37(4):511-5. doi: 10.1002/ajmg.1320370416. Am J Med Genet. 1990. PMID: 2260597

7

Persistent hyperinsulinemic hypoglycemia of infancy: long-term octreotide treatment without pancreatectomy.

Glaser B, Hirsch HJ, Landau H. Glaser B, et al. Among authors: landau h. J Pediatr. 1993 Oct;123(4):644-50. doi: 10.1016/s0022-3476(05)80970-9. J Pediatr. 1993. PMID: 8410523

8

Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.

Glaser B, Ryan F, Donath M, Landau H, Stanley CA, Baker L, Barton DE, Thornton PS. Glaser B, et al. Among authors: landau h. Diabetes. 1999 Aug;48(8):1652-7. doi: 10.2337/diabetes.48.8.1652. Diabetes. 1999. PMID: 10426386

9

Long-term neurodevelopmental outcome in conservatively treated congenital hyperinsulinism.

Mazor-Aronovitch K, Gillis D, Lobel D, Hirsch HJ, Pinhas-Hamiel O, Modan-Moses D, Glaser B, Landau H. Mazor-Aronovitch K, et al. Among authors: landau h. Eur J Endocrinol. 2007 Oct;157(4):491-7. doi: 10.1530/EJE-07-0445. Eur J Endocrinol. 2007. PMID: 17893264

10

Neonatal Hyperinsulinism.

Glaser B, Landau H, Permutt MA. Glaser B, et al. Among authors: landau h. Trends Endocrinol Metab. 1999 Mar;10(2):55-61. doi: 10.1016/s1043-2760(98)00102-7. Trends Endocrinol Metab. 1999. PMID: 10322395

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