Thornton PS - Search Results

1

Recommendations from the Pediatric Endocrine Society for Evaluation and Management of Persistent Hypoglycemia in Neonates, Infants, and Children.

Thornton PS, Stanley CA, De Leon DD, Harris D, Haymond MW, Hussain K, Levitsky LL, Murad MH, Rozance PJ, Simmons RA, Sperling MA, Weinstein DA, White NH, Wolfsdorf JI; Pediatric Endocrine Society. Thornton PS, et al. J Pediatr. 2015 Aug;167(2):238-45. doi: 10.1016/j.jpeds.2015.03.057. Epub 2015 May 6. J Pediatr. 2015. PMID: 25957977 Free article. No abstract available.

2

Familial and sporadic hyperinsulinism: histopathologic findings and segregation analysis support a single autosomal recessive disorder.

Thornton PS, Sumner AE, Ruchelli ED, Spielman RS, Baker L, Stanley CA. Thornton PS, et al. J Pediatr. 1991 Nov;119(5):721-4. doi: 10.1016/s0022-3476(05)80286-0. J Pediatr. 1991. PMID: 1941377 Free article.

3

Management of hyperinsulinism in infants.

Baker L, Thornton PS, Stanley CA. Baker L, et al. Among authors: thornton ps. J Pediatr. 1991 Nov;119(5):755-7. doi: 10.1016/s0022-3476(05)80291-4. J Pediatr. 1991. PMID: 1941380 Free article. No abstract available.

4

In vitro and in vivo effects of granulocyte colony-stimulating factor on neutrophils in glycogen storage disease type 1B: granulocyte colony-stimulating factor therapy corrects the neutropenia and the defects in respiratory burst activity and Ca2+ mobilization.

McCawley LJ, Korchak HM, Douglas SD, Campbell DE, Thornton PS, Stanley CA, Baker L, Kilpatrick L. McCawley LJ, et al. Among authors: thornton ps. Pediatr Res. 1994 Jan;35(1):84-90. doi: 10.1203/00006450-199401000-00017. Pediatr Res. 1994. PMID: 7510873

5

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.

Glaser B, Chiu KC, Liu L, Anker R, Nestorowicz A, Cox NJ, Landau H, Kaiser N, Thornton PS, Stanley CA, et al. Glaser B, et al. Among authors: thornton ps. Hum Mol Genet. 1995 May;4(5):879-86. doi: 10.1093/hmg/4.5.879. Hum Mol Genet. 1995. PMID: 7633448

6

Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene.

Glaser B, Chiu KC, Anker R, Nestorowicz A, Landau H, Ben-Bassat H, Shlomai Z, Kaiser N, Thornton PS, Stanley CA, et al. Glaser B, et al. Among authors: thornton ps. Nat Genet. 1994 Jun;7(2):185-8. doi: 10.1038/ng0694-185. Nat Genet. 1994. PMID: 7920639

7

Short- and long-term use of octreotide in the treatment of congenital hyperinsulinism.

Thornton PS, Alter CA, Katz LE, Baker L, Stanley CA. Thornton PS, et al. J Pediatr. 1993 Oct;123(4):637-43. doi: 10.1016/s0022-3476(05)80969-2. J Pediatr. 1993. PMID: 8410522 Free article.

8

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: thornton ps. Hum Mol Genet. 1996 Nov;5(11):1813-22. doi: 10.1093/hmg/5.11.1813. Hum Mol Genet. 1996. PMID: 8923011

9

A syndrome of congenital hyperinsulinism and hyperammonemia.

Weinzimer SA, Stanley CA, Berry GT, Yudkoff M, Tuchman M, Thornton PS. Weinzimer SA, et al. Among authors: thornton ps. J Pediatr. 1997 Apr;130(4):661-4. doi: 10.1016/s0022-3476(97)70256-7. J Pediatr. 1997. PMID: 9108870

10

Insulin-like growth factor binding protein-1 levels in the diagnosis of hypoglycemia caused by hyperinsulinism.

Levitt Katz LE, Satin-Smith MS, Collett-Solberg P, Thornton PS, Baker L, Stanley CA, Cohen P. Levitt Katz LE, et al. Among authors: thornton ps. J Pediatr. 1997 Aug;131(2):193-9. doi: 10.1016/s0022-3476(97)70153-7. J Pediatr. 1997. PMID: 9290603

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