Thornton PS - Search Results

1

International Guidelines for the Diagnosis and Management of Hyperinsulinism.

De Leon DD, Arnoux JB, Banerjee I, Bergada I, Bhatti T, Conwell LS, Fu J, Flanagan SE, Gillis D, Meissner T, Mohnike K, Pasquini TLS, Shah P, Stanley CA, Vella A, Yorifuji T, Thornton PS. De Leon DD, et al. Among authors: thornton ps. Horm Res Paediatr. 2024;97(3):279-298. doi: 10.1159/000531766. Epub 2023 Jul 14. Horm Res Paediatr. 2024. PMID: 37454648 Free article. Review.

2

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.

3

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.

4

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

5

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

6

Genetic heterogeneity in familial hyperinsulinism.

Nestorowicz A, Glaser B, Wilson BA, Shyng SL, Nichols CG, Stanley CA, Thornton PS, Permutt MA. Nestorowicz A, et al. Among authors: thornton ps. Hum Mol Genet. 1998 Jul;7(7):1119-28. doi: 10.1093/hmg/7.7.1119. Hum Mol Genet. 1998. PMID: 9618169

7

Clinical and molecular heterogeneity of familial hyperinsulinism.

Glaser B, Thornton PS, Herold K, Stanley CA. Glaser B, et al. Among authors: thornton ps. J Pediatr. 1998 Dec;133(6):801-2. doi: 10.1016/s0022-3476(98)70160-x. J Pediatr. 1998. PMID: 9843361 No abstract available.

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: thornton ps. Diabetes. 1999 Aug;48(8):1652-7. doi: 10.2337/diabetes.48.8.1652. Diabetes. 1999. PMID: 10426386

9

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: thornton ps. 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

10

Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome.

Hsu BY, Kelly A, Thornton PS, Greenberg CR, Dilling LA, Stanley CA. Hsu BY, et al. Among authors: thornton ps. J Pediatr. 2001 Mar;138(3):383-9. doi: 10.1067/mpd.2001.111818. J Pediatr. 2001. PMID: 11241047

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