Stanley CA - Search Results

1

Familial hyperinsulinism with apparent autosomal dominant inheritance: clinical and genetic differences from the autosomal recessive variant.

Thornton PS, Satin-Smith MS, Herold K, Glaser B, Chiu KC, Nestorowicz A, Permutt MA, Baker L, Stanley CA. Thornton PS, et al. Among authors: stanley ca. J Pediatr. 1998 Jan;132(1):9-14. doi: 10.1016/s0022-3476(98)70477-9. J Pediatr. 1998. PMID: 9469993

2

Clinical features and insulin regulation in infants with a syndrome of prolonged neonatal hyperinsulinism.

Hoe FM, Thornton PS, Wanner LA, Steinkrauss L, Simmons RA, Stanley CA. Hoe FM, et al. Among authors: stanley ca. J Pediatr. 2006 Feb;148(2):207-12. doi: 10.1016/j.jpeds.2005.10.002. J Pediatr. 2006. PMID: 16492430

3

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. Among authors: stanley ca. J Pediatr. 1991 Nov;119(5):721-4. doi: 10.1016/s0022-3476(05)80286-0. J Pediatr. 1991. PMID: 1941377 Free article.

4

Management of hyperinsulinism in infants.

Baker L, Thornton PS, Stanley CA. Baker L, et al. Among authors: stanley ca. 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.

5

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. Among authors: stanley ca. J Pediatr. 1993 Oct;123(4):637-43. doi: 10.1016/s0022-3476(05)80969-2. J Pediatr. 1993. PMID: 8410522 Free article.

6

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: stanley ca. J Pediatr. 1997 Apr;130(4):661-4. doi: 10.1016/s0022-3476(97)70256-7. J Pediatr. 1997. PMID: 9108870

7

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: stanley ca. J Pediatr. 1997 Aug;131(2):193-9. doi: 10.1016/s0022-3476(97)70153-7. J Pediatr. 1997. PMID: 9290603

8

Clinical and molecular heterogeneity of familial hyperinsulinism.

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

9

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: stanley ca. J Pediatr. 2001 Mar;138(3):383-9. doi: 10.1067/mpd.2001.111818. J Pediatr. 2001. PMID: 11241047

10

Nephrolithiasis, hypocitraturia, and a distal renal tubular acidification defect in type 1 glycogen storage disease.

Restaino I, Kaplan BS, Stanley C, Baker L. Restaino I, et al. J Pediatr. 1993 Mar;122(3):392-6. doi: 10.1016/s0022-3476(05)83422-5. J Pediatr. 1993. PMID: 8441093

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