Stanley CA - Search Results

1

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.

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

Hyperinsulinism in infancy: diagnosis by demonstration of abnormal response to fasting hypoglycemia.

Stanley CA, Baker L. Stanley CA, et al. Pediatrics. 1976 May;57(5):702-11. Pediatrics. 1976. PMID: 940710

4

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.

5

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.

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

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

9

Congenital hyperinsulinism and the surgeon: lessons learned over 35 years.

Lovvorn HN 3rd, Nance ML, Ferry RJ Jr, Stolte L, Baker L, O'Neill JA Jr, Schnaufer L, Stanley CA, Adzick NS. Lovvorn HN 3rd, et al. Among authors: stanley ca. J Pediatr Surg. 1999 May;34(5):786-92; discussion 792-3. doi: 10.1016/s0022-3468(99)90374-3. J Pediatr Surg. 1999. PMID: 10359182 Free article.

10

Suppression of insulin oversecretion by subcutaneous recombinant human insulin-like growth factor I in children with congenital hyperinsulinism due to defective beta-cell sulfonylurea receptor.

Katz LE, Ferry RJ Jr, Stanley CA, Collett-Solberg PF, Baker L, Cohen P. Katz LE, et al. Among authors: stanley ca. J Clin Endocrinol Metab. 1999 Sep;84(9):3117-24. doi: 10.1210/jcem.84.9.5949. J Clin Endocrinol Metab. 1999. PMID: 10487673 Clinical Trial.

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