Ganguly A - Search Results

1

Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the beta-cell sulfonylurea receptor.

Magge SN, Shyng SL, MacMullen C, Steinkrauss L, Ganguly A, Katz LE, Stanley CA. Magge SN, et al. Among authors: ganguly a. J Clin Endocrinol Metab. 2004 Sep;89(9):4450-6. doi: 10.1210/jc.2004-0441. J Clin Endocrinol Metab. 2004. PMID: 15356046

2

Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenase.

MacMullen C, Fang J, Hsu BY, Kelly A, de Lonlay-Debeney P, Saudubray JM, Ganguly A, Smith TJ, Stanley CA; Hyperinsulinism/hyperammonemia Contributing Investigators. MacMullen C, et al. Among authors: ganguly a. J Clin Endocrinol Metab. 2001 Apr;86(4):1782-7. doi: 10.1210/jcem.86.4.7414. J Clin Endocrinol Metab. 2001. PMID: 11297618

3

Hyperinsulinism and hyperammonemia syndrome: report of twelve unrelated patients.

De Lonlay P, Benelli C, Fouque F, Ganguly A, Aral B, Dionisi-Vici C, Touati G, Heinrichs C, Rabier D, Kamoun P, Robert JJ, Stanley C, Saudubray JM. De Lonlay P, et al. Among authors: ganguly a. Pediatr Res. 2001 Sep;50(3):353-7. doi: 10.1203/00006450-200109000-00010. Pediatr Res. 2001. PMID: 11518822

4

Aberrant mRNA splicing associated with coding region mutations in children with carnitine-acylcarnitine translocase deficiency.

Hsu BY, Iacobazzi V, Wang Z, Harvie H, Chalmers RA, Saudubray JM, Palmieri F, Ganguly A, Stanley CA. Hsu BY, et al. Among authors: ganguly a. Mol Genet Metab. 2001 Sep-Oct;74(1-2):248-55. doi: 10.1006/mgme.2001.3235. Mol Genet Metab. 2001. PMID: 11592821

5

Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency.

Cederbaum SD, Koo-McCoy S, Tein I, Hsu BY, Ganguly A, Vilain E, Dipple K, Cvitanovic-Sojat L, Stanley C. Cederbaum SD, et al. Among authors: ganguly a. Mol Genet Metab. 2002 Nov;77(3):195-201. doi: 10.1016/s1096-7192(02)00169-5. Mol Genet Metab. 2002. PMID: 12409266

6

Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor.

Thornton PS, MacMullen C, Ganguly A, Ruchelli E, Steinkrauss L, Crane A, Aguilar-Bryan L, Stanley CA. Thornton PS, et al. Among authors: ganguly a. Diabetes. 2003 Sep;52(9):2403-10. doi: 10.2337/diabetes.52.9.2403. Diabetes. 2003. PMID: 12941782

7

Histopathology of congenital hyperinsulinism: retrospective study with genotype correlations.

Suchi M, MacMullen C, Thornton PS, Ganguly A, Stanley CA, Ruchelli ED. Suchi M, et al. Among authors: ganguly a. Pediatr Dev Pathol. 2003 Jul-Aug;6(4):322-33. doi: 10.1007/s10024-002-0026-9. Pediatr Dev Pathol. 2003. PMID: 14692646

8

Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation.

Stanley CA, Thornton PS, Ganguly A, MacMullen C, Underwood P, Bhatia P, Steinkrauss L, Wanner L, Kaye R, Ruchelli E, Suchi M, Adzick NS. Stanley CA, et al. Among authors: ganguly a. J Clin Endocrinol Metab. 2004 Jan;89(1):288-96. doi: 10.1210/jc.2003-030965. J Clin Endocrinol Metab. 2004. PMID: 14715863

9

Congenital hyperinsulinism: intraoperative biopsy interpretation can direct the extent of pancreatectomy.

Suchi M, Thornton PS, Adzick NS, MacMullen C, Ganguly A, Stanley CA, Ruchelli ED. Suchi M, et al. Among authors: ganguly a. Am J Surg Pathol. 2004 Oct;28(10):1326-35. doi: 10.1097/01.pas.0000138000.61897.32. Am J Surg Pathol. 2004. PMID: 15371948

10

Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes.

Henwood MJ, Kelly A, Macmullen C, Bhatia P, Ganguly A, Thornton PS, Stanley CA. Henwood MJ, et al. Among authors: ganguly a. J Clin Endocrinol Metab. 2005 Feb;90(2):789-94. doi: 10.1210/jc.2004-1604. Epub 2004 Nov 23. J Clin Endocrinol Metab. 2005. PMID: 15562009

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