Cotterill AM - Search Results

1

Genotype-phenotype associations in patients with severe hyperinsulinism of infancy.

Greer RM, Shah J, Jeske YW, Brown D, Walker RM, Cowley D, Bowling FG, Liaskou D, Harris M, Thomsett MJ, Choong C, Bell JR, Jack MM, Cotterill AM. Greer RM, et al. Among authors: cotterill am. Pediatr Dev Pathol. 2007 Jan-Feb;10(1):25-34. doi: 10.2350/06-04-0083.1. Pediatr Dev Pathol. 2007. PMID: 17378627

2

The outcome in Australian children with hyperinsulinism of infancy: early extensive surgery in severe cases lowers risk of diabetes.

Jack MM, Greer RM, Thomsett MJ, Walker RM, Bell JR, Choong C, Cowley DM, Herington AC, Cotterill AM. Jack MM, et al. Among authors: cotterill am. Clin Endocrinol (Oxf). 2003 Mar;58(3):355-64. doi: 10.1046/j.1365-2265.2003.01725.x. Clin Endocrinol (Oxf). 2003. PMID: 12608942

3

Histologic findings in persistent hyperinsulinemic hypoglycemia of infancy: Australian experience.

Jack MM, Walker RM, Thomsett MJ, Cotterill AM, Bell JR. Jack MM, et al. Among authors: cotterill am. Pediatr Dev Pathol. 2000 Nov-Dec;3(6):532-47. doi: 10.1007/s100240010117. Pediatr Dev Pathol. 2000. PMID: 11000331 Clinical Trial.

4

Combined pituitary hormone deficiency in Australian children: clinical and genetic correlates.

McLennan K, Jeske Y, Cotterill A, Cowley D, Penfold J, Jones T, Howard N, Thomsett M, Choong C. McLennan K, et al. Clin Endocrinol (Oxf). 2003 Jun;58(6):785-94. doi: 10.1046/j.1365-2265.2003.01781.x. Clin Endocrinol (Oxf). 2003. PMID: 12780757

5

The association between ketoacidosis and 25(OH)-vitamin D levels at presentation in children with type 1 diabetes mellitus.

Huynh T, Greer RM, Nyunt O, Bowling F, Cowley D, Leong GM, Cotterill AM, Harris M. Huynh T, et al. Among authors: cotterill am. Pediatr Diabetes. 2009 Feb;10(1):38-43. doi: 10.1111/j.1399-5448.2008.00439.x. Epub 2008 Aug 27. Pediatr Diabetes. 2009. PMID: 18761649

6

21-hydroxylase genotyping in Australasian patients with congenital adrenal hyperplasia.

Jeske YW, McGown IN, Harris M, Bowling FG, Choong CS, Cowley DM, Cotterill AM. Jeske YW, et al. Among authors: cotterill am. J Pediatr Endocrinol Metab. 2009 Feb;22(2):127-41. doi: 10.1515/jpem.2009.22.2.127. J Pediatr Endocrinol Metab. 2009. PMID: 19449670 Free article.

7

Mini-dose glucagon rescue for mild hypoglycaemia in children with type 1 diabetes: the Brisbane experience.

Hartley M, Thomsett MJ, Cotterill AM. Hartley M, et al. Among authors: cotterill am. J Paediatr Child Health. 2006 Mar;42(3):108-11. doi: 10.1111/j.1440-1754.2006.00807.x. J Paediatr Child Health. 2006. PMID: 16509909

8

Utility of AVP gene testing in familial neurohypophyseal diabetes insipidus.

Chitturi S, Harris M, Thomsett MJ, Bowling F, McGown I, Cowley D, Leong GM, Batch J, Cotterill AM. Chitturi S, et al. Among authors: cotterill am. Clin Endocrinol (Oxf). 2008 Dec;69(6):926-30. doi: 10.1111/j.1365-2265.2008.03303.x. Epub 2008 May 20. Clin Endocrinol (Oxf). 2008. PMID: 18494865

9

Androgen receptor genotyping in a large Australasian cohort with androgen insensitivity syndrome; identification of four novel mutations.

Jeske YW, McGown IN, Cowley DM, Oley C, Thomsett MJ, Choong CS, Cotterill AM. Jeske YW, et al. Among authors: cotterill am. J Pediatr Endocrinol Metab. 2007 Aug;20(8):893-908. doi: 10.1515/jpem.2007.20.8.893. J Pediatr Endocrinol Metab. 2007. PMID: 17937062

10

Sertoli-Leydig cell tumor of the ovary, a rare cause of precocious puberty in a 12-month-old infant.

Choong CS, Fuller PJ, Chu S, Jeske Y, Bowling F, Brown R, Borzi P, Balazs ND, Suppiah R, Cotterill AM, Payton D, Robertson DM, Burger HG. Choong CS, et al. Among authors: cotterill am. J Clin Endocrinol Metab. 2002 Jan;87(1):49-56. doi: 10.1210/jcem.87.1.8162. J Clin Endocrinol Metab. 2002. PMID: 11788622

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