Cowley D - Search Results

1

Expanded newborn screening: outcome in screened and unscreened patients at age 6 years.

Wilcken B, Haas M, Joy P, Wiley V, Bowling F, Carpenter K, Christodoulou J, Cowley D, Ellaway C, Fletcher J, Kirk EP, Lewis B, McGill J, Peters H, Pitt J, Ranieri E, Yaplito-Lee J, Boneh A. Wilcken B, et al. Among authors: cowley d. Pediatrics. 2009 Aug;124(2):e241-8. doi: 10.1542/peds.2008-0586. Epub 2009 Jul 20. Pediatrics. 2009. PMID: 19620191

2

Adult-onset arginase deficiency.

Cowley DM, Bowling FG, McGill JJ, van Dongen J, Morris D. Cowley DM, et al. J Inherit Metab Dis. 1998 Aug;21(6):677-8. doi: 10.1023/a:1005492819527. J Inherit Metab Dis. 1998. PMID: 9762606 No abstract available.

3

Maternal gonadal mosaicism causing ornithine transcarbamylase deficiency.

Bowling F, McGown I, McGill J, Cowley D, Tuchman M. Bowling F, et al. Among authors: cowley d. Am J Med Genet. 1999 Aug 27;85(5):452-4. doi: 10.1002/(sici)1096-8628(19990827)85:5<452::aid-ajmg4>3.0.co;2-4. Am J Med Genet. 1999. PMID: 10405441

4

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: cowley d. 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

5

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: cowley d. 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

6

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: cowley d. Pediatr Dev Pathol. 2007 Jan-Feb;10(1):25-34. doi: 10.2350/06-04-0083.1. Pediatr Dev Pathol. 2007. PMID: 17378627

7

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: cowley dm. 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.

8

Is it time to commence newborn screening for congenital adrenal hyperplasia in Australia?

Wu JY, Sudeep, Cowley DM, Harris M, McGown IN, Cotterill AM. Wu JY, et al. Med J Aust. 2011 Sep 5;195(5):260-2. doi: 10.5694/mja11.10284. Med J Aust. 2011. PMID: 21895585

9

Non-anaemic iron deficiency identified by ZPP test in extremely premature infants: prevalence, dietary risk factors, and association with neurodevelopmental problems.

O'Keeffe MJ, O'Callaghan MJ, Cowley D, Tudehope DI, Gray P, Burns Y, Mohay H. O'Keeffe MJ, et al. Among authors: cowley d. Early Hum Dev. 2002 Dec;70(1-2):73-83. doi: 10.1016/s0378-3782(02)00072-5. Early Hum Dev. 2002. PMID: 12441206

10

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. Clin Endocrinol (Oxf). 2003 Mar;58(3):355-64. doi: 10.1046/j.1365-2265.2003.01725.x. Clin Endocrinol (Oxf). 2003. PMID: 12608942

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