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Conwell, Louise S., Greer, R. M., Walker, Ristan M., Fiumara, Frank, Campbell, Louise, Cowley, David, McGowan, Ivan M, Harris, Mark, Leong, Gary M., Batch, Jennifer A., McMahon, Sarah K., Dahiya, Rachana and Cotterill, Andrew M. (2012). [18F]-DOPA PET/CT imaging in congenital hyperinsulinism - first 2 years of the Queensland experience. In: Australasian Paediatric Endocrine Group Annual Scientific Meeting. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Queenstown, New Zealand, (). 28 July - 2 August 2012. 81  
Jeske, Y. W. A., McGown, I. N., Harris, M., Bowling, F. G., Choong, C. S. Y., Cowley, D. M. and Cotterill, A. M. (2009) 21-Hydroxylase Genotyping in Australasian Patients with Congenital Adrenal Hyperplasia. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 22 2: 127-141. 43   5 Cited 4 times in Scopus4
McWhinney, BC, Nagel, SL, Cowley, DM, Brown, JM and Chalmers, AH (1987) 2-Carbon Oxalogenesis Compared in Recurrent Calcium-Oxalate Stone Formers and Normal Subjects. Clinical Chemistry, 33 7: 1118-1120. 18   5
Buchanan, Kerry, Williams, Judith A., Greer, Ristan M., Fiumara, Frank, Campbell, Louise, Cowley, David, McGown, Ivan M., Batch, Jennifer A., McMahon, Sarah K. and Conwell, Louise S. (2012). A case of hyperinsulinism-hyperammonaemia syndrome. In: Australasian Paediatric Endocrine Group Annual Scientific Meeting. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Queenstown, New Zealand, (). July 29 - August 2 2012. 51  
Tudehope, DI, Mitchell, F and Cowley, DM (1986) A Comparative-Study of a Premature-Infant Formula and Preterm Breast-Milk for Low-Birth-Weight Infants. Australian Paediatric Journal, 22 3: 199-205. 11   4
Cowley D.M., Bowling F.G., McGiil J.J., Van Dongen J. and Morris D. (1998) Adult-onset arginase deficiency. Journal of Inherited Metabolic Disease, 21 6: 677-678. doi:10.1023/A:1005492819527 22   9 Cited 10 times in Scopus10 0
Fermo, E, Bianchi, P, Rodwell, R, Cowley, D and Zanella, A (2003). A lethal variant of pyruvate kinase deficiency associated with a missense mutation (G409A) and a large deletion in the LR-PK gene. In: Experimental Hematology. 32nd Annual Scientific Meeting of the International-Society-for-Experimental-Hematology, Paris France, (130-130). Jul 05-08, 2003. 6   0
McWhinney, BC, Cowley, DM and Chalmers, AH (1985) An Automated-Method for Measuring Plasma Citrate Without Protein Precipitation. Clinical Chemistry, 31 9: 1578-1579. 19   5
Jeske, Y. W. A., McGown, I. N., Cowley, D. M., Oley, C., Thomsett, M. J., Choong, C. S. Y. and Cotterill, A. M. (2007) Androgen receptor genotyping in a large Australasian cohort with androgen insensitivity syndrome; identification of four novel mutations. Journal of Pediatric Endocrinology & Metabolism, 20 8: 893-908. 14   6
Wu, Joyce Y., McGown, Ivan N., Lint, Lin, Achermann, John C., Harris, Mark, Cowley, David M., Aftimos, Salim, Neville, Kristen A., Choong, Catherine S. and Cotterill, Andrew M. (2013) A novel NR5A1 variant in an infant with elevated testosterone from an Australasian cohort of 46,XY patients with disorders of sex development. Clinical Endocrinology, 78 4: 545-550. doi:10.1111/cen.12012 67   3 Cited 3 times in Scopus3 1
Cotterill, A. M., Cowley, D., Harris, M., Huynh, T., Leong, G. M., McGown, I. and Nyunt, O. (2009) A novel V185DfsX4 mutation of the AAAS gene in a 2-year-old boy with Triple A Syndrome. Clinical Pediatric Endocrinology, 18 2: 73-75. doi:10.1297/cpe.18.73 62   Cited 0 times in Scopus0 0
Chalmers, AH, Cowley, DM and Brown, JM (1986) A Possible Etiologic Role for Ascorbate in Calculi Formation. Clinical Chemistry, 32 2: 333-336. 10   59
Cowley, DM, Davey, JF and Hjelm, NM (1983) A Radioimmunoassay of Human Pre-Albumin in Body-Fluids. Clinica Chimica Acta, 134 1-2: 69-76. doi:10.1016/0009-8981(83)90185-7 19   8 Cited 2 times in Scopus2 0
DeLeacy, EA, Moxon, LN, Ellis, VM, VanDongen, JMAM, Johnson, LP, Doddrell, DM and Cowley, DM (1995) A report of accidental ethylene glycol ingestion in 2 siblings. Pathology, 27 3: 273-276. 14   1
Huynh, Tony, Trebbin, Andrea, Cowley, David, Bowling, Francis, Leong, Gary M., Cotterill, Andrew M., Harris, Mark, De Bosscher, Karolien, Haegeman, Guy and Hoey, Andrew J. (2009). A selective glucocorticoid receptor modulator improves muscle function in a mouse model for Duchenne muscular dystrophy. In: Hormone Research. , , (163-163). . 6   0
Mcleod, D.S.A., Warner, J.V., Henman, M., Cowley, D., Gibbons, K. and Mcintyre, H.D. (2012) Associations of serum vitaminD concentrations with obstetric glucose metabolism in a subset of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort. Diabetic Medicine, 29 8: e199-e204. doi:10.1111/j.1464-5491.2011.03551.x 33   7 Cited 6 times in Scopus6 1
Stathis, SL, Cowley, DM and Broe, D (2000) Autism and adenylosuccinase deficiency. Journal of the American Academy of Child and Adolescent Psychiatry, 39 3: 274-275. doi:10.1097/00004583-200003000-00007 16   15 0
Gozzi T.G., Harris N.P., McGown I.N., Cowley D.M., Cotterill A.M., Campbell P.E., Anderson P.K. and Warne G.L. (2005) Autopsy diagnosis of 21-hydroxylase deficiency CAH in a case of apparent SIDS. Pediatric and Developmental Pathology, 8 3: 397-401. doi:10.1007/s10024-005-0004-0 15   9 Cited 9 times in Scopus9 0
Wu, J. Y., McGill, J., McWhinney, A. C., Neven, S. D. and Cowley, D. M. (2011). Cardiomyopathy as the Initial Presentation of Propionic Acidaemia in a Teenager. In: Journal of Inherited Metabolic Disease. , , (S138-S138). . 9   0
Burke, JR, Cowley, DM, Mottram, BM and Buckner, P (1986) Cellulose Phosphate and Chlorothiazide in Childhood Idiopathic Hypercalciuria. Australian and New Zealand Journal of Medicine, 16 1: 43-47. doi:10.1111/j.1445-5994.1986.tb01114.x 10   4 0
Cowley, DM, McWhinney, BC, Brown, JM and Chalmers, AH (1987) Chemical Factors Important to Calcium Nephrolithiasis - Evidence for Impaired Hydroxycarboxylic Acid Absorption Causing Hyperoxaluria. Clinical Chemistry, 33 2: 243-247. 7   34
Al-Shehri, S., Henman, M., Charles, B. G., Cowley, D., Shaw, P. N., Liley, H., Tomarchio, A., Punyadeera, C. and Duley, J. A. (2013) Collection and determination of nucleotide metabolites in neonatal and adult saliva by high performance liquid chromatography with tandem mass spectrometry. Journal of Chromatography B, 931 140-147. doi:10.1016/j.jchromb.2013.05.001 106   2 Cited 1 times in Scopus1 0
McLennan, K., Jeske, Y., Cowley, D. M., Thomsett, M., Cotterill, A. M. and Choong, C. (1999). Combined pituitary hormone deficiency: Clinical and genetic correlates. In: Australasian Paediatric Endocrine Group Annual Scientific Meeting. APEG 1999, Hyatt Coolum, Maroochydore, Qld., (A2). 8 - 10 Oct, 1999. 53  
McLennan, Kim, Jeske, Yvette, Cotterill, Andrew, Cowley, David, Penfold, James, Jones, Tim, Howard, Neville, Thomsett, Michael and Choong, Catherine (2003) Combined pituitary hormone deficiency in Australian children: clinical and genetic correlates. Clinical Endocrinology, 58 6: 785-794. doi:10.1046/j.1365-2265.2003.01781.x 57   29 Cited 31 times in Scopus31 0
Mottram, B., Weier, S. L. and Cowley, D. M. (1999). Comparision of DCA, variant II and diamat HbA1c. In: 37th Annual Scientific Conference Australian Association of Clinical Biochemists. 37th ASC Australian Association of Clinical Biochemists, Melbourne, (93). 5 - 9 October, 1999. 74  
Sinton, TJ, Deleacy, EA and Cowley, DM (1986) Comparison of Cr-51 Edta Clearance with Formulas in the Measurement of Glomerular-Filtration Rate. Pathology, 18 4: 445-447. 14   12
Huynh, Tony, McGown, Ivan, Cowley, David, Harris, Mark, Leong, Gary M. and Cotterill, Andrew M. (2009). Congenital adrenal hyperplasia genotyping strategy using MLPA and DNA sequencing: an Australian cohort. In: Hormone Research. , , (235-235). . 3   0
Deleacy, EA, Bowler, S, Brown, JM and Cowley, DM (1991) Corticotropin Deficiency - a Rare Cause of Hyponatremia Mimicking Siadh. Pathology, 23 1: 8-10. 14   9
Vuckovic, Slavica, Withers, Geoff, Harris, Mark, Khalil, Dalia, Gardiner, Damien, Flesch, Inge, Tepes, Sonia, Greer, Ristan, Cowley, David, Cotterill, Andrew and Hart, Derek N.J. (2007) Decreased blood dendritic cell counts in type 1 diabetic children. Clinical Immunology, 123 3: 281-288. doi:10.1016/j.clim.2007.03.002 129   36 Cited 38 times in Scopus38 0
Broe, D, Vandongen, J, Cowley, D, Vacca, A, Voreteliac, V, Maguire, D and Ellis, V (1992) Detection of Premature Rupture of Membranes by Measuring Diamine Oxidase in Vaginal Fluid - False-Negative Results Caused by Obstetric Antiseptic Creams. Clinical Chemistry, 38 5: 784-784. 17   8
Cowley, DM, McWhinney, BC, Brown, JM and Chalmers, AH (1989) Effect of Citrate On the Urinary-Excretion of Calcium and Oxalate - Relevance to Calcium-Oxalate Nephrolithiasis. Clinical Chemistry, 35 1: 23-28. 7   14
Deleacy, EA, Cowley, DM, Brown, JM, McWhinney, BC and Chalmers, AH (1989) Effect of Oral Citrate On Calcium-Absorption After An Oral Load of Calcium-Phosphate. Clinical Chemistry, 35 7: 1541-1541. 4   6
Cowley, DM, Nagle, BA, Chalmers, AH and Sinton, TJ (1985) Effects of Platelets On Collection of Specimens for Assay of Ammonia in Plasma. Clinical Chemistry, 31 2: 332-332. 12   2
Brown, JM, Chalmers, AH, Cowley, DM and McWhinney, BC (1986) Enteric Hyperoxaluria and Urolithiasis. New England Journal of Medicine, 315 15: 970-971. 8   5
Morgan, T. J., Vellaichamy, M., Cowley, D. M., Weier, S. L., Venkatesh, B. and Jones, M. A. (2009) Equivalent metabolic acidosis with four colloids and saline on ex vivo haemodilution. Anaesthesia and Intensive Care, 37 3: 407-414. 59   3 Cited 4 times in Scopus4
Deleacy, EA and Cowley, DM (1989) Evidence That the Oral Glucose-Tolerance Test Does Not Provide a Uniform Stimulus to Pancreatic-Islets in Pregnancy. Clinical Chemistry, 35 7: 1482-1485. 15   3
Wilcken, Bridget, Haas, Marion, Joy, Pamela, Wiley, Veronica, Bowling, Francis, Carpenter, Kevin, Christodoulou, John, Cowley, David, Ellaway, Carolyn, Fletcher, Janice, Kirk, Edwin P., Lewis, Barry, McGill, Jim, Peters, Heidi, Pitt, James, Ranieri, Enzo, Yaplito-Lee, Joy and Boneh, Avihu (2009) Expanded newborn screening: Outcome in screened and unscreened patients at age 6 years. Pediatrics, 124 2: E241-E248. doi:10.1542/peds.2008-0586 130   46 Cited 60 times in Scopus60 0
Deleacy, EA, Cowley, DM and Wynne, JM (1988) False-Positive Result of a Glucose-Tolerance Test. Medical Journal of Australia, 149 4: 225-226. 14   0
Jones, I, Cowley, D, Andersen, M, Vacca, A and Voroteliak, V (1996) Fibronectin as a predictor of preeclampsia: A pilot study. Australian & New Zealand Journal of Obstetrics & Gynaecology, 36 1: 1-3. doi:10.1111/j.1479-828X.1996.tb02909.x 10   8 0
Ellis, VM, Cowley, DM, Taylor, KM and Marlton, P (1992) Gamma-Heavy Chain Disease Developing in Association with Myelodysplastic Syndrome. British Journal of Haematology, 81 1: 125-126. doi:10.1111/j.1365-2141.1992.tb08184.x 18   5 0
Greer, Ristan M., Shah, Janaki, Jeske, Jeske, Yvette W., Brown, David, Walker, Rosslyn M., Cowley, David, Bowling, Francis G., Liaskou, Daphne, Harris, Mark, Thomsett, Michael J., Choong, Catherine, Bell, John R., Jack, Michelle M. and Cotterill, Andrew M. (2007) Genotype-Phenotype associations in patients with severe hyperinsulinism of infancy. Pediatric and Developmental Pathology, 10 1: 25-34. doi:10.2350/06-04-0083.1 139   7 Cited 10 times in Scopus10 0
Bode, Hans H., Rivkees, Scott A., Cowley, David M., Pardy, Karen and Johnson, Sandra (1999) Home monitoring of 17 hydroxyprogesterone levels in congenitx127 drenal hyperplasia with filter paper blood samples. Journal of Pediatrics, 134 2: 185-189. doi:10.1016/S0022-3476(99)70413-0 54   23 Cited 29 times in Scopus29 0
McIntyre, H. David, Chang, Allan M., Callaway, Leonie K., Cowley, David M., Dyer, Alan R., Radaelli, Tatjana, Farrell, Kristen A., Huston-Presley, Larraine, Amini, Saeid B., Kirwan, John P. and Catalano, Patrick M. (2010) Hormonal and metabolic factors associated with variations in insulin sensitivity in human pregnancy. Diabetes Care, 33 2: 356-360. doi:10.2337/dc09-1196 74   23 Cited 27 times in Scopus27 0
Maguire, DJ, Voroteliak, V, Cowley, D and Cannell, GR (1992). Human Placental Oxygen-Metabolism. In: Oxygen Transport to Tissue Xiii. 18Th Annual Meeting of the International Soc On Oxygen Transport to Tissue, Townsville Australia, (463-466). Jul 19-22, 1990. 3   0
Dawson, Paul A., Sim, Pearl, Mudge, David W. and Cowley, David (2013) Human SLC26A1 gene variants: a pilot study. Scientific World Journal, 2013 . doi:10.1155/2013/541710 34   0 Cited 0 times in Scopus0 0
Cowley, DM, Brown, JM, McWhinney, BC and Chalmers, AH (1988). Hydroxycarboxylate Malabsorption and Calcium-Oxalate Nephrolithiasis. In: Urological Research. , , (179-179). . 5   0
Cotterill, A. M., Cowley, D., Dahiya, R., Greer, R. M., Harris, M., Huynh, T., Leong, G., McGown, I., Nyunt, O., Venter, D. J. and Walker, R. (2008). Hyperinsulinism of infancy associated with a novel paternally inherited alteration in the KCNJ11 gene. In: Australasian Paediatric Endocrine Group Annual Scientific Meeting, Canberra, ACT, Australia, (). 17 - 19 November 2008. 51  
Cotterill, Andrew, Cowley, David and Greer, Ristan (2010). Hypoglycemia: assessment and management. In Charles G. D. Brook, Peter E. Clayton and Rosalind S. Brown (Ed.), Brook's Clinical Pediatric Endocrinology 6th ed. (pp. 505-529) Chichester, West Sussex, UK: Blackwell Publishing. doi:10.1002/9781444316728.ch19 13   Cited 0 times in Scopus0 0
Sivendran, S, Patterson, D, Spiegel, E, McGowan, I, Cowley, D and Colman, R (2004). Identification of 2 novel mutant human adenylosuccinate lyases(ASL) associated with autism and characterization of the equivalent mutant B-subtilis ASL. In: Faseb Journal. Annual Meeting of the American-Society-for-Biochemistry-and-Molecular-Biology/8th Congress of the International-Union-for-Biochemistry-and-Molecular-Biology, Boston Ma, (C241-C242). Jun 12-16, 2004. 8   0
Voroteliak, V, Cowley, DM and Florin, Thj (1993) Improved Colorimetric Determination of Urinary Thiosulfate to Study Intermediate Sulfur Metabolism in Humans. Clinical Chemistry, 39 12: 2533-2534. 928   14

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