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Items: 13

1.

Hereditary pituitary hyperplasia with infantile gigantism.

Gläsker S, Vortmeyer AO, Lafferty AR, Hofman PL, Li J, Weil RJ, Zhuang Z, Oldfield EH.

J Clin Endocrinol Metab. 2011 Dec;96(12):E2078-87. doi: 10.1210/jc.2011-1401. Epub 2011 Oct 5.

2.

Increased detection of cystic-fibrosis-related diabetes in Australia.

Rana M, Munns CF, Selvadurai HC, Simonds S, Cooper PJ, Woodhead HJ, Hameed S, Verge CF, Lafferty AR, Crock PA, Craig ME.

Arch Dis Child. 2011 Sep;96(9):823-6. doi: 10.1136/adc.2010.208652. Epub 2011 Jun 8.

PMID:
21653750
3.

Salmonella Rubislaw gastroenteritis linked to a pet lizard.

Moffatt CR, Lafferty AR, Khan S, Krsteski R, Valcanis M, Powling J, Veitch M.

Med J Aust. 2010 Jul 5;193(1):54-5. No abstract available.

PMID:
20618116
4.

Establishment of pediatric reference intervals on a large cohort of healthy children.

Southcott EK, Kerrigan JL, Potter JM, Telford RD, Waring P, Reynolds GJ, Lafferty AR, Hickman PE.

Clin Chim Acta. 2010 Oct 9;411(19-20):1421-7. doi: 10.1016/j.cca.2010.06.018. Epub 2010 Jun 22.

PMID:
20598674
5.

Contrasting longitudinal and cross-sectional relationships between insulin resistance and percentage of body fat, fitness, and physical activity in children-the LOOK study.

Telford RD, Cunningham RB, Shaw JE, Dunstan DW, Lafferty AR, Reynolds GJ, Hickman PE, Southcott E, Potter JM, Waring P, Telford RM.

Pediatr Diabetes. 2009 Dec;10(8):500-7. doi: 10.1111/j.1399-5448.2009.00513.x. Epub 2009 Apr 30.

PMID:
19460124
6.

Discordance of international adiposity classifications in Australian boys and girls - the LOOK study.

Telford RD, Cunningham RB, Daly RM, Reynolds GJ, Lafferty AR, Gravenmaker KJ, Budge MM, Javaid A, Bass SL, Telford RM.

Ann Hum Biol. 2008 May-Jun;35(3):334-41. doi: 10.1080/03014460802014625.

PMID:
18568596
7.

Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.

Edghill EL, Flanagan SE, Patch AM, Boustred C, Parrish A, Shields B, Shepherd MH, Hussain K, Kapoor RR, Malecki M, MacDonald MJ, Støy J, Steiner DF, Philipson LH, Bell GI; Neonatal Diabetes International Collaborative Group, Hattersley AT, Ellard S.

Diabetes. 2008 Apr;57(4):1034-42. Epub 2007 Dec 27.

8.

Prevalence and risk factors for microalbuminuria in a population-based sample of children and adolescents with T1DM in Western Australia.

Gallego PH, Bulsara MK, Frazer F, Lafferty AR, Davis EA, Jones TW.

Pediatr Diabetes. 2006 Jun;7(3):165-72.

PMID:
16787524
9.

An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma.

Ribeiro RC, Sandrini F, Figueiredo B, Zambetti GP, Michalkiewicz E, Lafferty AR, DeLacerda L, Rabin M, Cadwell C, Sampaio G, Cat I, Stratakis CA, Sandrini R.

Proc Natl Acad Sci U S A. 2001 Jul 31;98(16):9330-5.

10.

A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22).

Lafferty AR, Torpy DJ, Stowasser M, Taymans SE, Lin JP, Huggard P, Gordon RD, Stratakis CA.

J Med Genet. 2000 Nov;37(11):831-5.

11.
12.

Pituitary tumors in children and adolescents.

Lafferty AR, Chrousos GP.

J Clin Endocrinol Metab. 1999 Dec;84(12):4317-23. Review. No abstract available.

PMID:
10599681
13.

Thyroid nodules in childhood and adolescence--thirty years of experience.

Lafferty AR, Batch JA.

J Pediatr Endocrinol Metab. 1997 Sep-Oct;10(5):479-86. Review.

PMID:
9401903
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