Roy SM, Chesi A, Mentch F, Xiao R, Chiavacci R, Mitchell JA, Kelly A, Hakonarson H, Grant SF, Zemel BS, McCormack SE: Body Mass Index (BMI) Trajectories in Infancy Differ by Population Ancestry and May Presage Disparities in Early Childhood Obesity. J Clin Endocrinol Metab January 2015 [E-pub ahead of print]
Rustico SE, Kelly A, Monk HM, Calabria AC
: Calcitriol Treatment in Metabolic Bone Disease of Prematurity with Elevated Parathyroid Hormone: A Preliminary Study. Journal of Clinical & Translational Endocrinology 2: 14-20, January 2015 [E-pub ahead of print] Notes: DOI information: 10.1016/j.jcte.2014.12.001.
Kelly A, Kovatch KJ, Garber SJ: Metabolic Bone Disease Screening Practices Among U.S. Neonatologists. Clinical Pediatrics 53(11): 1077-83, October 2014.
Millington K, Miller V, Rubenstein RC, Kelly A: Patient and parent perceptions of the diagnosis and management of cystic fibrosis-related diabetes Journal of Clinical & Translational Endocrinology 1(3): 100-107, September 2014 Notes: DOI: 10.1016/j.jcte.2014.07.003.
Kelly A, Winer KK, Kalkwarf H, Oberfield SE, Lappe J, Gilsanz V, Zemel BS
: Age-based Reference Ranges for Annual Height Velocity in U.S. Children. Journal of Clinical Endocrinology and Metabolism 99(6): 2104-12, June 2014.
Wren TA, Kalkwarf HJ, Zemel BS, Lappe JM, Oberfield S, Shepherd JA, Winer KK, Gilsanz V; Bone Mineral Density in Childhood Study Group: Longitudinal tracking of dual-energy X-ray absorptiometry bone measures over 6 years in children and adolescents: persistence of low bone mass to maturity. J Pediatr 164(6): 1280-5, June 2014.
Sheikh S, Zemel BS, Stallings VA, Rubenstein RC, Kelly A: Body composition and pulmonary function in Cystic Fibrosis Frontiers in Pediatrics: Pediatric Pulmonology 2(33), April 2014 Notes: doi: 10.3389/fped.2014.00033. eCollection 2014.
Huang T, Kelly A, Becker SA, Cohen MS, Stanley CA: Hypertrophic cardiomyopathy in neonates with congenital hyperinsulinism. Archives of disease in childhood. Fetal and neonatal edition 98(4): F351-4, Jul 2013.
Suratwala D, Chan JSH, Kelly A, Meltzer L, Gallagher PR, Traylor J, Rubenstein RC, and Marcus CL: Nocturnal Saturation and Glucose Tolerance in Children with Cystic Fibrosis. Thorax 66(7): 574-8, July 2011.
Brodsky, Jill; Dougherty, Shayne; Makani, Ramkrishna; Rubenstein, Ronald; Kelly, Andrea
: Elevation of One-Hour Plasma Glucose During Oral Glucose Tolerance Testing is Associated with Worse Pulmonary Function in Cystic Fibrosis. Diabetes Care 34(2): 292-5, 2011.
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Last updated: 02/03/2015
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