faculty photo

Michael Alan Levine

Professor of Pediatrics at the Children's Hospital of Philadelphia
Department: Pediatrics

Contact information
The Children's Hospital of Philadelphia
34th & Civic Center Blvd.
Philadelphia, PA 19104
Office: 215-590-3618
Fax: 215-590-3053
Education:
A.B.
Rutgers College, New Brunswick, NJ, 1972.
M.D.
Drexel University (formerly Hahnemann) College of Medicine, Philadelpia, PA, 1976.
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Selected Publications

Dasgupta D, Wee MJ, Reyes M, Li Y, Simm PJ, Sharma A, Schlingmann KP, Janner M, Biggin A, Lazier J, Gessner M, Chrysis D, Tuchman S, Baluarte HJ, Levine MA, Tiosano D, Insogna K, Hanley DA, Carpenter TO, Ichikawa S, Hoppe B, Konrad M, Savendahl L, Munns CF, Lee H, Juppner H, Bergwitz C: Mutations in SLC34A3/NPT2c Are Associated with Kidney Stones and Nephrocalcinosis. Journal of the American Society of Nephrology 25(10): 2366-75, Oct 2014.

Mancilla EE, Brodsky JL, Mehta S, Pignolo RJ, Levine MA: Teriparatide as a Systemic Treatment for Lower Extremity Non-Union Fractures: A Case Series. Endocrine Practice Page: 1-22, Oct 2014 Notes: Epub ahead of print.

Li D, Opas EE, Tuluc F, Metzger DL, Hou C, Hakonarson H, Levine MA: Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization. J Clin Endocrinol Metab 99(9): E1774-83, Sep 2014.

Roizen J, Levine MA: A meta-analysis comparing the Biochemistry of Primary Hyperparathyroidism in Youths to the Biochemistry of Primary Hyperparathyroidism in Adults. J Clin Endocrinol Metab Page: jc20142268, Sep 2014 Notes: Epub ahead of print.

Yuan Z, Opas EE, Vrikshajanani C, Libutti SK, Levine MA: Generation of mice encoding a conditional null allele of Gcm2. Transgenic Res 23(4): 631-41, Aug 2014.

Fan B, Shepherd JA, Levine MA, Steinberg D, Wacker W, Barden HS, Ergun D, Wu XP: National Health and Nutrition Examination Survey whole-body dual-energy X-ray absorptiometry reference data for GE Lunar systems. J Clin Densitom 17(3): 344-77, Jul-Sep 2014 Notes: Epub 2013 Oct 23.

Hawkes CP, Levine MA: Ketotic hypercalcemia: a case series and description of a novel entity. J Clin Endocrinol Metab 99(5): 1531-6, May 2014.

Li D, Weber DR, Deardorff MA, Hakonarson H, Levine MA: Exome sequencing reveals a nonsense mutation in MMP13 as a new cause of autosomal recessive metaphyseal anadysplasia. European Journal of Human Genetics Apr 2014 Notes: Epub ahead of print.

Li Q, Brodsky JL, Conlin LK, Pawel B, Glatz AC, Gafni RI, Schurgers L, Uitto J, Hakonarson H, Deardorff MA, Levine MA: Mutations in the ABCC6 gene as a cause of generalized arterial calcification of infancy: genotypic overlap with pseudoxanthoma elasticum. Journal of Investigative Dermatology 134(3): 658-65, Mar 2014.

Gannon AW, Monk HM, Levine MA: Cinacalcet monotherapy in neonatal severe hyperparathyroidism: a case study and review. J Clin Endocrinol Metab 99(1): 7-11, Jan 2014.

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Last updated: 10/29/2014
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