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.
Permanent link
 

Selected Publications

Mancilla Edna E, Brodsky Jill L, Mehta Samir, Pignolo Robert J, Levine Michael A: Teriparatide as a Systemic Treatment for Lower Extremity Non-Union Fractures: A Case Series. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists Page: 1-22, Oct 2014.

Roizen Jeffrey, Levine Michael A: A meta-analysis comparing the Biochemistry of Primary Hyperparathyroidism in Youths to the Biochemistry of Primary Hyperparathyroidism in Adults. The Journal of clinical endocrinology and metabolism Page: jc20142268, Sep 2014.

Yuan Ziqiang, Opas Evan E, Vrikshajanani Chakravarthy, Libutti Steven K, Levine Michael A: Generation of mice encoding a conditional null allele of Gcm2. Transgenic research 23(4): 631-41, Aug 2014.

Fan Bo, Shepherd John A, Levine Michael A, Steinberg Dee, Wacker Wynn, Barden Howard S, Ergun David, Wu Xin P: National Health and Nutrition Examination Survey whole-body dual-energy X-ray absorptiometry reference data for GE Lunar systems. Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry 17(3): 344-77, Jul-Sep 2014.

Hawkes Colin Patrick, Levine Michael A: Ketotic hypercalcemia: a case series and description of a novel entity. The Journal of clinical endocrinology and metabolism 99(5): 1531-6, May 2014.

Li Dong, Weber David R, Deardorff Matthew A, Hakonarson Hakon, Levine Michael A: Exome sequencing reveals a nonsense mutation in MMP13 as a new cause of autosomal recessive metaphyseal anadysplasia. European journal of human genetics : EJHG Apr 2014.

Gannon Anthony W, Monk Heather M, Levine Michael A: Cinacalcet monotherapy in neonatal severe hyperparathyroidism: a case study and review. The Journal of clinical endocrinology and metabolism 99(1): 7-11, Jan 2014.

Li, Q., Brodsky, J. L., Conlin, L. K., Pawel, B., Glatz, A. C., Gafni, R. I., Schurgers, L., Uitto, J., Hakonarson, H., Deardorff, M. A., Levine, M. A.: 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, 2014.

Dasgupta, D., Wee, M. J., Reyes, M., Li, Y., Simm, P. J., Sharma, A., Schlingmann, K. P., Janner, M., Biggin, A., Lazier, J., Gessner, M., Chrysis, D., Tuchman, S., Baluarte, H. J., Levine, M. A., Tiosano, D., Insogna, K., Hanley, D. A., Carpenter, T. O., Ichikawa, S., Hoppe, B., Konrad, M., Savendahl, L., Munns, C. F., Lee, H., Juppner, H., Bergwitz, C.: Mutations in SLC34A3/NPT2c Are Associated with Kidney Stones and Nephrocalcinosis. Journal of the American Society of Nephrology 2014.

Roizen Jeffrey D, Shah Vipul, Levine Michael A, Carlow Dean C: Determination of reference intervals for serum total calcium in the vitamin D-replete pediatric population. The Journal of clinical endocrinology and metabolism 98(12): E1946-50, Dec 2013.

back to top
Last updated: 10/24/2014
The Trustees of the University of Pennsylvania