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
Rutgers College, New Brunswick, NJ, 1972.
Drexel University (formerly Hahnemann) College of Medicine, Philadelpia, PA, 1976.
Permanent link

Selected Publications

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.

Hawkes, C. P., Levine, M. A.: Ketotic Hypercalcemia: A Case Series and Description of a Novel Entity. Journal of Clinical Endocrinology and Metabolism Page: jc20134275, 2014.

Gannon, A. W., Monk, H. M., Levine, M. A.: Cinacalcet monotherapy in neonatal severe hyperparathyroidism: a case study and review. Journal of Clinical Endocrinology and Metabolism 99(1): 7-11, 2014.

Li, D., Opas, E. E., Tuluc, F., Metzger, D. L., Hou, C., Hakonarson, H., Levine, M. A.: Autosomal Dominant Hypoparathyroidism Caused by Germline Mutation in GNA11: Phenotypic and Molecular Characterization. Journal of Clinical Endocrinology and Metabolism Page: jc20141029, 2014.

Li, D., Weber, D. R., Deardorff, M. A., Hakonarson, H., Levine, M. A.: Exome sequencing reveals a nonsense mutation in MMP13 as a new cause of autosomal recessive metaphyseal anadysplasia. European Journal of Human Genetics 2014.

Yuan, Z., Opas, E. E., Vrikshajanani, C., Libutti, S. K., Levine, M. A.: Generation of mice encoding a conditional null allele of Gcm2. Transgenic Research 2014.

Fan, B., Shepherd, J. A., Levine, M. A., Steinberg, D., Wacker, W., Barden, H. S., Ergun, D., Wu, X. P.: National Health and Nutrition Examination Survey Whole-Body Dual-Energy X-Ray Absorptiometry Reference Data for GE Lunar Systems. Journal of Clinical Densitometry 2013.

Kelly, A., Levine, M. A.: Hypocalcemia in the critically ill patient. Journal of Intensive Care Medicine 28(3): 166-77, 2013.

Roizen, J. D., Shah, V., Levine, M. A., Carlow, D. C.: Determination of reference intervals for serum total calcium in the vitamin D-replete pediatric population. Journal of Clinical Endocrinology and Metabolism 98(12): E1946-50, 2013.

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Last updated: 05/23/2014
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