Michael Alan Levine, M.D., FAAP, FACP, FACE

faculty photo
Emeritus Professor CE of Pediatrics
Department: Pediatrics

Contact information
The Children's Hospital of Philadelphia
3615 Civic Center Boulevard
Abramson Research Building, Room 510A
Philadelphia, PA 19104
Office: 215-590-3174
Fax: 215-590-3053
Lab: (267) 426-2382
Rutgers College, New Brunswick, NJ, 1972.
Drexel University (formerly Hahnemann) College of Medicine, Philadelpia, PA, 1976.
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Selected Publications

Casella, A., Long, C., Zhou, J., Lai, M., O'Lear, L., Caplan, I., Levine, M. A., Roizen, J. D.: Differential Frequency of CYP2R1 Variants Across Populations Reveals Pathway Selection for Vitamin D Homeostasis. J Clin Endocrinol Metab 105(5): 1302-15, 2020.

Rampp, R. D., Mancilla, E. E., Adzick, N. S., Levine, M. A., Kelz, R. R., Fraker, D. L., Iyer, P., Lindeman, B. M., Mejia, V. A., Chen, H., Wachtel, H.: Single Gland, Ectopic Location: Adenomas are Common Causes of Primary Hyperparathyroidism in Children and Adolescents. World J Surg 44(5): 1518-1525, 2020.

Li, D., Bupp, C., March, M. E., Hakonarson, H., Levine, M. A.: Intragenic deletions of GNAS in pseudohypoparathyroidism type 1A identify a new region affecting methylation of exon A/B. J Clin Endocrinol Metab 2020.

Gordon, R. J., Li, D., Doyle, D., Zaritsky, J., Levine, M. A.: Digenic Heterozygous Mutations in SLC34A3 and SLC34A1 Cause Dominant Hypophosphatemic Rickets with Hypercalciuria. J Clin Endocrinol Metab 105(7), 2020.

Gordon, R. J., Levine, M. A.: Burosumab treatment of children with X-linked hypophosphataemic rickets. Lancet 393(10189): 2364-2366, 2019.

Roizen, J. D., Long, C., Casella, A., O'Lear, L., Caplan, I., Lai, M., Sasson, I., Singh, R., Makowski, A. J., Simmons, R., Levine, M. A.: Obesity Decreases Hepatic 25-Hydroxylase Activity Causing Low Serum 25-Hydroxyvitamin D. Journal of Bone and Mineral Research Page: e3686, 2019.

Youssefian, L., Vahidnezhad, H., Saeidian, A. H., Pajouhanfar, S., Sotoudeh, S., Mansouri, P., Amirkashani, D., Zeinali, S., Levine, M. A., Peris, K., Colombo, R., Uitto, J.: Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations. J Hepatol 71(2): 366-370, 2019.

Mannstadt, M., Clarke, B. L., Bilezikian, J. P., Bone, H., Denham, D., Levine, M. A., Peacock, M., Rothman, J., Shoback, D. M., Warren, M. L., Watts, N. B., Lee, H. M., Sherry, N., Vokes, T. J.: Safety and Efficacy of 5 Years of Treatment With Recombinant Human Parathyroid Hormone in Adults With Hypoparathyroidism. J Clin Endocrinol Metab 104(11): 5136-5147, 2019.

Li, D., March, M. E., Gutierrez-Uzquiza, A., Kao, C., Seiler, C., Pinto, E., Matsuoka, L. S., Battig, M. R., Bhoj, E. J., Wenger, T. L., Tian, L., Robinson, N., Wang, T., Liu, Y., Weinstein, B. M., Swift, M., Jung, H. M., Kaminski, C. N., Chiavacci, R., Perkins, J. A., Levine, M. A., Sleiman, P. M. A., Hicks, P. J., Strausbaugh, J. T., Belasco, J. B., Dori, Y., Hakonarson, H.: ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor. Nat Med 25(7): 1116-1122, 2019.

Hashim, R., Levine, M. A., Somasundarum, K., Lamahewage, A., Atapattu, N.: Neonatal severe hyperparathyroidism due to a homozygous mutation of calcium-sensing receptor; a challenging case. Ceylon Med J 64(4): 155-157, 2019.

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Last updated: 06/16/2020
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