faculty photo

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

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
Education:
A.B.
Rutgers College, New Brunswick, NJ, 1972.
M.D.
Drexel University (formerly Hahnemann) College of Medicine, Philadelpia, PA, 1976.
Post-Graduate Training
Intern, Medicine, Johns Hopkins Hospital, Baltimore, MD, 1976-1977.
Resident, Medicine, Johns Hopkins Hospital, Baltimore, MD, 1977-1979.
Fellow, Endocrinology and Metabolism (Pediatrics & Medicine), NIH Inter-Institute Program, Bethesda, MD, 1979-1982.
Fellow, Genetics, National Institutes of Health Inter-Institute Program, Bethesda, MD, 1981-1982.
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Selected Publications

Stoffers, A. J., Weber, D. R., Levine, M. A.: An Update on Vitamin D Deficiency in the twenty-first century: nature and nurture. Current Opinion in Endocrinology, Diabetes, and Obesity 29(1): 36-43, 2022.

Hawkes, Colin P, Al Jubeh, Jamal M, Li, Dong, Tucker, Susan E, Rajiyah, Tara, Levine, Michael A: Novel PTH gene mutations causing isolated hypoparathyroidism. Journal of Clinical Endocrinology and Metabolism 2022.

London, Shira, Levine, Michael A, Li, Dong, Spiegel, Ronen, Lebel, Asaf, Halevy, Rephael, Tenenbaum-Rakover, Yardena: Hypocalcemia as the Initial Presentation of Type 2 Bartter Syndrome: A Family Report. The Journal of Clinical Endocrinology & Metabolism 107(4): e1679-e1688, 2022.

Ralph, Douglas, Levine, Michael A, Richard, Gabriele, Morrow, Michelle, Flynn, Elizabeth, Uitto, Jouni, Li, Qiaoli: Mutation update: Variants of the ENPP1 gene in pathologic calcification, hypophosphatemic rickets, and cutaneous hypopigmentation with punctate keratoderma. Human Mutation 2022.

Ralph, D., Nitschke, Y., Levine, M. A., Caffet, M., Wurst, T., Saeidian, A. H., Youssefian, L., Vahidnezhad, H., Terry, S. F., Rutsch, F., Uitto, J., Li, Q.: ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification. PLoS Genet. 2022;18(4):e1010192. 18(4): e1010192, 2022.

Ramirez-Suarez, Karen I, Cohen, Sara A, Barrera, Christian A, Levine, Michael A, Goldberg, David J, Otero, Hansel J: Longitudinal assessment of vascular calcification in generalized arterial calcification of infancy. Pediatric Radiology Page: 1-13, 2022.

Ferreira CR, Hackbarth ME, Ziegler SG, Pan KS, Roberts MS, Rosing DR, Whelpley MS, Bryant JC, Macnamara EF, Wang S, Müller K, Hartley IR, Chew EY, Corden TE, Jacobsen CM, Holm IA, Rutsch F, Dikoglu E, Chen MY, Mughal MZ, Levine MA, Gafni RI, Gahl WA.: Prospective phenotyping of long-term survivors of generalized arterial calcification of infancy (GACI). Genet Med 23: 396-407, Feb 2021.

Hawkes CP, Roy SM, Dekelbab B, Frazier B, Grover M, Haidet J, Listman J, Madsen S, Roan M, Rodd C, Sopher A, Tebben P, Levine MA.: Hypercalcemia in Children Using the Ketogenic Diet: A Multicenter Study. J Clin Endocrinol Metab 106: e485-e495, Jan 2021.

Ferreira CR, Kavanagh D, Oheim R, Zimmerman K, Stürznickel J, Li X, Stabach P, Rettig RL, Calderone L, MacKichan C, Wang A, Hutchinson HA, Nelson T, Tommasini SM, von Kroge S, Fiedler IA, Lester ER, Moeckel GW, Busse B, Schinke T, Carpenter TO, Levine MA, Horowitz MC, Braddock DT.: Response of the ENPP1-Deficient Skeletal Phenotype to Oral Phosphate Supplementation and/or Enzyme Replacement Therapy: Comparative Studies in Humans and Mice. J Bone Miner Res Bone Miner Res, 2021.

Lenherr-Taube, Nina, Furman, Michelle, Assor, Esther, Elia, Yesmino, Collins, Carol, Thummel, Kenneth, Levine, Michael A, Sochett, Etienne: Mild idiopathic infantile hypercalcemia—part 2: a longitudinal observational study. The Journal of Clinical Endocrinology & Metabolism 106(10): 2938-2948, 2021.

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Last updated: 07/11/2022
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