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

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.
ML (Master of Law)
University of Pennsylania Carey Law School, 2024.
Permanent link
> Perelman School of Medicine   > Faculty   > Details

Selected Publications

Schigt H, Bald M, van der Eerden BCJ, Gal L, Ilenwabor BP, Konrad M, Levine MA, Li D, Mache CJ, Mackin S, Perry C, Rios FJ, Schlingmann KP, Storey B, Trapp CM, Verkerk AJMH, Zillikens MC, Touyz RM, Hoorn EJ, Hoenderop JGJ, de Baaij JHF.: Expanding the phenotypic spectrum of Kenny-Caffey syndrome: a case series and systematic literature review. J Clin Endocrinol Metab Mar 2023.

Zung A, Barash G, Banne E, Levine MA.: Novel Calcium-Sensing Receptor (CASR) Mutation in a Family with Autosomal Dominant Hypocalcemia Type 1 (ADH1): Genetic Study over Three Generations and Clinical Characteristics. Horm Res Paediatr Feb 2023.

Craven M, Vajravelu ME, Shekdar KV, Levine MA, Mumm S, Whyte MP, Mancilla EE.: Early identification of a 12-bp tandem duplication in TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK): Clinical characterization and response to bisphosphonate therapy. Bone 170: 116698, Feb 2023.

Mantoanelli L, de Almeida CM, Coelho MCA, Coutinho M, Levine MA, Collett-Solberg PF, Bordallo AP.: Vitamin D-Dependent Rickets Type 3: A Case Report and Systematic Review. Calcif Tissue Int Jan 2023.

Hawkes CP, Al Jubeh JM, Li D, Tucker SE, Rajiyah T, Levine MA.: Novel PTH Gene Mutations Causing Isolated Hypoparathyroidism. J Clin Endocrinol Metab 107: e2449-e2458, May 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, Apr 2022.

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, Feb 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.

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.

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Last updated: 03/16/2023
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