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.
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.
Permanent link

Selected Publications

George Sobenna, Weber David, Kaplan Paige, Hummel Kelly, Monk Heather M, Levine Michael A: Short Term Safety of Zoledronic Acid in Young Patients with Bone Disorders: An Extensive Institutional Experience. The Journal of clinical endocrinology and metabolism Page: jc20152680, Aug 2015.

Hawkes Colin P, Schnellbacher Sarah, Singh Ravinder J, Levine Michael A: 25-Hydroxyvitamin D Can Interfere With a Common Assay for 1,25-Dihydroxyvitamin D in Vitamin D Intoxication. The Journal of clinical endocrinology and metabolism 100(8): 2883-9, Aug 2015.

Gan Hoong-Wei, Bulwer Chloe, Jeelani Owase, Levine Michael Alan, Korbonits Márta, Spoudeas Helen Alexandra: Treatment-resistant pediatric giant prolactinoma and multiple endocrine neoplasia type 1. International journal of pediatric endocrinology 2015(1): 15, July 2015.

Thacher Tom D, Fischer Philip R, Singh Ravinder J, Roizen Jeffrey, Levine Michael A: CYP2R1 Mutations Impair Generation of 25-hydroxyvitamin D and Cause an Atypical Form of Vitamin D Deficiency. The Journal of clinical endocrinology and metabolism 100(7): E1005-13, May 2015.

Li D, Weber DR, Deardorff MA, Hakonarson H, Levine MA: Exome sequencing reveals a nonsense mutation in MMP13 as a new cause of autosomal recessive metaphyseal anadysplasia. Eur J Hum Genet 23(2): 264-6, Feb 2015 Notes: Epub ahead of print.

Li Qiaoli, Sundberg John P, Levine Michael A, Terry Sharon F, Uitto Jouni: The effects of bisphosphonates on ectopic soft tissue mineralization caused by mutations in the ABCC6 gene. Cell cycle (Georgetown, Tex.) 14(7): 1082-9, 2015.

Dasgupta D, Wee MJ, Reyes M, Li Y, Simm PJ, Sharma A, Schlingmann KP, Janner M, Biggin A, Lazier J, Gessner M, Chrysis D, Tuchman S, Baluarte HJ, Levine MA, Tiosano D, Insogna K, Hanley DA, Carpenter TO, Ichikawa S, Hoppe B, Konrad M, Savendahl L, Munns CF, Lee H, Juppner H, Bergwitz C: Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis. J Am Soc Nephrol 25(10): 2366-75, Oct 2014 Notes: Epub 2014 Apr 3.

Dasgupta Debayan, Wee Mark J, Reyes Monica, Li Yuwen, Simm Peter J, Sharma Amita, Schlingmann Karl-Peter, Janner Marco, Biggin Andrew, Lazier Joanna, Gessner Michaela, Chrysis Dionisios, Tuchman Shamir, Baluarte H Jorge, Levine Michael A, Tiosano Dov, Insogna Karl, Hanley David A, Carpenter Thomas O, Ichikawa Shoji, Hoppe Bernd, Konrad Martin, Sävendahl Lars, Munns Craig F, Lee Hang, Jüppner Harald, Bergwitz Clemens: Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis. Journal of the American Society of Nephrology : JASN 25(10): 2366-75, Oct 2014.

Mancilla EE, Brodsky JL, Mehta S, Pignolo RJ, Levine MA: Teriparatide as a Systemic Treatment for Lower Extremity Non-Union Fractures: A Case Series. Endocr Pract 21(2): 1-22, Oct 2014 Notes: Epub ahead of print.

Li D, Opas EE, Tuluc F, Metzger DL, Hou C, Hakonarson H, Levine MA: Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization. J Clin Endocrinol Metab 99(9): E1774-83, Sep 2014 Notes: Epub 2014 May 13.

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Last updated: 12/02/2015
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