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Charles A. Stanley

Emeritus Professor CE of Pediatrics
Department: Pediatrics

Contact information
Children's Hospital of Philadelphia
34th Street & Civic Center Blvd
Philadelphia, PA 19104
Office: 2155903420
Fax: 2155903053
Education:
B.A. (Biochemical Sciences)
Harvard University, 1964.
M.D. (Medicine)
University of Virginia School of Medicine, 1970.
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Description of Research Expertise

genetic disorders of carbohydrate and fatty acid metabolism, insulin secretion

Description of Clinical Expertise

hypoglycemia, glycogenoses, fatty acid oxidation disorders, diabetes mellitus

Selected Publications

Changhong Li, Amanda M. Ackermann, Kara E. Boodhansingh, Tricia R. Bhatti, Chengyang Liu, Jonathan Schug, Nicolai Doliba, Bing Han, Karen E. Cosgrove, Indraneel Banerjee, Franz M. Matschinsky, Itzhak Nissim, Klaus H. Kaestner, Ali Naji, N. Scott Adzick, Mark J. Dunne, Charles A. Stanley and Diva D. De León: Functional and Metabolomic Consequences of ATP-dependent Potassium Channel Inactivation in Human Islets. Diabetes [Epub ahead of print], April 25 2017.

Barrosse-Antle M, Su C, Chen P, Boodhansingh KE, Smith TJ, Stanley CA, De León DD, Li C: A severe case of hyperinsulinism due to hemizygous activating mutation of glutamate dehydrogenase. Pediatric Diabetes Feb 6 (on-line) 2017.

Boodhansingh K, Ferrara C, Stanley CA, et al: Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2 (UCP2). The Journal of Clinical Endocrinology & Metabolism Jan 2017 Notes: Accepted for publication.

Kalish JM, Boodhansingh KE, Bhatti TR, Ganguly A, Conlin LK, Becker SA, Givler S, Mighion L, Palladino AA, Adzick NS, De León DD, Stanley CA, Deardorff MA.: Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith-Wiedemann syndrome. J Med Genet 53(1), Jan 2016.

Bhatti T, Ganapathy K, Huppmann A, Conlin L, Boodhansingh S, MacMullen C, Becker S, Ernst L, Adzick NS, Ruchelli A, Ganguly A, Stanley CA: Histologic and Molecular Profile of Peditric Insulinomas: Evidence of a Paternal Parent-of-Origin Effect. Journal of Clinical Endoccrinology & Metabolism Page: jc20152914, Jan 12 2016.

Martin GM, Rex EA, Devaraneni P, Denton JS, Boodhansingh KE, DeLeon DD, Stanley CA, Shyng SL.: Pharmacological Correction of Trafficking Defects in ATP-sensitive Potassium Channels Caused by Sulfonylurea Receptor 1 Mutations. Journal of Biological Chemistry 291(42): 21971-21983, 2016.

Wong SY, Beamer LJ, Gadomski T, Honzik T, Mohamed M, Wortmann SB, Brocke Holmefjord KS, Mork M, Bowling F, Sykut-Cegielska J, Koch D, Ackermann A, Stanley CA, Rymen D, Zeharia A, Al-Sayed M, Marquardt T, Jaeken J, Lefeber D, Conrad DF, Kozicz T, Morava E: Defining the Phenotype and Assessing Severity in Phosphoglucomutase-1 Deficiency. Journal of Pediatrics 175: 130-136, 2016.

Lord K, Radcliffe J, Gallagher PR, Adzick NS, Stanley CA, De León: High Risk of Diabetes and Neurobehavioral Deficits in Individuals With Surgically Treated Hyperinsulinism. J Clin Endocrinol Metab 11(100): 4133-9, Nov 2015.

Kalish JM, Boodhansingh KE, Bhatti TR, Ganguly A, Conlin LK, Becker SA, Givler S, Mighion L, Palladino AA, Adzick NS, De León DD, Stanley CA, Deardorff MA: Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith– Wiedemann syndrome. J Med Genet Nov 2015.

Ferrara C, Patel P, Becker S, Stanley CA, Kelly A: Biomarkers of Insulin for the Diagnosis of Hyperinsulinemic Hypoglycemia in Infants and Children. J Pediatr Oct 2015.

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Last updated: 04/28/2017
The Trustees of the University of Pennsylvania