Katherine Lord, MD

faculty photo
Assistant Professor of Clinical Pediatrics
Department: Pediatrics

Contact information
Division of Endocrinology/Diabetes
The Children's Hospital of Philadelphia
3401 Civic Center Blvd
Philadelphia, PA 19104
Northwestern University, 2000.
Northwestern University Feinberg School of Medicine, 2007.
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Selected Publications

Adzick NS, De Leon DD, States L, Lord K, Bhatti T, Becker S, Stanley CA: Surgical treatment of congenital hyperinsulinism: Results from 500 pancreatectomies in neonates and children. Journal of Pediatric Surgery 54: 27-32, 2019.

Herrera A, Vajravelu ME, Givler S, Mitteer L, Avitabile C, Lord K, De Leon DD: Prevalence of Adverse Events in Children With Congenital Hyperinsulinism Treated With Diazoxide. Journal of Clinical Endocrinology and Metabolism 103(12): 4365-4372, December 2018.

Grand K, Levitt Katz LE, Crowley TB, Moss E, Lessig M, Bamba V, Lord K, Zackai EH, Emanuel BS, Valverde K, McDonald-McGinn DM: The impact of hypocalcemia on full scale IQ in patients with 22q11.2 deletion syndrome. American Journal of Medical Genetics Page: 2167–2171, April 2018.

Lord K, De Leon DD, Stanley, CA: Hypoglycemia. Pediatric Endocrinology, A Practical Clinical Guide, 3rd Edition 2018.

Lord K, De Leon DD: Hyperinsulinism in the Neonate. Clinics in Perinatology 45: 61-74, 2018.

Lord K, Stewart N, Langdon D, De Leon DD: Lanreotide is a Safe and Effective Treatment for Congenital Hyperinsulinism. 10th International Joint Meeting of Pediatric Endocrinology September 2017.

Lord K, Palladino AA: Disorders of Thyroid Hormone. Comprehensive Pediatric Hospital Medicine, 2nd Ed. 2017.

Hanley P, Lord K, Bauer AJ: Thyroid Disorders in Children and Adolescents: A Review. JAMA Pediatrics 170(10): 1008-1019, October 2016.

Vajravelu ME, Lord K, Givler S, De Leon DD: Protein-induced Hypoglycemia in KATP Hyperinsulinism is Mediated by the GLP-1 Receptor. Eastern Society of Pediatric Research, Philadelphia PA March 2016.

Sharma S, Place E, Lord K, Leroy BP, Falk MJ, Pradhan M.: Claudin 19-based familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a sibling pair. Clinical Nephrology 85(6): 346-52, 2016.

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Last updated: 01/15/2019
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