T. Andrew Burrow, MD
Title
Assistant Professor of Clinical Pediatrics
Email
thomas.burrow@cchmc.org
Phone
513-636-9437
Fax
513-636-7297
Credentials
MD: University of Arkansas for Medical Sciences, Little Rock, AR, 2003.
Residency: Pediatrics and Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 2008.
Fellowship: Medical Biochemical Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 2009.
Certification: Pediatrics, 2007.
Awards and Honors
- Alpha Omega Alpha Honor Medical Society, 2003.
- Genzyme/American College of Medical Genetics Foundation Clinical Genetics Fellow in Biochemical Genetics, 2008.
- Cincinnati Children's Fellow Award for Scholoarly Excellence, 2009.
Research
Clinical trials; lysosomal storage diseases; biomarkers in gaucher diseases
Publications, Most Recent
Burrow TA, Hopkin RJ, Bove KE, Miles L, Wong BL, Choudhary A, Bali D, Li SC, Chen YT: Non-Lethal Congenital Hypotonia Due to Glycogen Storage Disease Type IV. Am J Med Genet A, 2007:140(8):878-82.
Burrow TA, Cohen M, Deutsch G, Bokulic R, Choudhary A, Falcone R, Grabowski GA: Gaucher Disease: Progressive Mesenteric and Mediastinal Lymphadenopathy Despite Enzyme Therapy. J Peds, 2007:150:202-6.
Burrow TA, Bove KE, Grabowski, GA. The Lysosomal Storage Diseases. In: Suchy FJ, Sokol RJ, and Balistreri WF eds, Liver Disease in Children, 3rd ed., Cambridge University Press, New York; 2007:714-735.
Burrow TA, Hopkin, RJ, Leslie, ND, Tinkle, BT, and Grabowski, GA: Enzyme Reconstitution/Replacement Therapy for Lysosomal Storage Diseases. Curr Opin Pediatr, 2007:19:628-635.
Burrow, TA,Saal, HM, deAlarcon, A, Martin, L, Cotton, RT, Hopkin, RJ: A Characterization of Congenital Anomalies in Individuals with Choanal Atresia. Arch Otolaryngol Head Neck Surg. 2009;135(6):543-547.
Professional Organization Memberships
- American Society of Human Genetics
- American College of Medical Genetics
- American Academy of Pediatrics
Special Interests
Lysosomal storage diseases; inborn errors of metabolism
