Clinical Interests

Lysosomal storage diseases; inborn errors of metabolism

Research Interests

Clinical trials; lysosomal storage diseases; biomarkers in gaucher diseases

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; Clinical Genetics 2009
 

Burrow TA, Bailey LA, Kinnett DG, Hopkin RJ. Acute progression of neuromuscular findings in infantile Pompe disease. Pediatr Neurol. 2010 Jun;42(6):455-8.

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. 

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.