Harry “Adrian” Lesmana, MD

Harry “Adrian” Lesmana, MD

  • Clinical MD Fellow

Departments

Education

Pediatrics Hematology/Oncology Fellowship - St. Jude Children's Research Hospital
Combined Pediatrics/Human Genetics Residency - Cincinnati Children's Hospital
Pediatrics Intership - Cipto Mangunkusumo General Hospital/University of Indonesia
MD - University of Indonesia
Bachelor of Medicine - University of Indonesia

Selected Publications

Lesmana H, Lee MV, Hosseini SA, Burrow TA, Hallinan B, Bove K, Schapiro M, Hopkin RJ. CNTNAP1-Related Congenital Hypomyelinating Neuropathy. Pediatric Neurology Apr;93:43-49, 2019.

Schulze KV, Szafranski P, Lesmana H, Hopkin RJ, Hamvas A, Wambach JA, Shinawi M, Zapata G, Carvalho CMB, Liu Q, Karolak JA, Lupski JR, Hanchard NA, Stankiewicz P. Novel parent-of-origin-specific differentially methylated loci on chromosome 16. Clinical Epigenetics Apr 8;11(1):60, 2019.

Lesmana H, Dyer L, Morales DLS, Ryan TD, Hopkin RJ. Neonatal Myocardial Infarction in Williams-Beuren Syndrome. Progress in Pediatric Cardiology, 2019.

Lesmana H, Dyer L, Li X, Denton J, Griffiths J, Chonat S, Seu KG, Heeney MM, Zhang K, Hopkin RJ, Kalfa TA. Alu element insertion in PKLR gene as a novel cause of pyruvate kinase deficiency in Middle Eastern patients. Hum Mutat 39:389-393, 2018. doi:10.1002/humu.23392

Shaheen, R., Sebai, M. A., Patel, N., Ewida, N., Kurdi, W., Altweijri, I., Sogaty, S., Almardawi, E., Seidahmed, M. Z., Alnemri, A., Madirevula, S., Ibrahim, N., Abdulwahab, F., Hashem, M., Al-Sheddi, T., Alomar, R., Alobeid, E., Sallout, B., AlBaqawi, B., AlAali, W, Ajaji N, Lesmana H, Hopkin RJ, Dupuis L, Mendoza-Londono R, Al Rukban H, Yoon G, Faqeih E, Alkuraya FS. The genetic landscape of familial congenital hydrocephalus. Annals of Neurology 81, 890-897, 2017. doi:10.1002/ana.24964

Kartapradja H, Marzuki NS, Pertile MD, Francis D, Suciati LP, Anggaratri HW, Ambarwati DD, Idris FP, Lesmana H, Trimarsanto H, Paramayuda C, Harahap AR. Exceptional complex chromosomal rearrangements in three generations. Case Rep Genet 2015:321014, 2015. doi:10.1155/2015/321014

Last update: October 2019

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