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Office10833 Le Conte 32263 Ave
Los Angeles, CA 90095Phone(310) 206-6581Fax(310) 206-8616
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Education & Training
- Harbor - UCLA Medical CenterResidency, Pediatrics/Medical Genetics, 2002 - 2005
- Cedars-Sinai Medical CenterFellowship, Medical Genetics, 2005
- Children's Hospital of Los AngelesResidency, Pediatrics, 1993
- Children's Hospital of Los AngelesInternship, Pediatrics, 1990 - 1991
- University of California San Diego School of MedicineClass of 1990
Certifications & Licensure
- CA State Medical License 1991 - 2023
- American Board of Medical Genetics and Genomics Clinical Biochemical Genetics
- American Board of Medical Genetics and Genomics Clinical Genetics
Awards, Honors, & Recognition
- Fellow (FAAP) American Academy of Pediatrics
- Long-term Outcome of N-Carbamylglutamate Treatment in Propionic Acidemia and Methylmalonic Acidemia Start of enrollment: 2012 Sep 01Berry, G.T.,Gallagher, R.C.,Enns, G.M.,Wong, D.A.,Yudkoff, M.P.
- Short-term Outcome of N-Carbamylglutamate in the Treatment of Acute Hyperammonemia Start of enrollment: 2012 Sep 01Yudkoff, M.P.,Berry, G.T.,Gallagher, R.C.,Enns, G.M.,Wong, D.A.
- Oxidative Stress, Inflammation and Acute Decompensation in Urea Cycle Disorders Start of enrollment: 2012 Feb 01Lee, B.,Harding, C.,Heggie, C.,Coughlin, C.,Diaz, G.A.,Diaz, G.,Payan, I.,Simpson, K.,Merritt, L.,Brody, L.,Yudkoff, M.,Mullins, M.,Ambreen, M.,Dorrani, N.,Schrager, N.,Gallagher, R.C.,Berry, S.,Marrone, ...
- Longitudinal Study of Urea Cycle Disorders Start of enrollment: 2006 Feb 01Ambreen, M.,Anastasoaie, V.,Batshaw, M.L.,Berry, S.,Brody, L.,Burgard, P.,Coughlin, C.,Dorrani, N.,Heggie, C.,Marrone, T.,Mullins, M.,Payan, I.,Schrager, N.,Seminara, J.,Simpson, K.,Stricker, T.,Tuchman, M.
Publications & Presentations
- 9 citationsImpact of Diagnosis and Therapy on Cognitive Function in Urea Cycle Disorders.Roland Posset, Andrea L. Gropman, Sandesh C.S. Nagamani, Lindsay C. Burrage, Jirair K. Bedoyan, Derek Wong, Gerard T. Berry, Matthias R. Baumgartner, Marc Yudkoff, Mat...> ;Annals of Neurology. 2019 Jul 1
- 8 citationsVariant in human POFUT1 reduces enzymatic activity and likely causes a recessive microcephaly, global developmental delay with cardiac and vascular features.Hideyuki Takeuchi, Derek Wong, Michael Schneider, Hudson H. Freeze, Megumi Takeuchi, Steven J Berardinelli, Atsuko Ito, Hane Lee, Stanley F. Nelson, Robert S. Haltiwanger> ;Glycobiology. 2018 May 1
- 10 citationsOutcomes of four patients with homocysteine remethylation disorders detected by newborn screeningDerek Wong, Silvia Tortorelli, Lisa R. Bishop, Elizabeth A. Sellars, Lisa A. Schimmenti, Natalie M. Gallant, Carlos E. Prada, Robert J. Hopkin, Nancy D. Leslie, Susan ...> ;Genetics in Medicine. 2016 Feb 1
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- Ronald Reagan UCLA Medical CenterLos Angeles, California
- Ventura County Medical CenterVentura, California
- Mattel Childrens Hospital University of California Los AngelesLos Angeles, California
- UCLA Medical Center-Santa MonicaSanta Monica, California
- Cedars-Sinai Medical CenterLos Angeles, California
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