Loki Home

Research Interests

Funding Opportunities

FAQ

UI Login Guest Login

Browse by Investigator Last Name



Browse Research


Photo of Oleg Shchelochkov

Oleg Shchelochkov

This person no longer has an active appointment with the University of Iowa.

Education

M.D., Medicine, Tashkent Pediatric Medical Institute, USSR (Uzbekistan)
Residency, Pediatric Intensive Care and Anesthesiology, Tashkent Pediatric Medical Institute, USSR (Uzbekistan)
Pesidency, Pediatrics, Univ of Iowa Hospital and Clinics
Fellowship, Medical Genetics, Baylor College of Medicine, Houston, TX
Fellowship, Clinical Biochemical Genetics, Baylor College of Medicine, Houston, TX

Research Interests


MeSH Terms from Publications



Research Summary

Development of novel therapies for the urea cycle disorders; clinical and molecular characterization of genomic disorders.

Recent Publications


Show publications
  1. Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions. Eur J Hum Genet 20(12):1240-7, 2012. [PubMed]
  2. A randomized controlled trial to evaluate the effects of high-dose versus low-dose of arginine therapy on hepatic function tests in argininosuccinic aciduria. Mol Genet Metab 107(3):315-21, 2012. [PubMed]
  3. 2q24 deletions: Further characterization of clinical findings and their relation to the SCN cluster. Am J Med Genet A 158A(11):2767-74, 2012. [PubMed]
  4. Nitric-oxide supplementation for treatment of long-term complications in argininosuccinic aciduria. Am J Hum Genet 90(5):836-46, 2012. [PubMed]
  5. Hepatocellular carcinoma in a research subject with ornithine transcarbamylase deficiency. Mol Genet Metab 105(2):263-5, 2012. [PubMed]
  6. Replication of clinical associations with 17-hydroxyprogesterone in preterm newborns. J Pediatr Endocrinol Metab 25(3-4):301-5, 2012. [PubMed]
  7. Requirement of argininosuccinate lyase for systemic nitric oxide production. Nat Med 17(12):1619-26, 2011. [PubMed]
  8. A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features. Am J Med Genet A 155A(9):2224-8, 2011. [PubMed]
  9. Deoxyguanosine kinase deficiency presenting as neonatal hemochromatosis. Mol Genet Metab 103(3):262-7, 2011. [PubMed]
  10. Desmosterolosis-phenotypic and molecular characterization of a third case and review of the literature. Am J Med Genet A 155A(7):1597-604, 2011. [PubMed]