• 2196 Citations
  • 23 Scopus h-Index
20022020

Research output per year

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Research Output

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2018

Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: Unique presenting laboratory values and a review of biochemical and clinical features

Conboy, E., Vairo, F., Schultz, M., Agre, K., Ridsdale, R., Deyle, D., Oglesbee, D., Gavrilov, D., Klee, E. W. & Lanpher, B., Jan 1 2018, JIMD Reports. Springer, p. 63-69 7 p. (JIMD Reports; vol. 40).

Research output: Chapter in Book/Report/Conference proceedingChapter

8 Scopus citations
2016

Human genetic disorders

Volk, A. K., Mitchell, E. B., Thomas, B. C., Runke, C. K., Essendrup, A. A., Kotzer, K. E., Deyle, D. R., Coon, L., Pruthi, R. K., Oglesbee, D., Zetzsche, L., Kemppainen, J. & Gavrilova, R. M., Feb 13 2016, Essentials of Anatomic Pathology: Fourth Edition. Springer International Publishing, p. 595-663 69 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

1 Scopus citations
2014

Newborn screening by tandem mass spectrometry and molecular confirmation

Hofherr, S. & Oglesbee, D., Jan 1 2014, Molecular Diagnostics: 12 Tests That Changed Everything. Springer New York, p. 209-222 14 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

1 Scopus citations
2007

Laboratory diagnosis of inborn errors of metabolism

Oglesbee, D. & Rinaldo, P., Jan 1 2007, Liver Disease in Children, Third Edition. Cambridge University Press, p. 531-544 14 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

1 Scopus citations