• 1937 Citations
  • 21 Scopus h-Index
20022019
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Research Output 2002 2019

  • 1937 Citations
  • 21 Scopus h-Index
  • 42 Article
  • 4 Chapter
  • 2 Comment/debate
  • 1 Conference article
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Chapter
2018
2 Citations (Scopus)

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. R., 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

Hydroxymethylglutaryl-CoA Synthase
HDL Cholesterol
Organic acids
Biomarkers
Fasting
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

Inborn Genetic Diseases
Medical Genetics
2014
1 Citation (Scopus)

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

Tandem Mass Spectrometry
2007
1 Citation (Scopus)

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

Inborn Errors Metabolism
Clinical Laboratory Techniques
Inborn Errors Amino Acid Metabolism
Fatty Acids
Metabolic Diseases