Jerry Vockley

A proposed nosology of inborn errors of metabolism

Nenad Blau, Carlos R. Ferreira, Clara D.M. van Karnebeek, 2018, Genetics in Medicine.

Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy

Thomas Meitinger, Julien Gagneur, Holger Prokisch, 2015, American journal of human genetics.

c-Myc Programs Fatty Acid Metabolism and Dictates Acetyl-CoA Abundance and Fate*

Jie Lu, Jerry Vockley, E. Prochownik, 2014, The Journal of Biological Chemistry.

Isovaleric acidemia: New aspects of genetic and phenotypic heterogeneity

Jerry Vockley, J. Vockley, R. Ensenauer, 2006, American journal of medical genetics. Part C, Seminars in medical genetics.

Human Acyl-CoA Dehydrogenase-9 Plays a Novel Role in the Mitochondrial β-Oxidation of Unsaturated Fatty Acids*

Jerry Vockley, Thomas J Corydon, Miao He, 2005, Journal of Biological Chemistry.

Phenylalanine hydroxylase deficiency: diagnosis and management guideline

John J. Mitchell, Jerry Vockley, Barbara K Burton, 2013, Genetics in Medicine.

Phenylketonuria Scientific Review Conference: state of the science and future research needs.

Melissa L McPheeters, Mary Lou Lindegren, Anita MacDonald, 2014, Molecular genetics and metabolism.

Mammalian Electron Transferring Flavoprotein·Flavoprotein Dehydrogenase Complexes Observed by Microelectrospray Ionization-Mass Spectrometry and Surface Plasmon Resonance*

Linda Benson, Jerry Vockley, L. Benson, 2004, Journal of Biological Chemistry.

Recommendations for the nutrition management of phenylalanine hydroxylase deficiency

Jerry Vockley, J. Vockley, K. Moseley, 2014, Genetics in Medicine.