GerardVockleyMDPhD(He/Him)

PubMed

• Pegvaliase for the treatment of phenylketonuria: Final results of a long-term phase 3 clinical trial program.
  Hope Northrup, Rani Singh, Janet A Thomas, Kaleigh Bulloch Whitehall, Joshua Lilienstein, Kristin Lindstrom, Drew G Levy, Shaun Jones, Barbara K Burton, Cary O Harding...> ;Molecular Genetics and Metabolism Reports. 2024 Jun 1
• Clinical case report of intractable paroxysmal sympathetic hyperactivity in TANGO2 deficiency disorder.
  Kaitlin Morrison, Carol May, Lina Ghaloul-Gonzalez, Hitoshi Koshiya, Robert Safier, Amanda Brown, Jerry Vockley> ;American Journal of Medical Genetics. Part A. 2024 Apr 18
• Early diagnosis and treatment by newborn screening (NBS) or family history is associated with improved visual outcomes for long-chain 3-hydroxyacylCoA dehydrogenase de...
  Melanie B Gillingham, Dongseok Choi, Ashley Gregor, Nida Wongchaisuwat, Danielle Black, Hannah L Scanga, Ken K Nischal, Mark E Pennesi, Jose-Alain Sahel, Georgianne Ar...> ;Journal of Inherited Metabolic Disease. 2024 Apr 16
• Major clinical events and healthcare resource use among patients with long-chain fatty acid oxidation disorders in the United States: Results from LC-FAOD Odyssey prog...
  Yang, E., Kruger, E., Yin, D., Mace, K., Tierney, M., Liao, N., Cibelli, E., Drozd, D., Ross, N., Deering, K., Herout, P., Harshaw, Q., Shillington, A., Thomas, N., Ma...> ;Molecular Genetics and Metabolism. 2024 Feb 23
• 1 citations
  A proposal for an updated staging system for LCHADD retinopathy.
  Nida Wongchaisuwat, Melanie B Gillingham, Paul Yang, Lesley Everett, Ashley Gregor, Cary O Harding, Jose Alain Sahel, Ken K Nischal, Hannah L Scanga, Danielle Black, J...> ;Ophthalmic Genetics. 2024 Apr 1
• Optimizing metabolism is a complex issue.
  Vockley, J.> ;Nature Metabolism. 2024 Feb 1
• Impact of genetic and non-genetic factors on phenotypic diversity in NBAS-associated disease.
  Hammann, N., Lenz, D., Baric, I., Crushell, E., Vici, C., Distelmaier, F., Feillet, F., Freisinger, P., Hempel, M., Khoreva, A., Laass, M., Lacassie, Y., Lainka, E., L...> ;Molecular Genetics and Metabolism. 2024 Mar 1
• Metabolic features of treatment-refractory major depressive disorder with suicidal ideation.
  Wang, L., Li, K., Monk, J., Lingampelly, S., Segreti, A., Bloom, K., Tarnopolsky, M., Finegold, D., Peters, D., Pan, L., Naviaux, J., Vockley, J., Naviaux, R.> ;Translational Psychiatry. 2023 Dec 15
• The Myc-Like Mlx Network Impacts Aging and Metabolism.
  Huabo Wang, Taylor Stevens, Jie Lu, Alexander Roberts, Clinton Van't Land, Radhika Muzumdar, Zhenwei Gong, Jerry Vockley, Edward V Prochownik> ;Biorxiv. 2023 Nov 27
• Anomalous peroxidase activity of cytochrome c is the primary pathogenic target in Barth syndrome.
  Valerian E Kagan, Yulia Y Tyurina, Karolina Mikulska-Ruminska, Deena Damschroder, Eduardo Vieira Neto, Alessia Lasorsa, Alexander A Kapralov, Vladimir A Tyurin, Andrew...> ;Nature Metabolism. 2023 Dec 1
• 1 citations
  Genetic landscape of pediatric acute liver failure of indeterminate origin.
  Dominic Lenz, Lea D Schlieben, Masaru Shimura, Alyssa Bianzano, Dmitrii Smirnov, Robert Kopajtich, Riccardo Berutti, Rüdiger Adam, Denise Aldrian, Ivo Baric, Ulrich Ba...> ;Hepatology. 2024 May 1
• 4 citations
  Efficacy and safety of a synthetic biotic for treatment of phenylketonuria: a phase 2 clinical trial.
  Jerry Vockley, Neal Sondheimer, Marja Puurunen, George A Diaz, Ilona Ginevic, Dorothy K Grange, Cary Harding, Hope Northrup, John A Phillips 3rd, Shawn Searle, Janet A...> ;Nature Metabolism. 2023 Oct 1
• Amino acid ratio combinations as biomarkers for discriminating patients with pyruvate dehydrogenase complex deficiency from other inborn errors of metabolism.
  Anisha Verma, April N Lehman, Hatice Gokcan, Lorna Cropcho, Danielle Black, Steven F Dobrowolski, Jerry Vockley, Jirair K Bedoyan> ;Molecular Genetics & Genomic Medicine. 2024 Jan 1
• 1 citations
  Heptanoic and medium branched-chain fatty acids as anaplerotic treatment for medium chain acyl-CoA dehydrogenase deficiency.
  Anuradha Karunanidhi, Shakuntala Basu, Xue-Jun Zhao, Olivia D'Annibale, Clinton Van't Land, Jerry Vockley, Al-Walid Mohsen> ;Molecular Genetics and Metabolism. 2023 Nov 1
• 9 citations
  Premature aging and reduced cancer incidence associated with near-complete body-wide Myc inactivation.
  Huabo Wang, Jie Lu, Taylor Stevens, Alexander Roberts, Jordan Mandel, Raghunandan Avula, Bingwei Ma, Yijen Wu, Jinglin Wang, Clinton Van't Land, Toren Finkel, Jerry E ...> ;Cell Reports. 2023 Aug 29
• 8 citations
  Rapid Whole-Genomic Sequencing and a Targeted Neonatal Gene Panel in Infants With a Suspected Genetic Disorder.
  Jill L Maron, Stephen Kingsmore, Bruce D Gelb, Jerry Vockley, Kristen Wigby, Jennifer Bragg, Annemarie Stroustrup, Brenda Poindexter, Kristen Suhrie, Jae H Kim, Thomas...> ;JAMA. 2023 Jul 11
• Myelin Disruption, Neuroinflammation, and Oxidative Stress Induced by Sulfite in the Striatum of Rats Are Mitigated by the pan-PPAR agonist Bezafibrate.
  Nícolas Manzke Glänzel, Belisa Parmeggiani, Mateus Grings, Bianca Seminotti, Morgana Brondani, Larissa D Bobermin, César A J Ribeiro, André Quincozes-Santos, Jerry Voc...> ;Cells. 2023 Jun 6
• 3 citations
  Triheptanoin for the treatment of long-chain fatty acid oxidation disorders: Final results of an open-label, long-term extension study.
  Jerry Vockley, Barbara K Burton, Gerard Berry, Nicola Longo, John Phillips, Amarilis Sanchez-Valle, Kimberly A Chapman, Pranoot Tanpaiboon, Stephanie Grunewald, Elaine...> ;Journal of Inherited Metabolic Disease. 2023 Sep 1
• 7 citations
  Efficacy and Safety of Elamipretide in Individuals With Primary Mitochondrial Myopathy: The MMPOWER-3 Randomized Clinical Trial.
  Amel Karaa, Enrico Bertini, Valerio Carelli, Bruce H Cohen, Gregory M Enns, Marni J Falk, Amy Goldstein, Gráinne Siobhan Gorman, Richard Haas, Michio Hirano, Thomas Kl...> ;Neurology. 2023 Jul 18
• Response to Beretich and Beretich.
  Jerry Vockley, Nicola Brunetti-Pierri, Wendy K Chung, Angus J Clarke, Nina Gold, Robert C Green, Stephen Kagan, Tara Moroz, Christian P Schaaf, Martin Schulz, Elfride ...> ;Genetics in Medicine. 2023 Oct 1
• 2 citations
  Challenges and strategies for clinical trials in propionic and methylmalonic acidemias.
  Jerry Vockley, Barbara Burton, Agnieszka Jurecka, Jitendra Ganju, Beth Leiro, Roberto Zori, Nicola Longo> ;Molecular Genetics and Metabolism. 2023 Jul 1
• 1 citations
  Messenger RNA rescues medium-chain acyl-CoA dehydrogenase deficiency in fibroblasts from patients and a murine model.
  Xue-Jun Zhao, Ai-Walid Mohsen, Stephanie Mihalik, Keaton Solo, Shakuntala Basu, Ermal Aliu, Huifang Shi, Catherine Kochersberger, Anuradha Karunanidhi, Clinton Van't L...> ;Human Molecular Genetics. 2023 Jul 4
• Clinical, biochemical and molecular characterization of 12 patients with pyruvate carboxylase deficiency treated with triheptanoin.
  M Laura Duque Lasio, Angela C Leshinski, Leigh Anne Flore, April Lehman, Natasha Shur, Parul B Jayakar, Bryan E Hainline, Alice A Basinger, William G Wilson, George A ...> ;Molecular Genetics and Metabolism. 2023 Jun 1
• Mitochondrial ROS Triggers KIN Pathogenesis in FAN1-Deficient Kidneys.
  Merlin Airik, Haley Arbore, Elizabeth Childs, Amy B Huynh, Yu Leng Phua, Chi Wei Chen, Katherine Aird, Sivakama Bharathi, Bob Zhang, Peter Conlon, Stanislav Kmoch, Ken...> ;Antioxidants. 2023 Apr 8
• 1 citations
  Resting and total energy expenditure of patients with long-chain fatty acid oxidation disorders (LC-FAODs).
  James P DeLany, Angela Horgan, Ashley Gregor, Jerry Vockley, Cary O Harding, Melanie B Gillingham> ;Molecular Genetics and Metabolism. 2023 Mar 1
• Join now to see all

Journal Articles

• DNA methylation in the pathophysiology of hyperphenylalaninemia in the PAH mouse model of phenylketonuria  
  Dobrowolski SF, Lyons-Weiler J, Spridik K, Vockley J, Skvorak K, Biery A, Mol Genet Metab, 1/1/2016
• Neurometabolic Disorders: Potentially Treatable Abnormalities in Patients With Treatment-Refractory Depression and Suicidal Behavior  
  Pan LA, Martin P, Zimmer T, Segreti AM, Kassiff S, McKain BW, Baca CA, Rengasamy M, Hyland K, Walano N, Steinfeld R, Hughes M, Dobrowolski SK, Pasquino M, Diler R, Per..., American Journal of Psychiatry, 1/1/2016
• Metformin inhibits Branched Chain Amino Acid (BCAA) derived ketoacidosis and promotes metabolic homeostasis in MSUD  
  Sonnet SD, O' Leary NM, Gutierrez AM, Nguyen MS, Mateen S, Hsu Y, Mitchell PK, Lopez JA, Vockley J, Kennedy K, Ramanathan A, Scientific reports, 1/1/2016
• Precision medicine in the age of big data: The present and future role of large-scale unbiased sequencing in drug discovery and development  
  Vicini P, Fields O, Lai E, Litwack ED, Martin AM, Morgan TM, Pacanowski MA, Papaluca M, Perez OD, Ringel MS, Robson M, Sakul H, Vockley J, Zaks T, Dolsten M, Sogaard M, Clin Pharmacol Ther, 1/1/2016
• Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorder  
  Lee B, Diaz GA, Rhead W, Lichter-Konecki U, Feigenbaum A, Berry SA, Le Mons C, Bartley JA, Longo N, Nagamani SC, Berquist W, Gallagher R, Bartholomew D, Harding CO, Ko..., Genet Med, 1/1/2015
• Long-term major clinical outcomes in patients with long chain fatty acid oxidation disorders before and after transition to triheptanoin treatment-A retrospective char...  
  Vockley J, Marsden D, McCracken E, DeWard S, Barone A, Hsu K, Kakkis E, Mol Genet Metab, 1/1/2015
• c-Myc programs fatty acid metabolism and dictates acetyl-CoA abundance and fate  
  Vockley J, et al, Journal of Biological Chemistry, 1/1/2014
• Introduction: Neurodevelopmental issues in inborn errors of metabolism  
  Arnold GL, Vockley J, Introduction: Neurodevelopmental issues in inborn errors of metabolism, 1/1/2013
• Infantile Hypophosphatasia Secondary to a Novel Compound Heterozygous Mutation Presenting with Pyridoxine-Responsive Seizures  
  Belachew D, Kazmerski T, Libman I, Goldstein AC, Stevens ST, Deward S, Vockley J, Sperling MA, Balest AL, JIMD reports, 1/1/2013
• Neuropsychiatric Symptoms in Inborn Errors of Metabolism: Incorporation of Genomic and Metabolomic Analysis into Therapeutics and Prevention  
  Pan L, Vockley J, Current genetic medicine reports, 1/1/2013
• Newborn Screening Follow-up Guideline—Second Edition; CLSI document NBS02-A2  
  Tuerck J, Wilcken B, Webster DR, Forsman I, Kemper AR, Millington D, Ostrup J, Therrell BL, Torresani T, Vockley J, Clinical and Laboratory Standards Institute, 1/1/2013
• Ammonia control and neurocognitive outcome among urea cycle disorder patients treated with glycerol phenylbutyrate  
  Diaz GA, Krivitzky LS, Mokhtarani M, Rhead W, Bartley J, Feigenbaum A, Longo N, Berquist W, Berry SA, Gallagher R, Lichter-Konecki U, Bartholomew D, Harding CO, Cederb..., Hepatology, 1/1/2012
• Liver transplantation for classical maple syrup urine disease: long-term follow-up in 37 patients and comparative United network for organ sharing experience  
  Mazariegos GV, Morton DH, Sindhi R, Soltys K, Nayyar N, Bond G, Shellmer D, Shneider B, Vockley J, Strauss KA, The Journal of pediatrics, 1/1/2012
• Book review: Inborn metabolic diseases Diagnosis and treatment (5th edition)  
  Vockley J, Molecular genetics and metabolism, 1/1/2012
• Thoroughly modern medicine  
  Arnold GL, Vockley J, Molecular genetics and metabolism, 1/1/2011
• Efficient and gentle siRNA delivery by magnetofection  
  Ensenauer R, Hartl D, Vockley J, Roscher A, Fuchs U, Biotechnic & histochemistry, 1/1/2011
• Role of isovaleryl-CoA dehydrogenase and short branched-chain acyl-CoA dehydrogenase in the metabolism of valproic acid: implications for the branched-chain amino acid...  
  Luis PB, Ruiter JP, Ijlst L, Tavares de Almeida I, Duran M, Mohsen AW, Vockley J, Wanders RJ, Silva MF, Drug metabolism and disposition: the biological fate of chemicals, 1/1/2011
• GTP-cyclohydrolase deficiency responsive to sapropterin and 5-HTP supplementation: relief of treatment-refractory depression and suicidal behaviour  
  Pan L, McKain BW, Madan-Khetarpal S, McGuire M, Diler RS, Perel JM, Vockley J, Brent DA, BMJ case reports, 1/1/2011
• Trading places: liver transplantation as a treatment, not a cure, for metabolic liver disease  
  Shneider BL, Vockley J, Mazariegos GV, Liver transplantation : official publication of the American Association for the Study of Liver, 1/1/2011
• Evidence for physical association of mitochondrial fatty acid oxidation and oxidative phosphorylation complexes  
  Wang Y, Mohsen AW, Mihalik SJ, Goetzman ES, Vockley J, The Journal of biological chemistry, 1/1/2010
• Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples  
  Talkowski ME, McClain L, Allen T, Bradford LD, Calkins M, Edwards N, Georgieva L, Go R, Gur R, Kirov G, Chowdari K, Kwentus J, Lyons P, Mansour H, McEvoy J, O'Donovan ..., American journal of medical genetics Part B, Neuropsychiatric genetics, 1/1/2009
• Short-chain acyl-coenzyme A dehydrogenase deficiency  
  Jethva R, Bennett MJ, Vockley J, Molecular Genetics & Metabolism, 1/1/2008
• Molecular basis of dimethylglycine dehydrogenase deficiency associated with pathogenic variant H109R  
  McAndrew RP, Vockley J, Kim JJ, Journal of Inherited Metabolic Disease, 1/1/2008
• Detection and characterization of silencers and enhancer-blockers in the greater CFTR locus  
  Petrykowska HM, Vockley CM, Elnitski L, Genome Res, 1/1/2008
• Short-chain acyl-CoA dehydrogenase gene mutation (c319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish...  
  Tein I, Elpeleg O, Ben-Zeev B, Korman SH, Lossos A, Lev D, Lerman-Sagie T, Leshinsky-Silver E, Vockley J, Berry GT, Lamhonwah AM, Matern D, Roe CR, Gregersen N, Mol Genet Metab, 1/1/2008
• Join now to see all

Books/Book Chapters

• The Online Metabolic and Molecular Bases of Inherited Disease 
  Chapter: Mitochondrial Fatty Acid Oxidation Disorders 
  Vockley J, Bennett MJ, Gillingham MBEditors: Beaudet AL, Vogelstein B, Kinzler KW, Antonarakis SE, Ballabio A, Gibson KM,  Mitchell G.The McGraw-Hill Companies, Inc., New York, NY2016
• Pediatric Endocriniology and Inborn Errors of Metabolism  
  Chapter: Mitochondrial Fatty Acid Oxidation Defects 
  Vockley J, Longo N, Andresen BS, Bennett MJEditors: Sarafoglou K, Hoffman GF, Roth K.McGraw-Hill Companies2016
• The Online Metabolic and Molecular Basis of Inherited Disease 
  Chapter: Mitochondrial Fatty Acid Oxidation Disorders 
  Vockley J, Gillingham MB, Matern DEditors: Valle D.McGraw Hill, New York, NY2016
• Modern Nutrition in Health and Disease 
  Chapter: Inherited lipid disorders of beta-oxidation 
  Page 970 - 980Vockley J, Wolfe L, Renaud DLEditors: Ross AC, Caballero B, Cousins R, Tucker K, Ziegler T.Wolters kluwer/Lippincott Williams & Wilkins, Philadelphia, PA2013
• Intellectual & Developmental Research Reviews 
  Editors: Vockley J, Arnold G (Guest Editor).2013
• The Online Metabolic and Molecular Basis of Inherited Disease 
  Chapter: Branched Chain Organic Acidurias 
  Vockley J, Zschocke J, Knerr I, Walsh Vockley C, Gibson KMEditors: Valle D.McGraw Hill, New York, NY2012
• Diagnosis and Treatment of Inborn Errors of Metabolism 
  Chapter: Vademecum Metabolicum 
  Editors: Vockley J (Co-Editor), Zschocke J, Hoffmann GF.Milupa Metabolics GmbH & Co., GermanyEdition 3rd,2011
• Modern Nutrition in Health and Disease 
  Chapter: Defects of Beta-oxidation 
  Page 1057 - 1070Vockley JEditors: Shils ME, Olson JA, Shihe M and Ross AC.Williams and Wilkins, Baltimore, MDEdition 11th,2010
• Digenic inheritance 
  Vockley J2010
• Medium-chain acyl-CoA dehydrogenase deficiency 
  Vockley J2010
• Emery and Rimoin’s Principles and Practice of Medical Genetics 
  Chapter: Organic acidemias and disorders of fatty acid oxidation 
  Vockley JEditors: Rimoin, D.Churchill Livingstone, London, England2010
• The Metabolic and Molecular Basis of Inherited Disease 
  Chapter: Branched Chain Organic Acidemias 
  Vockley J, Gibson KM, Knerr I, Zschocker JEditors: Valle D.McGraw Hill, NYEdition 8th,2010
• Manual of Metabolic Paediatrics 
  Chapter: The Vademecum Metabolicum 
  Vockley JEditors: Vockley J (Co-Editor), Zschocke J, Hoffmann GF.Milupa Metabolics GmbH & Co., GermanyEdition 2nd,2004
• Methods in Enzymology 
  Chapter: Mammalian branched-chain acyl-CoA dehydrogenases: Molecular Cloning and Characterization of the Recombinant Enzymes 
  Vockley J, Mohsen A-W Binzak BA, Willard JM, and Fauq, AHEditors: Sokatch JR,Harris RA.Academic Press, San Diego, CA2000
• Flavins and Flavoproteins 
  Chapter: Biochemical characteristics of recombinant human isovaleryl-CoA dehydrogenase pre-treated with ethylenediaminetetraacetate 
  Page 515 - 518Mohsen A-W, Vockley JEditors: Ghisla S, Kroneck P, Macheroux P, Sund H.Rudolf Weber, New York, NY1999
• Flavins and Flavoproteins 1999. Proceedings of the Thirteenth International Symposium, Konstanz 
  Chapter: Biochemical Characteristics of Recombinant Human Isovaleryl-CoA Dehydrogenase Pre-Treated with Ethylenediaminetetraacetate 
  Page 515 - 518Mohsen A-W, Vockley JEditors: Ghisla S, Kroneck P, Macheroux P, Sund H.Agency for Scientific Publications, Berlin, Germany1999
• Flavins and Flavoproteins, 1996 
  Tiffany KA, Ming W, Paschke R, Mohsen A-W, Vockley J, Kim J-JPUniversity of Calgary Press, Calgary, Canada1997
• Flavins and Flavoproteins 
  Chapter: The acyl-CoA dehydrogenases: some mechanistic aspects 
  Page 597 - 603Thorpe C, Schaller RA, Mohsen A-W, Vockley JUniversity of Calgary Press, Calgary, Canada1996
• GeneReviews(R) 
  Chapter: Short-Chain Acyl-CoA Dehydrogenase Deficiency 
  Wolfe L, Jethva R, Oglesbee D, Vockley JEditors: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K.GeneReviews, Seattle, WA1993
• Flavins and Flavoproteins 
  Chapter: Three dimensional structures of acyl-CoA dehydrogenases: structural basis of substrate specificity 
  Page 273 - 282Kim J-JP, Wang M, Paschke R, Djordjevic S, Bennett DW, Vockley JEditors: Yagi K.Walter deGruyter, New York, NY1993
• Principles and Practice of Medical Genetics 
  Chapter: Organic Acidemias and Disorders of Fatty Acid Oxidation 
  Editors: Emory and Rimoin.Harcourt Health Sciences CompaniesEdition 5th,
• Pediatric Endocrinology and Inborn Errors of Metabolism 
  Chapter: Mitochondrial Fatty Acid Oxidation Defects 
  Vockley J, Longo N, Andresen B, and Bennett MJEditors: Sarafoglou, Hoffman, and Roth.McGraw-Hill Professional
• Join now to see all

Lectures

• Novel therapies for disorders of fatty acid oxidation 
  Ponte Vedre, FL - 1/1/2016
• Advances in fatty acid oxidation research 
  Boston, MA - 1/1/2016
• A Plain Population Genome Project 
  South Bend, IN - 1/1/2016
• Results from a randomized trial of triheptanoin compared to MCT oil in patients with long chain fatty acid oxidation defects 
  Salt Lake City, UT - 1/1/2015
• Mitochondrial respiratory chain disorders in the Old Order Amish Population 
  Salt Lake City, UT - 1/1/2015
• Emerging clinical trials for fatty acid oxidation disorders 
  Lyon, France - 1/1/2015
• Infantile hypophosphatasia 
  Memphis, TN - 1/1/2014
• Transplant for metabolic disease 
  Ottowa, CA - 1/1/2014
• The mitochondrial architecture of energy metabolism 
  Pittsburgh, PA - 1/1/2014
• Development of a New PKU Guideline 
  1/1/2013
• Moonlighting in mitochondria; ACAD9 plays a duel role in energy metabolism in mitochondria 
  Barcelona, Spain - 1/1/2013
• Molecular Architecture of Mitochondrial Energy Metabolism 
  Barcelona, Spain - 1/1/2013
• Novel therapy of long chain fatty acid oxidation disorders using triheptanoin 
  Barcelona, Spain - 1/1/2013
• The molecular Architecture of Mitochondrial Energy Metabolism 
  Barcelona, Spain - 1/1/2013
• Long chain fatty acid oxidation disorders 
  1/1/2012
• Personalized medicine and inborn errors of metabolism 
  1/1/2012
• Clinical trials for mitochondrial myopathies 
  1/1/2011
• New developments in the treatment of fatty acid oxidation disorders 
  Albuquerque, NM - 1/1/2010
• Changes in the mitochondrial proteome in fatty acid oxidation deficient mice 
  Istanbul, Turkey - 1/1/2010
• New enzymes of long chain fatty acid metabolism 
  San Diego, CA - 1/1/2009
• Characterization of a multi-functional protein complex containing the mitochondrial respiratory chain and fatty acid oxidation 
  San Diego, CA - 1/1/2009
• The latest outcome and clinical trials in PKU treatment 
  Phoenix, AZ - 1/1/2008
• A new inborn error of sterol metabolism 
  Asilomar, CA - 1/1/2008
• Energy metabolism as a complex genetic trait 
  Lisbon, Spain - 1/1/2008
• Tissue specificity of mitochondrial Beta-oxidation 
  Fulda, Germany - 1/1/2008
• Join now to see all

Other

• Mitochondrial myopathies. PREP Audio Series 
  Vockley J, Cohen B, and Wang, L-J, American Academy of Pediatrics
  1/1/2010
• The acyl-CoA dehydrogenases: Some mechanistic aspects 
  Thorpe C, Schaller RA, Mohsen A-W, Vockley J, University of Calgary Press
  Calgary, Canada - 1/1/1997