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Expert Review of Clinical Pharmacology
|
July 9, 2025
A pharmacological profile of triheptanoin for the treatment of long-chain fatty acid oxidation disorders
Raelynn Forsyth, Jerry Vockley
Developmental Disabilities Research Reviews
|
June 26, 2013
Introduction: Neurodevelopmental issues in inborn errors of metabolism
Georgianne L Arnold, Jerry Vockley
The Journal of Pediatrics
|
September 23, 2020
Mitochondrial Disease and Coenzyme Q10 Deficiency: Commentary
Audrey C Woerner, Jerry Vockley
Science Translational Medicine
|
May 25, 2022
Lysine acylation causes collateral damage in inborn errors of metabolism
Eric S Goetzman, Jerry Vockley
Molecular Genetics and Metabolism
|
August 3, 2011
Thoroughly modern medicine
Georgianne L Arnold, Jerry Vockley
Cell Metabolism
|
June 2, 2026
Is an emerging pharmacotherapeutic era for rare mitochondrial diseases here?
Jirair K Bedoyan, Jerry Vockley
Drugs
|
March 14, 2019
Phenylketonuria: Current Treatments and Future Developments
Uta Lichter-Konecki, Jerry Vockley
Pediatric Clinics of North America
|
March 6, 2018
Inborn Errors of Metabolism with Myopathy: Defects of Fatty Acid Oxidation and the Carnitine Shuttle System
Areeg El-Gharbawy, Jerry Vockley
Clinical Therapeutics
|
August 4, 2022
Survey of Health Care Provider Understanding of Gene Therapy Research for Inherited Metabolic Disorders
Joyanna Hansen, Radha Ramachandran, Jerry Vockley
Biochimie
|
December 3, 2014
Kinetic and spectral properties of isovaleryl-CoA dehydrogenase and interaction with ligands
Al-Walid A Mohsen, Jerry Vockley
Page
of 30
Search research articles
Search
Showing results (11-20 of 293) with videos related to
Sort By:
Page
of 30
Expert Review of Clinical Pharmacology
|
July 9, 2025
A pharmacological profile of triheptanoin for the treatment of long-chain fatty acid oxidation disorders
Raelynn Forsyth, Jerry Vockley
Developmental Disabilities Research Reviews
|
June 26, 2013
Introduction: Neurodevelopmental issues in inborn errors of metabolism
Georgianne L Arnold, Jerry Vockley
The Journal of Pediatrics
|
September 23, 2020
Mitochondrial Disease and Coenzyme Q10 Deficiency: Commentary
Audrey C Woerner, Jerry Vockley
Science Translational Medicine
|
May 25, 2022
Lysine acylation causes collateral damage in inborn errors of metabolism
Eric S Goetzman, Jerry Vockley
Molecular Genetics and Metabolism
|
August 3, 2011
Thoroughly modern medicine
Georgianne L Arnold, Jerry Vockley
Cell Metabolism
|
June 2, 2026
Is an emerging pharmacotherapeutic era for rare mitochondrial diseases here?
Jirair K Bedoyan, Jerry Vockley
Drugs
|
March 14, 2019
Phenylketonuria: Current Treatments and Future Developments
Uta Lichter-Konecki, Jerry Vockley
Pediatric Clinics of North America
|
March 6, 2018
Inborn Errors of Metabolism with Myopathy: Defects of Fatty Acid Oxidation and the Carnitine Shuttle System
Areeg El-Gharbawy, Jerry Vockley
Clinical Therapeutics
|
August 4, 2022
Survey of Health Care Provider Understanding of Gene Therapy Research for Inherited Metabolic Disorders
Joyanna Hansen, Radha Ramachandran, Jerry Vockley
Biochimie
|
December 3, 2014
Kinetic and spectral properties of isovaleryl-CoA dehydrogenase and interaction with ligands
Al-Walid A Mohsen, Jerry Vockley
Page
of 30