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Publications by P. Bross
Characterization of Wild-Type Human Medium-Chain Acyl-CoA Dehydrogenase (MCAD) and Mutant Enzymes Present in McAD-Deficient Patients by Two-Dimensional Gel Electrophoresis: Evidence for Posttranslational Modification of the Enzyme
Biochemical Medicine and Metabolic Biology
Related publications
Diagnosis of Medium Chain Acyl-Coa Dehydrogenase (MCAD) Deficiency in an Asymptomatic Neonate
Annals of Clinical Biochemistry
Medicine
Clinical Biochemistry
Nucleotide Sequence of Medium-Chain Acyl-CoA Dehydrogenase mRNA and Its Expression in Enzyme-Deficient Human Tissue.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
MEDIUM CHAIN ACYL-CoA DEHYDROGENASE (MCD) DEFICIENCY
Pediatric Research
Child Health
Pediatrics
Perinatology
Essential Fatty Acid Deficiency in Very Long-Chain Acyl-Coa Dehydrogenase Deficient Patients
International Journal of Food and Nutritional Science
Outcome of Medium Chain Acyl-CoA Dehydrogenase Deficiency After Diagnosis
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Immunochemical and Molecular Analysis of Medium-Chain Acyl CoA Dehydrogenase Deficiency.
Journal of Clinical Biochemistry and Nutrition
Medicine
Nutrition
Clinical Biochemistry
Dietetics
Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Evaluation of Genotype-Phenotype Correlation in Patients Detected by Newborn Screening
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Tissue Carnitine Homeostasis in Very-Long-Chain Acyl-CoA Dehydrogenase–Deficient Mice
Pediatric Research
Child Health
Pediatrics
Perinatology
In Vitro and in Vivo Consequences of Variant Medium-Chain Acyl-CoA Dehydrogenase Genotypes
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
