Multiple acyl-CoA dehydrogenase deficiency: a neonatal onset case responsive to treatment

Some international approaches to aminoglycoside monitoring in the extended dosing interval era.

Therapeutic drug monitoring·1999

Contamination of antibiotics resulting in severe pediatric methadone poisoning.

The Annals of pharmacotherapy·1999

Long-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency neuropathy: response to cod liver oil.

Neurology·1999

Fetal polycystic kidney disease associated with glutaric aciduria type II: an inborn error of energy metabolism.

American journal of perinatology·1996

Detection of metabolic disorders among selectively screened people with idiopathic mental retardation.

Mental retardation·1994

Pancreatitis in patients with organic acidemias.

The Journal of pediatrics·1994

Occurrence of Infusion Associated Reactions and Antidrug Antibodies in Enzyme Replacement Therapy for Fabry Disease and the Effect of Preventive Measures.

Journal of inherited metabolic disease·2026

From Common Pathway to Divergent Diseases: Metabolic Aspects of Inborn Errors of CoA Biosynthesis.

Journal of inherited metabolic disease·2026

Proteo-Metabolomic Profiling of PMM2-CDG Reveals Dysregulation of Retinoic Acid Synthesis, Myo-Inositol, and the Hexosamine Pathway.

Journal of inherited metabolic disease·2026

High-Protein Diet Ameliorates Cardiomyopathy in a Cardiac-Specific AGL Knockout Mouse Model: Association With Upregulated Hepatic Gluconeogenesis.

Journal of inherited metabolic disease·2026

Behavioral Phenotyping of the Pahenu2 Mouse Model for Phenylketonuria-A Scoping Review and Future Perspectives.

Journal of inherited metabolic disease·2026

Baat-Deficient Mice Recapitulate Elevated 7α-Hydroxy-3-Oxo-4-Cholestenoic Acid Observed in a Japanese Patient With BAAT Deficiency.

Journal of inherited metabolic disease·2026

LKB1 Dysregulation in Duchenne Muscular Dystrophy Models: Disease Specificity and Epigenetic Control by HDAC Inhibitors.

Annals of the New York Academy of Sciences·2026

Reframing MASLD: A Hepatic Condition With Systemic Clinical Impact.

Journal of clinical and experimental hepatology·2026

Mitochondrial dysfunction in schizophrenia and psychotic disorders: Implications for antipsychotic drug mechanisms.

Psychiatria Danubina·2026

Benefit of Psyllium with Weight Loss Diet in Preventing Liver Dysfunction in Overweight or Obese Adults with Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD).

International journal of preventive medicine·2026

A pan-tissue multi-omics resource atlas of coordinated immune, metabolic, and fibrotic alterations in diet-induced MASH.

iScience·2026

PKM2: A gatekeeper in macrophage metabolic reprogramming.

Journal of pharmaceutical analysis·2026

Related Experiment Videos

Multiple acyl-CoA dehydrogenase deficiency: a neonatal onset case responsive to treatment

Related Concept Videos

Some international approaches to aminoglycoside monitoring in the extended dosing interval era.

Contamination of antibiotics resulting in severe pediatric methadone poisoning.

Long-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency neuropathy: response to cod liver oil.

Fetal polycystic kidney disease associated with glutaric aciduria type II: an inborn error of energy metabolism.

Detection of metabolic disorders among selectively screened people with idiopathic mental retardation.

Pancreatitis in patients with organic acidemias.

Occurrence of Infusion Associated Reactions and Antidrug Antibodies in Enzyme Replacement Therapy for Fabry Disease and the Effect of Preventive Measures.

From Common Pathway to Divergent Diseases: Metabolic Aspects of Inborn Errors of CoA Biosynthesis.

Proteo-Metabolomic Profiling of PMM2-CDG Reveals Dysregulation of Retinoic Acid Synthesis, Myo-Inositol, and the Hexosamine Pathway.

High-Protein Diet Ameliorates Cardiomyopathy in a Cardiac-Specific AGL Knockout Mouse Model: Association With Upregulated Hepatic Gluconeogenesis.

Behavioral Phenotyping of the Pahenu2 Mouse Model for Phenylketonuria-A Scoping Review and Future Perspectives.

Baat-Deficient Mice Recapitulate Elevated 7α-Hydroxy-3-Oxo-4-Cholestenoic Acid Observed in a Japanese Patient With BAAT Deficiency.

LKB1 Dysregulation in Duchenne Muscular Dystrophy Models: Disease Specificity and Epigenetic Control by HDAC Inhibitors.

Reframing MASLD: A Hepatic Condition With Systemic Clinical Impact.

Mitochondrial dysfunction in schizophrenia and psychotic disorders: Implications for antipsychotic drug mechanisms.

Benefit of Psyllium with Weight Loss Diet in Preventing Liver Dysfunction in Overweight or Obese Adults with Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD).

A pan-tissue multi-omics resource atlas of coordinated immune, metabolic, and fibrotic alterations in diet-induced MASH.

PKM2: A gatekeeper in macrophage metabolic reprogramming.

Related Experiment Videos

Multiple acyl-CoA dehydrogenase deficiency: a neonatal onset case responsive to treatment

Related Concept Videos

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