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Last Updated: 10/31/2025

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Found 332 publications

Very-Late Onset Multiple Acyl-Coenzyme A Dehydrogenase Deficiency Associated With Sertraline Use: A Case Report.

Very-Late Onset Multiple Acyl-Coenzyme A Dehydrogenase Deficiency Associated With Sertraline Use: A Case Report.

Journal: Journal of clinical neuromuscular disease
Published: September 03, 2025

Riboflavin in neurological diseases: therapeutic advances, metabolic insights, and emerging genetic strategies.

Riboflavin in neurological diseases: therapeutic advances, metabolic insights, and emerging genetic strategies.

Journal: Frontiers in neurology
Published: July 10, 2025

Transient neonatal multiple acyl-CoA dehydrogenase deficiency due to riboflavin deficiency in an infant on total parenteral nutrition.

Transient neonatal multiple acyl-CoA dehydrogenase deficiency due to riboflavin deficiency in an infant on total parenteral nutrition.

Journal: BMJ case reports
Published: May 05, 2025

Exposure to sertraline and ranolazine is common among adult patients with genetically uncharacterized lipid storage myopathy.

Exposure to sertraline and ranolazine is common among adult patients with genetically uncharacterized lipid storage myopathy.

Journal: Journal of the neurological sciences
Published: April 14, 2025

Clinical, biochemical, and molecular findings in adults with hyperammonemia: A French bi-centric retrospective study.

Clinical, biochemical, and molecular findings in adults with hyperammonemia: A French bi-centric retrospective study.

Journal: Molecular genetics and metabolism
Published: April 10, 2025

Practical challenges and ethical considerations in treating early-onset MADD with exogenous ketones.

Practical challenges and ethical considerations in treating early-onset MADD with exogenous ketones.

Journal: Molecular genetics and metabolism
Published: April 02, 2025

Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): A Case Report With a Complex Biochemical Profile.

Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): A Case Report With a Complex Biochemical Profile.

Journal: JIMD reports
Published: April 01, 2025

Adolescent late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency manifesting with severe multi-organ failure: a case report.

Adolescent late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency manifesting with severe multi-organ failure: a case report.

Journal: Frontiers in pediatrics
Published: March 03, 2025

New insight in lipid storage myopathy.

New insight in lipid storage myopathy.

Journal: Neuromuscular disorders : NMD
Published: January 27, 2025

Carnitine Deficiency Caused by Salcaprozic Acid Sodium Contained in Oral Semaglutide in a Patient with Multiple Acyl-CoA Dehydrogenase Deficiency.

Carnitine Deficiency Caused by Salcaprozic Acid Sodium Contained in Oral Semaglutide in a Patient with Multiple Acyl-CoA Dehydrogenase Deficiency.

Journal: International journal of molecular sciences
Published: January 23, 2025

Growth differentiation factor 15: a valuable biomarker for the diagnosis and prognosis of late-onset form of multiple Acyl-CoA dehydrogenation deficiency.

Growth differentiation factor 15: a valuable biomarker for the diagnosis and prognosis of late-onset form of multiple Acyl-CoA dehydrogenation deficiency.

Journal: Orphanet journal of rare diseases
Published: December 26, 2024

Late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition: a case series from the West of Scotland.

Late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition: a case series from the West of Scotland.

Journal: Neuromuscular disorders : NMD
Published: December 20, 2024
Showing 1-12 of 332

Last Updated: 10/31/2025