Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation.
Journal of inherited metabolic disease·2007
Phenotype and genotype variation in primary carnitine deficiency.
Genetics in medicine : official journal of the American College of Medical Genetics·2001
Kapitza Pendulum Route to Supercurrent Tunnel Diodes.
Physical review letters·2026
PPG-AFNet: a lightweight and intelligible network for atrial fibrillation identification using photoplethysmography signals.
Biomedical engineering letters·2026
Electrical characterisation of fermentation process from milk to yogurt: a monitoring approach.
Journal of food science and technology·2026
Nano-thick freestanding and reusable epidermal electronics via edge-supporting strategy.
Microsystems & nanoengineering·2026