Disease: Myopathic carnitine deficiency
- A case history of myopathic carnitine deficiency benefited by glucocorticoids and L-carnitine supplementation
- A Case of Carnitine Palmitoyltransferase II Deficiency in Bahrain With a Novel Mutation
- A rare presentation of Carnitine palmitoyltransferase II (CPT-2) deficiency with normal acylcarnitine profile in a 10-year-old boy with muscle weakness and bilateral hearing loss; a case report
- Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiency
- Cardiac function and incidence of unexplained myocardial scarring in patients with primary carnitine deficiency - a cardiac magnetic resonance study
- Carnitin-Palmitoyl Transferase type 2 deficiency: a rare cause of acute renal failure due to rhabdomyolysis
- Carnitine deficiency
- Carnitine deficiency syndromes
- Carnitine metabolism and deficiency syndromes
- Carnitine metabolism and human carnitine deficiency
- Carnitine Palmitoyltransferase II Deficiency
- Carnitine palmitoyltransferase II deficiency and post-COVID vaccination rhabdomyolysis
- Case Study of an Elderly Patient With New Onset Weakness
- Cause of recurrent rhabdomyolysis, carnitine palmitoyltransferase II deficiency and novel pathogenic mutation
- Do renal and cardiac malformations in the fetus signal carnitine palmitoyltransferase II deficiency? A rare lethal fatty acid oxidation defect
- Efficacy of bezafibrate in two patients with mitochondrial trifunctional protein deficiency
- Encephalopathy and fatal myopathy in two siblings. Their association with partial deficiency of muscle carnitine
- Genetic disorders of carnitine metabolism and their nutritional management
- Infantile idiopathic myopathic carnitine deficiency: treatment with L-carnitine
- Intracellular free [Ca2+] in human skeletal muscle with myopathic carnitine deficiency
- Mitochondrial energetic impairment in a patient with late-onset glutaric acidemia Type 2
- Muscle Carnitine Palmitoyltransferase II (CPT II) Deficiency: A Conceptual Approach
- Myopathic carnitine deficiency associated with lymphocytic malignant non-Hodgkin lymphoma and monoclonal immunoglobulin G-K
- Phenotype of carnitine palmitoyltransferase II (CPT II) deficiency: A questionnaire-based survey
- Primary carnitine deficiency in a male adult
- Rhabdomyolysis Associated with Recent <em>SARS-COV-2</em> Infection in a Patient with Carnitine Palmitoyltransferase II Deficiency
- Treatment of myopathic carnitine deficiency: quantitation of response to prednisone and carnitine
- Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency