• 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