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Elevated plasma carnitine in the hepatic form of carnitine palmitoyltransferase‐1 deficiency
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ana.410300512openalex-snapshot
Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake
inferredcites →https://doi.org/10.1016/0005-2736(77)90257-7openalex-snapshot
Specificity and characteristics of the carnitine transport in human heart cells (CCL 27) in culture
inferredcites →https://doi.org/10.1016/1043-2760(91)90062-ropenalex-snapshot
Fatty acid oxidation: Clinical, biochemical, and molecular aspects
inferredcites →https://doi.org/10.1016/s0022-3476(81)80834-7openalex-snapshot
Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiency
inferredcites →https://doi.org/10.1016/s0065-3101(24)00155-5openalex-snapshot
New Genetic Defects in Mitochondrial Fatty Acid Oxidation and Carnitine Deficiency
inferredcites →https://doi.org/10.1056/nejm198811173192006openalex-snapshot
Primary Carnitine Deficiency Due to a Failure of Carnitine Transport in Kidney, Muscle, and Fibroblasts
inferredcites →https://doi.org/10.1172/jci115090openalex-snapshot
Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiopathological approach to carnitine palmitoyltransferase II deficiencies.
inferredcites →https://doi.org/10.1177/088307388900400310openalex-snapshot
Deficiency of Carnitine Palmitoyltransferase I
inferredcites →https://doi.org/10.1203/00006450-198311000-00008openalex-snapshot
Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Children with Non-Ketotic Hypoglycemia and Low Carnitine Levels
inferredcites →https://doi.org/10.1203/00006450-198809000-00006openalex-snapshot
Hepatic and Muscular Presentations of Carnitine Palmitoyl Transferase Deficiency: Two Distinct Entities
inferredcites →https://doi.org/10.1212/wnl.31.7.819openalex-snapshot
Primary systemic carnitine dehciency. II. Renal handling of carnitine
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1006/mgme.1999.2938openalex-snapshot
Carnitine Palmitoyltransferase Deficiencies
inferred← citeshttps://doi.org/10.1006/mgme.2001.3149openalex-snapshot
Hepatic Carnitine Palmitoyl Transferase 1 (CPT1 A) Deficiency in North American Hutterites (Canadian and American): Evidence for a Founder Effect and Results of a Pilot Study on a DNA-Based Newborn Screening Program
inferred← citeshttps://doi.org/10.1006/mgme.2001.3235openalex-snapshot
Aberrant mRNA Splicing Associated with Coding Region Mutations in Children with Carnitine-Acylcarnitine Translocase Deficiency
inferred← citeshttps://doi.org/10.1007/8904_2016_564openalex-snapshot
Reliable Diagnosis of Carnitine Palmitoyltransferase Type IA Deficiency by Analysis of Plasma Acylcarnitine Profiles
inferred← citeshttps://doi.org/10.1007/978-1-4612-1642-1_37openalex-snapshot
Inborn Errors of Lipid Metabolism (Mitochondrial Fatty Acid Oxidation)
inferred← citeshttps://doi.org/10.1007/978-1-4615-6005-0_2openalex-snapshot
Molecular Biology of Carnitine Palmitoyltransferases and Role of Carnitine in Gene Transcription
inferred← citeshttps://doi.org/10.1007/978-3-540-28785-8_13openalex-snapshot
Disorders of Mitochondrial Fatty Acid Oxidation and Related Metabolic Pathways
inferred← citeshttps://doi.org/10.1007/978-3-642-15720-2_13openalex-snapshot
Disorders of Mitochondrial Fatty Acid Oxidation and Related Metabolic Pathways
inferred← citeshttps://doi.org/10.1007/978-3-662-03147-6_11openalex-snapshot
Disorders of Fatty Acid Oxidation
inferred← citeshttps://doi.org/10.1007/978-3-662-04285-4_11openalex-snapshot
Disorders of Fatty Acid Oxidation
inferred← citeshttps://doi.org/10.1007/bf00710058openalex-snapshot
Disorders of mitochondrial long‐chain fatty acid oxidation
inferred← citeshttps://doi.org/10.1007/s100380200047openalex-snapshot
Expression analysis of two mutations in carnitine palmitoyltransferase IA deficiency
inferred← citeshttps://doi.org/10.1007/s11154-018-9448-1openalex-snapshot
Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle
inferred← citeshttps://doi.org/10.1016/b978-0-12-417044-5.00040-8openalex-snapshot
Lipid Storage Myopathies Due to Fatty Acid Oxidation Defects
inferred← citeshttps://doi.org/10.1016/b978-0-444-59565-2.00035-6openalex-snapshot
Disorders of fatty acid oxidation
inferred← citeshttps://doi.org/10.1016/b978-1-4377-0435-8.00091-3openalex-snapshot
Metabolic Myopathies
inferred← citeshttps://doi.org/10.1016/j.mam.2004.06.004openalex-snapshot
Carnitine palmitoyltransferases 1 and 2: biochemical, molecular and medical aspects
inferred← citeshttps://doi.org/10.1016/j.ymgme.2005.07.022openalex-snapshot
Novel metabolic and molecular findings in hepatic carnitine palmitoyltransferase I deficiency
inferred← citeshttps://doi.org/10.1016/j.ymgmr.2023.101032openalex-snapshot
A different perspective into clinical symptoms in CPT I deficiency
inferred← citeshttps://doi.org/10.1016/s0022-3476(05)82532-6openalex-snapshot
Fatty acid oxidation disorders: A new class of metabolic diseases
inferred← citeshttps://doi.org/10.1016/s0074-7742(02)53017-8openalex-snapshot
Defects of β-oxidation including carnitine deficiency
inferred← citeshttps://doi.org/10.1016/s0146-0005(99)80046-9openalex-snapshot
Neonatal metabolic myopathies
inferred← citeshttps://doi.org/10.1016/s0960-8966(01)00308-xopenalex-snapshot
Defects of mitochondrial β-oxidation: a growing group of disorders
inferred← citeshttps://doi.org/10.1017/cbo9780511547409.034openalex-snapshot
Inborn Errors of Mitochondrial Fatty Acid Oxidation
inferred← citeshttps://doi.org/10.1023/a:1005552106301openalex-snapshot
Defects in activation and transport of fatty acids
inferred← citeshttps://doi.org/10.1023/a:1005556207210openalex-snapshot
Recognition and management of fatty acid oxidation defects: A series of 107 patients
inferred← citeshttps://doi.org/10.1023/a:1005606805951openalex-snapshot
Carnitine palmitoyltransferase I deficiency in neonate identified by dried blood spot free carnitine and acylcarnitine profile
inferred← citeshttps://doi.org/10.1023/a:1012476029536openalex-snapshot
Lethal neonatal presentation of carnitine palmitoyltransferase I deficiency
inferred← citeshttps://doi.org/10.1023/b:boli.0000042979.42120.55openalex-snapshot
Successful long‐term treatment of hepatic carnitine palmitoyltransferase I deficiency and a novel mutation
inferred← citeshttps://doi.org/10.1053/sp.2000.6367openalex-snapshot
Hypoglycemia in association with various organic and amino acid disorders
inferred← citeshttps://doi.org/10.1080/09553002.2022.2063430openalex-snapshot
Logistic role of carnitine shuttle system on radiation-induced L-carnitine and acylcarnitines alteration
inferred← citeshttps://doi.org/10.1093/clinchem/47.10.1763openalex-snapshot
Hepatic Carnitine Palmitoyltransferase I Deficiency: Acylcarnitine Profiles in Blood Spots Are Highly Specific
inferred← citeshttps://doi.org/10.1097/00075197-200211000-00002openalex-snapshot
Diagnosis and management of defects of mitochondrial β-oxidation
inferred← citeshttps://doi.org/10.1139/g08-023openalex-snapshot
Mutations of the withered ( whd ) gene in Drosophila melanogaster confer hypersensitivity to oxidative stress and are lesions of the carnitine palmitoyltransferase I (CPT I) gene
inferred← citeshttps://doi.org/10.1146/annurev.nutr.18.1.179openalex-snapshot
GENETIC DISORDERS OF CARNITINE METABOLISM AND THEIR NUTRITIONAL MANAGEMENT
inferred← citeshttps://doi.org/10.1201/b13564-40openalex-snapshot
Carnitine palmitoyl transferase I deficiency
inferred← citeshttps://doi.org/10.1201/b13565-47openalex-snapshot
Carnitine palmitoyl transferase I deficiency
inferred← citeshttps://doi.org/10.1201/b15310-40openalex-snapshot
Carnitine palmitoyl transferase I deficiency
inferred← citeshttps://doi.org/10.1203/00006450-200001000-00010openalex-snapshot
Hepatic Carnitine Palmitoyltransferase I Deficiency Presenting as Maternal Illness in Pregnancy
inferred← citeshttps://doi.org/10.1515/jpem-2025-0382openalex-snapshot
Pitfalls in the diagnosis of carnitine palmitoyltransferase 1 deficiency
inferred← citeshttps://doi.org/10.30476/ijms.2021.88464.1919openalex-snapshot
Association of Abnormal Serum L-Carnitine Levels with Idiopathic Changes in Left Ventricular Geometry in Pediatric and Adolescent Patients.
inferred← citeshttps://doi.org/10.4062/biomolther.2009.17.2.181openalex-snapshot
Characterization of Plasma Carnitine Level in Obese Adolescent Korean Women
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