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Lipidomic analysis identifies long-chain acylcarnitine as a target for ischemic stroke

Journal of advanced research, 2024-07, Vol.61, p.133-149

2024

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Profiling of Acylcarnitines in First Episode Psychosis before and after Antipsychotic Treatment

Journal of proteome research, 2017-10, Vol.16 (10), p.3558-3566

2017

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Novel mutations associated with carnitine-acylcarnitine translocase and carnitine palmitoyl transferase 2 deficiencies in Malaysia

Clinical biochemistry, 2021-12, Vol.98, p.48-53

2021

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Quantitation and evaluation of perinatal medium-chain and long-chain acylcarnitine blood concentrations in 12,000 full-term breastfed newborns

Journal of Pediatric Endocrinology and Metabolism, 2021-08, Vol.34 (8), p.1023-1030

2021

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Circulating long chain acylcarnitines and outcomes in diabetic heart failure: an HF-ACTION clinical trial substudy

Cardiovascular diabetology, 2021-08, Vol.20 (1), p.161-161, Article 161

2021

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Zonisamide Administration Improves Fatty Acid β-Oxidation in Parkinson's Disease

Cells (Basel, Switzerland), 2018-12, Vol.8 (1), p.14

2018

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Hyperinsulinemia and skeletal muscle fatty acid trafficking

American journal of physiology: endocrinology and metabolism, 2013-08, Vol.305 (4), p.E540-E548

2013

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Characterization of plasma acylcarnitines in patients under valproate monotherapy using ESI-MS/MS

Clinical biochemistry, 2001-11, Vol.34 (8), p.635-638

2001

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Effects of L-carnitine on mechanical recovery of isolated rat hearts in relation to the perfusion with glucose and palmitate

Molecular and cellular biochemistry, 1998-08, Vol.185 (1-2), p.65-75

1998

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Uptake and release of carnitine by vascular endothelium in culture; effects of protons and oxygen free radicals

Molecular and cellular biochemistry, 1995-01, Vol.142 (2), p.99-106

1995

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Effect of dietary lysine level and protein restriction on the lipids and carnitine levels in the liver of pregnant rats

Annals of nutrition and metabolism, 1989, Vol.33 (3), p.162-169

Ortega, Myriam Fernández

1989

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Tissue lipid accumulation by l-aminocarnitine, an inhibitor of carnitine-palmitoyltransferase-2. Studies in intact rats and isolated mitochondria

Biochimica et biophysica acta, 1992-07, Vol.1127 (1), p.81-86

1992

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MYOCARDIAL FREE CARNITINE AND FATTY ACYLCARNITINE LEVELS IN PATIENTS WITH CHRONIC HEART FAILURE

JAPANESE CIRCULATION JOURNAL, 1990/12/20, Vol.54(12), pp.1471-1476

1990

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Plasma Acylcarnitine Profiles Suggest Incomplete Long-Chain Fatty Acid β-Oxidation and Altered Tricarboxylic Acid Cycle Activity in Type 2 Diabetic African-American Women

The Journal of nutrition, 2009-06, Vol.139 (6), p.1073-1081

2009

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Tissue acylcarnitine status in a mouse model of mitochondrial β-oxidation deficiency during metabolic decompensation due to influenza virus infection

Molecular genetics and metabolism, 2018-09, Vol.125 (1-2), p.144-152

2018

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A case of very-long-chain acyl-coenzyme a dehydrogenase deficiency with novel compound heterozygous mutations

Journal of the neurological sciences, 2016-09, Vol.368, p.165-167

2016

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Altered body composition and energy expenditure but normal glucose tolerance among humans with a long-chain fatty acid oxidation disorder

American journal of physiology: endocrinology and metabolism, 2013-11, Vol.305 (10), p.E1299-E1308

2013

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Synergistic heterozygosity in mice with inherited enzyme deficiencies of mitochondrial fatty acid β-oxidation

Molecular genetics and metabolism, 2005-05, Vol.85 (1), p.7-11

2005

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Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

Molecular genetics and metabolism, 2003-06, Vol.79 (2), p.114-123

2003

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Mutational spectrum and DNA-based prenatal diagnosis in carnitine–acylcarnitine translocase deficiency

Molecular genetics and metabolism, 2003, Vol.78 (1), p.68-73

2003

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Fat oxidation defect presenting with overwhelming ketonuria

Archives of disease in childhood, 2002-11, Vol.87 (5), p.428-429

2002

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Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype

Clinica chimica acta, 2001-10, Vol.312 (1), p.55-67

2001

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PRENATAL DIAGNOSIS OF MITOCHONDRIAL FATTY ACID OXIDATION DEFECTS

Prenatal diagnosis, 1996-02, Vol.16 (2), p.117-124

1996

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Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremia

The American journal of clinical nutrition, 1998-03, Vol.67 (3), p.386-390

1998

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Lipidomic analysis identifies long-chain acylcarnitine as a target for ischemic stroke

Profiling of Acylcarnitines in First Episode Psychosis before and after Antipsychotic Treatment

Novel mutations associated with carnitine-acylcarnitine translocase and carnitine palmitoyl transferase 2 deficiencies in Malaysia

Quantitation and evaluation of perinatal medium-chain and long-chain acylcarnitine blood concentrations in 12,000 full-term breastfed newborns

Circulating long chain acylcarnitines and outcomes in diabetic heart failure: an HF-ACTION clinical trial substudy

Zonisamide Administration Improves Fatty Acid β-Oxidation in Parkinson's Disease

Hyperinsulinemia and skeletal muscle fatty acid trafficking

Characterization of plasma acylcarnitines in patients under valproate monotherapy using ESI-MS/MS

Effects of L-carnitine on mechanical recovery of isolated rat hearts in relation to the perfusion with glucose and palmitate

Uptake and release of carnitine by vascular endothelium in culture; effects of protons and oxygen free radicals

Effect of dietary lysine level and protein restriction on the lipids and carnitine levels in the liver of pregnant rats

Tissue lipid accumulation by l-aminocarnitine, an inhibitor of carnitine-palmitoyltransferase-2. Studies in intact rats and isolated mitochondria

MYOCARDIAL FREE CARNITINE AND FATTY ACYLCARNITINE LEVELS IN PATIENTS WITH CHRONIC HEART FAILURE

Plasma Acylcarnitine Profiles Suggest Incomplete Long-Chain Fatty Acid β-Oxidation and Altered Tricarboxylic Acid Cycle Activity in Type 2 Diabetic African-American Women

Tissue acylcarnitine status in a mouse model of mitochondrial β-oxidation deficiency during metabolic decompensation due to influenza virus infection

A case of very-long-chain acyl-coenzyme a dehydrogenase deficiency with novel compound heterozygous mutations

Altered body composition and energy expenditure but normal glucose tolerance among humans with a long-chain fatty acid oxidation disorder

Synergistic heterozygosity in mice with inherited enzyme deficiencies of mitochondrial fatty acid β-oxidation

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

Mutational spectrum and DNA-based prenatal diagnosis in carnitine–acylcarnitine translocase deficiency

Fat oxidation defect presenting with overwhelming ketonuria

Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype

PRENATAL DIAGNOSIS OF MITOCHONDRIAL FATTY ACID OXIDATION DEFECTS

Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremia

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