Results 1 to 10 of about 162,227 (374)

Carnitine Inborn Errors of Metabolism

open access: yesMolecules, 2019
Carnitine plays essential roles in intermediary metabolism. In non-vegetarians, most of carnitine sources (~75%) are obtained from diet whereas endogenous synthesis accounts for around 25%.
Mohammed Almannai   +2 more
doaj   +2 more sources

Evaluation of Carnitine Status in Postnatal Piglets from Sows Fed Clofibrate [PDF]

open access: yesCurrent Issues in Molecular Biology
Milk carnitine content decreases quickly with lactation days and is accompanied by PPARα downregulation. This study aimed to investigate the effects of the maternal supplementation of the PPARα agonist, clofibrate, on milk carnitine content and carnitine
Brandon Pike   +6 more
doaj   +2 more sources

Simultaneous Analysis of L-Carnitine and Acetyl-L-Carnitine in Food Samples by Hydrophilic Interaction Nano-Liquid Chromatography [PDF]

open access: yesMethods and Protocols
L-Carnitine (L-CAR) and acetyl-L-carnitine (Acetyl L-CAR) are the essential cofactor compounds in lipid metabolism and are used in the treatment of various diseases.
Cemil Aydoğan   +2 more
doaj   +2 more sources

Evaluation of the Effect of L-Carnitine Supplementation in Preterm Neonates Suffering from Respiratory Distress Syndrome [PDF]

open access: yesInternational Journal of Medical Arts, 2022
Background: Carnitine is one of hydrophilic amino acid derivatives participating in pulmonary surfactant production in infants. The deficiency of Carnitine might lead to the incidence and severity of respiratory distress syndrome [RDS] in preterm infants.
Safaa Beshir   +3 more
doaj   +1 more source

Successful treatment of propofol-related infusion syndrome in critically ill patient receiving low-dose propofol infusion: a case report [PDF]

open access: yesAcute and Critical Care, 2023
Propofol is widely used to sedate agitated patients in intensive care units. However, it can cause a rare but fatal complication, propofol-related infusion syndrome (PRIS).
Nahyeon Park, Tae Sun Ha
doaj   +1 more source

The Comparative Effect of L-carnitine in Different Stages of Pregnancy on Alcohol-induced Memory Impairment in Adult Rat Offspring [PDF]

open access: yesمجله دانشکده پزشکی اصفهان, 2022
Background: Neuroprotective effects of L-carnitine on damage caused by fetal exposure to ethanol have been demonstrated. The purpose of this study was to evaluate the effects of different doses of L-carnitine at different stages of pregnancy on the ...
Zahra Iranpour   +3 more
doaj   +1 more source

The Effects of L-Carnitine, Acetyl-L-Carnitine, and Propionyl-L-Carnitine on Body Mass in Type 2 Diabetes Mellitus Patients

open access: yesFrontiers in Nutrition, 2021
Purpose: The study aimed to explore the effects of l-carnitine, acetyl-l-carnitine, and propionyl-l-carnitine on Body Mass in type 2 diabetes mellitus (T2DM) patients.Methods: Randomized controlled trial (RCT) studies of l-carnitine, acetyl-l-carnitine ...
Dong-Dong Wang   +4 more
doaj   +1 more source

Stable isotope-labeled carnitine reveals its rapid transport into muscle cells and acetylation during contraction

open access: yesHeliyon, 2023
Carnitine plays multiple roles in skeletal muscle metabolism, including fatty acid transport and buffering of excess acetyl-CoA in the mitochondria. The skeletal muscle cannot synthesize carnitine; therefore, carnitine must be taken up from the blood ...
Yasuro Furuichi   +5 more
doaj   +1 more source

Change in Anemia by Carnitine Supplementation in Patients Undergoing Peritoneal Dialysis: A Retrospective Observational Study

open access: yesFrontiers in Medicine, 2021
Background: Carnitine supplementation improves various dialysis-related symptoms including erythropoietin-resistant anemia in patients who are undergoing hemodialysis.
Shohei Kaneko   +6 more
doaj   +1 more source

Clinical and molecular characteristics of carnitineacylcarnitine translocase deficiency with c.270delC and a novel c.408C>A variant

open access: yesThe Turkish Journal of Pediatrics, 2021
Background. Carnitine-acylcarnitine translocase deficiency (CACTD) is a rare, autosomal recessive, and highly lethal fatty acid oxidation (FAO) disorder caused by defective acylcarnitine transport across the mitochondrial membrane.
Berrak Bilginer Gürbüz   +7 more
doaj   +1 more source

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