Cardiomyopathy and carnitine deficiency-Reference-Cited by-同舟云学术

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Cardiomyopathy and carnitine deficiency

Published:2008-06 Issue:2 Volume:94 Page:162-166
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Amat di San Filippo Cristina,Taylor Matthew R.G.,Mestroni Luisa,Botto Lorenzo D.,Longo Nicola

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference25 articles.

1. Mitochondrial fatty acid oxidation disorders;Roe,2001

2. Primary and secondary alterations of neonatal carnitine metabolism;Scaglia;Semin. Perinatol.,1999

3. Genetic epidemiology of the carnitine transporter OCTN2 gene in a Japanese population and phenotypic characterization in Japanese pedigrees with primary systemic carnitine deficiency;Koizumi;Hum. Mol. Genet.,1999

4. Carnitine transporter defect diagnosed by newborn screening with electrospray tandem mass spectrometry;Wilcken;J. Pediatr.,2001

5. Screening newborns for inborn errors of metabolism by tandem mass spectrometry;Wilcken;N. Engl. J. Med.,2003

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1. A Rare Treatable Cause of Cardiomyopathy: Primary Carnitine Deficiency;Molecular Syndromology;2023-11-27

2. L-carnitine이 3T3-L1 지방세포 분화에 미치는 영향;Korean Journal of Food and Cookery Science;2023-06-30

3. Targeting mitochondrial impairment for the treatment of cardiovascular diseases: From hypertension to ischemia-reperfusion injury, searching for new pharmacological targets;Biochemical Pharmacology;2023-02

4. Infantile primary carnitine deficiency: A severe cardiac presentation unresponsive to carnitine supplementation;JIMD Reports;2022-11-09

5. The effects of l-Carnitine supplementation on inflammatory markers, clinical status, and 28 days mortality in critically ill patients: A double-blind, randomized, placebo-controlled trial;Clinical Nutrition ESPEN;2022-06

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