(Q34216280)

31 July 2017

1 reference

title

Metabolic cardiomyopathies (English)

1 reference

31 July 2017

B Guertl

1

1 reference

PubMed ID

11298185

31 July 2017

C Noehammer

series ordinal

2

1 reference

PubMed ID

11298185

31 July 2017

G Hoefler

series ordinal

3

1 reference

31 July 2017

1 December 2000

1 reference

International Journal of Experimental Pathology

31 July 2017

1 reference

31 July 2017

81

1 reference

31 July 2017

6

1 reference

31 July 2017

349-372

1 reference

Alcoholic cardiomyopathy in mice myocardial glycogen, lipids and certain enzymes

31 July 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Alcoholic cardiomyopathy in mice. Electron microscopic observations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Effects of fatty acids on Na/Ca exchange in cardiac sarcolemmal membranes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Malonyl-CoA metabolism in cardiac myocytes and its relevance to the control of fatty acid oxidation

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Respiratory-chain and pyruvate metabolism defects: Italian collaborative survey on 72 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Unusual expression of Gaucher's disease: cardiovascular calcifications in three sibs homozygous for the D409H mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Barth syndrome: clinical observations and genetic linkage studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

The effects of novel vasodilator long chain acyl carnitine esters in the isolated perfused heart of the rat

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Metabolic myopathies: a clinical approach; part I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Secondary respiratory chain defect in a boy with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: possible diagnostic pitfalls

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Paradoxical role of lipid metabolism in heart function and dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Effects of some L-carnitine derivatives on heart membrane ATPases

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Glucose transport and glucose transporter GLUT4 are regulated by product(s) of intermediary metabolism in cardiomyocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Cellular fatty acid-binding proteins: their function and physiological significance

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Heart CD36 expression is increased in murine models of diabetes and in mice fed a high fat diet

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Brief report: a deficiency of carnitine-acylcarnitine translocase in the inner mitochondrial membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Mucopolysaccharidosis type IV as a cause of mitral stenosis in an adult

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Echocardiographic abnormalities in type IV mucopolysaccharidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Diabetes and cardiovascular disease. The Framingham study

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Role of diabetes in congestive heart failure: the Framingham study

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Substrate proteins for calmodulin-sensitive and phospholipid-sensitive Ca2+-dependent protein kinases in heart, and inhibition of their phosphorylation by palmitoylcarnitine

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Mitochondrial dysfunction induced by fatty acid ethyl esters, myocardial metabolites of ethanol

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Presence of nonoxidative ethanol metabolism in human organs commonly damaged by ethanol abuse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Mitochondrial respiratory chain disorders I: mitochondrial DNA defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Regulation of fatty acid oxidation in the mammalian heart in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Hypertriglyceridemia is exacerbated by slow lipolysis of triacylglycerol-rich lipoproteins in fed but not fasted streptozotocin diabetic rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Molecular heterogeneity in very-long-chain acyl-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden death

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Molecular lesion in patients with medium-chain acyl-CoA dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Effect of palmitoylcarnitine on the passive electrical properties of isolated guinea pig ventricular myocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Ca2+ uptake by cardiac sarcoplasmic reticulum from patients with idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Identification of two variant short chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Lethal neonatal deficiency of carnitine palmitoyltransferase II associated with dysgenesis of the brain and kidneys.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Metabolism of the heart in health and disease. I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Alterations in Ca2+ binding by and composition of the cardiac sarcolemmal membrane in chronic diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Palmitylcarnitine inhibition of the calcium pump in cardiac sarcoplasmic reticulum: A possible role in myocardial ischemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

The glucose fatty-acid cycle. Its role in insulin sensitivity and the metabolic disturbances of diabetes mellitus

21 January 2018

2 references

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

21 January 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Evidence for cardiomyopathy in familial diabetes mellitus

28 October 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase: a cause of lethal myopathy and cardiomyopathy in early childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Molecular and physiological alterations in murine ventricular dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Myocardial substrate metabolism: implications for diabetic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

The diabetic heart: metabolic causes for the development of a cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

A role for Sp and nuclear receptor transcription factors in a cardiac hypertrophic growth program

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

MCD encodes peroxisomal and cytoplasmic forms of malonyl-CoA decarboxylase and is mutated in malonyl-CoA decarboxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

The symptomatology, morphology and biochemistry of glycogenosis type II (Pompe) in the adult

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Development of obstruction to ventricular outflow and impairment of inflow in glycogen storage disease of the heart: serial echocardiographic studies from birth to death at 6 months

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Direct activation of Ca2+ channels by palmitoyl carnitine, a putative endogenous ligand

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Decreased myocardial glucose uptake during ischemia in diabetic swine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Regulation of energy substrate metabolism in the diabetic heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

The genetic basis of pediatric cardiovascular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Combined deficiency of beta-galactosidase and neuraminidase: natural history of the disease in the first 18 years of an American patient with late infantile onset form

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Molecular characterization of inherited carnitine palmitoyltransferase II deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

The effects of alcoholism on skeletal and cardiac muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Effect of increased afterload on cardiac lipoprotein lipase and VLDL receptor expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Cardiac fatty acid uptake and transport in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Maroteaux-lamy syndrome: five novel mutations and their structural localization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Mitochondrial defects in cardiomyopathy and neuromuscular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: mitochondrial DNA genes sustain seventeen times more mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

A missense mutation in the OCTN2 gene associated with residual carnitine transport activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Hypertrophic cardiomyopathy with type I CD36 deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Endocardial fibroelastosis and Niemann-Pick disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Cardiomyopathy in childhood, mitochondrial dysfunction, and the role of L-carnitine

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Inhibition of bovine heart Na+,K+-ATPase by palmitylcarnitine and palmityl-CoA

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

A new case of malonyl coenzyme A decarboxylase deficiency presenting with cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Metabolism of VLDL is increased in streptozotocin-induced diabetic rat hearts.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Metabolic aspects of myocardial disease and a role for L-carnitine in the treatment of childhood cardiomyopathy.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Two novel missense mutations of the OCTN2 gene (W283R and V446F) in a patient with primary systemic carnitine deficiency

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

A transgenic model of acetaldehyde overproduction accelerates alcohol cardiomyopathy

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Requirement for the heart-type fatty acid binding protein in cardiac fatty acid utilization

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

A sensitive immunoassay for rat fatty acid translocase (CD36) using phage antibodies selected on cell transfectants: abundant presence of fatty acid translocase/CD36 in cardiac and red skeletal muscle and up-regulation in diabetes

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

The feasibility of replacement therapy for inherited disorder of glycolysis: triosephosphate isomerase deficiency (review).

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Hemochromatosis: genetics helps to define a multifactorial disease.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

The effects of alcohol on the heart.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Fatty acid mitochondrial beta-oxidation and hypoglycaemia in children

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Cardiac hypertrophy and failure--a disease of adaptation. Modifications in membrane proteins provide a molecular basis for arrhythmogenicity.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Palmitoyl carnitine modifies sodium currents and induces transient inward current in ventricular myocytes.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

A mechanism for reduced myocardial carnitine levels in diabetic animals.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Deficiency of medium chain fatty acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

The natural history of the severe form of Hunter's syndrome: a study based on 52 cases.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Alterations in cardiac sarcolemmal Ca2+ pump activity during diabetes mellitus

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

I-cell disease: clinical studies of 21 Japanese cases.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Lipolysis in isolated myocardial cells from diabetic rat hearts

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Myocardial metabolism in insulin-deficient diabetic humans without coronary artery disease

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Influence of experimental diabetes on sarcoplasmic reticulum function in rat ventricular muscle

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Gaucher's disease with mitral and aortic involvement: Echocardiographic findings

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Molecular basis of mitochondrial fatty acid oxidation defects

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

In vitro effects of palmitylcarnitine on cardiac plasma membrane Na,K-ATPase, and sarcoplasmic reticulum Ca2+-ATPase and Ca2+ transport

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency

28 October 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517748

Effect of Fatty Acids on Contractility and Rhythm of the Heart

28 October 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

Fatty Acid and Glucose Metabolism in the Perfused Heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.2000.00186.X

The effects of acute and chronic diabetes on myocardial metabolism in rats

21 January 2018

1 reference

12 December 2020

Calcification of the ascending aorta and aortic and mitral valves in Gaucher's disease

1 reference

12 December 2020

Lipoprotein composition as a component in the lipoprotein clearance defect in experimental diabetes

1 reference

12 December 2020

Inhibition of sarcolemmal Na+-K+-ATPase by palmitoyl carnitine: potentiation by propranolol

1 reference

12 December 2020

Effects of diabetes on myocardial glucose transport system in rats: implications for diabetic cardiomyopathy

1 reference

12 December 2020

Cardiomyopathy in propionic acidaemia

1 reference

12 December 2020

Synthesis of ventricular mitochondrial proteins in vivo: effect of acute ethanol toxicity

1 reference

12 December 2020

Acetyl-CoA carboxylase regulation of fatty acid oxidation in the heart

1 reference

12 December 2020

Glycolysis and glucose oxidation during reperfusion of ischemic hearts from diabetic rats

1 reference

12 December 2020

Inherited cardiomyopathies

1 reference

12 December 2020

Perinatal hypothyroidism impairs the normal transition of GLUT4 and GLUT1 glucose transporters from fetal to neonatal levels in heart and brown adipose tissue. Evidence for tissue-specific regulation of GLUT4 expression by thyroid hormone

1 reference

12 December 2020

Rat heart fatty acid-binding protein content is increased in experimental diabetes

1 reference

12 December 2020

The capillary transport system for free fatty acids in the heart

1 reference

12 December 2020

Contribution of oxidative metabolism and glycolysis to ATP production in hypertrophied hearts

1 reference

12 December 2020

Malonic aciduria and cardiomyopathy

1 reference

12 December 2020

Novel mutations in mitochondrial cytochrome b in fatal post partum cardiomyopathy

1 reference

12 December 2020

Mitochondrial complex deficiencies in a male with cardiomyopathy and 3-methylglutaconic aciduria

1 reference

12 December 2020

A patient with lethal cardiomyopathy and a carnitine-acylcarnitine translocase deficiency

1 reference

12 December 2020

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype

1 reference

12 December 2020

Regulation of very-low-density lipoprotein receptor in hypertrophic rat heart

1 reference

12 December 2020

Myocardial cell damage by fatty acid ethyl esters

1 reference

12 December 2020

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts

1 reference

12 December 2020

Prenatal hypertrophic cardiomyopathy and pericardial effusion in carbohydrate-deficient glycoprotein syndrome

1 reference

12 December 2020

Plasma creatine kinase and cardiomyopathy in glycogen storage disease type III

1 reference

12 December 2020

Mitochondrial function in children with idiopathic dilated cardiomyopathy.

1 reference

12 December 2020

Lethal dilated cardiomyopathy due to long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Fatty acid oxidation enzyme gene expression is downregulated in the failing heart

1 reference

12 December 2020

Insulin-induced recruitment of glucose transporter 4 (GLUT4) and GLUT1 in isolated rat cardiac myocytes. Evidence of the existence of different intracellular GLUT4 vesicle populations

1 reference

12 December 2020

Abnormal myocardial kinetics of 123I-heptadecanoic acid in subjects with impaired glucose tolerance

1 reference

12 December 2020

Alterations in sarcoplasmic reticulum gene expression in human heart failure. A possible mechanism for alterations in systolic and diastolic properties of the failing myocardium

1 reference

12 December 2020

Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy

1 reference

12 December 2020

Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation

1 reference

12 December 2020

Neonatal lethal mitochondrial trifunctional protein deficiency mimicking a respiratory chain defect

1 reference

12 December 2020

Dilated cardiomyopathy caused by plasma membrane carnitine transport defect

1 reference

12 December 2020

Detection and assessment by positron emission tomography of a genetically determined defect in myocardial fatty acid utilization (long-chain acyl-CoA dehydrogenase deficiency)

1 reference

12 December 2020

Identification of two novel mutations in the hypoglycemic phenotype of very long chain acyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Gaucher disease with oculomotor apraxia and cardiovascular calcification (Gaucher type IIIC)

1 reference

12 December 2020

Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders.

1 reference

12 December 2020

Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms

1 reference

12 December 2020

Clinical and molecular heterogeneity in very–long-chain acyl-coenzyme a dehydrogenase deficiency

1 reference

12 December 2020

Inhibition of enzyme activities by free fatty acids

1 reference

12 December 2020

Increased glycolytic metabolism in cardiac hypertrophy and congestive failure

1 reference

12 December 2020

Type 3 mucopolysaccharidosis: report of a case with severe mitral valve involvement

1 reference

12 December 2020

Cardiac involvement in Sandhoff's disease. Inborn error of glycosphingolipid metabolism

1 reference

12 December 2020

Effects of excess free fatty acids on mechanical and metabolic function in normal and ischemic myocardium in swine

1 reference

12 December 2020

Lipid-membrane interactions and the pathogenesis of ischemic damage in the myocardium

1 reference

12 December 2020

Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathy

1 reference

12 December 2020

Differential regulation of calcium-dependent and calcium-independent cyclic nucleotide phosphodiesterases from heart by palmitoylcarnitine and palmitoyl coenzyme A

1 reference

12 December 2020

Endogenous triacylglycerol metabolism in diabetic heart

1 reference

12 December 2020

Carnitine deficiency presenting as familial cardiomyopathy: a treatable defect in carnitine transport

1 reference

12 December 2020

Infantile cardiomyopathy and neuromyopathy with beta-galactosidase deficiency

1 reference

12 December 2020

Myocardial metabolites of ethanol

1 reference

12 December 2020

Echocardiographic features in the cardiac type of glycogen storage disease II

1 reference

12 December 2020

Mucopolysaccharidosis type VI presenting in infancy with endocardial fibroelastosis and heart failure

1 reference

12 December 2020

Cardiac involvement by Gaucher's disease documented by right ventricular endomyocardial biopsy

1 reference

12 December 2020

Salient effects of L-carnitine on adenine-nucleotide loss and coenzyme A acylation in the diabetic heart perfused with excess palmitic acid. A phosphorus-31 NMR and chemical extract study

1 reference

12 December 2020

Histologic and biochemical correlates of left ventricular chamber dynamics in man

1 reference

12 December 2020

The varied clinical and laboratory manifestations of type II Gaucher's disease

1 reference

12 December 2020

Abnormal intracellular calcium handling in myocardium from patients with end-stage heart failure

1 reference

12 December 2020

Clinical heterogeneity in infantile galactosialidosis

1 reference

12 December 2020

Hurler syndrome with cardiomyopathy in infancy

1 reference

12 December 2020

Combined aortic and mitral valve replacement in an adult with Scheie's disease

1 reference

12 December 2020

Cardiac involvement in glycogen storage disease type III

1 reference

12 December 2020

Mechanism of arrhythmias induced by palmitylcarnitine in guinea pig papillary muscle

1 reference

12 December 2020

Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy

1 reference

12 December 2020

Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome

1 reference

12 December 2020

Mitochondrial mutation in fatal infantile cardiomyopathy

1 reference

12 December 2020

Myocardial free carnitine and fatty acylcarnitine levels in patients with chronic heart failure

1 reference

12 December 2020

Insulin action on glucose transport in isolated cardiac myocytes: signalling pathways and diabetes-induced alterations

1 reference

12 December 2020

Myocardial triglyceride turnover and contribution to energy substrate utilization in isolated working rat hearts

1 reference

12 December 2020

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

1 reference

12 December 2020

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Cardiomyopathy in glycogen-storage disease type III: clinical and echographic study of 18 patients

1 reference

12 December 2020

Primary carnitine deficiency: Heterozygote and intrafamilial phenotypic variation

1 reference

12 December 2020

Lethal neonatal multiorgan deficiency of carnitine palmitoyltransferase II

1 reference

12 December 2020

Valvular heart disease in four patients with Maroteaux-Lamy syndrome

1 reference

12 December 2020

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Different clinical expression in three unrelated patients

1 reference

12 December 2020

Glycogen storage disease type III (glycogen debranching enzyme deficiency): correlation of biochemical defects with myopathy and cardiomyopathy

1 reference

12 December 2020

Differences in cardiac calcium release channel (ryanodine receptor) expression in myocardium from patients with end-stage heart failure caused by ischemic versus dilated cardiomyopathy

1 reference

12 December 2020

Gaucher's disease with mitral valve calcification

1 reference

12 December 2020

Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy

1 reference

12 December 2020

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA

1 reference

12 December 2020

Fatty acid beta-oxidation deficiency masquerading as fulminant myocarditis

1 reference

12 December 2020

Transcriptional regulation of metabolic processes: implications for cardiac metabolism

1 reference

12 December 2020

The energy substrate switch during development of heart failure: gene regulatory mechanisms (Review)

1 reference

12 December 2020

Acute, severe cardiomyopathy as main symptom of late-onset very long-chain acyl-coenzyme A dehydrogenase deficiency

1 reference

12 December 2020

Cytochrome P450, peroxisome proliferation, and cytoplasmic fatty acid-binding protein content in liver, heart and kidney of the diabetic rat

1 reference

12 December 2020

Protein-mediated palmitate uptake and expression of fatty acid transport proteins in heart giant vesicles

1 reference

12 December 2020

Scintigraphic evidence for a specific long-chain fatty acid transporting system deficit and the genetic background in a patient with hypertrophic cardiomyopathy

1 reference

12 December 2020

10.1046/J.1365-2613.2000.00186.X

Identifiers

DOI

1 reference

31 July 2017

0 references

1 reference

PubMed ID

11298185