Add to ORKGHypertrophic cardiomyopathy associated with a mitochondrial myopathy of voluntary muscles and congenital catarac
Primary cardiomyopathy is an important cause of mortality in children and adults. Apart from inherit...
A 43-year-old female patient diagnosed with chronic progressive external ophthalmoplegia (CPEO) beca...
Defects of the mitochondrial respiratory chain in cardiac muscle are an important, yet still overloo...
Abstract. Metabolic cardiomyopathies include amino acid, lipid and mitochondrial disorders, as well ...
The autosomal recessive syndrome characterized by mitochondrial myopathy of cardiac and skeletal mus...
Hypertrophic cardiomyopathy is generally considered to be a primary disease of cardiac muscle, altho...
Contains fulltext : 58868.pdf (publisher's version ) (Closed access)We describe tw...
We describe two siblings with a Sengers-like syndrome, who presented with congenital hypertrophic ca...
Cardiomyopathies are defined as diseases of the myocardium associated with cardiac dysfunction and a...
Mitochondrial myopathies are clinically heterogeneous disorders that can affect multiple systems bes...
Two brothers, 25 and 19 years old, were affected by asymmetrical hypertrophic cardiomyopathy. The ol...
Hypertrophic cardiomyopathy is the most common form of cardiomyopathy, occurring in childhood, occur...
A striking feature of mitochondrial disorders is the vast heterogeneity in their clinical symptoms t...
Mitochondrial diseases (MD) are a group of genetic and acquired disorders which present significant ...
Hypertrophic cardiomyopathy (HCM) is a genetic disorder characterized by left ventricular hypertroph...
Primary cardiomyopathy is an important cause of mortality in children and adults. Apart from inherit...
A 43-year-old female patient diagnosed with chronic progressive external ophthalmoplegia (CPEO) beca...
Defects of the mitochondrial respiratory chain in cardiac muscle are an important, yet still overloo...
Abstract. Metabolic cardiomyopathies include amino acid, lipid and mitochondrial disorders, as well ...
The autosomal recessive syndrome characterized by mitochondrial myopathy of cardiac and skeletal mus...
Hypertrophic cardiomyopathy is generally considered to be a primary disease of cardiac muscle, altho...
Contains fulltext : 58868.pdf (publisher's version ) (Closed access)We describe tw...
We describe two siblings with a Sengers-like syndrome, who presented with congenital hypertrophic ca...
Cardiomyopathies are defined as diseases of the myocardium associated with cardiac dysfunction and a...
Mitochondrial myopathies are clinically heterogeneous disorders that can affect multiple systems bes...
Two brothers, 25 and 19 years old, were affected by asymmetrical hypertrophic cardiomyopathy. The ol...
Hypertrophic cardiomyopathy is the most common form of cardiomyopathy, occurring in childhood, occur...
A striking feature of mitochondrial disorders is the vast heterogeneity in their clinical symptoms t...
Mitochondrial diseases (MD) are a group of genetic and acquired disorders which present significant ...
Hypertrophic cardiomyopathy (HCM) is a genetic disorder characterized by left ventricular hypertroph...
Primary cardiomyopathy is an important cause of mortality in children and adults. Apart from inherit...
A 43-year-old female patient diagnosed with chronic progressive external ophthalmoplegia (CPEO) beca...
Defects of the mitochondrial respiratory chain in cardiac muscle are an important, yet still overloo...