Objectives: To determine the prevalence of Lysosomal Acid Lipase (LAL) deficiency in patients with severe dyslipidemia and premature coronary heart disease
AbstractLysosomal acid lipase deficiency (LAL-D) is a rare autosomal recessive lysosomal storage dis...
Objectives: Evidence suggests that lysosomal acid lipase deficiency (LAL-D) is often underdiagnosed ...
Lysosomal storage diseases (LSDs) are a group of heterogeneous and multisystemic disorders caused by...
Georg Strebinger, Elena Müller, Alexandra Feldman, Elmar AignerFirst Department of Medicine, Pa...
International audienceBACKGROUND: Lysosomal acid lipase deficiency (LALD, OMIM#278000) is a rare lys...
Lysosomal acid lipase (LAL) is a lysosomal enzyme essential for the degradation of cholesteryl ester...
To characterize key clinical manifestations of lysosomal acid lipase deficiency (LAL D) in children ...
Lysosomal acid lipase deficiency (LAL-D) is stilla little recognized genetic disease with significan...
Lysosomal Acid Lipase (LAL) is a key enzyme involved in lipid metabolism, responsible for hydrolysin...
Introduction: Lysosomal acid lipase deficiency (LAL-D) causes progressive cholesteryl ester and trig...
Highlights: - Dyslipidemia phenotype of patients with familial hypercholesterolemia and lysosomal ac...
† These authors contributed equally to this work. ‡ Joint senior authors. Abstract: Lysosomal Acid L...
Dyslipidaemia is one of many independent cardiovascular risk factors that have been identified for C...
Background: Lysosomal acid lipase deficiency (LAL-D) is a rare genetic disease associated with lipid...
AbstractLysosomal acid lipase deficiency (LAL-D) is a rare autosomal recessive lysosomal storage dis...
Objectives: Evidence suggests that lysosomal acid lipase deficiency (LAL-D) is often underdiagnosed ...
Lysosomal storage diseases (LSDs) are a group of heterogeneous and multisystemic disorders caused by...
Georg Strebinger, Elena Müller, Alexandra Feldman, Elmar AignerFirst Department of Medicine, Pa...
International audienceBACKGROUND: Lysosomal acid lipase deficiency (LALD, OMIM#278000) is a rare lys...
Lysosomal acid lipase (LAL) is a lysosomal enzyme essential for the degradation of cholesteryl ester...
To characterize key clinical manifestations of lysosomal acid lipase deficiency (LAL D) in children ...
Lysosomal acid lipase deficiency (LAL-D) is stilla little recognized genetic disease with significan...
Lysosomal Acid Lipase (LAL) is a key enzyme involved in lipid metabolism, responsible for hydrolysin...
Introduction: Lysosomal acid lipase deficiency (LAL-D) causes progressive cholesteryl ester and trig...
Highlights: - Dyslipidemia phenotype of patients with familial hypercholesterolemia and lysosomal ac...
† These authors contributed equally to this work. ‡ Joint senior authors. Abstract: Lysosomal Acid L...
Dyslipidaemia is one of many independent cardiovascular risk factors that have been identified for C...
Background: Lysosomal acid lipase deficiency (LAL-D) is a rare genetic disease associated with lipid...
AbstractLysosomal acid lipase deficiency (LAL-D) is a rare autosomal recessive lysosomal storage dis...
Objectives: Evidence suggests that lysosomal acid lipase deficiency (LAL-D) is often underdiagnosed ...
Lysosomal storage diseases (LSDs) are a group of heterogeneous and multisystemic disorders caused by...