Objectives: Evidence suggests that lysosomal acid lipase deficiency (LAL-D) is often underdiagnosed because symptoms may be nonspecific. We aimed to investigate the prevalence of LAL-D in children with unexplained liver disease and to identify demographic and clinical features with a prospective, multicenter, cross-sectional study
Aim of review. To acquaint general practitioners with a rarely diagnosed disease - the hereditary de...
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 ...
Objectives: Evidence suggests that lysosomal acid lipase deficiency (LAL-D) is often underdiagnosed ...
Objectives: Evidence suggests that lysosomal acid lipase deficiency (LAL-D) is often underdiagnosed ...
The aim of this study was to characterize key clinical manifestations of lysosomal acid lipase defic...
Georg Strebinger, Elena Müller, Alexandra Feldman, Elmar AignerFirst Department of Medicine, Pa...
Background and aims Childhood/Adult-onset Lysosomal Acid Lipase Deficiency (LAL-D) is a recessive di...
Lysosomal acid lipase deficiency (LAL-D) is stilla little recognized genetic disease with significan...
Lysosomal acid lipase (LAL) is a key enzyme in lipid metabolism. Initial reports have suggested a ro...
International audienceBACKGROUND: The childhood/adult-onset lysosomal acid lipase deficiency (LALD; ...
Background: Lysosomal acid lipase deficiency (LAL-D) is a rare genetic disease associated with lipid...
Lysosomal acid lipase deficiency (LAL D) is an orphan disease connected with accumulation of cholest...
Lysosomal Acid Lipase (LAL) is a key enzyme involved in lipid metabolism, responsible for hydrolysin...
BACKGROUND & AIMS: Lysosomal acid lipase deficiency (LAL-D) is an autosomal recessive condition that...
Aim of review. To acquaint general practitioners with a rarely diagnosed disease - the hereditary de...
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 ...
Objectives: Evidence suggests that lysosomal acid lipase deficiency (LAL-D) is often underdiagnosed ...
Objectives: Evidence suggests that lysosomal acid lipase deficiency (LAL-D) is often underdiagnosed ...
The aim of this study was to characterize key clinical manifestations of lysosomal acid lipase defic...
Georg Strebinger, Elena Müller, Alexandra Feldman, Elmar AignerFirst Department of Medicine, Pa...
Background and aims Childhood/Adult-onset Lysosomal Acid Lipase Deficiency (LAL-D) is a recessive di...
Lysosomal acid lipase deficiency (LAL-D) is stilla little recognized genetic disease with significan...
Lysosomal acid lipase (LAL) is a key enzyme in lipid metabolism. Initial reports have suggested a ro...
International audienceBACKGROUND: The childhood/adult-onset lysosomal acid lipase deficiency (LALD; ...
Background: Lysosomal acid lipase deficiency (LAL-D) is a rare genetic disease associated with lipid...
Lysosomal acid lipase deficiency (LAL D) is an orphan disease connected with accumulation of cholest...
Lysosomal Acid Lipase (LAL) is a key enzyme involved in lipid metabolism, responsible for hydrolysin...
BACKGROUND & AIMS: Lysosomal acid lipase deficiency (LAL-D) is an autosomal recessive condition that...
Aim of review. To acquaint general practitioners with a rarely diagnosed disease - the hereditary de...
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 ...