Acid cholesteryl ester hydrolase deficiency, type 2

Known as: Acid lipase disease, Lysosomal acid lipase deficiency, LIPA deficiency 
 

Topic mentions per year

Topic mentions per year

1999-2018
01219992018

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2018
2018
AIMS Lysosomal acid lipase deficiency (LALD) is an autosomal recessive disorder of cholesterol ester storage associated with… (More)
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2018
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2018
INTRODUCTION Lysosomal acid lipase deficiency (LAL-D) causes progressive cholesteryl ester and triglyceride accumulation in the… (More)
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2017
2017
BACKGROUND Lysosomal acid lipase deficiency (LALD) is an autosomal recessive disorder and an unrecognized cause of dyslipidemia… (More)
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2017
2017
Lysosomal acid lipase deficiency (LALD) is an ultra-rare disease caused by a congenital disorder of the lipid metabolism… (More)
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2017
Review
2017
INTRODUCTION With the growing obesity epidemic, nonalcoholic fatty liver disease (NAFLD) is rapidly becoming one of the leading… (More)
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2017
2017
Lysosomal acid lipase deficiency (LAL-D) is still a little recognized genetic disease with significant morbidity and mortality in… (More)
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2017
2017
Lysosomal acid lipase deficiency (LAL-D) is an inherited, autosomal recessive lysosomal storage disorder characterized by… (More)
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2016
2016
Lysosomal acid lipase deficiency (LAL-D) is a classic lysosomal storage disorder characterized by accumulation of cholesteryl… (More)
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Review
2014
Review
2014
Lysosomal acid lipase deficiency (LAL-D) is a rare autosomal recessive lysosomal storage disease caused by deleterious mutations… (More)
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2014
Review
2014
Lysosomal acid lipase (LAL) is responsible for the hydrolysis of cholesterol esters and triglycerides. LAL is coded by the LIPA… (More)
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