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What does LAL stand for?

LAL stands for Lysosomal Acid Lipase

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Lysosomal acid lipase (LAL) is an essential enzyme that hydrolyzes triglycerides (TGs) and cholesteryl esters (CEs) in lysosomes. Genetic LAL mutations lead to Wolman...
Identifying Lysosomal Acid Lipase Deficiency in Clinical Practice CME. James A. Underberg, MD, MS; Nirav K. Desai, MD. CME Released: 12/22/2014; Valid for credit...
Lysosomal Acid Lipase (LAL) deficiency is an autosomal recessive lysosomal storage disease caused by a deficiency of LAL, an enzyme responsible for lipid breakdown.
Lysosomal Acid Lipase Deficiency: An Under-diagnosed Cause of Liver Dysfunction. Lysosomal acid lipase deficiency is characterized by the accumulation of cholesteryl...
Lysosomal Acid Lipase Deficiency (LAL D): LAL D is an inherited (genetic) disorder which means that it is passed down within a family. It is autosomal recessive which...
Lysosomal acid lipase: at the crossroads of normal and atherogenic cholesterol metabolism
Clinical Utility. Lysosomal Acid Lipase (LAL) deficiency is an autosomal recessive lysosomal storage disease caused by a deficiency of LAL, an enzyme responsible for...
Wolman disease is a type of autosomal recessive disorder caused by mutations of the lysosomal acid lipase (LIPA) gene.
LAL Solace is an online support group to help patients with LAL Deficiency (Lysosomal Acid Lipase Disease) and Wolman Disease.
Lysosomal Acid Lipase Deficiency (LALD) is a genetic disease which is characterized by abnormal lipid accumulation in many parts of the body due to a marked decrease...
Mutations in the LIPA gene (10q23.31) cause autosomal recessive lysosomal acid lipase deficiency. The phenotype varies in clinical onset and the severity of the disease.
Lysosomal Acid Lipase Deficiency Impairs Regulation of ABCA1 Gene and Formation of High Density Lipoproteins in Cholesteryl Ester Storage Disease*
Lysosomal acid lipase deficiency symptoms, causes, diagnosis, and treatment information for Lysosomal acid lipase deficiency (Wolman disease) with alternative...
quot;Mutations at the lysosomal acid cholesteryl ester hydrolase; "Different missense mutations in histidine-108 of lysosomal acid lipase cause cholesteryl ester...
Clinical Information. Deficiency of lysosomal acid lipase (LAL) results in 2 clinically distinct phenotypes; Wolman disease (WD) and cholesteryl ester storage disease...
Lysosomal acid lipase (LAL, E.C. 3.1.1.13) is a hydrolase involved in the intracellular degradation of lipoproteins. LAL was first described in fibroblasts (1), and...
In a new Original Article, a phase 3 trial of enzyme-replacement therapy in children and adults with lysosomal acid lipase deficiency, which causes cirrhosis and...
Lysosomal lipase is a form of lipase which functions intracellularly, in the lysosomes. Clinical significance. A deficiency associated with Lysosomal Acid Lipase...
Burton et al. (2015) reported the results of a 20-week phase 3 trial of sebelipase alfa in lysosomal acid lipase deficiency in a multicenter randomized double-blind...
Deficiency of lysosomal acid lipase causes 2 distinct phenotypes in humans: Wolman disease and cholesteryl ester storage disease (CESD). Wolman disease is an early...
Clinical characteristics. The phenotypic spectrum of lysosomal acid lipase (LAL) deficiency ranges from the infantile-onset form (Wolman disease) to later-onset forms...
Lysosomal acid lipase deficiency is a lipid storage disease caused by reduced or missing lysosomal acid lipase. When there is a deficiency of this enzyme, the body...
Lysosomal acid lipase (LAL) is a lysosomal enzyme that is involved in intracellular lipid metabolism. Complete deficiency of the LAL enzyme causes Wolman disease...
A deficiency associated with Lysosomal Acid Lipase Deficiency, Wolman disease, and cholesteryl ester storage disease. Chlorpromazine is an inhibitor of lysosomal lipase.
Lysosomal acid lipase deficiency (LAL-D) is a rare autosomal recessive lysosomal storage disease caused by deleterious mutations in the LIPA gene. The age at on
9/26/2014 1 Lysosomal Acid Lipase Deficiency: Biology, Clinical Manifestations, Diagnosis, and Novel Approach to Treatment Mark A. Goldberg, M.D.
Summary. Lysosomal acid lipase A (LIPA) deficiency is a lipid storage disease that can result in 1) an early-onset severe form, Wolman disease (see this term), or 2...
613497 - lipase a, lysosomal acid; lipa - lysosomal acid lipase; lal;; cholesterol ester hydrolase - lipa
Lysosomal acid lipase deficiency An under-diagnosed cause of liver dysfunction Irene De Biase, MD, PhD, FACMG. Assistant Professor of Pathology, University of Utah
Clinical trials: Lysosomal acid lipase deficiency (LALD) The mission of our clinical research is to foster discoveries in the novel therapies of inflammatory bowel...
Lysosomal acid lipase (LAL) is responsible for the hydrolysis of cholesterol esters and triglycerides. LAL is coded by the LIPA gene on chromosome 10q23.31. Its...
Useful For. Evaluation of patients with a clinical presentation suggestive of lysosomal acid lipase deficiency