Clinical Trials on Lipidoses

Conditions: Lipid Storage Disease

Conditions: Neutral Lipid Storage Disease

Conditions: Neutral Lipid Storage Disease

Conditions: Sphingomyelin Lipidosis

Conditions: Sphingomyelin Lipidosis

Conditions: Sphingomyelin Lipidosis

Conditions: Sphingomyelin Lipidosis

Conditions: Cardiovascular Risk Factor; Cholesterol; Lipidosis

Conditions: Primary Triglyceride Deposit Cardiomyovasculopathy (TGCV); Neutral Lipid Storage Disease With Myopathy (NLSD-M)

Conditions: Cholesterol; Lipidosis; Arterial Hypertension; Blood Glucose, High

Conditions: Lipoidosis

Conditions: Inflammatory Bowel Diseases; Crohn Disease; Polyunsaturated Acid Lipidosis

Conditions: Gaucher Disease; Cerebroside Lipidosis Syndrome; Glucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease

Conditions: Gaucher Disease Type I; Cerebroside Lipidosis Syndrome; Clucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease; Gaucher Disease, Non-Neuronopathic Form

Conditions: Gaucher Disease, Type 1; Cerebroside Lipidosis Syndrome; Glucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease; Gaucher Disease, Non-Neuronopathic Form

Conditions: Gaucher Disease, Type 1; Cerebroside Lipidosis Syndrome; Glucocerebrosidase Deficiency Disease; Glucosylceramide Beta-Glucosidase Deficiency Disease; Gaucher Disease, Non-Neuronopathic Form

Conditions: Cardiovascular Risk Factor; Cardiovascular Diseases; Coronary Heart Disease; Stroke; Diabetes; Blood Pressure; Cholesterol; Lipidosis; Inflammation; Adiposity

Conditions: Metabolism, Inborn Errors; Lipid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency; Glycogenin-1 Deficiency (Glycogen Storage Disease Type XV); Carnitine Palmitoyl Transferase 2 Deficiency; VLCAD Deficiency; Medium-chain Acyl-CoA Dehydrogenase Deficiency; Multiple Acyl-CoA Dehydrogenase Deficiency; Carnitine Transporter Deficiency; Neutral Lipid Storage Disease; Glycogen Storage Disease Type II; Glycogen Storage Disease Type III; Glycogen Storage Disease Type IV; Glycogen Storage Disease Type V; Muscle Phosphofructokinase Deficiency; Phosphoglucomutase 1 Deficiency; Phosphoglycerate Mutase Deficiency; Phosphoglycerate Kinase Deficiency; Phosphorylase Kinase Deficiency; Beta Enolase Deficiency; Lactate Dehydrogenase Deficiency; Glycogen Synthase Deficiency

Conditions: Krabbe Disease

Conditions: Lysosomal Storage Diseases; Gaucher Disease; Sphingolipidoses

Conditions: Mixed Hyperlipoproteinemia

Conditions: Mixed Hyperlipidemia

Conditions: Mixed Hyperlipidemia

Conditions: Mixed Hyperlipidemia

Conditions: Niemann-Pick Disease; Niemann-Pick Disease, Type C