International Registry Study of Neutral Lipid Storage Disease (NLSD) / Triglyceride Deposit Cardiomyovasculopathy (TGCV) and Related Diseases
Condition(s):Neutral Lipid Storage DiseaseLast Updated:November 9, 2023Recruiting
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Condition(s):Neutral Lipid Storage DiseaseLast Updated:November 9, 2023Recruiting
Condition(s):Neutral Lipid Storage DiseaseLast Updated:May 14, 2013Completed
Condition(s):Primary Triglyceride Deposit Cardiomyovasculopathy (TGCV); Neutral Lipid Storage Disease With Myopathy (NLSD-M)Last Updated:July 8, 2019Terminated
Condition(s):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 DeficiencyLast Updated:October 16, 2019Unknown status
Condition(s):Lysosomal Acid Lipase DeficiencyLast Updated:November 18, 2019Terminated
Condition(s):Lysosomal Acid Lipase Deficiency; Wolman DiseaseLast Updated:January 30, 2019Completed
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