Screening of Lysosomal Storage Disorders Diseases in Minority Groups
Condition(s):Lysosomal Storage DiseasesLast Updated:January 22, 2019Unknown status
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Condition(s):Lysosomal Storage DiseasesLast Updated:January 22, 2019Unknown status
Condition(s):Lysosomal Storage DiseasesLast Updated:January 22, 2019Unknown status
Condition(s):Mucopolysaccharidosis I; Mucopolysaccharidosis II; Mucopolysaccharidosis IV A; Mucopolysaccharidosis VI; Mucopolysaccharidosis VII; Pompe Disease Infantile-Onset; Neuronopathic Gaucher Disease; Wolman DiseaseLast Updated:December 12, 2023Recruiting
Condition(s):Lysosomal Storage DisordersLast Updated:February 23, 2021Unknown status
Condition(s):Lysosomal Storage Diseases; Inborn Errors of MetabolismLast Updated:June 29, 2017Withdrawn
Condition(s):Neonatal Screening; Lysosomal Storage DiseasesLast Updated:October 20, 2021Unknown status
Condition(s):MPS I; MPS II; MPS IVA; MPS VI; Mps VII; Gaucher Disease, Type 2; Gaucher Disease, Type 3; Pompe Disease Infantile-Onset; Wolman DiseaseLast Updated:September 21, 2023Recruiting
Condition(s):Lysosomal Storage Disorders; Gaucher Disease; Parkinson DiseaseLast Updated:March 27, 2024Enrolling by invitation
Condition(s):Lysosomal Storage Disorders; Gaucher Disease; Fabry Disease; Pompe Disease; Niemann-Pick DiseaseLast Updated:April 4, 2017Unknown status
Condition(s):Fabry Disease; Gaucher Disease; Niemann-Pick Disease, Type C; Lysosomal Storage DiseasesLast Updated:June 7, 2021Withdrawn
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