Example: Heart Attack
Clinical Trials on Scheie Syndrome
Total 19 results
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NCT00912925CompletedConditions: Mucopolysaccharidosis I; Hurlers Syndrome; Hurler-Scheie Syndrome
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NCT00258011CompletedConditions: Mucopolysaccharidosis I; Hurler Syndrome; Hurler-Scheie Syndrome; Scheie Syndrome
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NCT00146757CompletedConditions: Mucopolysaccharidosis I; Hurler Syndrome; Hurler-Scheie Syndrome; Scheie Syndrome
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NCT00146770CompletedConditions: Mucopolysaccharidosis I; Hurler's Syndrome; Hurler-Scheie Syndrome; Scheie Syndrome
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NCT00144781CompletedConditions: Mucopolysaccharidosis I; Hurler's Syndrome; Hurler-Scheie Syndrome; Scheie Syndrome
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NCT00144768CompletedConditions: Mucopolysaccharidosis I; Hurler's Syndrome; Hurler-Scheie Syndrome; Scheie's Syndrome
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NCT02597114CompletedConditions: Mucopolysaccharidosis I
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NCT00418821Unknown statusConditions: Mucopolysaccharidosis I; Hurler's Syndrome; Hurler-Scheie Syndrome; Scheie
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NCT00852358CompletedConditions: Cognitive Decline; Mucopolysaccharidosis I; Hurler-Scheie Syndrome; Scheie Syndrome; Lysosomal Storage Disease
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NCT00786968TerminatedConditions: Spinal Cord Compression; Mucopolysaccharidosis I; Hurler-Scheie Syndrome; Scheie Syndrome; Lysosomal Storage Disease
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NCT00144794RecruitingConditions: Mucopolysaccharidosis I (MPS I)
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NCT01372228Active, not recruitingConditions: Hurler Syndrome (MPS I); Hurler-Scheie Syndrome; Hunter Syndrome (MPS II); Sanfilippo Syndrome (MPS III); Krabbe Disease (Globoid Leukodystrophy); Metachromatic Leukodystrophy (MLD); Adrenoleukodystrophy (ALD and AMN); Sandhoff Disease; Tay Sachs Disease; Pelizaeus Merzbacher (PMD); Niemann-Pick Disease; Alpha-mannosidosis
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NCT01938014CompletedConditions: Mucopolysaccharidosis Type I (MPS I); Mucopolysaccharidosis Type II (MPS II); Mucopolysaccharidosis Type III (MPS III); Mucopolysaccharidosis Type VI (MPS VI); Krabbe Disease
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NCT01870375CompletedConditions: Mucopolysaccharidosis Type I; Mucopolysaccharidosis Type II; Mucopolysaccharidosis Type VI; Mucopolysaccharidosis Type IV; Mucopolysaccharidosis Type VII
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NCT02298712Active, not recruitingConditions: Mucopolysaccharidosis Type I; Gargoylism; Metabolism, Inborn Errors
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NCT04628871Enrolling by invitationConditions: Hemophilia B; Mucopolysaccharidosis I; Mucopolysaccharidosis II
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NCT02702115Active, not recruitingConditions: MPS I
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NCT00654433TerminatedConditions: Inherited Metabolic Diseases; Lysosomal Storage Disorders; Peroxisomal Storage Diseases; Inborn Errors of Metabolism; Mucopolysaccharidosis
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NCT02095015TerminatedConditions: Mucopolysaccharidosis (MPS)