Example: Heart Attack
Clinical Trials on Beta-galactosidase-1 Deficiency
Total 17 results
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NCT04310163RecruitingConditions: GM1 Gangliosidosis
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NCT04273269Not yet recruitingConditions: GM1 Gangliosidosis
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NCT04041102RecruitingConditions: GM1 Gangliosidosis
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NCT04320329Not yet recruitingConditions: Morquio B Disease; GM1 Gangliosidosis Type III
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NCT04713475RecruitingConditions: GM1 Gangliosidosis; GM1 Gangliosidosis, Type I; GM1 Gangliosidosis, Type 2; Beta-Galactosidase-1 (GLB1) Deficiency
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NCT04470713RecruitingConditions: GM1 Gangliosidosis; GM2 Gangliosidosis; Gaucher Disease, Type 2; Tay-Sachs Disease; AB Variant Gangliosidosis GM2; Sandhoff Disease
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NCT03952637RecruitingConditions: Lysosomal Diseases; Gangliosidosis; GM1
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NCT02030015RecruitingConditions: GM1 Gangliosidoses; GM2 Gangliosidoses; Tay-Sachs Disease; Sandhoff Disease
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NCT00668187RecruitingConditions: Tay-Sachs Disease; Sandhoff Disease; Late Onset Tay-Sachs Disease; GM1 Gangliosidosis; GM2 Gangliosidosis
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NCT00383448CompletedConditions: Adrenoleukodystrophy; Metachromatic Leukodystrophy; Globoid Cell Leukodystrophy; Tay Sachs Disease; Sandhoffs Disease; Wolman Disease; I-Cell Disease; Sanfilippo Syndrome; GM1 Gangliosidosis
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NCT04624789RecruitingConditions: Gangliosidoses; GM1 Gangliosidosis; Morquio B Disease; Sialidosis; Galactosialidosis; Gm2-Gangliosidosis, Variant B1; Tay-Sachs Disease; Sandhoff Disease; GM2 Activator Deficiency
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NCT03333200RecruitingConditions: MLD; Krabbe Disease; ALD; MPS I; MPS II; MPS III; Vanishing White Matter Disease; GM3 Gangliosidosis; PKAN; Tay-Sachs Disease; NP Deficiency; Osteopetrosis; Alpha-Mannosidosis; Sandhoff Disease; Niemann-Pick Diseases; MPS IV; Gaucher Disease; GAN; GM1 Gangliosidoses; Morquio Disease; S-Adenosylhomocysteine Hydrolase Deficiency; Batten Disease; Pelizaeus-Merzbacher Disease; Leukodystrophy; Lysosomal Storage Diseases; Purine Nucleoside Phosphorylase Deficiency; Multiple Sulfatase Deficiency Disease
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NCT00176904CompletedConditions: Adrenoleukodystrophy; Metachromatic Leukodystrophy; Globoid Cell Leukodystrophy; Gaucher's Disease; Fucosidosis; Wolman Disease; Niemann-Pick Disease; Batten Disease; GM1 Gangliosidosis; Tay Sachs Disease; Sandhoff Disease
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NCT01626092CompletedConditions: Lysosomal Storage Disease; Peroxisomal Disorder
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NCT00029965RecruitingConditions: Neurological Regression; Myoclonus; Cherry Red Spot; Brain Atrophy
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NCT00654433TerminatedConditions: Inherited Metabolic Diseases; Lysosomal Storage Disorders; Peroxisomal Storage Diseases; Inborn Errors of Metabolism; Mucopolysaccharidosis
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NCT01891422Unknown statusConditions: Aspartylglucosaminuria; Fucosidosis; Galactosialidosis; Alpha Mannosidosis; Beta Mannosidosis; Mucolipidosis II; Mucolipidosis III; Schindler Disease; Sialidosis