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Your search returned 4 studies. (Get alerts for new studies):HSCT for High Risk Inherited Inborn ErrorsConditions: Adrenoleukodystrophy - Metachromatic Leukodystrophy - Globoid Cell Leukodystrophy - Tay Sachs Disease - Sandhoffs Disease - Wolman Disease - I-Cell Disease - Sanfilippo Syndrome - GM1 Gangliosidosis1 Location availableAllogeneic Bone Marrow Transplant for Inherited Metabolic DisordersConditions: Mucopolysaccharidosis - Hurler Syndrome - Hunter Syndrome - Maroteaux-Lamy Syndrome - Sly Syndrome - Alpha Mannosidosis - Fucosidosis - Aspartylglucosaminuria - Adrenoleukodystrophy (ALD) - Globoid Cell Leukodystrophy (GLD) - Krabbe Disease - Metachromati1 Location availableA Multicenter Access and Distribution Protocol for Unlicensed Cryopreserved Cord Blood Units (CBUs)Conditions: Hematological Malignancies - Certain Lysosomal Storage and Peroxisomal Enzyme Deficiency Disorders - Hurler Syndrome (MPS I) - Krabbe Disease (Globoid Leukodystrophy) - X-linked Adrenoleukodystrophy - Primary Immunodeficiency Diseases - Bone Marrow Failur123 Locations availableExercise Study of Function and Pathology for Women With X-linked AdrenoleukodystrophyConditions: X-linked Adrenoleukodystrophy1 Location available
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