Status | Study |
Recruiting |
Study Name: Biomarker for Glycogen Storage Diseases Condition: Fructose Metabolism, Inborn Errors Glycogen Storage Disease Date: 2015-03-02 |
Recruiting |
Study Name: Biomarker for Mucolipidosis Disorder Type I, II, III or IV Condition: Mucolipidosis Type I Mucolipidosis Date: 2014-10-23 |
Completed |
Study Name: Longitudinal Studies of the Glycoproteinoses Condition: Aspartylglucosaminuria Fucosidosis Galactosialidosis Date: 2013-05-22 |
Recruiting |
Study Name: Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford Condition: Rare Disorders Undiagnosed Disorders Disorders of Unknown Date: 2013-02-13 |
Completed |
Study Name: Reduced-Intensity Hematopoietic Stem Cell Transplant for High Risk Lysosomal and Peroxisomal Disorders Condition: Lysosomal Storage Disease Peroxisomal Disorder Date: 2012-06-20 Interventions: Drug: Campath-1H A daily dose |
Recruiting |
Study Name: The Natural History of Mucolipidosis Type IV Condition: Mucolipidosis Type IV Date: 2010-02-10 |
Completed |
Study Name: HSCT for High Risk Inherited Inborn Errors Condition: Adrenoleukodystrophy Metachromatic Leukodystrophy Globoid Date: 2006-09-29 Interventions: Drug: Clofarabine days -7 thro |
Completed |
Study Name: Stem Cell Transplantation for Hurler Condition: Mucopolysaccharidosis I Mucopolysaccharidosis VI Mannosido Date: 2005-09-12 Interventions: Procedure: Stem Cell Transplant |
Completed |
Study Name: The Natural History and Pathogenesis of Mucolipidosis Type IV Condition: Mucolipidosis Type IV Date: 2001-05-04 |
Completed |
Study Name: Study of Pulmonary Complications in Pediatric Patients With Storage Disorders Undergoing Allogeneic Hematopoietic Stem Cell Transplantation Condition: I Cell Disease Fucosidosis Globoid Cell Leukodystrophy Date: 2000-06-02 |