Clinical Trials Browser

Adrenoleukodystrophy, Fucosidosis, Gaucher Disease, Leukodystrophy, Globoid Cell, Leukodystrophy, Metachromatic, Mucopolysaccharidosis I, Metabolism, Inborn Errors, Mucolipidoses, Mucopolysaccharidoses, Mucopolysaccharidosis VI, Niemann-Pick Diseases, Sphingolipidoses, Wolman Disease, Genetic Diseases, Inborn, Rare Diseases, Mannosidase Deficiency Diseases

NCT00007046 2005-06-24

Genetic Study of Patients and Families With Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma of the Bone

Completed

Sarcoma

Arthritis, Bone Neoplasms, Connective Tissue Diseases, Constriction, Pathologic, Genetic Diseases, Inborn, Rare Diseases, Histiocytoma, Histiocytoma, Malignant Fibrous

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Fluorodeoxyglucose-Positron Emission Tomography (FDG-PET) to Evaluate Autoimmune Lymphoproliferative Syndrome (ALPS) and ALPS-associated Lymphoma

Study of Pulmonary Complications in Pediatric Patients With Storage Disorders Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

Genetic Study of Patients and Families With Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma of the Bone