Clinical Trials Browser

NIH × Observational × Genetic Diseases, Inborn × Clear all

Asthma, Lung Diseases, Pulmonary Fibrosis, Sarcoidosis, Lymphangioleiomyomatosis, Genetic Diseases, Inborn

NCT01369953 2018-07-26

Informed Consent for Whole Genome Sequencing: Ideals and Norms Referenced by Early Participants

Completed

30 enrolled

Head & Neck

Hyperparathyroidism 2, Coronary Artery Disease, Proteus Syndrome, Genetic Diseases, Inborn

NCT00068146 2018-07-05

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

Completed

77 enrolled

Lymphoid

Lymphadenopathy, Lymphoma, Lymphoproliferative Disorders, Syndrome, Genetic Diseases, Inborn

NCT00005900 2005-06-24

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

Unknown

10 enrolled

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

Clinical Trials

Role of Helicobacter Pylori and Its Toxins in Lung and Digestive System Diseases

Informed Consent for Whole Genome Sequencing: Ideals and Norms Referenced by Early Participants

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