NCT01165060
- Conditions
- Adrenal Gland Diseases, Adrenal Insufficiency, Adrenoleukodystrophy, +23 more
- Locations
-
- Academisch Medisch Centrum Amsterdam, North Holland, Netherlands
Clinical trial condition
Genetic Diseases, X-Linked
Explore clinical trials studying Genetic Diseases, X-Linked. Study availability and eligibility vary by location and protocol.
1,242 public trials
227 recruiting studies
Genetic Diseases, X-Linked trial results
NCT00654784
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), Genetic Diseases, Inborn, +8 more
- Locations
-
- Children's Hospital, University Hospital Leuven, Belgium
NCT00749476
- Conditions
- Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +7 more
- Locations
-
- Dr. Lambert Le Kremlin-Bicêtre, France
- Pr Chambost Marseille, France
- Dr. Hassoun Montmorency, France
- Pr Schved Montpellier, France
NCT00758225
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- University Hospitals Leuven Leuven, Belgium
NCT01080859
- Conditions
- Acute Coronary Syndrome, Amino Acid Metabolism, Inborn Errors, Brain Diseases, +16 more
- Locations
-
- Satakunta Central Hospital Pori, Finland
NCT00866606
- Conditions
- Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, Coagulation Protein Disorders, +7 more
- Locations
-
- Pfizer Investigational Site Guangzhou, China
- Pfizer Investigational Site Suzhou, Jiangsu, China
- Pfizer Investigational Site Tianjin, Tianjin Municipality, China
- Pfizer Investigational Site Hangzhou, Zhejiang, China
Completed
Creatine Metabolism in Rett Syndrome
NCT01198015
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
- Locations
-
- Maastricht University Medical Center Maastricht, Limburg, Netherlands
NCT00168077
- Conditions
- Acquired Coagulation Factor Deficiency, Blood Coagulation Disorders, Blood Coagulation Disorders, Inherited, +8 more
- Locations
-
- Clinical Trials Registration Coordinator Feldkirch, Austria
- Clinical Trials Registration Coordinator Vienna, Austria
- Clinical Trials Registration Coordinator Halle, Germany
- Clinical Trials Registration Coordinator Hanover, Germany
NCT00303446
- Conditions
- Bulbo-Spinal Atrophy, X-Linked, Central Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +11 more
- Locations
-
- National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States
NCT00261508
- Conditions
- Asperger Syndrome, Autism Spectrum Disorder, Autistic Disorder, +15 more
- Locations
-
Not specified