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NCT02435940
- Conditions
- Abetalipoproteinemia, Abnormalities, Multiple, Achromatopsia, +100 more
- Locations
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- Foundation Fighting Blindness Columbia, Maryland, United States
Recruiting
Longitudinal Natural History Study of Patients With Peroxisome Biogenesis Disorders (PBD)
NCT01668186
- Conditions
- ACBD5 (AcylCoA Binding Domain 5) Deficiency, ATP Binding Cassette Subfamily D Member 3 Gene Mutation, Abnormalities, Multiple, +48 more
- Locations
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- Research Institute of the McGill University Health Center Montreal, Quebec, Canada
Recruiting
The Myelin Disorders Biorepository Project
NCT03047369
- Conditions
- 4H Syndrome, ADLD, AGS, +173 more
- Locations
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- Children's Hospital of Los Angeles Los Angeles, California, United States
- Children's Hospital of Orange County Orange, California, United States
- Stanford University (Lucile Packard Children's Hospital) Palo Alto, California, United States
- University of California, Davis (UC Davis Health) Sacramento, California, United States
Recruiting
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
NCT01793168
- Conditions
- 1p36 Deletion Syndrome, 3-Methylglutaconic Aciduria, Type V, 4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome, +698 more
- Locations
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- Sanford Health Sioux Falls, South Dakota, United States
- Online Patient Enrollment System Sydney, Australia
NCT02699190
- Conditions
- 4H Syndrome, ADLD, AGS, +173 more
- Locations
-
- The Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States