Spherocytosis, Hereditary
2 clinical trials · Condition
◉ Watch Spherocytosis, Hereditary
| Record | Firm | Date |
|---|---|---|
| Integrative Diagnosis for SCD and Other RADs (NCT07206095) | Hospital Universitari Vall d'Hebron Research Institute | 2020-11-13 |
| ERN-EuroBloodNet Registry on Patients With Rare Red Blood Cell Defects and COVID-19 (NCT06831799) | Hospital Universitari Vall d'Hebron Research Institute | 2020-04-15 |
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