University Medical Center Hamburg-Eppendorf, Department of Pediatric Hematology and Oncology, Martinistr 52

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome)	Cytopenia, Familial Thrombotic Thrombocytopenic Purpura, Hemic and Lymphatic Diseases, Hemorrhage, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Skin Manifestations, anemia, blood coagulation disease, blood platelet disease, congenital thrombotic thrombocytopenic purpura, hematologic disorder, hemolytic anemia, purpura, thrombocytopenia, thrombocytopenic purpura, thrombophilia, thrombotic microangiopathy, thrombotic thrombocytopenic purpura	Recruiting	Not stated	2023-10-11		NCT01257269

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