Congenital thrombotic thrombocytopenic purpura (cTTP) is an ultra-rare
thrombomicroangiopathy caused by an inherited deficiency of a disintegrin and …

Hereditary Thrombotic Thrombocytopenic Purpura Hereditary thrombotic thrombocytopenic
purpura is an autosomal recessive disorder caused by the absence of a functional protease …

The article focuses on providing guidelines to healthcare professionals for the diagnosis of
various types and sub groups of Thrombotic thrombocytopenic purpura (TTP), occurring …

Background Congenital thrombotic thrombocytopenic purpura (TTP) results from severe
hereditary deficiency of ADAMTS13. The efficacy and safety of recombinant ADAMTS13 and …

Recombinant ADAMTS13 and Severe Neonatal TTP Thrombotic thrombocytopenic purpura
was diagnosed in a neonate with hereditary ADAMTS13 deficiency. Treatment with …

The American Society for Apheresis (ASFA) conducted a 1 day consensus conference on
Thrombotic Thrombocytopenic Purpura (TTP) during its annual meeting in Atlanta, GA, on …

The objective of this guideline is to provide healthcare professionals with clear, up‐to‐date
and practical guidance on the management of thrombotic thrombocytopenic purpura (TTP) …

Thrombotic thrombocytopenic purpura (TTP) is a rare hematologic disorder (annual
incidence of 11.3 cases per 1 million population), characterized by microangiopathic …

Background: Thrombotic thrombocytopenic purpura (TTP) is a rare life‐threatening disease.
Of surviving patients, 45% develops an exacerbation or a late recurrence. Severe ADAMTS …

Background: ADAMTS13 mutations play a role in thrombotic thrombocytopenic purpura
(TTP) pathogenesis. Objectives: To establish a phenotype–genotype correlation in a cohort …