Results 81 to 90 of about 1,394,911 (165)
BackgroundChronic immune thrombocytopenia (ITP) is characterized by persistent thrombocytopenia and bleeding risk, and a subset of patients remains refractory or relapses despite multiple lines of therapy.
Nashwa Al-Sharji +3 more
doaj +1 more source
Total remission of severe immune thrombocytopenia after short term treatment with romiplostim
Immune thrombocytopenia (ITP) in adults is an acquired chronic immune-mediated disorder defined by isolated thrombocytopenia. In recent years, an improved understanding of the pathophysiology of ITP has been achieved and is now accepted that the disorder
Efthymia Vlachaki +6 more
doaj +1 more source
Thrombocytopenia is a tough complication after hematopoietic stem cell transplantation (HSCT) with elusive pathogenesis and lack of well-established therapies.
Yifang Yao (11776165) +7 more
core +1 more source
Background: There have been no licensed treatment options in the UK for treating thrombocytopenia in people with chronic liver disease requiring surgery.
Nigel Armstrong +15 more
doaj +1 more source
In steady-state adult hematopoiesis, most hematopoietic stem cells (HSCs) are in the resting phase of the cell cycle. Upon enhanced hematopoietic demand, HSCs can be induced to divide and self-renew or differentiate.
Takizawa, H +5 more
core +1 more source
Introduction: The management of adult (≥18 years) immune thrombocytopenia patients relies on platelet count, the risk of bleeding and presence of bleeding.
Rosângela de Albuquerque Ribeiro +5 more
doaj +1 more source
Thrombocytopenia and Procedural Prophylaxis in the Era of Thrombopoietin Receptor Agonists
Thrombocytopenia is common in patients with advanced liver disease. These patients frequently require invasive diagnostic or therapeutic procedures in the setting of thrombocytopenia.
Kathy M. Nilles +2 more
doaj +1 more source
Genetic studies of familial myeloproliferative disorders [PDF]
Hereditary thrombocythemia (HT) is an autosomal dominant disorder with clinical features resembling sporadic essential thrombocythemia. HT families share similar clinical symptoms caused by heterogeneous genetic alterations.
Liu, Kun
core +1 more source
Hetrombopag for the treatment of chemotherapy-induced thrombocytopenia in patients with solid tumors
Based on real-world research, we aimed to systematically evaluate the efficacy and safety of hetrombopag for the treatment of chemotherapy-induced thrombocytopenia (CIT) in patients with solid tumors.
Yuan Liu +6 more
doaj +1 more source
IntroductionPrimary immune thrombocytopenia is an autoimmune bleeding disorder characterized by variable immune-mediated platelet destruction. These patients have reported thrombotic complications, both venous and arterial, in addition to bleeding ...
Roberto Castelli +16 more
doaj +1 more source

