Immune-mediated thrombotic thrombocytopenic purpura: a narrative review of diagnosis and treatment in adults

R Blennerhassett, J Curnow… - Seminars in thrombosis …, 2020 - thieme-connect.com
Immune-mediated thrombotic thrombocytopenic purpura (iTTP) is a rare and potentially
lethal disease characterized by fragmentary hemolysis, moderate-to-severe …

Open ADAMTS13, induced by antibodies, is a biomarker for subclinical immune-mediated thrombotic thrombocytopenic purpura

E Roose, AS Schelpe, E Tellier… - Blood, The Journal …, 2020 - ashpublications.org
Recently, we showed that ADAMTS13 circulates in an open conformation during the acute
phase of immune-mediated thrombotic thrombocytopenic purpura (iTTP). Although the …

Current and future perspectives on ADAMTS13 and thrombotic thrombocytopenic purpura

E Roose, BS Joly - Hämostaseologie, 2020 - thieme-connect.com
Thrombotic thrombocytopenic purpura (TTP) is a rare, relapsing, and life-threatening
disorder with an annual incidence of 10 cases per million people. TTP is a thrombotic …

Guidelines on the laboratory aspects of assays used in haemostasis and thrombosis

P Baker, S Platton, C Gibson, E Gray… - British journal of …, 2020 - pubmed.ncbi.nlm.nih.gov
Guidelines on the laboratory aspects of assays used in haemostasis and thrombosis Guidelines
on the laboratory aspects of assays used in haemostasis and thrombosis Br J Haematol. 2020 …

Assessment and monitoring of patients with immune-mediated thrombotic thrombocytopenic purpura (iTTP): strategies to improve outcomes

S Kucukyurt, AE Eskazan - Journal of Blood Medicine, 2020 - Taylor & Francis
Background Acquired or immune-mediated TTP (iTTP) is a life-threatening thrombotic
microangiopathy, characterized by the presence of microangiopathic hemolytic anemia and …

Опыт применения российского биоаналога оригинального препарата экулизумаба для лечения больных атипичным гемолитико-уремическим синдромом

ЮВ Лаврищева, АА Яковенко… - Терапевтический архив, 2020 - cyberleninka.ru
Атипичный гемолитико-уремический синдром (аГУС)-хроническое системное
заболевание генетической природы, в основе которого лежит неконтролируемая …

Managing pregnancy-associated clinical emergencies in systemic lupus erythematosus: a case-based approach

M Choi, E Butler, A Clarke, LP Girard… - Expert Review of …, 2020 - Taylor & Francis
Introduction: Systemic lupus erythematosus (SLE)-related thrombocytopenia during
pregnancy and the postpartum period have been associated with adverse pregnancy …

A genome-wide association study in chronic thromboembolic pulmonary hypertension and the ADAMTS13-VWF axis

M Newnham - 2020 - repository.cam.ac.uk
Chronic thromboembolic pulmonary hypertension (CTEPH) is an important and severe
consequence of pulmonary embolism (PE), resulting from failure of thrombus resolution …

The experience of using the Russian biosimilar of the original drug eculizumab for the treatment of patients with atypical hemolytic-uremic syndrome

YV Lavrishcheva, AA Yakovenko, DA Kudlai - Terapevticheskii arkhiv, 2020 - ter-arkhiv.ru
Atypical hemolytic-uremic syndrome (aHUS) is a chronic systemic disease of a genetic
nature, which is based on uncontrolled activation of the alternative complement pathway …

Chronic Neurological Impairment in Patients with Thrombotic Thrombocytopenic Purpura: Findings in Quantitative MRI

J Hamilton - 2020 - search.proquest.com
Thrombotic thrombocytopenic purpura (TTP) is a life-threatening, microvascular blood
disorder that affects approximately 5 people per million per year. The disorder is …