[HTML][HTML] Thrombotic thrombocytopenic purpura: pathophysiology, diagnosis, and management
S Sukumar, B Lämmle, SR Cataland - Journal of clinical medicine, 2021 - mdpi.com
Thrombotic thrombocytopenic purpura (TTP) is a rare thrombotic microangiopathy
characterized by microangiopathic hemolytic anemia, severe thrombocytopenia, and …
characterized by microangiopathic hemolytic anemia, severe thrombocytopenia, and …
[HTML][HTML] Platelet activation mechanisms and consequences of immune thrombocytopenia
Autoimmune disorders are often associated with low platelet count or thrombocytopenia. In
immune-induced thrombocytopenia (IIT), a common mechanism is increased platelet …
immune-induced thrombocytopenia (IIT), a common mechanism is increased platelet …
[HTML][HTML] ISTH guidelines for treatment of thrombotic thrombocytopenic purpura
Background Despite advances in treatment options for thrombotic thrombocytopenic purpura
(TTP), there are still limited high quality data to inform clinicians regarding its appropriate …
(TTP), there are still limited high quality data to inform clinicians regarding its appropriate …
[HTML][HTML] ISTH guidelines for the diagnosis of thrombotic thrombocytopenic purpura
Background Despite an increase in our understandings of pathogenesis of thrombotic
thrombocytopenic purpura (TTP), the approaches for initial diagnosis and management of …
thrombocytopenic purpura (TTP), the approaches for initial diagnosis and management of …
[HTML][HTML] Recombinant ADAMTS13 for hereditary thrombotic thrombocytopenic purpura
LM Asmis, A Serra, A Krafft, A Licht… - … England Journal of …, 2022 - Mass Medical Soc
A 27-year-old patient with a history of severe obstetrical complications and arterial
thrombosis received a diagnosis of hereditary thrombotic thrombocytopenic purpura (TTP) …
thrombosis received a diagnosis of hereditary thrombotic thrombocytopenic purpura (TTP) …
Comparison of DLin-MC3-DMA and ALC-0315 for siRNA delivery to hepatocytes and hepatic stellate cells
F Ferraresso, AW Strilchuk, LJ Juang… - Molecular …, 2022 - ACS Publications
Ionizable cationic lipids are essential for efficient in vivo delivery of RNA by lipid
nanoparticles (LNPs). DLin-MC3-DMA (MC3), ALC-0315, and SM-102 are the only ionizable …
nanoparticles (LNPs). DLin-MC3-DMA (MC3), ALC-0315, and SM-102 are the only ionizable …
Recombinant ADAMTS13 in congenital thrombotic thrombocytopenic purpura
Background Congenital thrombotic thrombocytopenic purpura (TTP) results from severe
hereditary deficiency of ADAMTS13. The efficacy and safety of recombinant ADAMTS13 and …
hereditary deficiency of ADAMTS13. The efficacy and safety of recombinant ADAMTS13 and …
Hereditary thrombotic thrombocytopenic purpura
JA Kremer Hovinga, JN George - New England Journal of …, 2019 - Mass Medical Soc
Hereditary Thrombotic Thrombocytopenic Purpura Hereditary thrombotic thrombocytopenic
purpura is an autosomal recessive disorder caused by the absence of a functional protease …
purpura is an autosomal recessive disorder caused by the absence of a functional protease …
Annual incidence and severity of acute episodes in hereditary thrombotic thrombocytopenic purpura
E Tarasco, L Bütikofer, KD Friedman… - Blood, The Journal …, 2021 - ashpublications.org
Hereditary thrombotic thrombocytopenic purpura (hTTP) is a rare thrombotic
microangiopathy characterized by severe congenital ADAMTS13 deficiency and recurring …
microangiopathy characterized by severe congenital ADAMTS13 deficiency and recurring …
Reduced ADAMTS13 activity during TTP remission is associated with stroke in TTP survivors
H Upreti, J Kasmani, K Dane… - Blood, The Journal …, 2019 - ashpublications.org
With timely and effective treatment, most patients with thrombotic thrombocytopenic purpura
(TTP) survive the acute TTP episode. In addition to the risk of relapse, TTP survivors have …
(TTP) survive the acute TTP episode. In addition to the risk of relapse, TTP survivors have …