Dosing algorithm for complement inhibitor

S Jodele, T Fukuda, K Mizuno - US Patent App. 18/499,353, 2024 - Google Patents
Described are methods and systems for the treatment of individuals having a disorder
characterized by complement system dysregulation. The described methods and systems …

Compositions for interferon blockade and methods of using same

S Jodele - US Patent 12,037,389, 2024 - Google Patents
Disclosed are compositions that may include one or more inhibitors of interferon activity for
the treatment of a disease state, for example, a disorder associated with increased interferon …

thrombotic microangiopathy

VV Voitsekhovskii, LB Filatov, AV Pivnik, PV Avdonin… - old.bloodjournal.ru
This paper presents a literature review on state of art in issues of etiology, pathogenesis,
clinical features and diagnosis of thrombotic thrombocytopenic purpura (ТТP or …

congenital thrombotic thrombocytopenic purpura

VV Voitsekhovskii, LB Filatov, AV Pivnik, PV Avdonin… - old.bloodjournal.ru
This paper presents a literature review on state of art in issues of etiology, pathogenesis,
clinical features and diagnosis of thrombotic thrombocytopenic purpura (ТТP or …

microangiopathic hemolytic anemia

VV Voitsekhovskii, LB Filatov, AV Pivnik, PV Avdonin… - old.bloodjournal.ru
This paper presents a literature review on state of art in issues of etiology, pathogenesis,
clinical features and diagnosis of thrombotic thrombocytopenic purpura (ТТP or …

Eculizumab como opción terapéutica en paciente con crisis renal esclerodérmica asociada a síndrome hemolítico urémico

AM Bucheli, SM Alfonso, LMS Rivera - Revista Colombiana de …, 2020 - Elsevier
La crisis renal esclerodérmica (CRS) es una manifestación rara de la esclerosis sistémica
(ES). Se presenta como hipertensión arterial de nuevo inicio, empeoramiento o aceleración …

thrombotic thrombocytopenic purpura

VV Voitsekhovskii, LB Filatov, AV Pivnik, PV Avdonin… - old.bloodjournal.ru
This paper presents a literature review on state of art in issues of etiology, pathogenesis,
clinical features and diagnosis of thrombotic thrombocytopenic purpura (ТТP or …

Upshaw-Schulman syndrome

VV Voitsekhovskii, LB Filatov, AV Pivnik, PV Avdonin… - old.bloodjournal.ru
This paper presents a literature review on state of art in issues of etiology, pathogenesis,
clinical features and diagnosis of thrombotic thrombocytopenic purpura (ТТP or …

HELLP syndrome

VV Voitsekhovskii, LB Filatov, AV Pivnik, PV Avdonin… - old.bloodjournal.ru
This paper presents a literature review on state of art in issues of etiology, pathogenesis,
clinical features and diagnosis of thrombotic thrombocytopenic purpura (ТТP or …

Does severe ADAMTS13 deficiency in thrombotic microangiopathy rule out complement-mediated atypical hemolytic uremic syndrome

V Arumugam, R Bhowmick, I Agarwal… - Saudi Journal of …, 2019 - journals.lww.com
In evaluating a patient with thrombotic microangiopathy (TMA), it is necessary to rule out
thrombotic thrombocytopenic purpura before a diagnosis of atypical hemolytic uremic …