نتایج جستجو برای: thrombotic microangiopathies

تعداد نتایج: 14502  

2013
Diana Karpman Johan Rebetz Li Wang Christoph Licht David Motto Ramesh Tati Ann-Charlotte Kristoffersson Anne-lie Ståhl

Journal: :American journal of nephrology 2015
Ahmet Emre Eskazan Ayse Salihoglu

include classical ADAMTS13 deficient acquired (primaryidiopathic) TTP, Shiga toxin-mediated TMA (also called hemolytic-uremic syndrome (HUS)), drug-mediated TMA and complement-mediated TMA (so called atypical HUS). In addition to these, systemic infections, disseminated cancer, severe preeclampsia inc. Hemolysis, Elevated Liver enzymes, and Low Platelets (HELLP) syndrome, malignant hypertension...

Journal: :Journal of the American Society of Nephrology : JASN 2016
Fengxiao Bu Nicolo Ghiringhelli Borsa Michael B Jones Erika Takanami Carla Nishimura Jill J Hauer Hela Azaiez Elizabeth A Black-Ziegelbein Nicole C Meyer Diana L Kolbe Yingyue Li Kathy Frees Michael J Schnieders Christie Thomas Carla Nester Richard J H Smith

The thrombotic microangiopathies (TMAs) and C3 glomerulopathies (C3Gs) include a spectrum of rare diseases such as atypical hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, C3GN, and dense deposit disease, which share phenotypic similarities and underlying genetic commonalities. Variants in several genes contribute to the pathogenesis of these diseases, and identification of thes...

Journal: :P & T : a peer-reviewed journal for formulary management 2010
Geno J Merli James B Groce

Thanks to their predictable pharmacokinetics and ease of use, low-molecular-weight heparins (LMWHs) have established uses in the prevention and treatment of thrombotic diseases and as a replacement for unfractionated heparin (UFH). Although LMWHs as a class have similar antithrombotic effects, they comprise a diverse group of agents with distinct biochemical and pharmacological profiles. In lig...

Journal: :Dalton transactions 2014
Jung-Ho Son Jiarui Wang William H Casey

Here we report synthesis and characterization of early transition-metal(TM)-substituted decaniobates as a continuation of our previous report of tetramethylammonium (TMA) salt of FeNb9 and NiNb9: TMA6[H2Cr(III)Nb9O28]·14H2O (1, CrNb9), TMA8[Mn(III)Nb9O28]·29H2O (2, MnNb9) and TMA7[H2Co(II)Nb9O28]·25H2O (3, CoNb9). Among the TM-substituted decaniobates, CoNb9 or NiNb9 exhibit a higher photocatal...

Journal: :Arquivos brasileiros de cardiologia 2006
Ricardo Pereira Silva Carlos Roberto Martins Rodrigues

We describe the clinical case of two siblings with different presentations of thrombotic phenomena, in which prothrombin mutation was observed.

2014
Galit Sarig

Thrombotic microangiopathies (TMAs) comprise a group of distinct disorders characterized by microangiopathic hemolytic anemia, thrombocytopenia, and microvascular thrombosis. For many years distinction between these TMAs, especially between thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS), remained purely clinical and hard to make. Recent discoveries shed light on d...

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