Results 81 to 90 of about 8,784 (177)

ATYPICAL HEMOLYTIC-UREMIC SYNDROME IN THE FEMALE PATIENT WITH CONCURRENT MENOMETRORRHAGIA (clinical case)

Вестник анестезиологии и реаниматологии, 2018
The article describes the follow-up over the development of atypical hemolytic-uremic syndrome in the female patient suffering menometrorrhagia which manifested with concurrent metrorrhagia and was accompanied with acute renal failure.
A. V. Pyregov, T. A. Fedorova, A. Yu. Korolev, K. I. Grischuk   +3 more
doaj   +1 more source

Pathogenic Variants in Complement Genes and Risk of Atypical Hemolytic Uremic Syndrome Relapse after Eculizumab Discontinuation

, 2016
International audienceBACKGROUND AND OBJECTIVES: The complement inhibitor eculizumab has dramatically improved the outcome of atypical hemolytic uremic syndrome.
Delmas, Yahsou, Cailliez, Mathilde, Rafat, Cédric, Karras, Alexandre, Chantal Loirat, Cédric Rafat, Delmas, Y., Valérie Châtelet, Hogan, Julien, Barbet, Christelle, Christelle Barbet, Chatelet, V., Loirat, C., Frémeaux-Bacchi, Véronique, Makdassi, Raifah, Servais, Aude, Véronique Frémeaux-Bacchi, Fila, Marc, François Provôt, Marc Fila, Coindre, J. P., Châtelet, Valérie, Rondeau, Eric, Provôt, François, Fila, M., Louillet, F., Cailliez, M., Karras, A., Provot, F., Julien Hogan, Feriell Louillet, Hogan, J., Mathilde Cailliez, Fakhouri, F., Yahsou Delmas, Alexandre Karras, Fakhouri, Fadi, Jean-Philippe Coindre, Loirat, Chantal, Raifah Makdassi, Rafat, C., Servais, A., Louillet, Feriell, Barbet, C., Fadi Fakhouri, Coindre, Jean-Philippe, Rondeau, E., Eric Rondeau, Fremeaux-Bacchi, V., Aude Servais, Makdassi, R.   +50 more
core   +1 more source

Atypical hemolytic uremic syndrome and mutation analysis of factor H gene in two Tunisian families

, 2010
Imen Habibi1,Imen Sfar1,Walid Ben Alaya1, Jihen Methlouthi2, Abdelkrim Ayadi2, Mounira Brahim2, Jacques Blouin3, Raoudha Dhagbouj1, Thouraya Ben Rhomdhane1, Mouna Makhlouf1, Houda Aouadi1, Saloua Ayed-Jendoubi1, Véronique Fremeaux-bacchi3 ...
et al, Walid Ben Alaya, Imen Habibi, Imen Sfar   +3 more
core  

Complement mutations in Diacylglycerol Kinase-E-associated atypical hemolytic uremic syndrome.

, 2014
32 p.-4 tab-3 fig.-2 tab. suppl.Background and objectives Atypical hemolytic uremic syndrome is characterized by vascular endothelial damage caused by complement dysregulation.
Roldán, María Luisa Justa, Rodríguez de Córdoba, Santiago, Sheila Pinto, Sánchez-Corral, Pilar, Maria Luisa Justa Roldan, Marta Adragna, Adragna, Marta, López, Laura, Laura Lopez, Hoppe, Bernd, Antonia Peña, Peña, Antonia, López-Trascasa, Margarita, Sánchez Chinchilla, Daniel, Margarita Lopez Trascasa, Daniel Sánchez Chinchilla, Santiago Rodríguez de Córdoba, Bernd Hoppe, Pilar Sánchez-Corral, Pinto, Sheila   +19 more
core   +1 more source

[Hemolytic uremic syndrome with an atypical presentation].

Revue medicale de Liege, 2010
The hemolytic uremic syndrome (HUS) is rare and of guarded prognosis in adults. It expresses a renal thrombotic microangiopathy. We report the case of a young patient whose clinical presentation and exploration make a diagnosis of HUS likely. The atypical presentation provides an opportunity not only to discuss all diagnostic elements based on recent ...
NOGUE KAMDJE, Alain, BRASSEUR, Edmond, fournier,, D'Orio, Vincenzo   +3 more
openaire   +2 more sources

Critical appraisal of eculizumab for atypical hemolytic uremic syndrome

, 2016
Lilian M Pereira Palma,1 Craig B Langman2  1Pediatric Nephrology, State University of Campinas (UNICAMP), Campinas, São Paulo, Brazil; 2The Feinberg School of Medicine, Northwestern University, and the Ann and Robert H.
Palma LMP, Langman CB
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Plasma Volume to Achieve Remission in Atypical Hemolytic Uremic Syndrome

, 2019
Introduction: Atypical hemolytic uremic syndrome (HUS) is defined as a heterogeneous group of disorders. Plasma infusion or plasma exchange is the rescue therapy for this life-threatening syndrome.
Nakysa, Hooman, Mahdaynia, Soheila, Hoseini-Shamsabadi, Rozita, Otukesh, Hasan, Nickavar, Azar   +4 more
core   +1 more source

Case report of atypical hemolytic uremic syndrome with retinal arterial and venous occlusion treated with eculizumab

, 2015
Gregory T Greenwood Nephrology Associates, PLLC, Winston-Salem, NC, USA Abstract: Atypical hemolytic uremic syndrome (aHUS) is a rare disease caused by chronic, uncontrolled activation of the alternative complement pathway, leading to thrombotic ...
Greenwood GT
core  

Atypical hemolytic uremic syndrome in first trimester pregnancy successfully treated with eculizumab

, 2017
Background Atypical hemolytic uremic syndrome is a rare disorder which is known to cause acute thrombotic microangiopathy during pregnancy with poor maternal and fetal outcomes.
Katherine Linder, Karass, M, Andries, Gabriela, Karass, Michael, Nelson, John, Pawar, Rahul, Savneek Chugh, Gabriela Andries, Srikanth Yandrapalli, Michael Karass, Linder, Katherine, Delong Liu, Pawar, R, Chugh, Savneek, John Nelson, Liu, Delong, Rahul Pawar, Yandrapalli, Srikanth   +17 more
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An adult case of atypical hemolytic uremic syndrome presented with posterior reversible encephalopathy syndrome: Successful response to late-onset eculizumab treatment

Hematology Reports, 2018
Atypical hemolytic uremic syndrome is a rare and progressive disease caused by uncontrolled alternative complement activation. Dysregulatıon of the complement activation results in thrombotic microangiopathy and multiorgan damage.
Serife Solmaz Medeni, Sinem Namdaroglu, Tugba Cetintepe, Can Ozlu, Funda Tasli, Zehra Hilal Adibelli, Oktay Bilgir, Erhan Tatar   +7 more
doaj   +1 more source