Results 111 to 120 of about 39,585 (213)

MALIGNANT ARTERIAL HYPERTENSION IN A CHILD WITH ATYPICAL HEMOLYTIC-UREMIC SYNDROME

Мать и дитя в Кузбассе, 2022
Atypical hemolytic-uremic syndrome (aHUS) is a rare orphan disease. In the Altai Region, two cases of aHUS among children have been recorded. The disease is characterized by a severe course with high mortality, frequent development of complications and a
Олеся Алексеевна Зенченко, Евгений Васильевич Скударнов, Галина Ивановна Выходцева, Юлия Васильевна Волкова, Людмила Михайловна Новикова, Ольга Михайловна Малюга   +5 more
doaj  

Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains [PDF]

, 2007
Matthew C. Pickering, Elena Goicoechea de Jorge, Rubén Martínez-Barricarte, Sergio Recalde, Alfredo García‐Layana, Kirsten L. Rose, Jill Moss, Mark Walport, H. Terence Cook, Santiago Rodrı́guez de Córdoba, Marina Botto   +10 more
openalex   +1 more source

The Functional State of Neutrophils Correlates With the Severity of Renal Dysfunction in Children With Hemolytic Uremic Syndrome [PDF]

, 2007
Gabriela Fernández, Sonia Gómez, María Victoria Carballo Calero Ramos, Leticia V. Bentancor, Romina Jimena Fernández‐Brando, Verónica I. Landoni, Laura López, Flavia B. Ramírez, Mario Díaz, Marta Alduncín, Irene Grimoldi, Ramón Exeni, Martı́n A. Isturiz, Marina S. Palermo   +13 more
openalex   +1 more source

The Janus-faced nature of complement in hemodialysis: interplay between complement, inflammation, and bioincompatibility unveiling a self-amplifying loop contributing to organ damage

Frontiers in Nephrology
In hemodialysis (HD), complement activation, bioincompatibility, and inflammation are intricately intertwined. In the 1970s, as HD became a routine therapy, the observation of complement pathway activation and transient leukopenia by cellulosic dialysis ...
Bernard Canaud, Peter Stenvinkel, Rebecca Scheiwe, Sonja Steppan, Sudhir Bowry, Giuseppe Castellano   +5 more
doaj   +1 more source

Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom [PDF]

, 2010
,, Goodship, Tim H J, Machin, Sam, Taylor, C Mark, Wigmore, Stephen J   +4 more
core   +1 more source

Should eculizumab be discontinued in patients with atypical hemolytic uremic syndrome? [PDF]

, 2017
Eva Rodríguez, Clara Barrios, María José Soler   +2 more
openalex   +1 more source

Prepartum Eculizumab for prevention of atypical hemolytic uremic syndrome: A case report [PDF]

, 2016
Gianluigi Ardissino, Giulia Maria Baffero, Manuela Wally Ossola, Benedetta Agnoli, Francesca Tel, Michela Perrone, Stefania Salardi, Martina Sgarbanti, Martina Sgarbanti   +8 more
openalex   +1 more source

SP218ANALYSIS OF SERUM ACTIVITY OF ADAMTS13 OF SHIGA TOXIN-PRODUCING ESCHERICHIA COLI (STEC) HEMOLYTIC UREMIC SYNDROME (HUS) IN CHILDREN [PDF]

, 2016
O.M. Orlova, Khadizha Emirova, П. В. Авдонин, Evgeniya Tolstova, Tatiana Pancratenko, Tatiana Abaseeva, Alexandr Muzurov, Alexandr Burov, Alexandr Burov   +8 more
openalex   +1 more source

Hemolytic Uremic Syndrome Associated with Pneumococcal Pneumonia. A Case Report

Medisur, 2013
Hemolytic uremic syndrome is a condition characterized by hemolytic microangiopathic anemia, thrombocytopenia and acute renal failure. In its classic form it is associated with diarrhea and it has a good prognosis.
Ariel Efrén Uriarte Méndez, Andrés Prieto Apesteguía, Jesús Vila Díaz, Jorge Luis Capote Padrón, Kendrie Villavicencio Cardoso, Alnilam Fernández González   +5 more
doaj   +2 more sources

A Case of Carfilzomib-Induced Atypical Hemolytic Uremic Syndrome

Annals of Internal Medicine: Clinical Cases
Atypical hemolytic uremic syndrome (aHUS) is a rare non-Shiga toxin thrombotic microangiopathy caused by uncontrolled activation of the alternative complement pathway.
Kwasi Opare-Addo, Sammudeen Ibrahim, Basilio Addo, Jorge Chancay Rodriguez   +3 more
doaj   +1 more source