Results 21 to 30 of about 13,380 (189)

Eculizumab in gemcitabine-induced thrombotic microangiopathy: experience of the French thrombotic microangiopathies reference centre

open access: yesBMC Nephrology, 2021
Background Gemcitabine is a broadly prescribed chemotherapy, the use of which can be limited by renal adverse events, including thrombotic microangiopathy (TMA). Methods This study evaluated the efficacy of eculizumab, a monoclonal antibody targeting the
Maximilien Grall   +14 more
doaj   +1 more source

Meningococcemia in a vaccinated child receiving eculizumab and review of the literature

open access: yesThe Turkish Journal of Pediatrics, 2023
Background. Atypical hemolytic uremic syndrome (aHUS) is a rare and severe disease characterized by uncontrolled activation and dysregulation of the alternative complement pathway and development of thrombotic microangiopathy. Eculizumab, which is
Diana Üçkardeş   +5 more
doaj   +1 more source

Comparison of demographic and outcome in the Brazilian aHUS cohort patients according to the treatment (without the use of Eculizumab, prophylactic Eculizumab, and Eculizumab treatment).

open access: yes, 2021
Comparison of demographic and outcome in the Brazilian aHUS cohort patients according to the treatment (without the use of Eculizumab, prophylactic Eculizumab, and Eculizumab treatment).
Hong Si Nga (4592092)   +9 more
core   +1 more source

Eculizumab hepatotoxicity in pediatric aHUS. [PDF]

open access: yes, 2015
BACKGROUND Eculizumab is a humanized anti-C5 antibody approved for the treatment of atypical hemolytic uremic syndrome (aHUS). Its use is increasing in children following reports of its safety and efficacy.
Hayes, Wesley   +5 more
core   +2 more sources

Consistent improvement with eculizumab across muscle groups in myasthenia gravis [PDF]

open access: yes, 2020
Objective: To assess whether eculizumab, a terminal complement inhibitor, improves patient- and physician-reported outcomes (evaluated using the myasthenia gravis activities of daily living profile and the quantitative myasthenia gravis scale ...
Patrick K.   +501 more
core   +5 more sources

Aplicaciones terapéuticas del eculizumab [PDF]

open access: yes, 2022
Introducción: El eculizumab es un anticuerpo monoclonal de tipo IgG diseñado para el tratamiento de la hemoglobinuria paroxística nocturna (HPN), en el que su diana farmacológica forma parte del sistema del complemento.
Campos González, Natalia   +11 more
core   +1 more source

Atypical haemolytic uraemic syndrome in the eculizumab era: presentation, response to treatment and evaluation of an eculizumab withdrawal strategy [PDF]

open access: yes, 2019
The complement inhibitor, eculizumab, has revolutionised the management of atypical haemolytic uraemic syndrome (aHUS), although the optimum treatment duration is debated.
Shah, R   +4 more
core   +2 more sources

Eculizumab in Pediatric Kidney Disorders: A Review: Eculizumab in Kidney Disorders

open access: yes, 2022
Eculizumab is a humanized monoclonal antibody targeting the C5 (complement 5) memberof complement proteins and inhibiting its cleavage to C5a and C5b. Eculizumab has beenproven to be effective in a wide array of nephrologic, neurologic, and hematologic ...
Mohkam, Masoumeh   +6 more
core   +1 more source

Case Report: Variable Pharmacokinetic Profile of Eculizumab in an aHUS Patient

open access: yesFrontiers in Immunology, 2021
BackgroundWith the introduction of eculizumab, a C5-inhibitor, morbidity and mortality improved significantly for patients with atypical hemolytic uremic syndrome (aHUS).
Romy N. Bouwmeester   +8 more
doaj   +1 more source

Eculizumab dosing in infants

open access: yesIndian Journal of Nephrology, 2018
Eculizumab is the therapy of choice for patients with atypical hemolytic uremic syndrome (aHUS). Dosing recommendations stem from two trials: one retrospective trial (19 children and 5 infants) and one prospective trial (22 patients and 5 infants). This case report highlights the need for more precise dosing recommendations in children, particularly in
Kobrzynski, M   +3 more
openaire   +3 more sources

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