Kolexia
Servais Aude Néphrologie
Servais Aude
Néphrologie
Hôpital Necker Enfants Malades
Paris, France
209 Activités
0 Followers
Scientifique
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Production scientifique
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{{person.topmesh1.name}} Cystinose Maladies du rein Défaillance rénale chronique Insuffisance rénale chronique Syndrome néphrotique Glomérulonéphrite membranoproliférative Glomérulonéphrite Insuffisance rénale Syndrome hémolytique et urémique atypique

Collaborateurs

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Boyer Olivia
Boyer Olivia
Hôpital Necker Enfants Malades, Paris, France
Fremeaux-Bacchi Veronique
Fremeaux-Bacchi Veronique
Hôpital Européen Georges Pompidou, Paris, France
Delmas Muriel-Yahsou
Delmas Muriel-Yahsou
Hôpital Pellegrin, Bordeaux, France
Arnoux Jean-Baptiste
Arnoux Jean-Baptiste
Hôpital Necker Enfants Malades, Paris, France

Industries

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Bouchara-Recordati
7 collaboration(s)
Dernière en 2023
Chiesi
6 collaboration(s)
Dernière en 2022
IQVIA
4 collaboration(s)
Dernière en 2021
Vertex
4 collaboration(s)
Dernière en 2022

Dernières activités

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Assessment of epidemiology and outcomes of adult patients with kidney-limited thrombotic microangiopathies.
Kidney international   29 février 2024
CYSTEA-BONE: A European, Multicenter, Prospective Clinical Study to Evaluate Cysteamine Toxicity on Human Osteoclasts. The CYSTEA-BONE Clinical Study.
Essai Clinique (Hospices Civils de Lyon)   27 février 2024
Reassuring pregnancy outcomes in women with mild COL4A3-5 related disease (Alport Syndrome) as the genetic type of disease can aid personalized counseling.
Kidney international   19 février 2024
TOTEM: Therapeutic Orientation Test in Thrombotic Microangiopathy
Essai Clinique (CHU Montpellier)   25 janvier 2024
DAILY-LUMA: Retrospective and Prospective Follow-up of Patients With Primary Hyperoxaluria Type 1 Treated With Lumasiran in France - DAILY-LUMA
Essai Clinique (Hospices Civils de Lyon)   17 janvier 2024
Influence of primary kidney disease in Chronic Kidney Disease pregnancies: pregnancy outcomes in women with COL4A3-5 related disease (Alport Syndrome)
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
Pubertal origin of growth retardation in inborn errors of protein metabolism: A longitudinal cohort study.
Molecular genetics and metabolism   01 janvier 2024
Worldwide disparities in access to treatment and investigations for nephropathic cystinosis: a 2023 perspective.
Pediatric nephrology (Berlin, Germany)   18 novembre 2023
Systemic primary carnitine deficiency induces severe arrhythmia due to shortening of QT interval.
Molecular genetics and metabolism   10 novembre 2023
Fertility Management in Cystinosis: A Clinical Perspective.
Kidney international reports   03 novembre 2023