Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Laure Collard"'
Autor:
Evelien Snauwaert, Stefanie De Buyser, An Desloovere, Wim Van Biesen, Ann Raes, Griet Glorieux, Laure Collard, Koen Van Hoeck, Maria Van Dyck, Nathalie Godefroid, Johan Vande Walle, Sunny Eloot
Publikováno v:
Toxins, Vol 16, Iss 8, p 349 (2024)
To promote improved trial design in upcoming randomized clinical trials in childhood chronic kidney disease (CKD), insight in the within- and inter-patient variability of uremic toxins with its nutritional, treatment- and patient-related confounding
Externí odkaz:
https://doaj.org/article/0bfac0465d854f04b277e2546986042d
Autor:
Elisabeth L. Metry, Sander F. Garrelfs, Hessel Peters-Sengers, Sally-Anne Hulton, Cecile Acquaviva, Justine Bacchetta, Bodo B. Beck, Laure Collard, Georges Deschênes, Casper Franssen, Markus J. Kemper, Graham W. Lipkin, Giorgia Mandrile, Nilufar Mohebbi, Shabbir H. Moochhala, Michiel J.S. Oosterveld, Larisa Prikhodina, Bernd Hoppe, Pierre Cochat, Jaap W. Groothoff
Publikováno v:
Kidney International Reports, Vol 7, Iss 2, Pp 210-220 (2022)
Introduction: In primary hyperoxaluria type 1 (PH1), oxalate overproduction frequently causes kidney stones, nephrocalcinosis, and kidney failure. As PH1 is caused by a congenital liver enzyme defect, combined liver–kidney transplantation (CLKT) ha
Externí odkaz:
https://doaj.org/article/b741147b79de4dfb83077c53198d2dea
Autor:
Evelien Snauwaert, Els Holvoet, Wim Van Biesen, Ann Raes, Griet Glorieux, Johan Vande Walle, Sanne Roels, Raymond Vanholder, Varvara Askiti, Karolis Azukaitis, Aysun Bayazit, Nur Canpolat, Michel Fischbach, Nathalie Godefroid, Saoussen Krid, Mieczyslaw Litwin, Lukasz Obrycki, Fabio Paglialonga, Bruno Ranchin, Charlotte Samaille, Franz Schaefer, Claus Peter Schmitt, Brankica Spasojevic, Constantinos J. Stefanidis, Maria Van Dyck, Koen Van Hoeck, Laure Collard, Sunny Eloot, Rukshana Shroff
Publikováno v:
Toxins, Vol 11, Iss 4, p 235 (2019)
Protein-bound uremic toxins (PBUTs) play a role in the multisystem disease that children on hemodialysis (HD) are facing, but little is known about their levels and protein binding (%PB). In this study, we evaluated the levels and %PB of six PBUTs cr
Externí odkaz:
https://doaj.org/article/49bdd5457df04f20994d3eb31259d206
Autor:
Anne-Laure Collard
Publikováno v:
Espace populations sociétés, Vol 2020 (2021)
In 2014, the vine protection devices of La Londe-les-Maures are carried away, ripped off by unprecedented floods on the territory. The winegrowers quickly worked to rebuild them, reproducing the domestication of rivers initiated by their predecessors
Externí odkaz:
https://doaj.org/article/24cd69885e3e4e1395aab656fc60754b
Autor:
Lisa J. Deesker, Sander F. Garrelfs, Giorgia Mandrile, Michiel J.S. Oosterveld, Pierre Cochat, Georges Deschênes, Jérôme Harambat, Sally-Anne Hulton, Asheeta Gupta, Bernd Hoppe, Bodo B. Beck, Laure Collard, Rezan Topaloglu, Larisa Prikhodina, Eduardo Salido, Thomas Neuhaus, Jaap W. Groothoff, Justine Bacchetta
Publikováno v:
Kidney International Reports, 7(7), 1608-1618. Elsevier Inc.
Introduction: Infantile oxalosis is the most severe form of primary hyperoxaluria type 1 (PH1), with onset of end-stage kidney disease (ESKD) during infancy. We aimed to analyze the outcome of these patients as our current understanding is limited ow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64c422b749989458ea98a6fdaf2d557f
https://doi.org/10.1016/j.ekir.2022.04.012
https://doi.org/10.1016/j.ekir.2022.04.012
Autor:
Elke De Bruyne, Lore Willem, Koen Van Hoeck, Sarah Reynaert, Sylvie Vankerckhove, Brigitte Adams, Stéphanie Leroi, Laure Collard, Aline Michaux, Nathalie Godefroid, Djalila Mekahli, Noël Knops, Sunny Eloot, Ann Raes, Johan Vande Walle, Eline Van Hoecke, Evelien Snauwaert, Elena Levtchenko
Publikováno v:
Pediatric nephrology
Background This cross-sectional study investigated quality of life (QoL) and illness-related parental stress in children with kidney diseases by (1) comparing mean levels of these two variables between several kidney disease categories; (2) exploring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec8bc610dae314d759b1b43fd26dd523
https://doi.org/10.1007/s00467-023-05911-3
https://doi.org/10.1007/s00467-023-05911-3
Autor:
Gema Ariceta, Laure Collard, Saoussen Abroug, Shabbir H. Moochhala, Edward Gould, Abir Boussetta, Mohamed Ben Hmida, Sudarsana De, Tracy E. Hunley, Faical Jarraya, Gloria Fraga, Ana Banos, Elisabeth Lindner, Bastian Dehmel, Gesa Schalk
Publikováno v:
PEDIATRIC NEPHROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Scientia
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Scientia
Background Primary hyperoxalurias (PHs) are rare genetic diseases that increase the endogenous level of oxalate, a waste metabolite excreted predominantly by the kidneys and also the gut. Treatments aim to improve oxalate excretion, or reduce oxalate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81f1afa0cbbe74e917bec91eb873c8a3
https://doi.org/10.1007/s00467-022-05591-5
https://doi.org/10.1007/s00467-022-05591-5
Autor:
Markus J. Kemper, Georges Deschênes, Laure Collard, Larisa Prikhodina, Hessel Peters-Sengers, Sander F. Garrelfs, Pierre Cochat, Justine Bacchetta, Elisabeth L. Metry, Shabbir H. Moochhala, Jaap W. Groothoff, Sally-Anne Hulton, Casper F. M. Franssen, Graham Lipkin, Nilufar Mohebbi, Cécile Acquaviva, Giorgia Mandrile, Bernd Hoppe, Michiel J. S. Oosterveld, Bodo B. Beck
Publikováno v:
Kidney International Reports, Vol 7, Iss 2, Pp 210-220 (2022)
Kidney International Reports, 7(2), 210-220. ELSEVIER SCIENCE INC
Kidney International Reports, 7(2), 210-220. Elsevier Inc.
Kidney International Reports, 7(2), 210-220. ELSEVIER SCIENCE INC
Kidney International Reports, 7(2), 210-220. Elsevier Inc.
Introduction: In primary hyperoxaluria type 1 (PH1), oxalate overproduction frequently causes kidney stones, nephrocalcinosis, and kidney failure. As PH1 is caused by a congenital liver enzyme defect, combined liver–kidney transplantation (CLKT) ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeb680725496cbc4e095b95a78e6eec0
http://www.sciencedirect.com/science/article/pii/S2468024921015126
http://www.sciencedirect.com/science/article/pii/S2468024921015126
Autor:
Nassim Ait-Mouheb, Sami Bouarfa, Anne-Laure Collard, Christelle Guigui, Jérôme Labille, Rémi Lombard-Latune, Jean-Denis Mathias, Bruno Molle, Pascal Molle, Jaime Nivala, Dominique Patureau, Alain Rapaport, Nicolas Roche, Mathieu Sperandio, Severine Tomas, Jérôme Harmand
Publikováno v:
MATEC Web of Conferences
MATEC Web of Conferences, 2023, 379, ⟨10.1051/matecconf/202337908001⟩
MATEC Web of Conferences, 2023, 379, ⟨10.1051/matecconf/202337908001⟩
International audience; The reuse of wastewater aims to mobilize and treat, for certain uses and under certain conditions, water that has already been used. Rather than discharging wastewater into the natural environment, this practice aims to recove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b78c1b9b5b98339c41de0658bb92754
https://amu.hal.science/hal-04099633/file/matecconf_sfgp23_08001.pdf
https://amu.hal.science/hal-04099633/file/matecconf_sfgp23_08001.pdf
The added value of using computer modeling to study the relationship between water and society is not always shared between modelers and other disciplines in the humanities such as qualitative sociology. Although both can share the same research obje
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98cf1f3cfc74f831de3b6e6b809f1642
https://doi.org/10.5194/iahs2022-222
https://doi.org/10.5194/iahs2022-222