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Emmanuelle Plaisier

Showing results (41-50 of 66) with videos related to

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Human Pathology|January 9, 2018
Decreased expression of megalin and cubilin and altered mitochondrial activity in tenofovir nephrotoxicityAlexandre Cez, Isabelle Brocheriou, François-Xavier Lescure, et al.
Journal of the American Society of Nephrology : JASN|June 30, 2016
Rituximab for Severe Membranous Nephropathy: A 6-Month Trial with Extended Follow-UpKarine Dahan, Hanna Debiec, Emmanuelle Plaisier, et al.
Talanta|January 22, 2017
Multiplex and accurate quantification of acute kidney injury biomarker candidates in urine using Protein Standard Absolute Quantification (PSAQ) and targeted proteomicsBenoît Gilquin, Mathilde Louwagie, Michel Jaquinod, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 10, 2019
Prevalence of tubulopathy and association with renal function loss in HIV-infected patientsFrançois-Xavier Lescure, Soraya Fellahi, Gilles Pialoux, et al.
Neurobiology of Disease|January 7, 2017
Col4a1 mutation generates vascular abnormalities correlated with neuronal damage in a mouse model of HANAC syndromeAlix Trouillet, Henri Lorach, Elisabeth Dubus, et al.
Kidney International Reports|September 11, 2018
Apolipoprotein CII Amyloidosis Associated With p.Lys41Thr MutationSanjeev Sethi, Surendra Dasari, Emmanuelle Plaisier, et al.
Nephron Extra|April 4, 2012
Rituximab treatment for membranous nephropathy: a French clinical and serological retrospective study of 28 patientsPierre-Antoine Michel, Karine Dahan, Pierre-Yves Ancel, et al.
Medicine|November 14, 2009
Clinical and morphologic spectrum of renal involvement in patients with mixed cryoglobulinemia without evidence of hepatitis C virus infectionMarie Matignon, Patrice Cacoub, Magali Colombat, et al.
The New England Journal of Medicine|December 28, 2007
COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle crampsEmmanuelle Plaisier, Olivier Gribouval, Sonia Alamowitch, et al.
Journal of the American Society of Nephrology : JASN|May 24, 2014
Improving mutation screening in familial hematuric nephropathies through next generation sequencingVincent Morinière, Karin Dahan, Pascale Hilbert, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Human Pathology|January 9, 2018
Decreased expression of megalin and cubilin and altered mitochondrial activity in tenofovir nephrotoxicityAlexandre Cez, Isabelle Brocheriou, François-Xavier Lescure, et al.
Journal of the American Society of Nephrology : JASN|June 30, 2016
Rituximab for Severe Membranous Nephropathy: A 6-Month Trial with Extended Follow-UpKarine Dahan, Hanna Debiec, Emmanuelle Plaisier, et al.
Talanta|January 22, 2017
Multiplex and accurate quantification of acute kidney injury biomarker candidates in urine using Protein Standard Absolute Quantification (PSAQ) and targeted proteomicsBenoît Gilquin, Mathilde Louwagie, Michel Jaquinod, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 10, 2019
Prevalence of tubulopathy and association with renal function loss in HIV-infected patientsFrançois-Xavier Lescure, Soraya Fellahi, Gilles Pialoux, et al.
Neurobiology of Disease|January 7, 2017
Col4a1 mutation generates vascular abnormalities correlated with neuronal damage in a mouse model of HANAC syndromeAlix Trouillet, Henri Lorach, Elisabeth Dubus, et al.
Kidney International Reports|September 11, 2018
Apolipoprotein CII Amyloidosis Associated With p.Lys41Thr MutationSanjeev Sethi, Surendra Dasari, Emmanuelle Plaisier, et al.
Nephron Extra|April 4, 2012
Rituximab treatment for membranous nephropathy: a French clinical and serological retrospective study of 28 patientsPierre-Antoine Michel, Karine Dahan, Pierre-Yves Ancel, et al.
Medicine|November 14, 2009
Clinical and morphologic spectrum of renal involvement in patients with mixed cryoglobulinemia without evidence of hepatitis C virus infectionMarie Matignon, Patrice Cacoub, Magali Colombat, et al.
The New England Journal of Medicine|December 28, 2007
COL4A1 mutations and hereditary angiopathy, nephropathy, aneurysms, and muscle crampsEmmanuelle Plaisier, Olivier Gribouval, Sonia Alamowitch, et al.
Journal of the American Society of Nephrology : JASN|May 24, 2014
Improving mutation screening in familial hematuric nephropathies through next generation sequencingVincent Morinière, Karin Dahan, Pascale Hilbert, et al.
Pageof 7