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Corinne Antignac

Showing results (11-20 of 215) with videos related to

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Medecine Sciences : M/S|March 11, 2006
[Mutations in genes in the renin-angiotensin system and renal tubular dysgenesis]Olivier Gribouval, Corinne Antignac, Marie-Claire Gubler
Stem Cell Research|June 26, 2020
Generation of an induced pluripotent stem cell (iPSC) line (IMAGINi007) from a patient with steroid-resistant nephrotic syndrome carrying the homozygous p.R138Q mutation in the podocin-encoding NPHS2 geneGiulia Menara, Nathalie Lefort, Corinne Antignac, et al.
Annals of the New York Academy of Sciences|October 26, 2010
Hereditary kidney diseases: highlighting the importance of classical Mendelian phenotypesGeneviève Benoit, Eduardo Machuca, Laurence Heidet, et al.
Nephrologie & Therapeutique|April 15, 2019
APOL1 risk genotype in Europe: Data in patients with focal segmental glomerulosclerosis and after renal transplantationAude Servais, Olivier Gribouval, François Gaillard, et al.
NDT Plus|May 8, 2015
What is the risk that I will transmit nephrotic syndrome to my children, Doctor?Geneviève Benoit, Vincent Morinière, Marina Charbit, et al.
Pediatric Nephrology (Berlin, Germany)|December 3, 2015
Macroscopic hematuria with normal renal biopsy-following the chain to the diagnosis: QuestionsJeanne Truong, Georges Deschênes, Patrice Callard, et al.
Biochemical and Biophysical Research Communications|October 7, 2004
Glutathione precursors replenish decreased glutathione pool in cystinotic cell linesMarie Chol, Nathalie Nevo, Stéphanie Cherqui, et al.
European Journal of Human Genetics : EJHG|September 19, 2013
Clinical utility gene card for: cystinosisElena Levtchenko, Lambertus van den Heuvel, Francesco Emma, et al.
Kidney International|June 4, 2026
From Dysphagia to Kidney Disease: Alport Syndrome with LeiomyomatosisIdris Boudhabhay, Corinne Antignac, Sylvain Bodard, et al.
Pediatric Nephrology (Berlin, Germany)|December 3, 2015
Macroscopic hematuria with normal renal biopsy-following the chain to the diagnosis: AnswersJeanne Truong, Georges Deschênes, Patrice Callard, et al.
Pageof 22

Showing results (11-20 of 215) with videos related to

Sort By:
Pageof 22
Medecine Sciences : M/S|March 11, 2006
[Mutations in genes in the renin-angiotensin system and renal tubular dysgenesis]Olivier Gribouval, Corinne Antignac, Marie-Claire Gubler
Stem Cell Research|June 26, 2020
Generation of an induced pluripotent stem cell (iPSC) line (IMAGINi007) from a patient with steroid-resistant nephrotic syndrome carrying the homozygous p.R138Q mutation in the podocin-encoding NPHS2 geneGiulia Menara, Nathalie Lefort, Corinne Antignac, et al.
Annals of the New York Academy of Sciences|October 26, 2010
Hereditary kidney diseases: highlighting the importance of classical Mendelian phenotypesGeneviève Benoit, Eduardo Machuca, Laurence Heidet, et al.
Nephrologie & Therapeutique|April 15, 2019
APOL1 risk genotype in Europe: Data in patients with focal segmental glomerulosclerosis and after renal transplantationAude Servais, Olivier Gribouval, François Gaillard, et al.
NDT Plus|May 8, 2015
What is the risk that I will transmit nephrotic syndrome to my children, Doctor?Geneviève Benoit, Vincent Morinière, Marina Charbit, et al.
Pediatric Nephrology (Berlin, Germany)|December 3, 2015
Macroscopic hematuria with normal renal biopsy-following the chain to the diagnosis: QuestionsJeanne Truong, Georges Deschênes, Patrice Callard, et al.
Biochemical and Biophysical Research Communications|October 7, 2004
Glutathione precursors replenish decreased glutathione pool in cystinotic cell linesMarie Chol, Nathalie Nevo, Stéphanie Cherqui, et al.
European Journal of Human Genetics : EJHG|September 19, 2013
Clinical utility gene card for: cystinosisElena Levtchenko, Lambertus van den Heuvel, Francesco Emma, et al.
Kidney International|June 4, 2026
From Dysphagia to Kidney Disease: Alport Syndrome with LeiomyomatosisIdris Boudhabhay, Corinne Antignac, Sylvain Bodard, et al.
Pediatric Nephrology (Berlin, Germany)|December 3, 2015
Macroscopic hematuria with normal renal biopsy-following the chain to the diagnosis: AnswersJeanne Truong, Georges Deschênes, Patrice Callard, et al.
Pageof 22