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Laurence Heidet

Showing results (1-10 of 99) with videos related to

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Nephrologie & Therapeutique|November 7, 2016
[Alport syndrome: Hereditary nephropathy associated with mutations in genes coding for type IV collagen chains]Laurence Heidet, Marie-Claire Gubler
Journal of the American Society of Nephrology : JASN|May 28, 2009
The renal lesions of Alport syndromeLaurence Heidet, Marie-Claire Gubler
Nephrologie & Therapeutique|June 2, 2007
[Alport syndrome or progressive hereditary nephritis with hearing loss]Marie-Claire Gubler, Laurence Heidet, Corinne Antignac
Kidney Medicine|April 28, 2025
Molecular Genetics Solves the Conundrum of Two Brothers Affected With Proteinuria Coming With a Very Different Flavor: A Case ReportLudwig Haydock, Guillaume Dorval, Laurence Heidet, 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.
Journal of Nephrology|July 13, 2002
Hereditary nephritis with macrothrombocytopenia: phenotypic variety and the genotypic defectCarlo Basile, Palmira Schiavone, Laurence Heidet, et al.
Medecine Sciences : M/S|March 21, 2023
[Major advances in pediatric nephro-genetics]Marguerite Hureaux, Laurence Heidet, Rosa Vargas-Poussou, et al.
Pediatric Nephrology (Berlin, Germany)|June 12, 2016
Hyperechogenic kidneys and polyhydramnios associated with HNF1B gene mutationLeire Gondra, Stéphane Décramer, Gihad E Chalouhi, et al.
Clinical Genetics|September 11, 2022
Bi-allelic pathogenic variants in ITGA8 cause slowly progressive renal disease of unknown etiologySara Gómez-Conde, Olivier Dunand, Aurélie Hummel, et al.
Clinical Kidney Journal|June 14, 2016
A wide spectrum of phenotypes in a family with renal coloboma syndrome caused by a PAX2 mutationJennifer Adam, Andrew C Browning, Daniela Vaideanu, et al.
Pageof 10

Showing results (1-10 of 99) with videos related to

Sort By:
Pageof 10
Nephrologie & Therapeutique|November 7, 2016
[Alport syndrome: Hereditary nephropathy associated with mutations in genes coding for type IV collagen chains]Laurence Heidet, Marie-Claire Gubler
Journal of the American Society of Nephrology : JASN|May 28, 2009
The renal lesions of Alport syndromeLaurence Heidet, Marie-Claire Gubler
Nephrologie & Therapeutique|June 2, 2007
[Alport syndrome or progressive hereditary nephritis with hearing loss]Marie-Claire Gubler, Laurence Heidet, Corinne Antignac
Kidney Medicine|April 28, 2025
Molecular Genetics Solves the Conundrum of Two Brothers Affected With Proteinuria Coming With a Very Different Flavor: A Case ReportLudwig Haydock, Guillaume Dorval, Laurence Heidet, 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.
Journal of Nephrology|July 13, 2002
Hereditary nephritis with macrothrombocytopenia: phenotypic variety and the genotypic defectCarlo Basile, Palmira Schiavone, Laurence Heidet, et al.
Medecine Sciences : M/S|March 21, 2023
[Major advances in pediatric nephro-genetics]Marguerite Hureaux, Laurence Heidet, Rosa Vargas-Poussou, et al.
Pediatric Nephrology (Berlin, Germany)|June 12, 2016
Hyperechogenic kidneys and polyhydramnios associated with HNF1B gene mutationLeire Gondra, Stéphane Décramer, Gihad E Chalouhi, et al.
Clinical Genetics|September 11, 2022
Bi-allelic pathogenic variants in ITGA8 cause slowly progressive renal disease of unknown etiologySara Gómez-Conde, Olivier Dunand, Aurélie Hummel, et al.
Clinical Kidney Journal|June 14, 2016
A wide spectrum of phenotypes in a family with renal coloboma syndrome caused by a PAX2 mutationJennifer Adam, Andrew C Browning, Daniela Vaideanu, et al.
Pageof 10