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C Antignac

Showing results (31-40 of 103) with videos related to

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American Journal of Human Genetics|March 11, 2000
Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisisS Saunier, J Calado, F Benessy, et al.
Journal Francais D'Ophtalmologie|March 8, 2000
[Pigmentosum retinis and tubulo-interstitial nephronophtisis in Sensenbrenner syndrome: a case report]C Costet, F Betis, E Bérard, et al.
Advances in Experimental Medicine and Biology|February 23, 1999
Mutations in the vasopressin V2 receptor and aquaporin-2 genes in twelve families with congenital nephrogenic diabetes insipidusR Vargas-Poussou, L Forestier, M D Dautzenberg, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 16, 1998
Diffuse leiomyomatosis of the esophagus: disorder of cell-matrix interaction?P Thorner, L Heidet, F Moreno Merlo, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1984
[Captopril treatment of arterial hypertension in children after renal transplantation]M F Gagnadoux, C Antignac, J L Bacri, et al.
Clinical Nephrology|July 1, 1988
De novo membranous glomerulonephritis in renal allografts in childrenC Antignac, N Hinglais, M C Gubler, et al.
Pediatric Nephrology (Berlin, Germany)|April 1, 1996
Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish populationA Fuchshuber, P Niaudet, O Gribouval, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1985
[Diffuse arterial calcified elastopathy]C Antignac, M C Gubler, L Garel, et al.
European Journal of Ophthalmology|July 9, 2008
Bilateral macular detachment caused by bilateral optic nerve malformation in a papillorenal syndrome due to a new PAX2 mutationS Samimi, C Antignac, C Combe, et al.
Human Molecular Genetics|April 1, 1995
Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndromeB Knebelmann, L Forestier, L Drouot, et al.
Pageof 11

Showing results (31-40 of 103) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|March 11, 2000
Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisisS Saunier, J Calado, F Benessy, et al.
Journal Francais D'Ophtalmologie|March 8, 2000
[Pigmentosum retinis and tubulo-interstitial nephronophtisis in Sensenbrenner syndrome: a case report]C Costet, F Betis, E Bérard, et al.
Advances in Experimental Medicine and Biology|February 23, 1999
Mutations in the vasopressin V2 receptor and aquaporin-2 genes in twelve families with congenital nephrogenic diabetes insipidusR Vargas-Poussou, L Forestier, M D Dautzenberg, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 16, 1998
Diffuse leiomyomatosis of the esophagus: disorder of cell-matrix interaction?P Thorner, L Heidet, F Moreno Merlo, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1984
[Captopril treatment of arterial hypertension in children after renal transplantation]M F Gagnadoux, C Antignac, J L Bacri, et al.
Clinical Nephrology|July 1, 1988
De novo membranous glomerulonephritis in renal allografts in childrenC Antignac, N Hinglais, M C Gubler, et al.
Pediatric Nephrology (Berlin, Germany)|April 1, 1996
Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish populationA Fuchshuber, P Niaudet, O Gribouval, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1985
[Diffuse arterial calcified elastopathy]C Antignac, M C Gubler, L Garel, et al.
European Journal of Ophthalmology|July 9, 2008
Bilateral macular detachment caused by bilateral optic nerve malformation in a papillorenal syndrome due to a new PAX2 mutationS Samimi, C Antignac, C Combe, et al.
Human Molecular Genetics|April 1, 1995
Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndromeB Knebelmann, L Forestier, L Drouot, et al.
Pageof 11