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Pierre Cochat

Showing results (211-220 of 225) with videos related to

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Clinical Journal of the American Society of Nephrology : CJASN|February 27, 2015
CKD and Its Risk Factors among Patients with CystinuriaCaroline Prot-Bertoye, Saïd Lebbah, Michel Daudon, et al.
Pediatric Radiology|November 16, 2017
Standardization of pediatric uroradiological terms: a multidisciplinary European glossaryPierre-Hugues Vivier, Thomas A Augdal, Fred E Avni, et al.
Journal of Pediatric Urology|November 28, 2017
Standardization of pediatric uroradiological terms: A multidisciplinary European glossaryPierre-Hugues Vivier, Thomas A Augdal, Fred E Avni, et al.
BJU International|February 26, 2019
Adverse events associated with currently used medical treatments for cystinuria and treatment goals: results from a series of 442 patients in FranceCaroline Prot-Bertoye, Saïd Lebbah, Michel Daudon, et al.
Human Mutation|June 18, 2010
Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrumVerena Matejas, Bernward Hinkes, Faisal Alkandari, et al.
Arthritis and Rheumatism|May 14, 2013
Protein kinase cδ deficiency causes mendelian systemic lupus erythematosus with B cell-defective apoptosis and hyperproliferationAlexandre Belot, Paul R Kasher, Eleanor W Trotter, et al.
The Journal of Allergy and Clinical Immunology|April 6, 2015
PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunityAnne-Laure Mathieu, Estelle Verronese, Gillian I Rice, et al.
Orphanet Journal of Rare Diseases|September 25, 2012
Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia?Marie Morimoto, Zhongxin Yu, Peter Stenzel, et al.
Pediatric Nephrology (Berlin, Germany)|October 24, 2017
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndromeGuillaume Dorval, Olivier Gribouval, Vanesa Martinez-Barquero, et al.
Human Mutation|January 4, 2012
Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific databaseMatthew Bower, Rémi Salomon, Judith Allanson, et al.
Pageof 23

Showing results (211-220 of 225) with videos related to

Sort By:
Pageof 23
Clinical Journal of the American Society of Nephrology : CJASN|February 27, 2015
CKD and Its Risk Factors among Patients with CystinuriaCaroline Prot-Bertoye, Saïd Lebbah, Michel Daudon, et al.
Pediatric Radiology|November 16, 2017
Standardization of pediatric uroradiological terms: a multidisciplinary European glossaryPierre-Hugues Vivier, Thomas A Augdal, Fred E Avni, et al.
Journal of Pediatric Urology|November 28, 2017
Standardization of pediatric uroradiological terms: A multidisciplinary European glossaryPierre-Hugues Vivier, Thomas A Augdal, Fred E Avni, et al.
BJU International|February 26, 2019
Adverse events associated with currently used medical treatments for cystinuria and treatment goals: results from a series of 442 patients in FranceCaroline Prot-Bertoye, Saïd Lebbah, Michel Daudon, et al.
Human Mutation|June 18, 2010
Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrumVerena Matejas, Bernward Hinkes, Faisal Alkandari, et al.
Arthritis and Rheumatism|May 14, 2013
Protein kinase cδ deficiency causes mendelian systemic lupus erythematosus with B cell-defective apoptosis and hyperproliferationAlexandre Belot, Paul R Kasher, Eleanor W Trotter, et al.
The Journal of Allergy and Clinical Immunology|April 6, 2015
PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunityAnne-Laure Mathieu, Estelle Verronese, Gillian I Rice, et al.
Orphanet Journal of Rare Diseases|September 25, 2012
Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia?Marie Morimoto, Zhongxin Yu, Peter Stenzel, et al.
Pediatric Nephrology (Berlin, Germany)|October 24, 2017
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndromeGuillaume Dorval, Olivier Gribouval, Vanesa Martinez-Barquero, et al.
Human Mutation|January 4, 2012
Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific databaseMatthew Bower, Rémi Salomon, Judith Allanson, et al.
Pageof 23