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Vincent Guigonis

Showing results (41-50 of 84) with videos related to

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Acta Dermato-Venereologica|May 18, 2019
Keratitis-Ichthyosis-Deafness Syndrome: Early Death Caused by the GJB2 Mutation p.Gly12ArgClothilde Godillot, Maella Severino-Freire, Vincent Michaud, et al.
Pediatric Nephrology (Berlin, Germany)|August 29, 2009
Cryptosporidiosis in paediatric renal transplantationFlavio Bandin, Theresa Kwon, Marie-Denise Linas, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 11, 2024
Vaginal screening for group B streptococcus using PCR in pregnant women with unknown colonization status: Impact on newborn monitoring for early-onset sepsisAnne Laure Blanquart, Fabien Garnier, Thomas Lauvray, et al.
The Journal of Pediatrics|December 3, 2014
Neonatal hemochromatosis: diagnostic work-up based on a series of 56 cases of fetal death and neonatal liver failureSophie Heissat, Sophie Collardeau-Frachon, Julien Baruteau, et al.
The Journal of Clinical Endocrinology and Metabolism|May 11, 2016
Topical Sodium Thiosulfate: A Treatment for Calcifications in Hyperphosphatemic Familial Tumoral Calcinosis?Jérémy Jost, Claire Bahans, Marie Courbebaisse, et al.
Journal of Medical Microbiology|January 15, 2009
Maternofetal infections due to Eikenella corrodensFabien Garnier, Geoffrey Masson, Antoine Bedu, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 10, 2010
Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseasesLaurence Heidet, Stéphane Decramer, Audrey Pawtowski, et al.
Journal of the American Society of Nephrology : JASN|December 24, 2005
Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohortTim Ulinski, Sandra Lescure, Sandrine Beaufils, et al.
Lancet (London, England)|October 7, 2004
Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathiesHanna Debiec, Jeroen Nauta, Florence Coulet, et al.
Journal of Autoimmunity|October 24, 2017
NEPHRUTIX: A randomized, double-blind, placebo vs Rituximab-controlled trial assessing T-cell subset changes in Minimal Change Nephrotic SyndromeAhmed Boumediene, Pauline Vachin, Kelhia Sendeyo, et al.
Pageof 9

Showing results (41-50 of 84) with videos related to

Sort By:
Pageof 9
Acta Dermato-Venereologica|May 18, 2019
Keratitis-Ichthyosis-Deafness Syndrome: Early Death Caused by the GJB2 Mutation p.Gly12ArgClothilde Godillot, Maella Severino-Freire, Vincent Michaud, et al.
Pediatric Nephrology (Berlin, Germany)|August 29, 2009
Cryptosporidiosis in paediatric renal transplantationFlavio Bandin, Theresa Kwon, Marie-Denise Linas, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 11, 2024
Vaginal screening for group B streptococcus using PCR in pregnant women with unknown colonization status: Impact on newborn monitoring for early-onset sepsisAnne Laure Blanquart, Fabien Garnier, Thomas Lauvray, et al.
The Journal of Pediatrics|December 3, 2014
Neonatal hemochromatosis: diagnostic work-up based on a series of 56 cases of fetal death and neonatal liver failureSophie Heissat, Sophie Collardeau-Frachon, Julien Baruteau, et al.
The Journal of Clinical Endocrinology and Metabolism|May 11, 2016
Topical Sodium Thiosulfate: A Treatment for Calcifications in Hyperphosphatemic Familial Tumoral Calcinosis?Jérémy Jost, Claire Bahans, Marie Courbebaisse, et al.
Journal of Medical Microbiology|January 15, 2009
Maternofetal infections due to Eikenella corrodensFabien Garnier, Geoffrey Masson, Antoine Bedu, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 10, 2010
Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseasesLaurence Heidet, Stéphane Decramer, Audrey Pawtowski, et al.
Journal of the American Society of Nephrology : JASN|December 24, 2005
Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohortTim Ulinski, Sandra Lescure, Sandrine Beaufils, et al.
Lancet (London, England)|October 7, 2004
Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathiesHanna Debiec, Jeroen Nauta, Florence Coulet, et al.
Journal of Autoimmunity|October 24, 2017
NEPHRUTIX: A randomized, double-blind, placebo vs Rituximab-controlled trial assessing T-cell subset changes in Minimal Change Nephrotic SyndromeAhmed Boumediene, Pauline Vachin, Kelhia Sendeyo, et al.
Pageof 9