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Daniel G Bichet

Showing results (111-120 of 144) with videos related to

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Annals of Internal Medicine|December 21, 2006
Agalsidase-beta therapy for advanced Fabry disease: a randomized trialMaryam Banikazemi, Jan Bultas, Stephen Waldek, et al.
Pituitary|November 5, 2022
Changing the name of diabetes insipidusHiroshi Arima, Daniel G Bichet, Timothy Cheetham, et al.
International Journal of Molecular Sciences|August 29, 2020
Diurnal Variation of Urinary Fabry Disease Biomarkers during Enzyme Replacement Therapy CyclesMichel Boutin, Pamela Lavoie, Iskren Menkovic, et al.
Bioanalysis|October 17, 2023
Fabry disease biomarkers in patients switched from enzyme-replacement therapy to migalastat oral chaperone therapyChristiane Auray-Blais, Pamela Lavoie, Tristan Martineau, et al.
Molecular Genetics and Metabolism|November 21, 2007
Urinary globotriaosylceramide excretion correlates with the genotype in children and adults with Fabry diseaseChristiane Auray-Blais, Denis Cyr, Aimé Ntwari, et al.
Kidney International Reports|May 14, 2023
OVERTURE: A Worldwide, Prospective, Observational Study of Disease Characteristics in Patients With ADPKDRonald D Perrone, Dorothee Oberdhan, John Ouyang, et al.
American Journal of Medical Genetics. Part A|March 29, 2019
Safety of switching to Migalastat from enzyme replacement therapy in Fabry disease: Experience from the Phase 3 ATTRACT studyDerralynn A Hughes, Kathleen Nicholls, Gere Sunder-Plassmann, et al.
The Journal of Clinical Investigation|June 16, 2026
GLUT9b- and ABCG2-mediated collecting duct urate transport uncover a vasopressin-independent mechanism of renal water reabsorptionMohamad Hadla, Jean Marc Mardirossian, Daniel G Bichet, et al.
Journal of Medical Genetics|December 21, 2022
Long-term multisystemic efficacy of migalastat on Fabry-associated clinical events, including renal, cardiac and cerebrovascular outcomesDerralynn A Hughes, Daniel G Bichet, Roberto Giugliani, et al.
Journal of the American Society of Nephrology : JASN|May 23, 2000
Report of 33 novel AVPR2 mutations and analysis of 117 families with X-linked nephrogenic diabetes insipidusMarie-Françoise Arthus, Michèle Lonergan, M Joyce Crumley, et al.
Pageof 15

Showing results (111-120 of 144) with videos related to

Sort By:
Pageof 15
Annals of Internal Medicine|December 21, 2006
Agalsidase-beta therapy for advanced Fabry disease: a randomized trialMaryam Banikazemi, Jan Bultas, Stephen Waldek, et al.
Pituitary|November 5, 2022
Changing the name of diabetes insipidusHiroshi Arima, Daniel G Bichet, Timothy Cheetham, et al.
International Journal of Molecular Sciences|August 29, 2020
Diurnal Variation of Urinary Fabry Disease Biomarkers during Enzyme Replacement Therapy CyclesMichel Boutin, Pamela Lavoie, Iskren Menkovic, et al.
Bioanalysis|October 17, 2023
Fabry disease biomarkers in patients switched from enzyme-replacement therapy to migalastat oral chaperone therapyChristiane Auray-Blais, Pamela Lavoie, Tristan Martineau, et al.
Molecular Genetics and Metabolism|November 21, 2007
Urinary globotriaosylceramide excretion correlates with the genotype in children and adults with Fabry diseaseChristiane Auray-Blais, Denis Cyr, Aimé Ntwari, et al.
Kidney International Reports|May 14, 2023
OVERTURE: A Worldwide, Prospective, Observational Study of Disease Characteristics in Patients With ADPKDRonald D Perrone, Dorothee Oberdhan, John Ouyang, et al.
American Journal of Medical Genetics. Part A|March 29, 2019
Safety of switching to Migalastat from enzyme replacement therapy in Fabry disease: Experience from the Phase 3 ATTRACT studyDerralynn A Hughes, Kathleen Nicholls, Gere Sunder-Plassmann, et al.
The Journal of Clinical Investigation|June 16, 2026
GLUT9b- and ABCG2-mediated collecting duct urate transport uncover a vasopressin-independent mechanism of renal water reabsorptionMohamad Hadla, Jean Marc Mardirossian, Daniel G Bichet, et al.
Journal of Medical Genetics|December 21, 2022
Long-term multisystemic efficacy of migalastat on Fabry-associated clinical events, including renal, cardiac and cerebrovascular outcomesDerralynn A Hughes, Daniel G Bichet, Roberto Giugliani, et al.
Journal of the American Society of Nephrology : JASN|May 23, 2000
Report of 33 novel AVPR2 mutations and analysis of 117 families with X-linked nephrogenic diabetes insipidusMarie-Françoise Arthus, Michèle Lonergan, M Joyce Crumley, et al.
Pageof 15