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Pascal Houillier

Showing results (161-170 of 176) with videos related to

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Kidney International|June 26, 2016
Observations of a large Dent disease cohortAnne Blanchard, Emmanuel Curis, Tiphaine Guyon-Roger, et al.
Annales D'Endocrinologie|June 19, 2016
SFE/SFHTA/AFCE primary aldosteronism consensus: Introduction and handbookLaurence Amar, Jean Philippe Baguet, Stéphane Bardet, et al.
The Journal of Clinical Investigation|June 30, 2026
Cilia to basement membrane signaling is a biomechanical driver in models of autosomal dominant polycystic kidney diseaseManal Mazloum, Brice Lapin, Rushdi Alghamdi, et al.
Journal of the American Society of Nephrology : JASN|April 3, 2021
Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural DeafnessKarl P Schlingmann, Aparna Renigunta, Ewout J Hoorn, et al.
The Journal of Clinical Endocrinology and Metabolism|March 11, 2016
Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and DifferencesRosa Vargas-Poussou, Lamisse Mansour-Hendili, Stéphanie Baron, et al.
Journal of the American Society of Nephrology : JASN|October 5, 2021
Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNADaan Viering, Karl P Schlingmann, Marguerite Hureaux, et al.
Nature Genetics|March 13, 2012
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephronHélène Louis-Dit-Picard, Julien Barc, Daniel Trujillano, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 2, 2015
Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel FormationClaire Bardet, Frédéric Courson, Yong Wu, et al.
Journal of the American Society of Nephrology : JASN|October 5, 2021
mTOR-Activating Mutations in <i>RRAGD</i> Are Causative for Kidney Tubulopathy and CardiomyopathyKarl P Schlingmann, François Jouret, Kuang Shen, et al.
Presse Medicale (Paris, France : 1983)|January 21, 2014
[HAS report on vitamin D measurement: don't go from an extreme situation to another as extreme situation]Jean-Claude Souberbielle, Claude Laurent Benhamou, Bernard Cortet, et al.
Pageof 18

Showing results (161-170 of 176) with videos related to

Sort By:
Pageof 18
Kidney International|June 26, 2016
Observations of a large Dent disease cohortAnne Blanchard, Emmanuel Curis, Tiphaine Guyon-Roger, et al.
Annales D'Endocrinologie|June 19, 2016
SFE/SFHTA/AFCE primary aldosteronism consensus: Introduction and handbookLaurence Amar, Jean Philippe Baguet, Stéphane Bardet, et al.
The Journal of Clinical Investigation|June 30, 2026
Cilia to basement membrane signaling is a biomechanical driver in models of autosomal dominant polycystic kidney diseaseManal Mazloum, Brice Lapin, Rushdi Alghamdi, et al.
Journal of the American Society of Nephrology : JASN|April 3, 2021
Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural DeafnessKarl P Schlingmann, Aparna Renigunta, Ewout J Hoorn, et al.
The Journal of Clinical Endocrinology and Metabolism|March 11, 2016
Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and DifferencesRosa Vargas-Poussou, Lamisse Mansour-Hendili, Stéphanie Baron, et al.
Journal of the American Society of Nephrology : JASN|October 5, 2021
Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNADaan Viering, Karl P Schlingmann, Marguerite Hureaux, et al.
Nature Genetics|March 13, 2012
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephronHélène Louis-Dit-Picard, Julien Barc, Daniel Trujillano, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 2, 2015
Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel FormationClaire Bardet, Frédéric Courson, Yong Wu, et al.
Journal of the American Society of Nephrology : JASN|October 5, 2021
mTOR-Activating Mutations in <i>RRAGD</i> Are Causative for Kidney Tubulopathy and CardiomyopathyKarl P Schlingmann, François Jouret, Kuang Shen, et al.
Presse Medicale (Paris, France : 1983)|January 21, 2014
[HAS report on vitamin D measurement: don't go from an extreme situation to another as extreme situation]Jean-Claude Souberbielle, Claude Laurent Benhamou, Bernard Cortet, et al.
Pageof 18