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Caroline Silve

Showing results (41-50 of 53) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|May 5, 2018
Pro-FHH: A Risk Equation to Facilitate the Diagnosis of Parathyroid-Related HypercalcemiaJean-Philippe Bertocchio, Muriel Tafflet, Eugénie Koumakis, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 27, 2020
Hyperparathyroidism in Patients With X-Linked HypophosphatemiaAnne-Lise Lecoq, Philippe Chaumet-Riffaud, Anne Blanchard, et al.
The Journal of Clinical Endocrinology and Metabolism|January 17, 2015
Novel microdeletions affecting the GNAS locus in pseudohypoparathyroidism: characterization of the underlying mechanismsIntza Garin, Francesca M Elli, Agnes Linglart, et al.
Journal of Medical Genetics|October 26, 2010
Quantification of the methylation at the GNAS locus identifies subtypes of sporadic pseudohypoparathyroidism type IbStéphanie Maupetit-Méhouas, Virginie Mariot, Christelle Reynès, et al.
The Journal of Clinical Endocrinology and Metabolism|May 23, 2018
Progression of Mineral Ion Abnormalities in Patients With Jansen Metaphyseal ChondrodysplasiaHiroshi Saito, Hiroshi Noda, Philippe Gatault, et al.
Endocrine Connections|December 23, 2021
Practice patterns for chronic hypoparathyroidism: data from patients and physicians in FranceJean-Philippe Bertocchio, Natalie Grosset, Lionel Groussin, et al.
The Journal of Clinical Endocrinology and Metabolism|January 8, 2013
Frequent large germline HRPT2 deletions in a French National cohort of patients with primary hyperparathyroidismLéopoldine Bricaire, Marie-Françoise Odou, Catherine Cardot-Bauters, et al.
Clinical Endocrinology|April 30, 2020
Clinical characteristics of familial hypocalciuric hypercalcaemia type 1: A multicentre study of 77 adult patientsCéline Mouly, Rosa Vargas-Poussou, Anne Lienhardt, et al.
European Journal of Endocrinology|July 13, 2016
From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP networkSusanne Thiele, Giovanna Mantovani, Anne Barlier, et al.
The Journal of Clinical Endocrinology and Metabolism|October 9, 2012
PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistanceAgnès Linglart, Helena Fryssira, Olaf Hiort, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
The Journal of Clinical Endocrinology and Metabolism|May 5, 2018
Pro-FHH: A Risk Equation to Facilitate the Diagnosis of Parathyroid-Related HypercalcemiaJean-Philippe Bertocchio, Muriel Tafflet, Eugénie Koumakis, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 27, 2020
Hyperparathyroidism in Patients With X-Linked HypophosphatemiaAnne-Lise Lecoq, Philippe Chaumet-Riffaud, Anne Blanchard, et al.
The Journal of Clinical Endocrinology and Metabolism|January 17, 2015
Novel microdeletions affecting the GNAS locus in pseudohypoparathyroidism: characterization of the underlying mechanismsIntza Garin, Francesca M Elli, Agnes Linglart, et al.
Journal of Medical Genetics|October 26, 2010
Quantification of the methylation at the GNAS locus identifies subtypes of sporadic pseudohypoparathyroidism type IbStéphanie Maupetit-Méhouas, Virginie Mariot, Christelle Reynès, et al.
The Journal of Clinical Endocrinology and Metabolism|May 23, 2018
Progression of Mineral Ion Abnormalities in Patients With Jansen Metaphyseal ChondrodysplasiaHiroshi Saito, Hiroshi Noda, Philippe Gatault, et al.
Endocrine Connections|December 23, 2021
Practice patterns for chronic hypoparathyroidism: data from patients and physicians in FranceJean-Philippe Bertocchio, Natalie Grosset, Lionel Groussin, et al.
The Journal of Clinical Endocrinology and Metabolism|January 8, 2013
Frequent large germline HRPT2 deletions in a French National cohort of patients with primary hyperparathyroidismLéopoldine Bricaire, Marie-Françoise Odou, Catherine Cardot-Bauters, et al.
Clinical Endocrinology|April 30, 2020
Clinical characteristics of familial hypocalciuric hypercalcaemia type 1: A multicentre study of 77 adult patientsCéline Mouly, Rosa Vargas-Poussou, Anne Lienhardt, et al.
European Journal of Endocrinology|July 13, 2016
From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP networkSusanne Thiele, Giovanna Mantovani, Anne Barlier, et al.
The Journal of Clinical Endocrinology and Metabolism|October 9, 2012
PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistanceAgnès Linglart, Helena Fryssira, Olaf Hiort, et al.
Pageof 6