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Agnès Linglart

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 29, 2024
Autosomal recessive hypophosphatemic rickets type 2 due to ENPP1 deficiency (ARHR2)Thomas Edouard, Agnès Linglart
Current Osteoporosis Reports|April 17, 2016
HypophosphatasiaAgnès Linglart, Martin Biosse-Duplan
International Journal of Pediatric Endocrinology|March 7, 2017
Erratum to: A randomized pilot trial of growth hormone with anastrozole versus growth hormone alone, starting at the very end of puberty in adolescents with idiopathic short statureAnya Rothenbuhler, Agnès Linglart, Pierre Bougnères
International Journal of Pediatric Endocrinology|May 15, 2015
A randomized pilot trial of growth hormone with anastrozole versus growth hormone alone, starting at the very end of puberty in adolescents with idiopathic short statureAnya Rothenbuhler, Agnès Linglart, Pierre Bougnères
Annales D'Endocrinologie|April 28, 2015
Multiple hormonal resistances: Diagnosis, evaluation and therapyAgnès Linglart, Caroline Silve, Anya Rothenbuhler
Clinical Endocrinology|July 27, 2007
Similar clinical and laboratory findings in patients with symptomatic autosomal dominant and sporadic pseudohypoparathyroidism type Ib despite different epigenetic changes at the GNAS locusAgnès Linglart, Murat Bastepe, Harald Jüppner
Hormone Research in Paediatrics|April 4, 2013
GNAS -Related Loss-of-Function Disorders and the Role of ImprintingAgnès Linglart, Stéphanie Maupetit-Méhouas, Caroline Silve
Endocrinology and Metabolism Clinics of North America|November 5, 2018
PseudohypoparathyroidismAgnès Linglart, Michael A Levine, Harald Jüppner
The Journal of Clinical Endocrinology and Metabolism|May 27, 2010
Risk of corrected QT interval prolongation after pamidronate infusion in childrenAnya Rothenbuhler, Isis Marchand, Pierre Bougnères, et al.
Metabolism: Clinical and Experimental|April 1, 2019
Diagnosis, treatment-monitoring and follow-up of children and adolescents with X-linked hypophosphatemia (XLH)Anya Rothenbuhler, Dirk Schnabel, Wolfgang Högler, et al.
Pageof 21

Showing results (1-10 of 208) with videos related to

Sort By:
Pageof 21
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 29, 2024
Autosomal recessive hypophosphatemic rickets type 2 due to ENPP1 deficiency (ARHR2)Thomas Edouard, Agnès Linglart
Current Osteoporosis Reports|April 17, 2016
HypophosphatasiaAgnès Linglart, Martin Biosse-Duplan
International Journal of Pediatric Endocrinology|March 7, 2017
Erratum to: A randomized pilot trial of growth hormone with anastrozole versus growth hormone alone, starting at the very end of puberty in adolescents with idiopathic short statureAnya Rothenbuhler, Agnès Linglart, Pierre Bougnères
International Journal of Pediatric Endocrinology|May 15, 2015
A randomized pilot trial of growth hormone with anastrozole versus growth hormone alone, starting at the very end of puberty in adolescents with idiopathic short statureAnya Rothenbuhler, Agnès Linglart, Pierre Bougnères
Annales D'Endocrinologie|April 28, 2015
Multiple hormonal resistances: Diagnosis, evaluation and therapyAgnès Linglart, Caroline Silve, Anya Rothenbuhler
Clinical Endocrinology|July 27, 2007
Similar clinical and laboratory findings in patients with symptomatic autosomal dominant and sporadic pseudohypoparathyroidism type Ib despite different epigenetic changes at the GNAS locusAgnès Linglart, Murat Bastepe, Harald Jüppner
Hormone Research in Paediatrics|April 4, 2013
GNAS -Related Loss-of-Function Disorders and the Role of ImprintingAgnès Linglart, Stéphanie Maupetit-Méhouas, Caroline Silve
Endocrinology and Metabolism Clinics of North America|November 5, 2018
PseudohypoparathyroidismAgnès Linglart, Michael A Levine, Harald Jüppner
The Journal of Clinical Endocrinology and Metabolism|May 27, 2010
Risk of corrected QT interval prolongation after pamidronate infusion in childrenAnya Rothenbuhler, Isis Marchand, Pierre Bougnères, et al.
Metabolism: Clinical and Experimental|April 1, 2019
Diagnosis, treatment-monitoring and follow-up of children and adolescents with X-linked hypophosphatemia (XLH)Anya Rothenbuhler, Dirk Schnabel, Wolfgang Högler, et al.
Pageof 21