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Anya Rothenbuhler

Showing results (11-20 of 77) with videos related to

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The Journal of Pediatrics|December 6, 2011
A pilot study of discontinuous, insulin-like growth factor 1-dosing growth hormone treatment in young children with FGFR3 N540K-mutated hypochondroplasiaAnya Rothenbuhler, Agnès Linglart, Catherine Piquard, et al.
Hormone Research in Paediatrics|September 20, 2017
Continuous Subcutaneous Recombinant Parathyroid Hormone (1-34) Infusion in the Management of Childhood Hypoparathyroidism Associated with MalabsorptionVrinda Saraff, Anya Rothenbuhler, Wolfgang Högler, et al.
Joint Bone Spine|February 4, 2019
X-linked hypophosphatemia: Management and treatment prospectsAnne-Sophie Lambert, Volha Zhukouskaya, Anya Rothenbuhler, et al.
Clinical Endocrinology|July 29, 2015
Higher methylation of the IGF1 P2 promoter is associated with idiopathic short statureMeriem Ouni, Anne-Laure Castell, Anya Rothenbuhler, et al.
Orphanet Journal of Rare Diseases|September 12, 2024
Prevalence of hearing loss in pseudohypoparathyroidismCassandre Djian, Jugurtha Berkenou, Anya Rothenbuhler, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 2011
Long-term results of continuous subcutaneous recombinant PTH (1-34) infusion in children with refractory hypoparathyroidismAgnès Linglart, Anya Rothenbuhler, Iva Gueorgieva, et al.
Hormone Research in Paediatrics|August 18, 2024
Characterization of Digestive Manifestations in Patients with Impaired PTH/PTHrP Signaling Disorder/PseudohypoparathyroidismBérénice Goy, Jugurtha Berkenou, Anya Rothenbuhler, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Progressive Development of PTH Resistance in Patients With Inactivating Mutations on the Maternal Allele of GNASAlessia Usardi, Asmaa Mamoune, Elodie Nattes, et al.
Pediatric Radiology|December 2, 2021
Imaging patterns in pediatric hypophosphatasiaInès Mannes, Anya Rothenbuhler, Valérie Merzoug, et al.
European Journal of Endocrinology|January 20, 2016
Impaired quality of life in adults with X-linked hypophosphatemia and skeletal symptomsHélène Che, Christian Roux, Adrien Etcheto, et al.
Pageof 8

Showing results (11-20 of 77) with videos related to

Sort By:
Pageof 8
The Journal of Pediatrics|December 6, 2011
A pilot study of discontinuous, insulin-like growth factor 1-dosing growth hormone treatment in young children with FGFR3 N540K-mutated hypochondroplasiaAnya Rothenbuhler, Agnès Linglart, Catherine Piquard, et al.
Hormone Research in Paediatrics|September 20, 2017
Continuous Subcutaneous Recombinant Parathyroid Hormone (1-34) Infusion in the Management of Childhood Hypoparathyroidism Associated with MalabsorptionVrinda Saraff, Anya Rothenbuhler, Wolfgang Högler, et al.
Joint Bone Spine|February 4, 2019
X-linked hypophosphatemia: Management and treatment prospectsAnne-Sophie Lambert, Volha Zhukouskaya, Anya Rothenbuhler, et al.
Clinical Endocrinology|July 29, 2015
Higher methylation of the IGF1 P2 promoter is associated with idiopathic short statureMeriem Ouni, Anne-Laure Castell, Anya Rothenbuhler, et al.
Orphanet Journal of Rare Diseases|September 12, 2024
Prevalence of hearing loss in pseudohypoparathyroidismCassandre Djian, Jugurtha Berkenou, Anya Rothenbuhler, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 2011
Long-term results of continuous subcutaneous recombinant PTH (1-34) infusion in children with refractory hypoparathyroidismAgnès Linglart, Anya Rothenbuhler, Iva Gueorgieva, et al.
Hormone Research in Paediatrics|August 18, 2024
Characterization of Digestive Manifestations in Patients with Impaired PTH/PTHrP Signaling Disorder/PseudohypoparathyroidismBérénice Goy, Jugurtha Berkenou, Anya Rothenbuhler, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Progressive Development of PTH Resistance in Patients With Inactivating Mutations on the Maternal Allele of GNASAlessia Usardi, Asmaa Mamoune, Elodie Nattes, et al.
Pediatric Radiology|December 2, 2021
Imaging patterns in pediatric hypophosphatasiaInès Mannes, Anya Rothenbuhler, Valérie Merzoug, et al.
European Journal of Endocrinology|January 20, 2016
Impaired quality of life in adults with X-linked hypophosphatemia and skeletal symptomsHélène Che, Christian Roux, Adrien Etcheto, et al.
Pageof 8