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Ana Coral Barreda-Bonis

Showing results (1-10 of 8) with videos related to

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Cureus|April 28, 2025
CurQ+ With Resveratrol Diminish Joint Pain in a Child With Pseudoachondroplasia: A Case ReportJacqueline T Hecht, Ana-Coral Barreda-Bonis, Karen L Posey
European Journal of Medical Genetics|October 13, 2017
Multiple SLC26A2 mutations occurring in a three-generational familyAna Coral Barreda-Bonis, Jimena Barraza-García, Manuel Parrón, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 10, 2011
Familial glucocorticoid deficiency due to compound heterozygosity of two novel MC2R mutationsMiriam Aza-Carmona, Ana Coral Barreda-Bonis, Julio Guerrero-Fernández, et al.
Anales De Pediatria|December 7, 2024
Expert consensus for the management of patients with achondroplasia in treatment with vosoritideAna-Coral Barreda-Bonis, Josep Maria de Bergua Domingo, Enrique Galán-Gómez, et al.
Anales De Pediatria|June 12, 2026
Update and review of treatment in achondroplasiaSilvia Gallego-Gutiérrez, Ana Coral Barreda-Bonis, Isolina Riaño-Galán, et al.
Orphanet Journal of Rare Diseases|August 29, 2023
Transition of patients with metabolic bone disease from paediatric to adult healthcare services: current situation and proposals for improvementEnrique Casado, Carlos Gómez-Alonso, Guillem Pintos-Morell, et al.
Anales De Pediatria|November 8, 2022
Achondroplasia: Update on diagnosis, follow-up and treatmentAntonio Leiva-Gea, María F Martos Lirio, Ana Coral Barreda Bonis, et al.
European Journal of Endocrinology|June 2, 2017
Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinaseSarah M Leiter, Victoria E R Parker, Alena Welters, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Cureus|April 28, 2025
CurQ+ With Resveratrol Diminish Joint Pain in a Child With Pseudoachondroplasia: A Case ReportJacqueline T Hecht, Ana-Coral Barreda-Bonis, Karen L Posey
European Journal of Medical Genetics|October 13, 2017
Multiple SLC26A2 mutations occurring in a three-generational familyAna Coral Barreda-Bonis, Jimena Barraza-García, Manuel Parrón, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 10, 2011
Familial glucocorticoid deficiency due to compound heterozygosity of two novel MC2R mutationsMiriam Aza-Carmona, Ana Coral Barreda-Bonis, Julio Guerrero-Fernández, et al.
Anales De Pediatria|December 7, 2024
Expert consensus for the management of patients with achondroplasia in treatment with vosoritideAna-Coral Barreda-Bonis, Josep Maria de Bergua Domingo, Enrique Galán-Gómez, et al.
Anales De Pediatria|June 12, 2026
Update and review of treatment in achondroplasiaSilvia Gallego-Gutiérrez, Ana Coral Barreda-Bonis, Isolina Riaño-Galán, et al.
Orphanet Journal of Rare Diseases|August 29, 2023
Transition of patients with metabolic bone disease from paediatric to adult healthcare services: current situation and proposals for improvementEnrique Casado, Carlos Gómez-Alonso, Guillem Pintos-Morell, et al.
Anales De Pediatria|November 8, 2022
Achondroplasia: Update on diagnosis, follow-up and treatmentAntonio Leiva-Gea, María F Martos Lirio, Ana Coral Barreda Bonis, et al.
European Journal of Endocrinology|June 2, 2017
Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinaseSarah M Leiter, Victoria E R Parker, Alena Welters, et al.
Pageof 1