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Ariane Berdal

Showing results (101-110 of 115) with videos related to

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Frontiers in Endocrinology|November 15, 2021
Pathogenesis of Enamel-Renal Syndrome Associated Gingival Fibromatosis: A Proteomic ApproachVictor Simancas Escorcia, Clément Guillou, Lilia Abbad, et al.
Human Pathology|August 8, 2016
Defining a new aggressiveness classification and using NFATc1 localization as a prognostic factor in cherubismNatacha Kadlub, Quentin Sessiecq, Linda Dainese, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 11, 2014
The calcineurin inhibitor tacrolimus as a new therapy in severe cherubismNatacha Kadlub, Marie-Paule Vazquez, Louise Galmiche, et al.
European Journal of Human Genetics : EJHG|September 5, 2023
Oro-dental phenotyping and report of three families with RELT-associated amelogenesis imperfectaKemelly Karolliny Moreira Resende, Margot Charlotte Riou, Paulo Marcio Yamaguti, et al.
Acta Biomaterialia|August 13, 2023
Multi-scale characterization of Developmental Defects of Enamel and their clinical significance for diagnosis and treatmentSophia Houari, Karen DeRocher, Tran Thu Thuy, et al.
BMC Musculoskeletal Disorders|August 23, 2020
Cherubism as a systemic skeletal disease: evidence from an aggressive caseAnne Morice, Aline Joly, Manon Ricquebourg, et al.
Oral Diseases|November 21, 2024
Dental and Craniofacial Anomalies in Fanconi Anemia: A Systematic Review and Additional 46 ReportsPaula Alves da Silva Rocha, Nayara Conceição Marcos Santana, José Alcides Almeida de Arruda, et al.
Scientific Reports|April 25, 2024
Gingival proteomics reveals the role of TGF beta and YAP/TAZ signaling in Raine syndrome fibrosisCláudio Rodrigues Rezende Costa, Rym Chalgoumi, Amina Baker, et al.
The Journal of Craniofacial Surgery|September 4, 2025
Timeline of Amelogenesis Imperfecta ManagementAlexandra Jimenez-Armijo, Paola L Carvajal Monroy, Saranda Ombashi, et al.
Journal of Medical Genetics|August 18, 2016
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutationsPaulo Marcio Yamaguti, Francisco de Assis Rocha Neves, Dominique Hotton, et al.
Pageof 12

Showing results (101-110 of 115) with videos related to

Sort By:
Pageof 12
Frontiers in Endocrinology|November 15, 2021
Pathogenesis of Enamel-Renal Syndrome Associated Gingival Fibromatosis: A Proteomic ApproachVictor Simancas Escorcia, Clément Guillou, Lilia Abbad, et al.
Human Pathology|August 8, 2016
Defining a new aggressiveness classification and using NFATc1 localization as a prognostic factor in cherubismNatacha Kadlub, Quentin Sessiecq, Linda Dainese, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 11, 2014
The calcineurin inhibitor tacrolimus as a new therapy in severe cherubismNatacha Kadlub, Marie-Paule Vazquez, Louise Galmiche, et al.
European Journal of Human Genetics : EJHG|September 5, 2023
Oro-dental phenotyping and report of three families with RELT-associated amelogenesis imperfectaKemelly Karolliny Moreira Resende, Margot Charlotte Riou, Paulo Marcio Yamaguti, et al.
Acta Biomaterialia|August 13, 2023
Multi-scale characterization of Developmental Defects of Enamel and their clinical significance for diagnosis and treatmentSophia Houari, Karen DeRocher, Tran Thu Thuy, et al.
BMC Musculoskeletal Disorders|August 23, 2020
Cherubism as a systemic skeletal disease: evidence from an aggressive caseAnne Morice, Aline Joly, Manon Ricquebourg, et al.
Oral Diseases|November 21, 2024
Dental and Craniofacial Anomalies in Fanconi Anemia: A Systematic Review and Additional 46 ReportsPaula Alves da Silva Rocha, Nayara Conceição Marcos Santana, José Alcides Almeida de Arruda, et al.
Scientific Reports|April 25, 2024
Gingival proteomics reveals the role of TGF beta and YAP/TAZ signaling in Raine syndrome fibrosisCláudio Rodrigues Rezende Costa, Rym Chalgoumi, Amina Baker, et al.
The Journal of Craniofacial Surgery|September 4, 2025
Timeline of Amelogenesis Imperfecta ManagementAlexandra Jimenez-Armijo, Paola L Carvajal Monroy, Saranda Ombashi, et al.
Journal of Medical Genetics|August 18, 2016
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutationsPaulo Marcio Yamaguti, Francisco de Assis Rocha Neves, Dominique Hotton, et al.
Pageof 12