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Frontiers in Endocrinology
|
November 15, 2021
Pathogenesis of Enamel-Renal Syndrome Associated Gingival Fibromatosis: A Proteomic Approach
Victor 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 cherubism
Natacha 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 cherubism
Natacha 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 imperfecta
Kemelly 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 treatment
Sophia Houari, Karen DeRocher, Tran Thu Thuy, et al.
BMC Musculoskeletal Disorders
|
August 23, 2020
Cherubism as a systemic skeletal disease: evidence from an aggressive case
Anne 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 Reports
Paula 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 fibrosis
Cláudio Rodrigues Rezende Costa, Rym Chalgoumi, Amina Baker, et al.
The Journal of Craniofacial Surgery
|
September 4, 2025
Timeline of Amelogenesis Imperfecta Management
Alexandra 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 mutations
Paulo Marcio Yamaguti, Francisco de Assis Rocha Neves, Dominique Hotton, et al.
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of 12
Search research articles
Search
Showing results (101-110 of 115) with videos related to
Sort By:
Page
of 12
Frontiers in Endocrinology
|
November 15, 2021
Pathogenesis of Enamel-Renal Syndrome Associated Gingival Fibromatosis: A Proteomic Approach
Victor 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 cherubism
Natacha 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 cherubism
Natacha 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 imperfecta
Kemelly 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 treatment
Sophia Houari, Karen DeRocher, Tran Thu Thuy, et al.
BMC Musculoskeletal Disorders
|
August 23, 2020
Cherubism as a systemic skeletal disease: evidence from an aggressive case
Anne 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 Reports
Paula 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 fibrosis
Cláudio Rodrigues Rezende Costa, Rym Chalgoumi, Amina Baker, et al.
The Journal of Craniofacial Surgery
|
September 4, 2025
Timeline of Amelogenesis Imperfecta Management
Alexandra 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 mutations
Paulo Marcio Yamaguti, Francisco de Assis Rocha Neves, Dominique Hotton, et al.
Page
of 12