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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 29, 2024
Human genetic diseases of phosphate and pyrophosphate metabolism
Arnaud Molin
The Journal of Clinical Investigation
|
April 15, 2025
Clinical evidence for independent regulation of vitamin D by intestinal CYP24A1
Sandrine Lemoine, Arnaud Molin, Alice Koenig, et al.
Joint Bone Spine
|
December 12, 2018
Lamin A/C gene (LMNA) mutation associated with laminopathy: A rare cause of idiopathic acro-osteolysis
Julie-Charlotte Lambert, Pauline Baudart, Annachiara De Sandre-Giovannoli, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
February 16, 2019
Fluconazole as a New Therapeutic Tool to Manage Patients With NPTIIc (SLC34A3) Mutation: A Case Report
Aurélia Bertholet-Thomas, Nathalie Tram, Laurence Dubourg, et al.
Annales D'Endocrinologie
|
January 16, 2025
Chapter 5: The roles of genetics in primary hyperparathyroidism
Pauline Romanet, Lucie Coppin, Arnaud Molin, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2015
Patients with isolated oligo/hypodontia caused by RUNX2 duplication
Arnaud Molin, Serena Lopez-Cazaux, Olivier Pichon, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 26, 2013
Paternal GNAS mutations lead to severe intrauterine growth retardation (IUGR) and provide evidence for a role of XLαs in fetal development
Nicolas Richard, Arnaud Molin, Nadia Coudray, et al.
Kidney International
|
January 24, 2026
Primary hyperoxaluria(s): from trials to real-life data and pipeline therapies
Justine Bacchetta, Cécile Acquaviva-Bourdain, Nadia Abid, et al.
Joint Bone Spine
|
January 23, 2017
Calcium pyrophosphate deposition disease revealing a hypersensitivity to vitamin D
Pauline Baudart, Arnaud Molin, Johann Cesini, et al.
Calcified Tissue International
|
May 21, 2020
Prolonged 25-OH Vitamin D Deficiency Does Not Impair Bone Mineral Density in Adult Patients With Vitamin D 25-Hydroxylase Deficiency (CYP2R1)
Arnaud Wiedemann, Emeline Renard, Arnaud Molin, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 50) with videos related to
Sort By:
Page
of 5
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 29, 2024
Human genetic diseases of phosphate and pyrophosphate metabolism
Arnaud Molin
The Journal of Clinical Investigation
|
April 15, 2025
Clinical evidence for independent regulation of vitamin D by intestinal CYP24A1
Sandrine Lemoine, Arnaud Molin, Alice Koenig, et al.
Joint Bone Spine
|
December 12, 2018
Lamin A/C gene (LMNA) mutation associated with laminopathy: A rare cause of idiopathic acro-osteolysis
Julie-Charlotte Lambert, Pauline Baudart, Annachiara De Sandre-Giovannoli, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
February 16, 2019
Fluconazole as a New Therapeutic Tool to Manage Patients With NPTIIc (SLC34A3) Mutation: A Case Report
Aurélia Bertholet-Thomas, Nathalie Tram, Laurence Dubourg, et al.
Annales D'Endocrinologie
|
January 16, 2025
Chapter 5: The roles of genetics in primary hyperparathyroidism
Pauline Romanet, Lucie Coppin, Arnaud Molin, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2015
Patients with isolated oligo/hypodontia caused by RUNX2 duplication
Arnaud Molin, Serena Lopez-Cazaux, Olivier Pichon, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 26, 2013
Paternal GNAS mutations lead to severe intrauterine growth retardation (IUGR) and provide evidence for a role of XLαs in fetal development
Nicolas Richard, Arnaud Molin, Nadia Coudray, et al.
Kidney International
|
January 24, 2026
Primary hyperoxaluria(s): from trials to real-life data and pipeline therapies
Justine Bacchetta, Cécile Acquaviva-Bourdain, Nadia Abid, et al.
Joint Bone Spine
|
January 23, 2017
Calcium pyrophosphate deposition disease revealing a hypersensitivity to vitamin D
Pauline Baudart, Arnaud Molin, Johann Cesini, et al.
Calcified Tissue International
|
May 21, 2020
Prolonged 25-OH Vitamin D Deficiency Does Not Impair Bone Mineral Density in Adult Patients With Vitamin D 25-Hydroxylase Deficiency (CYP2R1)
Arnaud Wiedemann, Emeline Renard, Arnaud Molin, et al.
Page
of 5