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Water intake and progression of chronic kidney disease: the CKD-REIN cohort study
(Nephrology Dialysis Transplantation. vol. 37, n° 4, pp. 730-739, 2022-04-01)Article de revue -
Use of Human Gingival Fibroblasts for Pre-Vascularization Strategies in Oral Tissue Engineering
(Tissue Engineering and Regenerative Medicine. vol. 19, n° 3, pp. 525-535, 2022-06-01)Article de revue -
3D printing for orbital volume anatomical measurement
(Surgical and Radiologic Anatomy. vol. 44, n° 7, pp. 991-998, 2022-07-01)Article de revue -
A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodies.
(Platelets. vol. 32, n° 3, pp. 420-423, 2021-04-03)Article de revue -
Effect of modified bilateral sagittal split osteotomy on inferior alveolar nerve neurosensory disturbance
(British Journal of Oral and Maxillofacial Surgery. vol. 60, n° 8, pp. 1086-1091, 2022-10-01)Article de revue -
Computational Identification and 3D Morphological Characterization of Renal Glomeruli in Optically Cleared Murine Kidneys.
(Sensors. vol. 21, n° 22, 2021-11-09)Article de revue -
CHEDDA syndrome is an underrecognized neurodevelopmental disorder with a highly restricted ATN1 mutation spectrum
(Clinical Genetics. vol. 100, n° 4, pp. 468-477, 2021-07-01)Article de revue -
Dopachrome tautomerase variants in patients with oculocutaneous albinism
(Genetics in Medicine. vol. 23, n° 3, pp. 479-487, 2021)Article de revue -
Correspondence on « De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females » by Polla et al.
(Genetics in Medicine. vol. 23, n° 10, pp. 2003-2004, 2021-06-02)Article de revue -
A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodies
(Platelets. vol. 32, n° 3, pp. 420-423, 2021)Article de revue