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In vitro long term differentiation and functionality of three-dimensional bioprinted primary human hepatocytes: application for in vivo engraftment
(Biofabrication. vol. 14, n° 3, 2022-06)Article de revueLibre acceso -
Reliability and validity of the French adaptation of the Family Relationship Index–short form in patients’ with chronic kidney disease
(Journal of Health Psychology. vol. 27, n° 1, pp. 166-175, 2022-01-01)Article de revueLibre acceso -
Patient perspectives on chronic kidney disease and decision-making about treatment. Discourse of participants in the French CKD-REIN cohort study
(Journal of Nephrology. vol. 35, n° 5, pp. 1387-1397, 2022-06)Article de revueLibre acceso -
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 -
Pain evaluation after day-surgery using a mobile phone application
(Anaesthesia Critical Care & Pain Medicine. vol. 40, n° 3, 2021-06)Article de revue -
Novel variants in the BLOC1S3 gene in patients presenting a mild form of Hermansky-Pudlak syndrome
(Pigment Cell & Melanoma research. vol. 34, n° 1, pp. 132-135, 2021-01)Article de revue