Recherche
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Management of albinism: French guidelines for diagnosis and care
(Journal of the European Academy of Dermatology and Venereology. vol. 35, n° 7, pp. 1449-1459, 2021-05-27)Article de revue -
CHN1 and duane retraction syndrome: Expanding the phenotype to cranial nerves development disease
(European Journal of Medical Genetics. vol. 64, n° 4, 2021-04)Article de revue -
Clinical description and mutational profile of a moroccan series of patients with rubinstein taybi syndrome
(African Health Sciences. vol. 21, n° 2, pp. 960-967, 2021-08-02)Article de revueLibre accès -
A recurrent missense variant in EYA3 gene is associated with oculo-auriculo-vertebral spectrum
(Human Genetics. vol. 140, n° 6, pp. 933-944, 2021)Article de revue -
Erratum: Rémy et al. Isolation and Culture of Human Stem Cells from Apical Papilla under Low Oxygen Concentration Highlight Original Properties.
(Cells. vol. 10, n° 5, pp. 988, 2019-11-21)Article de revueLibre accès -
Atypical late diagnosis of Noonan syndrome revealed by bleedings due to platelet dysfunction.
(Journal of Thrombosis and Thrombolysis, 2021-08-08)Article de revue -
Osteopontin: A Promising Therapeutic Target in Cardiac Fibrosis
(Cells. vol. 8, n° 12, 2019-12-03)Article de revueLibre accès -
Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)
(European Journal of Human Genetics. vol. 29, n° 9, pp. 1470-1471, 2021-07-15)Article de revue -
Dual Inhibition of FLT3 and AXL by Gilteritinib Overcomes Hematopoietic Niche-Driven Resistance Mechanisms in -ITD Acute Myeloid Leukemia.
(Clinical Cancer Research, 2021-08-16)Article de revue -
Chronic kidney disease of unknown origin in agricultural communities: beyond tropical mist?
(Nephrology Dialysis Transplantation, 2020-10-27)Article de revueLibre accès