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Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel Formation
(Journal of Bone and Mineral Research. vol. 31, n° 3, pp. 498–513, 2015-10)Article de revue -
Clinical variability and probable founder effect in oculocutaneous albinism type 7.
(Clinical Genetics. vol. 97, n° 3, pp. 527-528, 2020-03-01)Article de revue -
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 revueOpen access -
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 -
How I manage pregnancy in women with Glanzmann thrombasthenia.
(Blood, 2022-03-14)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 revueOpen access -
Superior Vena Cava Thrombosis.
(The American Journal of Medicine, 2022-04-23)Article de revue -
Un nouveau type de substitut vasculaire obtenu par tissage de fils issus de la membrane amniotique humaine
(Université de Bordeaux)Thèses de doctorat