Parents
Sign in to add mentor| Serge Amselem | grad student | 2010 | UPMC Univ Paris 6 | |
| (Implication du récepteur de la ghréline en pathologie humaine : caractérisation d’une nouvelle étiologie des maladies de la croissance et de ses mécanismes moléculaires) | ||||
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| Brudon A, Legendre M, Mageau A, et al. (2024) High risk of lung cancer in surfactant-related gene variant carriers. The European Respiratory Journal |
| Thomas L, Cuisset L, Papon JF, et al. (2024) Skewed X-chromosome inactivation drives the proportion of -defective airway motile cilia and variable expressivity in primary ciliary dyskinesia. Journal of Medical Genetics |
| Diesler R, Legendre M, Si-Mohamed S, et al. (2024) Similarities and differences of interstitial lung disease associated with pathogenic variants in SFTPC and ABCA3 in adults. Respirology (Carlton, Vic.) |
| Desroziers T, Prévot G, Coulomb A, et al. (2023) Hypomorphic pathogenic variant in SFTPB leads to adult pulmonary fibrosis. European Journal of Human Genetics : Ejhg |
| Le Guen P, Borie R, Legendre M, et al. (2023) mutation revealed by a lymphoid interstitial pneumonia in an adult with rheumatoid arthritis. Erj Open Research. 9 |
| Muñoz-Garcia J, Heymann D, Giurgea I, et al. (2023) Pharmacological options in the treatment of osteogenesis imperfecta: a comprehensive review of clinical and potential alternatives. Biochemical Pharmacology. 115584 |
| Legendre M, Darde X, Ferreira M, et al. (2022) The clinical course of interstitial lung disease in an adult patient with an ABCA3 homozygous complex allele under hydroxychloroquine and a review of the literature. Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of Wasog. 39: e2022019 |
| Assrawi E, Louvrier C, El-Khouri E, et al. (2022) Mosaic variants in TNFRSF1A: An emerging cause of tumor necrosis factor receptor-associated periodic syndrome. Rheumatology (Oxford, England) |
| Legendre M, Thouvenin G, Taytard J, et al. (2022) High Nasal Nitric Oxide, Cilia Analyses and Genotypes in a Retrospective Cohort of Children with Primary Ciliary Dyskinesia. Annals of the American Thoracic Society |
| Charbit-Henrion F, Goguyer-Deschaumes R, Borensztajn K, et al. (2022) Systemic inflammatory syndrome in children with FARSA deficiency. Clinical Genetics |