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Serge Amselem

Affiliations:

UPMC Univ Paris 6, France

Area:

, Hereditary recurrent fevers, Inflammasome

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"Serge Amselem"

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Parents

Children

Cecile Cazeneuve	grad student	2001	Paris 12
Irène Netchine	grad student	2002	Université Paris-Est Créteil Val de Marne (UPEC)
Gaëlle Pennarun	grad student	2002	Université Paris-Est Créteil Val de Marne (UPEC)
Damien Sternberg	grad student	2002	Université Paris-Est Créteil Val de Marne (UPEC)
Stéphanie Papin	grad student	2003	Université Paris-Est Créteil Val de Marne (UPEC)
Kalotina Machinis	grad student	2004	Université Paris 7
Isabelle Jéru	grad student	2006	UPMC Univ Paris 6
Marie Legendre	grad student	2010	UPMC Univ Paris 6
Christelle Perez	grad student	2012	UPMC Univ Paris 6
Esther Kott	grad student	2013	UPMC Univ Paris 6
Fawaz Awad	grad student	2014	UPMC Univ Paris 6

Collaborators

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Publications

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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
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
Louvrier C, Awad F, Cosnes A, et al. (2022) RNF213-associated urticarial lesions with hypercytokinemia. The Journal of Allergy and Clinical Immunology
Louvrier C, Awad F, Amselem S, et al. (2022) Absence of NLRP3 somatic mutations and VEXAS-related UBA1 mutations in a large cohort of patients with Schnitzler syndrome. Allergy
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
Manali ED, Kannengiesser C, Borie R, et al. (2022) Genotype-Phenotype Relationships in Inheritable Idiopathic Pulmonary Fibrosis: A Greek National Cohort Study. Respiration; International Review of Thoracic Diseases. 1-13
Mabrouk I, Al-Harthi N, Mani R, et al. (2022) Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients. Journal of Human Genetics
Legendre M, Butt A, Borie R, et al. (2020) Functional assessment and phenotypic heterogeneity of and mutations in interstitial lung diseases and lung cancer. The European Respiratory Journal

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