Concepedia
Statistics
Publications
6
Citations
621
H-Index
Active since
1995
Affiliations
Inserm(Current)
Hôpital Necker-Enfants Malades
Hôpitaux Universitaires Henri-Mondor
Sorbonne Université
Université Paris Cité
E. Girodon is an author at Inserm specializing in cftr gene mutations, cystic fibrosis, and cystic fibrosis genetics.
Publications per year
1995–2022
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France
Mireille Claustres, Caroline Guittard, Dominique Bozon et al. · Human Mutation · 2000 · 250 citations
Life Sciences, Genetics, Molecular Genetics +11
Frequent Occurrence of the CFTRIntron 8 (TG)n 5T Allele in Men withCongenital Bilateral Absence of the Vas Deferens
Bruno Costes, E. Girodon, N. Ghanem et al. · European Journal of Human Genetics · 1995 · 150 citations
Medicine, Genetics, Molecular Genetics +13
Clinical Phenotype and Genotype of Children with Borderline Sweat Test and Abnormal Nasal Epithelial Chloride Transport
Isabelle Sermet‐Gaudelus, E. Girodon, Dorota Sands et al. · American Journal of Respiratory and Critical Care Medicine · 2010 · 68 citations
Medicine, Genetics, Pediatrics +15
Atypical Sinusitis in Adults Must Lead to Looking for Cystic Fibrosis and Primary Ciliary Dyskinesia
A. Coste, E. Girodon, S.A. Louis et al. · The Laryngoscope · 2004 · 57 citations
Medicine, Pathology, Pediatric Otolaryngology +15
ECFS standards of care on CFTR-related disorders: Diagnostic criteria of CFTR dysfunction
Isabelle Sermet‐Gaudelus, E. Girodon, F. Vermeulen et al. · Journal of Cystic Fibrosis · 2022 · 51 citations · Full text
Medicine, Clinical Sciences, Health Care Regulation +6
1–5 of 6