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au.\*:("CREVEAUX, I")

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Bronchiolite folliculaire : une observation pédiatrique = Follicular bronchiolitis paediatric case reportLABBE, A; DECHELOTTE, P; CREVEAUX, I et al.Revue des maladies respiratoires. 1992, Vol 9, Num 3, pp 324-326, issn 0761-8425Article

Le déficit héréditaire en céruléoplasmine = Hereditary ceruleoplasmin deficiencyABERGEL, A; SAPIN, V; BONNY, C et al.Hépato-gastro (Montrouge). 2000, Vol 7, Num 2, pp 93-100, issn 1253-7020Article

SCO-spondin is evolutionarily conserved in the central nervous system of the chordate phylumGOBRON, S; CREVEAUX, I; MEINIEL, R et al.Neuroscience. 1999, Vol 88, Num 2, pp 655-664, issn 0306-4522Article

Complex expression pattern of the SCO-spondin gene in the bovine subcommissural organ : toward an explanation for Reissner's fiber complexity?CREVEAUX, I; GOBRON, S; MEINIEL, R et al.Molecular brain research. 1998, Vol 55, Num 1, pp 45-53, issn 0169-328XArticle

Récidive d'une dystrophie de Groenouw de type I après photokératectomie thérapeutique : Étude en biologie moléculaire du rôle de l'épithélium cornéen = Early recurrence of Groenouw type I corneal dystrophy after phototherapeutic keratectomy. Molecular biology study suggests epithelial genesisCHIAMBARETTA, F; PILON, F; DERIOT, J.-B et al.Journal français d'ophtalmologie. 2004, Vol 27, Num 5, pp 449-456, issn 0181-5512, 8 p.Article

De novo interstitial direct duplication of Xq21.1q25 associated with skewed X-inactivation patternTACHDJIAN, G; ABOURA, A; BENKHALIFA, M et al.American journal of medical genetics. 2004, Vol 131A, Num 3, pp 273-280, issn 0148-7299, 8 p.Article

Fetal midgut volvulus as a sign for cystic fibrosisDURAND, M; COSTE, K; LEMERY, D et al.Prenatal diagnosis. 2008, Vol 28, Num 10, pp 973-974, issn 0197-3851, 2 p.Article

La photokératectomie thérapeutique dans le traitement de la dystrophie grillagée de type I = Phototherapeutic keratectomy in the treatment of lattice corneal dystrophy type ICHIAMBARETTA, F; ROZIER, B; PILON, F et al.Journal français d'ophtalmologie. 2004, Vol 27, Num 7, pp 747-753, issn 0181-5512, 7 p.Article

Screening for cystic fibrosis transmembrane conductance regulator gene mutations in men included in an intracytoplasmic sperm injection programmeBOUCHER, D; CREVEAUX, I; GRIZARD, G et al.Molecular human reproduction. 1999, Vol 5, Num 6, pp 587-593, issn 1360-9947Article

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