Corrélations phénotype–génotype de la rétinopathie pigmentaire non syndromique : à propos de dix familles tunisiennes

Autor: Chebil, A., Falfoul, Y., Habibi, I., Munier, F., Schorderet, D., El Matri, L.

Publikováno v: In Journal Francais d'Ophtalmologie March 2016 39(3):277-286

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Incidence of retinoblastoma has increased: results from 40 European countries

Autor: Stacey AW, BOWMAN R, FOSTER A, KIVELA TT, MUNIER F, CASSOUX N, FABIAN ID, AL HARBY L, ALARCON PORTABELLA S, ALIA DB, ALL ERIKSSON C, ANTONINO R, ASTBURY NJ, BALGAGUER J, BALWIERZ W, BARRANCO H, BASCARAN C, BECK POPOVIC M, BIEWALD EM, BOBROVA N, BORNFELD N, BRICHARD, Bénédicte

Publikováno v: Ophtalmology, no.21, p. 72-75 (2021)

Incidence of retinoblastoma has increased: results from 40 European countries

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1493::10ea55606acb8ad78f692b308a03f6a8
https://hdl.handle.net/2078.1/244976

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Phenotype‐genotype correlation of p.R124S mutation in granular type 1 corneal dystrophy of Tunisian origin

Autor: Falfoul, Y, Bouyacoub, Y., Munier, F, Sayeb, M, Ouederni, M, Chargui, M, Matri, L, Abdelhak, S, Cheour, M

Publikováno v: Acta Ophthalmologica Scandinavica-Supplement
Acta Ophthalmologica Scandinavica-Supplement-, 2018, Special Issue: Abstract from the 2018 European Association for Vision and Eye Research Conference, 96 (S261), pp.38. ⟨10.1111/aos.13972_134⟩

International audience; Purpose: We report the clinical features and phenotype‐genotype correlation in a large Tunisian family with granular corneal dystrophy type I.Methods: Twenty‐seven members of the Tunisian family underwent a complete ophtha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8386097616b952a6bc8de72881d46566
https://hal-riip.archives-ouvertes.fr/pasteur-02003045