Zobrazeno 1 - 10
of 252
pro vyhledávání: '"Deutman, A.F"'
Autor:
Nolthenius, Tutein1, Deutman, A.F.1
Publikováno v:
Ophthalmologica. 1983, Vol. 186 Issue 1, p11-16. 6p.
Autor:
Pinckers, A.1, Deutman, A.F.1
Publikováno v:
Ophthalmologica. 1977, Vol. 174 Issue 3, p145-150. 6p.
Autor:
Deutman, A.F.1, van Balen, A.T.M.1
Publikováno v:
Ophthalmologica. 1976, Vol. 173 Issue 3/4, p196-199. 4p.
Publikováno v:
Ophthalmologica. 1973, Vol. 167 Issue 5/6, p368-372. 5p.
Autor:
Pennings, R.J.E., Huygen, P.L.M., Orten, D.J., Wagenaar, M., Aarem, A. van, Kremer, J.M.J., Kimberling, W.J., Cremers, C.W.R.J., Deutman, A.F.
Publikováno v:
Acta Ophthalmologica Scandinavica, 82, 131-9
Acta Ophthalmologica Scandinavica, 82, 2, pp. 131-9
Acta Ophthalmologica Scandinavica, 82, 2, pp. 131-9
Contains fulltext : 58539.pdf (Publisher’s version ) (Closed access) PURPOSE: To evaluate visual impairment in Usher syndrome 1b (USH1b) and Usher syndrome 2a (USH2a). METHODS: We carried out a retrospective study of 19 USH1b patients and 40 USH2a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e513306145273954a4b1773eb232bffb
https://hdl.handle.net/2066/58539
https://hdl.handle.net/2066/58539
Publikováno v:
Nederlands Tijdschrift voor Geneeskunde, 146, 2354-8
Nederlands Tijdschrift voor Geneeskunde, 146, 49, pp. 2354-8
Nederlands Tijdschrift voor Geneeskunde, 146, 49, pp. 2354-8
Item does not contain fulltext Usher syndrome is an autosomal recessively inherited disease, characterised by sensorineural hearing loss, tapetoretinal degeneration and in some cases vestibular problems. Based on the clinical heterogeneity, the disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::175d436a7238adf35eaf1e91cdc9a6e5
https://hdl.handle.net/2066/144599
https://hdl.handle.net/2066/144599
Autor:
Driessen, C.A.G.G., Janssen, A.P.M., Winkens, H.J., Kuhlmann, E.D., Vugt, A.H.M. van, Pinckers, A.J.L.G., Deutman, A.F., Janssen, J.J.M.
Publikováno v:
Ophthalmology, 108, 8, pp. 1479-84
Ophthalmology, 108, 1479-84
Ophthalmology, 108, 1479-84
Item does not contain fulltext PURPOSE: Recent studies show that mutations in the gene encoding 11-cis retinol dehydrogenase are associated with fundus albipunctatus. The authors wanted to investigate whether additional, more severe, mutations in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a28fd3e4634011c74921f18f0a43765c
https://doi.org/10.1016/s0161-6420(01)00640-6
https://doi.org/10.1016/s0161-6420(01)00640-6