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Autor:
J. W. Delleman
Publikováno v:
Orbit. 3:211-212
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed83e26eec8651e8cbb89a63556a96fb
https://doi.org/10.3109/01676838409019203
https://doi.org/10.3109/01676838409019203
Publikováno v:
Acta ophthalmologica, 72(1), 98-102. Copenhagen Scriptor
Results of a pilot study to evaluate goniodysge-nesis as a cause of familial open-angle glaucoma are reported. Patients with a familial high tension open-angle glaucoma and a goniodysgenetic chamber angle (n = 11), a number of their relatives with gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7280d42797bcc622be63d01cfa4002a5
https://doi.org/10.1111/j.1755-3768.1994.tb02745.x
https://doi.org/10.1111/j.1755-3768.1994.tb02745.x
Publikováno v:
Clinical Genetics. 25:470-472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3498a15729102ad3c354dbfe89fcc6b1
https://doi.org/10.1111/j.1399-0004.1984.tb02019.x
https://doi.org/10.1111/j.1399-0004.1984.tb02019.x
Publikováno v:
Documenta Ophthalmologica. 85:13-19
The direct compensation method allows for an accurate determination of intraocular light scattering between 3.5 and 25 degrees of scattering angle and is suitable for untrained subjects. The method was used to study light scattering in four forms of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::570daabdc978db6c227927d8dc6571f4
https://doi.org/10.1007/bf01268096
https://doi.org/10.1007/bf01268096
Autor:
P T, de Jong, E M, Bleeker-Wagemakers, G F, Vrensen, R M, Broekhuyse, J D, Peereboom-Wynia, J W, Delleman
Publikováno v:
Ophthalmology. 97(9)
A 7-year-old girl was found to have a progressive axial crystalline cataract located in the embryonal, fetal, and infantile nucleus. She also had the unknown association of crystalline cataract with uncombable hair. Samples of the aspirate after extr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0e7ecef691da4f965b3f1235426fe39d
https://pubmed.ncbi.nlm.nih.gov/2234851
https://pubmed.ncbi.nlm.nih.gov/2234851
Autor:
E. J. M. Schuurman, Françoise Meire, J. W. Delleman, A. A. B. Bergen, G.J.B. van Ommen, J.B. ten Brink
Publikováno v:
Genomics, 18(2), 463-464. Academic Press Inc.
X-linked progressive cone dystrophy (XLPCD) is a rare hereditary eye disorder characterized by disturbed cone ERG, abnormal color vision, loss of visual acuity, and photophobia. Linkage analysis in only two XLPCD families has been described previousl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22c8803db7372345c86532c5213ae9f9
https://doi.org/10.1006/geno.1993.1504
https://doi.org/10.1006/geno.1993.1504
Autor:
M J Hageman, J W Delleman
Publikováno v:
Journal of Pediatric Ophthalmology & Strabismus. 15:341-345
In the Netherlands five families with 34 previously unreported patients with Waardenburg syndrome were traced. Twenty-three patients with the syndrome including dystopia canthorum (Type I) were ophthalmologically examined and three patients with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0045ff83eb15ac6c7addddbc597f59d7
https://doi.org/10.3928/0191-3913-19781101-03
https://doi.org/10.3928/0191-3913-19781101-03