Zobrazeno 1 - 10
of 37
pro vyhledávání: '"J W, Delleman"'
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
Publikováno v:
Documenta Ophthalmologica. 56:183-194
As part of a combined ophthalmological, genetic, clinical, biochemical, ultrastructural and electro-physiological study of albinism we have examined over one hundred albinos, together with their heterozygote family members. Given this substantial num
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a35e9a01452f2e5a7dec891df2c765f6
https://doi.org/10.1007/bf00154728
https://doi.org/10.1007/bf00154728
Publikováno v:
Journal of Pediatric Ophthalmology & Strabismus. 14:205-212
Three families with a total of five patients with Lowe's syndrome are described. We tried to trace female heterozygotes by ophthalmological abnormalities in order to realize prevention of this serious X-chromosomal recessive disease. Of the fourteen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::773e5b541fe3f2fee406a8606b866d1b
https://doi.org/10.3928/0191-3913-19770701-05
https://doi.org/10.3928/0191-3913-19770701-05
Publikováno v:
Documenta Ophthalmologica. 56:177-181
Colobomata of the optic disc result from failure of closure of the most anterior portion of the optic stalk. Therefore the great majority of these defects are found at the six o'clock position in the region of the embryonic defect. The authors examin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ad5b90d7c1db4cc123282efe3aab85f
https://doi.org/10.1007/bf00154727
https://doi.org/10.1007/bf00154727