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- aggregation classification "A1".
- aggregation creator B110242.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation date "2001".
- aggregation format "application/pdf".
- aggregation hasFormat 141072.bibtex.
- aggregation hasFormat 141072.csv.
- aggregation hasFormat 141072.dc.
- aggregation hasFormat 141072.didl.
- aggregation hasFormat 141072.doc.
- aggregation hasFormat 141072.json.
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- aggregation hasFormat 141072.txt.
- aggregation hasFormat 141072.xls.
- aggregation hasFormat 141072.yaml.
- aggregation isPartOf urn:issn:0721-832X.
- aggregation language "eng".
- aggregation rights "I have transferred the copyright for this publication to the publisher".
- aggregation subject "Biology and Life Sciences".
- aggregation title "Clinical and electrophysiological findings in autosomal dominant vitreoretinochoroidopathy: report of a new pedigree.".
- aggregation abstract "Purpose: To report the clinical and electrophysiological findings in a three-generation pedigree with autosomal dominant vitreoretinochoroidopathy. Methods: Sixteen members of a three-generation pedigree with autosomal dominant vitreoretinochoroidopathy were examined clinically, including measurement of the corneal diameter. In 14 persons, Goldmann perimetry, axial length determination and electro-oculography were carried out. Electroretinography, according to ISCEV standards, was performed in 11 of 12 affected persons. Results: Characteristic annular peripheral pigmentary changes were present in all affected members, as well as chorioretinal atrophy varying from a tigroid aspect to marked atrophy. Four patients presented a microcornea and shallow anterior chamber without microphthalmia. The visual fields appeared to narrow with ageing. The electro-oculography was pathological in the affected patients and normal in the unaffected. The electroretinographic amplitude responses tended to worsen with age, with maintenance of near normal latencies. Conclusion: The clinical presentation of autosomal dominant vitreoretinopathy is variable. Electrooculography seems to be a discriminative test. The condition may be associated with anterior segment abnormalities other than presenile cataract, such as microcornea, shallow anterior chamber and angle closure glaucoma.".
- aggregation authorList BK281826.
- aggregation endPage "582".
- aggregation issue "8".
- aggregation startPage "575".
- aggregation volume "239".
- aggregation aggregates 2087360.
- aggregation isDescribedBy 141072.
- aggregation similarTo s004170100318.
- aggregation similarTo LU-141072.