Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Hannelore Kraus"'
Publikováno v:
Documenta Ophthalmologica. 111:149-157
The purpose of this retrospective study was to determine the relevance of both visual-evoked potentials (VEP) and multifocal electroretinography (mfERG) to evaluate unexplained visual loss. Seventy-two consecutive patients (1996-2002) with visual dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b28a44827b3c0851c2b8bbc1e9888a86
https://doi.org/10.1007/s10633-005-5362-4
https://doi.org/10.1007/s10633-005-5362-4
Autor:
Nicole Mohr, H. Tillack, Ulrich Kellner, Bernhard H. F. Weber, Agnes B. Renner, Bernd Wissinger, Susanne Kohl, Michael H. Foerster, Hannelore Kraus
Publikováno v:
Retina. 24:929-939
Purpose: Detailed morphologic and functional evaluation of adult vitelliform macular dystrophy (AVMD). Methods: The records of 61 consecutive AVMD patients (inclusion criterion: vitelliform lesion smaller than one disk diameter at least in one eye) w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12d7a504af4628b5354999db0e108b13
https://doi.org/10.1097/00006982-200412000-00014
https://doi.org/10.1097/00006982-200412000-00014
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 238:94-97
· Background: A study was carried out to evaluate the regional variance of retinal dysfunction in chloroquine retinopathy. · Methods: In three patients with different stages of chloroquine retinopathy, ophthalmologic evaluations including recording
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4930a32bb6efff70f3383521ce57c9f4
https://doi.org/10.1007/s004170050016
https://doi.org/10.1007/s004170050016
Autor:
Hannelore Kraus, Ulrich Kellner, Margot Christ-Adler, Claudia Jandeck, Hagen Thieme, Bernd Wissinger, Michael H. Foerster
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 237:714-719
· Background: Leber’s hereditary optic neuropathy (LHON) mostly affects young males. In patients carrying one of the primary mutations the risk to develop LHON is 50% for males and 10% for females. We report a family with predominantly young girls
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ffd016a6977eea77ef49d2e54031fd6
https://doi.org/10.1007/s004170050301
https://doi.org/10.1007/s004170050301
Autor:
Horst Helbig, Heinrich Heimann, Hannelore Kraus, Michael H. Foerster, Norbert Bornfeld, Ulrich Kellner
Publikováno v:
British Journal of Ophthalmology. 82:650-654
AIMS—To describe the clinical picture and electrophysiological findings in Muller cell sheen dystrophy, a recently reported retinal dystrophy. METHOD—A basic ophthalmological evaluation as well as recording of standard electro-oculography and ele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7557b7d69aaf235a6b5072978d2dc90
https://doi.org/10.1136/bjo.82.6.650
https://doi.org/10.1136/bjo.82.6.650
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 236:109-114
• Background: Autosomal dominant vitreoretinochoroidopathy (ADVIRC) is a rare disorder previously described in four families residing in the USA and one family residing in Germany. We report the clinical and unexpected electrophysiological findings
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c14110a9928198c61ad3fea1d82f9103
https://doi.org/10.1007/s004170050050
https://doi.org/10.1007/s004170050050
Publikováno v:
Der Ophthalmologe. 94:796-800
Purpose: To analyze the value of electrophysiologic testing according to standards of the International Society for Clinical Electrophysiology of Vision (ISCEV) in infants less than 10 years of age. Patients and methods: In 64 infants less than 10 ye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30792995443d2ea4169e668662532f04
https://doi.org/10.1007/s003470050206
https://doi.org/10.1007/s003470050206
Publikováno v:
Der Ophthalmologe. 101
Die adulte vitelliforme Makuladystrophie (AVMD) wird haufig fehldiagnostiziert. Grosere Studien mit modernen morphologischen und funktionellen Diagnosetechniken existieren nicht. Die Daten von 67 konsekutiven AVMD-Patienten (1994–2003) wurden retro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3099ff48ea40056fb2d2b9ba7ad38d3
https://doi.org/10.1007/s00347-004-1025-1
https://doi.org/10.1007/s00347-004-1025-1
Publikováno v:
Der Ophthalmologe. 101
Hintergrund Ziel dieser Studie ist es, die klinisch-molekulargenetische Korrelation bei Patienten mit kongenitalen Zapfenfunktionsstorungen darzustellen.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7efe9c87a41a626b6b220361fa336f2
https://doi.org/10.1007/s00347-003-0976-y
https://doi.org/10.1007/s00347-003-0976-y
Autor:
Bernd Wissinger, Michael H. Foerster, Susanne Kohl, Hannelore Kraus, Sabine Tippmann, Ulrich Kellner
Publikováno v:
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. 242(9)
X-linked blue cone monochromatism (BCM) has to be differentiated from x-linked cone dystrophy and autosomal recessive rod monochromatism.In nine male patients with congenital cone dysfunction (one family, six single cases; age range: 9-55 years), mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e81ff02600c28d536491e4046ce0103
https://pubmed.ncbi.nlm.nih.gov/15069569
https://pubmed.ncbi.nlm.nih.gov/15069569