Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Claudia Grünauer-Kloevekorn"'
Autor:
Andrea Magdalena Waibel, Johanna Mirjam Stoye, Pablo Villavicencio-Lorini, Katrin Hoffmann, Carolin Obermaier, Saskia Biskup, Claudia Grünauer-Kloevekorn
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 239:1473-1477
ZusammenfassungDie X-chromosomal rezessive Retinoschisis (XLRS) ist eine seltene vitreoretinale Dystrophie, die durch molekulargenetische Veränderungen im RS1-Gen ausgelöst wird. Sie manifestiert sich meist in jungem Lebensalter mit einer symmetris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f636a5b42e01868da77d53e460fe0970
https://doi.org/10.1055/a-1901-1011
https://doi.org/10.1055/a-1901-1011
Autor:
Andrea Magdalena, Waibel, Johanna Mirjam, Stoye, Pablo, Villavicencio-Lorini, Katrin, Hoffmann, Carolin, Obermaier, Saskia, Biskup, Claudia, Grünauer-Kloevekorn
Publikováno v:
Klinische Monatsblatter fur Augenheilkunde. 239(12)
X-linked retinoschisis (XLRS) is a rare vitreoretinal dystrophy caused by molecular genetic changes in theDie X-chromosomal rezessive Retinoschisis (XLRS) ist eine seltene vitreoretinale Dystrophie, die durch molekulargenetische Veränderungen im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ddaaa4eaff2651076bf8244994fa01cf
https://pubmed.ncbi.nlm.nih.gov/36493766
https://pubmed.ncbi.nlm.nih.gov/36493766
Autor:
Claudia Grünauer-Kloevekorn, Ruth Kawan, Nina Kosanetzky, Anika Schröter, Thomas Neß, Isabell Funk, S. Heinzelmann
Publikováno v:
Der Ophthalmologe. 116:789-793
A 53-year-old patient consulted our practice clinic complaining of progressive visual loss, increased glare sensitivity and color sense disorder. Extensive diagnostic investigation, including multifocal ERG (mfERG) and macular thickness map with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c439986bd0fc12beb345568ba6a10dc1
https://doi.org/10.1007/s00347-018-0804-z
https://doi.org/10.1007/s00347-018-0804-z
Autor:
Anika, Schröter, Nina, Kosanetzky, Ruth, Kawan, Isabell, Funk, Claudia, Grünauer-Kloevekorn, Thomas, Neß, Sonja, Heinzelmann
Publikováno v:
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft. 116(8)
A 53-year-old patient consulted our practice clinic complaining of progressive visual loss, increased glare sensitivity and color sense disorder. Extensive diagnostic investigation, including multifocal ERG (mfERG) and macular thickness map with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::352a426f97075e621980f6ee89cee913
https://pubmed.ncbi.nlm.nih.gov/30426193
https://pubmed.ncbi.nlm.nih.gov/30426193
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 226:466-469
BACKGROUND: Fuchs endothelial corneal dystrophy is the most common disease of the corneal endothelium. Besides some sporadic cases, an autosomal dominant inheritance is frequently described. Mutations in the VSX-1 gene are identified as the underlyin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::415c40f44c2e7914b74da3a0b4f8a8bb
https://doi.org/10.1055/s-0028-1109427
https://doi.org/10.1055/s-0028-1109427
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 226:428-431
PURPOSE: Diseases of the retina, the optic nerve and the cornea may lead to a non-treatable loss of central vision. We report on low vision rehabilitation in 100 vision impaired patients. METHODS: Low vision rehabilitation was performed in 100 consec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d255d451bb79c743a42f4e8553b75140
https://doi.org/10.1055/s-0028-1109194
https://doi.org/10.1055/s-0028-1109194
Autor:
F. Tost, C Auw-Haedrich, Claudia Grünauer-Kloevekorn, M Wolter-Roessler, Ursula G. Froster, H E Völcker, W Heinritz, S Braeutigam, Giw Duncker, E Weidle
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 223:829-836
Purpose Different missense mutations in the TGFBI gene cause granular (Groenouw CDGG1, Avellino CDA, Reis-Bucklers CDB1) and lattice (Type I; Biber-Haab-Dimmer; CDL1) corneal dystrophies and, in some reports, corneal dystrophy Thiel-Behnke (CDB2). We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcc1c9406b043d4dd7ae1d7c54fd5168
https://doi.org/10.1055/s-2006-926694
https://doi.org/10.1055/s-2006-926694
Autor:
Claudia Grünauer-Kloevekorn, H. Frimmel, M. Bloching, U. Bilkenroth, Giw Duncker, A. Eichhorst, I. Clausen, E. Röpke
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 223:243-246
Background Pseudotumors of the orbit comprise a group of idiopathic inflammatory processes and are, except for endocrine orbitopathy, the most common reason for exophthalmos in adults. Orbital pseudotumors, also called idiopathic orbital inflammatory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a1b50d85136302416121843fa2bf5a0
https://doi.org/10.1055/s-2005-858722
https://doi.org/10.1055/s-2005-858722
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 222:54-57
Puprose: It is a challenge to prevent irreversible amblyopia in infants suffering from Peters anomaly. In some cases of centrally located corneal opacifications an optical sector iridectomy can not lead to a clear opticalaxis. The homologous penetrat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0bb8c9c26bd2ea3bb143da809ad4402
https://doi.org/10.1055/s-2004-813914
https://doi.org/10.1055/s-2004-813914
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 222:874-882
Introduction The purpose is to compare videokeratometric data (Fourier series harmonic analysis and wave-front analysis) in eyes with ectatic corneal disease (keratoconus; pellucid marginal corneal degeneration [PMCD]) and to determine parameters for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfc66e931d32a634832aeab2b1ed4b2b
https://doi.org/10.1055/s-2005-858822
https://doi.org/10.1055/s-2005-858822