Inhaltspezifische Aktionen


  • New Scleral Depressor Marker for Retinal Detachement Surgery
    Lytvynchuk L, Grzybowski A, Lorenz B, Ansari-Shahrezaei S, Binder S
    Ophthalmology Retina 2019;3:73-76
  • An ontological foundation for ocular phenotypes and rare eye diseases
    Sergouniotis P I, Maxime E, Leroux D, Olry A, Thompson R, Rath A, Robinson P N, Dollfus H, ERN-EYE Ontology Study Group
    Sergouniotis et al. Orphanet Journal of Rare Diseases (2019) 14:8
  • Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders
    Zeitz C, Michiels C, Neuillé M, Friedburg C, Condroyer C, Boyard F, Antonio A, Bouzidi N, Milicevic D, Veaux R, Tourville A, Zoumba A, Seneina I, Foussard M, Andrieu C, Preising M, Blanchard S, Saraiva JP, Mesrob L, Le Floch E, Jubin C, Meyer V, Blanché H, Boland A, Deleuze J-F, Sharon D, Drumare I, Defoort-Dhellemmes S, De Baere E, Leroy BP, Zanlonghi X, Casteels I, de Ravel TJ, Balikova I, Koenekoop R, Laffargue F, McLean R, Gottlob I, Bonneau D, Schordert DF, Munier FL, McKibbin M, Prescott K, Pelletier V, Dollfuss H, Perdomo‐Trujillo Y, Faure C, Reiff C, Wissinger B, Meunier I, Kohl S, Banin E, Zrenner E, Jurklies B, Lorenz B, Sahel JA, Audo I
    Human mutation, 2019 Jun;40(6):765-787
  • Beidseitige Sehminderung im 3. Lebensjahr gefolgt von einseitiger flacher Netzhautablösung im 3. Lenbensjahr - klinischer Verlauf bei einem Kind mit Compound heterozygoten RP1-Mutationen
    Starosta D, Lorenz B, Lytvynchuk L, Peising MN
    Klin Mon Aug 236(3):286-288, März 2019
  • The Phenotypic Spectrum of Ophthalmic Changes in CEP290 Mutations
    Preising MN, Schneider U, Friedburg C, Gruber H, Lindner S, Lorenz B
    Klin Monbl Augenheilkd. 2019 Mar;236(3):244-252

  • High-dose Anderson operation for nystagmus-related anomalous head turn
    Gräf M, Hausmann A, Lorenz B
    Graefe's Archive for Clinical and Experimental Ophthalmology, published online 14.06.2019

  • Splitting of the lateral rectus muscle with medial transposition to treat oculomotor palsy: a retrospective analysis of 29 consecutive cases
    Basiakos S, Gräf M, Preising MN, Lorenz B
    Graefe's Archive for Clinical and Experimental Ophthalmology, 2019 Sep;257(9):2005-2014
  • Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene
    Felden J, Baumann B, Ali M, Audo I, Ayuso C, Bocquet B, Casteels I, Garcia-Sandoval B, Jacobson SG, Jurklies B, Kellner U, Kessel L, Lorenz B, McKibbin M, Meunier I, de Ravel T, Rosenberg T, Rüther K, Vadala M, Wissinger B, Stingl K, Kohl S.
    Hum Mutat. 2019 Aug;40(8):1145-1155

  • Methods for achieving low endophthalmitis rates in phacoemulsification cataract surgery
    Grzybowski A, Kanclerz P, Lytvynchuk L
    Acta Ophthalmol. 2019 Jun (Epub ahead of print)
  • Dynamic intraoperative optical coherence tomography for inverted internal limiting membrane flap technique in large macular hole surgery
    Lytvynchuk L, Falkner-Radler CI, Krepler K, Glittenberg CG, Ahmed D, Petrovski G, Lorenz B, Ansari-Shahrezaei S, Binder S
    Graefes Arch Clin Exp Ophthtalmol. 2019 Nov;257(11):2589
  • Reduced Visual Acuity at the Age of 3 Years and Flat Unilateral Retinal Detachment at the Age of 9 Years - History of a Child with Compound Heterozygous RP1 Mutations
    Starosta DA, Lorenz B, Lytvynchuk L, Preising MN
    Klin Monbl Augenheilkd. 2019 Mar (3):286-288
  • Human Embryonic Sterm Cell-Derived Retinal Pigment Epithelium-Role in Dead Cell Clearace and Inflammation
    Szatmári-Tóth M, Ilmarinen T, Mikhailova A, Skottman H, Kauppinen A, Kaarniranta K, Kristóf E, Lytvynchuk L, Veréb Z, Fésüs L, Petrovski G
    Int J Mol Sci 2019 Feb 20;20(4)
  • Optimizing Measurement of Vascular Endothelial Growth Factor in Small Blood Samples of Premature Infants
    Lopez Yomayuza CC, Preissner KT, Lorenz B, Stieger K
    Sci Rep. 2019 May 1;9(1):6744
  • Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus
    Mayer AK, Mahajnah M, Thomas MG, Cohen Y, Habib A, Schulze M, Maconachie GDE, AlMoallem B, De Baere E, Lorenz B, Traboulsi EI, Kohl S, Azem A, Bauer P, Gottlob I, Sharkia R, Wissinger B
    Brain 2019 Jun 1;142(6)1528-1534
  • Cone-Mediated Function Correlates to Altered Foveal Morphology in Preterm-Born Children at School Age
    Bowl W, Raoof S, Lorenz B, Holve K, Schweinfurth S, Stieger K, Andrassi-Darida M
    Invest Ophthalmol Vis Sci. 2019 Apr 1;60(5):1614-1620
  • The Natural History of Inherited Retinal Dystrophy Due to Biallelic Mutations in the RPE65 Gene
    Chung DC, Berelsen M, Lorenz B, Pennesi ME, Leroy BP, Hame CP, Pierce E, Sallum J, Larsen M, Stieger K, Preising M, Weleber R, Yang P, Place E, Liu E, Schaefer G, Di Stefano-Pappas J, Elci OU, McCague S, Wellmann JA, High KA, Reape KZ
    Am J. Ophthalmol 2019 Mar;199:58-70
  • Toward geneome editing in X-linked RP-development of a mouse model with specific treatment relevant features
    Schlegel J, Hoffmann J, Röll D, Müller B, Günther S, Zhang W, Janise A, Vössing C, Fühler B, Neidhardt J, Khanna H, Lorenz B, Stieger K
    Transl Res. 2019 Jan;203:57-72
  • An ontological foundation for ocular phenotypes and rare eye diseases
    Sergouniotis PI, Maxime E, Leroux D, Olry A, Thompson R, Rath A, Robinson PN, Dollfus H; ERN-EYE Ontology Study Group.
    Orphanet J Rare Dis. 2019 Jan 9;14(1):8

  • Correction to: Visual impairment and blindness in institutionalized elderly in Germany
    Larsen PP, Thiele S, Krohne TU, Ziemssen F, Krummenauer F, Holz FG, Finger RP; OVIS-Study Group
    Graefes Arch Clin Exp Ophthalmol. 2019 May;257(5):1057

  • Symptomatische Minimalvariante einer Grubenpapille mit zentrozökalem Gesichtsfeldausfall infolge einer begrenzten progressiven Atrophie der retinalen Ganglienzellen - ein Fallbericht
    Starosta D, Lorenz B
    Klin Mon Ophthalmol, 2019 Jul 2. doi: 10.1055/a-0901-7582. Online ahead of print
  • Biallelic mutation of human SLC646 encoding the taurine transporter TAUTis linked to early retinal degeneration
    Preising MN, Görg B, Friedburg C, Qvartskhava N, Budde BS, Bonus BS, Bonus M, Toliat MR, Pfleger C, Altmüller J, Herebian D, Beyer M, Zöllner HJ, Wittsack HJ, Schaper J, Klee D, Zechner U, Nürnberg P, Schipper J, Schnitzler A, Gohlke H, Lorenz B, Häussinger D, Bolz HJ
    FASEB J 2019 Oct;33(10):11507-11527
  • Fundus-Controlled Dark Adaptometry in Young Children Without and with Spontaneously Regressed Retinopathy of Prematurity
    Bowl W, Lorenz B, Stieger K, Schweinfurth S, Holve K, Andrassi-Darida M
    Transl Vis Sci Technol. 2019 Jun 28;8(3):62
  • Answer to the Letter to the Editor relating: Lytvynchuk LM, Falkner-Radler CI, Krepler K, Glittenberg CG, Ahmed D et al. "Dynamic intraoperative optical coherence tomography for inverted internal limiting membrane flap techniue in large macular hole surgery" Graefe's Arch Clin Exp Ophthalmol 2019 May 29; written by Michaleska Z. and Nawrocki J
    Lytvynchuk LM, Binder S
    Graefes Arch Clin Exp Ophthalmol. 2019 Nov;257(11):2589
  • Precision of bag-in-the-lens intraocular lens power calculation in different age groups of pediatric catarct patients: Report of the Giessen Pediatric Catarct Study Group
    Lytvynchuk LM, Thiele MV, Schmidt W, Lorenz B
    J Cataract Refract Surg. 2019 Oct;45(10):1372-1379
  • Efficiency of the Hydraulic Centripetal Macular Displacemtne Technique in the Treatment of Traumatic Full-Thickness Macular Holes
    Ruban A, Lytvynchuk L, Zolnikova A, Richard G
    Retina. 2019 Oct;39 Suppl 1:S74-S83
  • Ophthalmic Genetics: Insights into Current (Latest) Methods of Diagnostics, Phenotyping and Therapy
    Lorenz B
    Klin Mon Aug, 2019 236(3): 234-235.
  • Microdeletion uncovers loss-of-function of a MYH11 missense variant in a patient with megacystis-microcolon-intestinal-hypoperistalsis syndrome
    Kloth K, Renner S, Burmester G, Steinemann D, Pabst B, Lorenz B, Simon R, Kolbe V, Hempel M, Rosenberger G. (2019) 16p13.11
    Clin Genet, 2019 96(1): 85-90
  • International Practice Patterns for the Management of Acute Postsurgical and Postintravitreal Injection Endophthalmitis: European Vitreo-Retinal Society Endophthalmitis Study Report 1
    Soliman MK, Gini G, Kuhn F, Iros M, Parolini B, Ozdek S, Michalewska Z, Bopp S, Adelman RA, Sallam AB; European Vitreo-Retinal Society Endophthalmitis Study Group
    Ophthalmol Retina. 2019 Jun;3(6):461-467