Inhaltspezifische Aktionen

2016

  • Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness
    Vincent A, Audo I, Tavares E, Maynes JT, Tumber A, Wright T, Li S, Michiels C, GNB3 Consortium, Condroyer C, MacDonald H, Verdet R, Sahel JA, Hamel CP, Zeitz C, Héon E
    Am J. Hum Genet. 2016 Apr 6
  • Albinism and the Range of Fundus Hypopigmentation, Macular Hypoplasia, and Nystagmus
    Preising MN, Lorenz B
    Klin Monbl Augenheilkd. 2016 Mar;232(3):243-50
  • Manifestation of bilateral choroidal osteoma in childhood: Progressive myopia due to staphyloma posticum
    Heichel J, Bredehorn-Mayr T, Stuhlträger U, Kunert KS, Jäger M, Lorenz B
    Ophthalmologe 2016 Feb;113(2):160-3
  • Treatment Options for Basal Cell Carcinomas of the Medial Canthus
    Papadopoulou C, Solbach C, Lorenz B, Luciani F
    Klin Monbl Augenheilkd. 2016 Jan;233(1):38-43
  • Evaluation of intraocular lens position during phacoemulsification using intraoperative spectral-domain optical coherence tomography
    Lytvynchuk LM, Glittenberg CG, Falkner-Radler CI, Neumaier-Ammerer B, Smretschnig E, Hagen S, Ansari-Shahrezaei S, Binder S
    J Cataract Refract Surg 2016; May 42:649-702
  • Retinal vascular development with 0,312 MG intravitreal bevacizumab to treat severe posterior retinopathy of prematurity: A longitudinal fluorescein angiographic study
    Lorenz B, Stieger, K, Jäger M, Mais C, Stieger S, Andrassi-Darida M
    Retina, 2017 Jan;37(1):97-111
  • Palsy of CVI caused by ecchordosis physaliphora
    Stahl-Hoffmann VD, Gräf M, Cesnulis E, Schuknecht B, Lorenz B
    Ophthalmologe. 2016 Jun;113(6):514-6
  • Ocular morphology and function in juvenile neuronal ceroid lipofuscinosis (CLN3) in the first decade of life
    Preising MN, Abura M, Jäger M, Wassill KH, Lorenz B
    Ophthalmic Genet, 2017 May-Jun;38(3):252-259

  • [Indication and Results of the Anderson Procedure].
    Gräf M, Lorenz B.
    Klin Monbl Augenheilkd. 2016 Oct;233(10):1115-1119

  • [Handheld Optical Coherence Tomography in Paediatric Ophthalmology: Experience of the Department of Ophthalmology in Giessen].
    Bowl W, Andrassi-Darida M, Holve K, Schweinfurth S, Knobloch R, Lorenz B.
    Klin Monbl Augenheilkd. 2016 Oct;233(10):1142-1148

  • OCT-Based Macular Structure-Function Correlation in Dependence on Birth Weight and Gestational Age-the Giessen Long-Term ROP Study.
    Bowl W, Stieger K, Bokun M, Schweinfurth S, Holve K, Andrassi-Darida M, Lorenz B.
    Invest Ophthalmol Vis Sci. 2016 Jul 1;57(9):OCT235-41. doi: 10.1167/iovs.15-18843

  • Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amourosis in Denmark.
    Astuti GD, Bertelsen M, Preising MN, Ajmal M, Lorenz B, Faradz SM, Qamar R, Collin RW, Rosenberg T, Cremers FP
    Eur J Hum Genet. 2016 Jul;24(7):1071-9

  • Correlation of central visual function and ROP risk factors in prematures with and without acute ROP at the Age of 6-13 years: the Giessen Long-term ROP study
    Bowl W, Lorenz B, Stieger K, Schweinfurth S, Holve K, Friedburg C, Andrassi-Darida M
    Br J Ophthalmol. 2016 Sp;100(9):1238-44

  • In vivo Genome editing as a potentitial Treatment strategy for inherited retinal dystrophies
    Yanik M, Müller B, Song F, Gall J, Wagner F, Wende W, Lorenz B, Stieger K
    Progress in Retinal and Eye Research 2017, 56: 1-18

  • Quantification of the vascular endothelial growth factor with a bioluminescence resonance energy transfer (BRET) based single molecule biosensor
    Wimmer T, Lorenz B, Stieger K.
    Biosens Bioelectron. 2016 Dec 15;86:609-15

  • Rebound macular edema following oral actazolamide therapy for juvenile X-linked retinoschisis in an Italian family
    Galantuomo MS, fossarello M, cuccu A, Farci R, Preising MN, Lorenz B, Napoli PE
    Clin Ophthalmol. 2016 Nov 25;10:2377-2382

  • Der Brücknertest zur Früherkennung und Amblyopieprävention
    Gräf M
    Pädiatr. Praxis 2016; 87:133-146

  • Anderson procedure for naystagmus-related head-turn: Decrease in long-term effect?
    Gräf M Lorenz B
    Cioplean A (Hrsg) Transactions 38th Meeting of the European Strabismological Association, Budapest, 29.09. - 01.10.2016: 187-190

  • Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome.
    Ansari M, Rainger J, Hanson IM, Williamson KA, Sharkey F, Harewood L, Sandilands A, Clayton-Smith J, Dollfus H, Bitoun P, Meire F, Fantes J, Franco B, Lorenz B, Taylos DS, Stewart F, Willoughby CE, mcEntagart M, Khaw PT, Clericuzio C, Van Maldergem L, Williams D, newbury-Exob R, Traboulsi El, Silva ED, Madlom MM, Goudie DR, Fleck BW, Wieczorek D, Kohlhase J, McTrusty AD, Gardiner C, YaleC, Moore AT, Russel-Eggitt I, Islam L, Lees M, Beales PL, Tuft SJ, Solano JB, Splitt M, Hertz JM, Prescott TE, Shears DJ, Nischal KK, Doco-Fenzy M, rieur F, Temple IK, Lachlan KL, Damante G, Morrison DA, van Heyingen V, FitzPatrick DR
    PLos One. 2016 Apr 28;11(4):e0153757

  • Investigations for the underlying genetic cause in a consangineous family with complete achromatosia.
    Preising MN, Zuliani, AM, Lorenz B.
    (ARVO): Abstract 3167
  • Evaluation of intraocular lens position during phacoemulsification using intraoperative spectral-domain optical coherence tomography
    Lytvynchuk LM, Glittenberg CG, Falkner-Radler CI, Neumaier-Ammerer B, Smretschnig E, Hagen S, Ansari-Shahrezaei S, Binder S.
    J Cataract Refract Surg. 2016 May; 42(5):694-702