Inhaltspezifische Aktionen

2009

 

  • Gentherapie bei degenerativen Erkrankungen der Netzhaut
    Stieger K, Lorenz B
    Zeitschr prakt Augenheilkd 2009, 30:561-573
  • Diagnosis and treatment of trochlear nerve palsy
    Gräf M
    Klin Monbl Augenheilkd. 2009 226(10):805-11
  • TRPM1 is mutated in patients  with autosomal recessive complete congenital stationary night blindness
    Audo I, Kohl S, Leroy B, Munier FL, Guillonneau X, Mohand-Said S, Bujakowska K, Nandrot EF, Lorenz B, Preising MN, Kellner U, Renner AB, Bernd A, Antonio A, Moskova-Doumanova V, Lancelot ME, Poloschek CM, Drumare I, Defoort-Dhellemmes S, Wissinger B, Leveillard T, Hamel CP, Schorderet DF, De Baere E, Berger W, Jacobson SG, Zrenner E, Sahel JA, Bhattachrya SS, Zeitz C
    Am J Hum Genet 2009 85(13):1-10

  • The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutation.
    Graw J, Schmidt W, Minogue PJ, Rodriguez J, Tong JJ, Klopp N, Illig T, Ebihara L, Berthoud VM, Beyer EC
    Mol Vis. 2009 Sep 14;15:1881-5
  • Spontan reversibles vitreomaculäres Traktionssyndrom
    Weinand F, Jung A, Becker R, Pavlovic S.
    Der Ophthalmologe 2009, Jan 106, (1):44-46
  • Genotyping microarray for CSNB-associated genes
    Zeitz C, Labs S, Lorenz B, Forster U, Ueksti J, Kroes HY, De Baere E, Leroy BP, Cremers FP, Wittmer M, van Genderen MM, Sahel JA, Audo I, Poloschek CM, Mohand-Saïd S, Fleischhauer JC, Hueffmeier U, Moskova-Doumanova V, Levin AV, Hamel CP, Leifert D, Munier FL, Schorderet D, Zrenner E, Friedburg C, Wissinger B, Kohl S, Berger W
    IOVS     2009, Dez 50, (12):5919-26

  • [A stochastic test for validity control of visual acuity statements.]
    Roland J, Hirsch U, Heinrich SP, Bach M, Gräf M
    Ophthalmologe. 2009 Jul 15. [Epub ahead of print]
  • Disease-Causing 7.4kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction with the FOXL2 Promotor: Implications for Mutation Screening
    D'haene B, Attanasio C, Beysen D, Dostie J, Lemire E, Bouchard P, Field M, Jones K, Lorenz B, Menten B, Buysse K, Pattyn F, Friedli M, Ucla C, Rossier C, Wyss C, Speleman F, De Paepe A, Dekker J, Antonarakis SE, De Baere E
    PLOS Genet     2009 5(6):e1000522 June 19 epub ahead of print
  • Expression of the diabetes risk gene wolframin (WFS1) in the human retina
    Schmidt-Kastner R, Kreczmanski P, Preising MN, Diederen R, Schmitz C, Reis D, Blanks J, Dorey KC
    Exp Eye Res     2009 June 11 epub ahead of print

  • "Fragebogen zum Kindlichen Sehvermögen (FKS)". [Assessment of quality of life with the German version of the Children's Visual Function Questionnaire]
    Pieh C, Fronius M, Chopovska Y, Pepler L, Klein M, Lüchtenberg M, Lagrèze WA, Felius J Ophthalmologe. 2009 May;106(5):420-

  • Wide-field digital imaging based telemedicine for screening for acute retinopathy of prematurity (ROP). Six-years results of a multicentre field study
    Lorenz B, Spasovska K, Elflein H, Schneider N
    Graefes Arch Clin Exp Ophthalmol     2009 May 22 epub ahead of print
  • In vivo Gene Regulation using Tetracycline-Regulatable Systems
    Stieger K, Belbellaa B, Le Guiner C, Moullier P, Rolling F
    Adv Drug Del Rev     2009 61(7-8):527-541
  • Fundus Autofluorescence in Carrier of Choroideremia and Correlation with Electrophysiologic and psyco-physical data
    Preising MN, Wegscheider E, Friedburg C, Poloschek CM, Wabbels BK, Lorenz B Ophthalmology 2009 Apr 18 epub ahead of print
  • Genetische Erkrankungen des retinalen Pigmentepithels
    Preising MN, Lorenz B
    Der Ophthalmologe     2009 Apr 106(4):311-319 German
  • A randomised comparison of bilateral recession vs. unilateral recession-resection as surgery for infantile esotropia
    Polling JR, Eijkemans MJ, Esser J, Gilles U, Kolling GH, Schulz E, Lorenz B, Roggenkämper P, Herzau V, Zubcov A, Ten Tusscher MP, Wittebol-Post D, Gusek-Schneider GC, Cruysberg JR, Simonsz HJ Br J Ophthalmol 2009 Mar 30 epub ahead of print
  • AAV-mediated gene therapy for retinal disorders in large animal models
    Stieger K , Lhériteau E, Moullier P, Rolling F
    ILAR J     2009 50:206-224
  • The RPGRIP1-deficient dog, a promising canine model for gene therapy
    Lhériteau E, Libeau L, Stieger K, Deschamps JY, Mendes-Madeira A, Provost N, Lemoine F, Mellersh C, Ellinwood NM, Cherel Y, Moullier P, Rolling F
    Mol Vis     2009 15:349-361
  • Systematic Review of Digital Imaging Screening Strategies for Retinopathy of Prematurity - letter to the editor
    Fielder AR, Hildebrand PL, Ells A, Lorenz B, Trese MT, Capone A, Gordon RA, Wilson C, Fleck BW, Chiang MF
    Pediatrics     2009 Feb;123:e360-361
  • Detection of intact rAAV particles up to 6 years after successful gene transfer in the retina of dogs and primates.
    Stieger K, Schroeder J, Provost N, Mendes-Madeira A, Belbellaa B, Le Meur G, Weber M, Deschamps JY, Lorenz B, Moullier P, Rolling F.
    Mol Ther    . 2009 Mar;17(3):516-23.
  • Effect of diagnostic occlusion in acquired trochlear nerve palsy.
    Gräf M , Weihs J.
    Graefes Arch Clin Exp Ophthalmol     . 2009 Feb;247(2):253-9. Epub 2008 Sep 23