Inhaltspezifische Aktionen


  • Choroidal Thickness with Swept-Source Optical Coherence Tomography versus Foveal Morphology in Young Children with a History of Prematurity
    Bowl W, Bowl M, Schweinfurth S, Holve K, Andrassi-Darida M, Stieger K, Lorenz B.
    Ophthalmic Res. 2018 Feb 7. doi: 10.1159/000484631. [Epub ahead of print]
  • Structure-Function Correlation in Hemianopic Vision Loss in Children Aged 3-6 Years Using OCT and SVOP, and Comparison with Adult Eyes
    Bowl W, Knobloch R, Schweinfurth S,
    Holve K, Stieger K, Lorenz B.
    Ophthalmic Res. epub: 2018 Jan 13
  • Clinical history and management recommendations of the smooth muscle diyfunction syndrome due to ACTA2 argininie 179 alterations
    Regalado ES, Mellor-Crummey L, De GJ, Braverman AC, Ades L, Benedict S, Bradley TJ, Brickner ME, Chatfield KC, Child A, Feist C, Holmes KW, Iannucci G, Lorenz B, Mark P, Morisaki T, Morisaki H, Morris SA, Mitchell AL, Ostergaard JR, Richer J, Sallee D, Shalhub S, Tekin M, Estrera A, Musolino P, Yetman A, Pyeritz R, Milewicz DM
    Genet Med. epub: 2018 Jan 4
  • Retinal Astrocytic Hamartoma in Neurofibromatosis Type 2 - Metaanalysis and a Case Report
    Starosta DA, Lorenz B.
    Klin Monbl. Augenheilkd. 2018 Mar; 235(3):290-300
  • Ophthalmic Genetics: Insights into Actual Methods of Diagnostics, Phenotyping and Therapy
    Lorenz B
    Klin Monbl. Augenheilkd. 2018 Mar; 235 (3):256-257
  • Visuelle Wahrnehmungsstörungen
    Weber P, John R, Konrad K, v. Livonius B, Lorenz B, Ruple B, Stock-Mühlnickel S, Karch D, Schroeder A
    Monatsschrift Kinderheilkunde, 166(5), 437-444
  • A noninterventional study to monitor patients with diabetic macular oedema starting treatment with  ranibizumab (POLARIS)
    Stefanickova J, Cunha-Vaz J, Ulbig M, Pearce I, Fernández-Vega Sanz A, Theodossiadis P, Kodjikian L, Izmailov A, Muston D, Vassilev Z, Lamotte B, Tückmantel C, Friedl S, Altemark A, Schwarz HJ, Katz T; POLARIS study investigators
    Acta Ophthalmol. 2018 Apr 25. doi: 10.1111/aos.13771. [Epub ahead of print]
  • Unexpected Genetic Cause in Two Female Siblings with High Myopia and Reduced Visual Acuity
    Preising MN, Friedburg CF, Bowl W, Lorenz B
    BioMed Research International, Vol. 2018
  • Clinical characterization of 66 Patients with congenital retinal disease due to the deep-intronic c.2991+1655A>G mutation in CEP290
    Valkenburg D, van Cauwenberg C, Lorenz B, van Genderen MM, Bertelsen M, Pott JR
    Invest Ophthalmol Vis Sci 2018 Sep 4;59(11):4384-4391
  • Reply
    Lorenz B

    Retina 2018 Aug;38(8):e65-e66
  • Development of a reporter system to explore MMEJ in the context of Replacing large genomic fragments
    Yanik M, Ponnam SPG, Wimmer T, Trimborn L, Müller C, Gambert I, Ginsberg J, Janise A, Domicke J, Wende W, Lorenz B, Stieger K
    Mol Ther Nucleic Acids 2018 Jun 1;11:407-415
  • Detection of DNA double strand breaks by γH2AX does not result in 35bp1 recruitment in mouse retinal tissues
    Müller B, Ellinwood NM, Lorenz B, Stieger K
    Front Neurosci 2018 May 1;K12:286
  • OCT Angiography in Young Children with a History of Retinopathy of Prematurity
    Bowl W, Bowl M, Schweinfurth S, Holve K, Knobloch R, Stieger K, Andrassi-Darida M, Lorenz B
    Opthalmology Retina 2018;2:972-978
  • Overview of congenital stationary night blindness with predominantly normal fundus appearance
    Zeitz C, Friedburg C, Preising MN, Lorenz B
    Klin Monbl Augenheilkd. 2018;235(3):281-289