2018
- 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