Inhaltspezifische Aktionen

2015

  • Shared Decision-Making, Control Preferences and Psychological Well-Being in Patients with RPE65 Deficiency Awaiting Experimental Gene Therapy
    Nelles M, Stieger K, Preising MN, Kruse J, Lorenz B
    Ophthalmic Res. 2015; 54(2):96-102
  • Retrobulbar Spot Sign Predicts Thrombolytic Treatment Effects and Etiology in Central Retinal Artery Occlusion.
    Nedelmann M, Graef M, Weinand F, Wassil KH, Kaps M, Lorenz B, Tanislav C
    Stroke. 2015 Aug; 46(8):2322-4
  • Recess-resect surgery with myopexy of the lateral rectus muscle to correct esotropia with high myopia
    Gräf M, Lorenz B
    Br J Ophthalmol. 2015 Dec;99(12):1702-5
  • Fundus-controlled two-color dark adaptometry with the Microperimeter MP1
    Bowl W, Stieger K, Lorenz B
    Grafes Arch Clin Exp Ophthalmol. 2015 Jun;(6):965-72
  • Functional Characterization of AAV-Expressed Recombinant Anti-VEGF Single-Chain Variable Fragments In Vitro
    Wimmer T, Lorenz B, Stieger K
    J. Ocul Pharmacol Ther. 2015 Jun;31(5):269-76
  • Retinal vessel pathologies in a rat model of periventricular leukomalacia: a new model for retinopathy of prematurity?
    Steck J, Blueml C, Kampmann, Greene B, Maier RF, Arnhold S, Gerstner B, Stieger K, Lorenz B
    Inves Ophthalmol Vis Sci. 2015 Feb 19;56(3):1830-41
  • The pros and cons of vertebrate animal models for functional and therapeutic research on inherited retinal dystrophies
    Slijkerman RW, Song F, Astuti GD, Huynen MA, van Wijk E, Stieger K, Collin RW
    Prog Retin Eye Res. 2015 Sep;48:137-59
  • Retinopathy of prematurity: Recent developments in diagnosis and treatment
    Lorenz B, Stieger K.
    Review of Ophthalmology 02/2015; 10(2):1-16
  • Bestrophin 1-Phenotypes and Functional Aspects in Bestrophinopathies
    Pasquay C, Wang LF, Lorenz B, Preising MN
    Ophthalmic Genet. 2015 Sep;(3):193-212
  • Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neurupathies
    Angebault C, Guichet PO, Talmat-Amar Y, Charif M, Gerber S, Fares-Taie L, Gueguen N, Halloy F, Moore D, Amati-Bonneau P, Manes G, Hebrard M, Bocquet B, Quiles M, Piro-Mégy C, Teigell M, Delettre C, Rossel M, Meunier I, Preising M, Lorenz B, Carelli V, Chinnery PF, Yu-Wai-Main P, Kaplan J, Roubertie A, Barakat A, Bonneau D, Reynier P, Rozet JM, Bomont P, Hamal CP, Lenaers G
    J Hum Genet. 2015 Nov 5;97(5):754-60
  • Recruitment of Suitable Families to IdentifyCausyative Genes in Hereditary Strabismus
    Preising MN, Steinmüller PH, Lorenz B
    Klin Monbl Augenheilkd. 2015 Oct;232(10):1158-64
  • Palsy of CVI caused by ecchordosis physaliphora
    Stahl-Hoffmann VD, Gräf M, Cesnulis E, Schuknecht B, Lorenz B
    Ophthalmologe 2015 Oct 26
  • Strabismus
    Gräf M, Lorenz B
    Monatsschr Kinderheilkd 2015;163:230-240
  • Erfolgreiche Behandlung von strabismus und Amblyopie in der Kindheit nur über Früherkennung
    Gräf M
    Kinder spezial 2015;52:11-13 in Kinderärztliche Praxis. Soziale Pädiatrie und Jugendmedizin 2015; 86(5)
  • Operative Behandlung bei Nystagmus
    Gräf M, Lorenz B
    Z prakt Augenheilkd 2015;36:312-314 und 36:Suppl 2:29-31
  • High-dosage Anderson operation for nystagmus associated head-turn
    Gräf M, Lorenz B
    Cioplean A (Hrsg) Transactions 37th Meeting of the European Strabismological Association, Venedig, October 2015: 155-158
  • Correlation of central visual funkction 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, Friecburg C, Andrassi-Darida M
    Br J Ophthalmol. 2015 Dec 1
  • Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark
    Austuti GD, Bertelsen M, Preising MN, Ajmal M, Lorenz B, Faradz SM, Qamar R, Collin RW, Rosenberg T, Cremers FB
    Eur J Hum Genet. 2015 Dec 2
  • Schwerwiegende seltene Augenerkrankungen bei Kindern und Jugendlichen mit meist sehr guten therapeutischen Möglichkeiten
    Lorenz B
    Kinder spezial 2015;52:17-19 in Kinderärztliche Praxis. Soziale Pädiatrie und Jugendmedizin 2015; 86(5)
  • Ophthalmologie und Genetik - Neuronale Zeroidlipofuszinosen (CLN)
    Preising, M.N., Lorenz, B.
    Ophtha 2015, (3):150-161
  • Erratum to: Do intraocular pressure measurements over 48 h make sense? Sind Augeninnendruckmessungen über 48 h sinnovll?
    Ophthalmologe. 112 (1):93-3212. epub: 2015
    Grossjohann, R., Tost, F., Lorenz, B.