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(2016)
Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1.
Ophthalmic Genetics 37, pp. 201-208.
Fulltext not available.
and Stöhr, Heidi
(2015)
Inherited Retinal or Optic Nerve Disorders – Five Steps to Diagnosis (Originaltitel: Erbliche Netzhaut- und Sehbahnerkrankungen – 5 Schritte zur Diagnose).
Klinische Monatsblätter für Augenheilkunde 232, pp. 250-258.
Fulltext not available.
Kellner, U., Renner, A. B., Herbst, S. M., Kellner, S., Weinitz, S. and Weber, Bernhard H. F.
(2012)
Hereditäre Netzhautdystrophien.
Klinische Monatsblätter für Augenheilkunde 229 (2), pp. 171-196.
Kellner, U., Kellner, S., Renner, A. B., Fiebig, B. S., Weinitz, S. and Weber, Bernhard H. F.
(2009)
Evidenzbasierte Diagnostik hereditärer Netzhautdystrophien 2009 =
, Fiebig, B., Weinitz, S. and Ruether, K.
(2009)
Lipofuscin- and melanin-related fundus autofluorescence in patients with ABCA4-associated retinal dystrophies.
American Journal of Ophthalmology 147 (5), pp. 895-902.
Fulltext not available.
, Fiebig, B., Weinitz, S. and Ruether, K.
(2009)
Lipofuscin- and melanin-related fundus autofluorescence visualize different retinal pigment epithelial alterations in patients with retinitis pigmentosa.
Eye (Lond) 23 (6), pp. 1349-1359.
Fulltext not available.
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