Suchergebnisse - "Kellner, Ulrich"

PubPharm (280)

1

Training of Medical Assistants in Ophthalmology : Survey of a Sample of Large Ophthalmic Centers

enthalten in: Gesundheitswesen (Bundesverband der Arzte des Offentlichen Gesundheitsdienstes (Germany)) | 2024

von Hahn, U. | Kellner, U.

2

Diagnostics and management of patients with inherited retinal diseases in Germany : Results of a nationwide survey of university and non-university eye departments and specialized practices

enthalten in: Die Ophthalmologie | 2023

von Künzel, S. | Mahren, E. | Morr, M. | +48

3

Less Frequent Vascular Disorders of the Retina - Part 1

enthalten in: Klinische Monatsblatter fur Augenheilkunde | 2023

von Heimann, H. | Schüler, A. | Kellner, U. | +2

4

Participation in a clinical trial-Is that something for me? : Video article

enthalten in: Die Ophthalmologie | 2023

von Lorenz, K. | Böhringer, D. | Wilhelm, B. | +57

5

Hereditary retinal, choroidal and visual pathway diseases : S1 guidelines of the German Society of Ophthalmology (DOG), the German Retina Society (RG) and the German Professional Association of Ophthalmologists (BVA). Version: 18 September 2021

enthalten in: Die Ophthalmologie | 2023

von Deutsche Ophthalmologische Gesellschaft (DOG) | Retinologische Gesellschaft e. V. (RG) | Berufsverband der Augenärzte Deutschlands e. V. (BVA) | +7

6

Exogenously induced retinopathies

enthalten in: Klinische Monatsblatter fur Augenheilkunde | 2022

von Kellner, U. | Kellner, S. | Weinitz, S. | +1

7

Investigation of Structural Alterations in Inherited Retinal Diseases : A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations

enthalten in: International journal of molecular sciences | 2022

von Gersch, J. | Hufendiek, K. | Delarocque, J. | +5

8

Safety and efficacy of risdiplam in patients with type 1 spinal muscular atrophy (FIREFISH part 2) : secondary analyses from an open-label trial

enthalten in: The Lancet. Neurology | 2022

von Masson, R. | Mazurkiewicz-Bełdzińska, M. | Rose, K. | +120

CommentIn: Lancet Neurol. 2022 Dec;21(12):1065-1066. - PMID 36244363

9

DNAJC30 disease-causing gene variants in a large Central European cohort of patients with suspected Leber's hereditary optic neuropathy and optic atrophy

enthalten in: Journal of medical genetics | 2022

von Kieninger, S. | Xiao, T. | Weisschuh, N. | +11

10

Diagnosis of inherited retinal dystrophies. Relevance of molecular genetic testing from the patient's perspective

enthalten in: Die Ophthalmologie | 2022

von Kellner, U. | Jansen, S. | Bucher, F. | +1

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