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Suggested authors matching "AUTH:Kellner U" with an ORCID

Ulrich Kellner
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Aflibercept Biosimilar MYL-1701P vs Reference Aflibercept in Diabetic Macular Edema: The INSIGHT Randomized Clinical Trial.
Bressler SB, Barve A, Ganapathi PC, Beckmann K, Apte RS, Marcus DM, Baumane K, Agarwal S, Oleksy P, Reichstein DA, Patel SS, Ernest J, Dégi R, Gupta V, Kishino G, Kamei M, Loganathan S, INSIGHT Study Group
JAMA Ophthalmol, 142(10):952-960, 01 Oct 2024
Cited by: 0 articles | PMID: 39264599 | PMCID: PMC11393752
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18-Years of single-centre DNA testing in over 7000 index cases with inherited retinal dystrophies and optic neuropathies.
Kiel C, Biasella F, Stöhr H, Rating P, Spital G, Kellner U, Hufendiek K, Huchzermeyer C, Jaegle H, Ruether K, Weber BHF
Sci Rep, 14(1):25529, 26 Oct 2024
Cited by: 0 articles | PMID: 39462066 | PMCID: PMC11513943
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[Training of Medical Assistants in Ophthalmology: Survey of a Sample of Large Ophthalmic Centers].
Hahn U, Kellner U
Gesundheitswesen, 86(8-09):587-592, 02 Apr 2024
Cited by: 0 articles | PMID: 38565191 | PMCID: PMC11404335
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[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].
Künzel SH, Mahren E, Morr M, Holz FG, Lorenz B, Arbeitsgruppe IRDs in Deutschland
Ophthalmologie, 120(11):1127-1137, 15 Aug 2023
Cited by: 0 articles | PMID: 37582888
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[Less Frequent Vascular Disorders of the Retina - Part 1].
Heimann H, Schüler A, Kellner U, Lommatzsch A, Krause L
Klin Monbl Augenheilkd, 16 Aug 2023
Cited by: 0 articles | PMID: 37586399
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[Participation in a clinical trial-Is that something for me? : Video article].
Lorenz K, Böhringer D, Wilhelm B, Arbeitsgemeinschaft DOG Klinische Studienzentren
Ophthalmologie, 120(5):552-555, 18 Apr 2023
Cited by: 0 articles | PMID: 37071185
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Blood taken immediately after fatal resuscitation attempts yields higher quality DNA for genetic studies as compared to autopsy samples.
Stanasiuk C, Milting H, Homm S, Persson J, Holtz L, Wittmer A, Fox H, Laser T, Knöll R, Pohl GM, Paluszkiewicz L, Jakob T, Bachmann-Mennenga B, Henzler D, Grautoff S, Veit G, Klingel K, Hori E, Kellner U, [...] Tiesmeier J
Int J Legal Med, 137(5):1569-1581, 11 Feb 2023
Cited by: 0 articles | PMID: 36773088 | PMCID: PMC10421769
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[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].
Deutsche Ophthalmologische Gesellschaft (DOG), Retinologische Gesellschaft e. V. (RG), Berufsverband der Augenärzte Deutschlands e. V. (BVA)
Ophthalmologie, 120(suppl 1):44-49, 16 Dec 2022
Cited by: 0 articles | PMID: 36525046
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[Exogenously induced retinopathies].
Kellner U, Kellner S, Weinitz S, Farmand G
Klin Monbl Augenheilkd, 239(12):1493-1511, 17 Nov 2022
Cited by: 0 articles | PMID: 36395811
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Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations.
Gersch J, Hufendiek K, Delarocque J, Framme C, Jacobsen C, Stöhr H, Kellner U, Hufendiek K
Int J Mol Sci, 23(24):16007, 16 Dec 2022
Cited by: 2 articles | PMID: 36555650 | PMCID: PMC9788460
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Safety and efficacy of risdiplam in patients with type 1 spinal muscular atrophy (FIREFISH part 2): secondary analyses from an open-label trial.
Masson R, Mazurkiewicz-Bełdzińska M, Rose K, Servais L, Xiong H, Zanoteli E, Baranello G, Bruno C, Day JW, Deconinck N, Klein A, Mercuri E, Vlodavets D, Wang Y, Dodman A, El-Khairi M, Gorni K, Jaber B, Kletzl H, [...] FIREFISH Study Group
Lancet Neurol, 21(12):1110-1119, 14 Oct 2022
Cited by: 26 articles | PMID: 36244364
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Impact of left atrial appendage fibrosis on atrial fibrillation in patients following coronary bypass surgery.
Eckstein J, Renner A, Zittermann A, Fink T, Sohns C, Niehaus K, Bednarz H, Neumann JM, Piran M, Kellner U, Gummert J
Clin Cardiol, 45(10):1029-1035, 21 Jul 2022
Cited by: 1 article | PMID: 35864729 | PMCID: PMC9574744
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The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy.
Wissinger B, Baumann B, Buena-Atienza E, Ravesh Z, Cideciyan AV, Stingl K, Audo I, Meunier I, Bocquet B, Traboulsi EI, Hardcastle AJ, Gardner JC, Michaelides M, Branham KE, Rosenberg T, Andreasson S, Dollfus H, Birch D, Vincent AL, [...] Kohl S
Proc Natl Acad Sci U S A, 119(27):e2115538119, 27 Jun 2022
Cited by: 7 articles | PMID: 35759666 | PMCID: PMC9271157
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[Near-infrared Fundus Autofluorescence: Clinical Application and Diagnostic Relevance].
Kellner S, Weinitz S, Farmand G, Kellner U
Klin Monbl Augenheilkd, 239(8):1059-1076, 24 May 2022
Cited by: 0 articles | PMID: 35609811
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National guideline for ophthalmological screening of premature infants in Germany (S2k level, AWMF guidelines register no. 024/010, March 2020) : Joint recommendation of the German Ophthalmological Society (DOG), German Retina Society (RG), Professional Association of Ophthalmologists in Germany (BVA), German Society of Pediatrics and Adolescent Medicine (DGKJ), Professional Association of Pediatricians (BVKJ), Federal Association "The Premature Infant", Society for Neonatology and Pediatric Intensive Care Medicine (GNPI).
Maier RF, Hummler H, Kellner U, Krohne TU, Lawrenz B, Lorenz B, Mitschdörfer B, Roll C, Stahl A
Ophthalmologie, 119(suppl 2):123-136, 04 May 2022
Cited by: 2 articles | PMID: 35507084
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[Scientific performance of ophthalmological research institutions in Germany 2018-2020 : Studies, publications, third-party funding and more-The research map of the German Ophthalmological Society (DOG)].
Schaub F, Mele B, Gass P, Ader M, Helbig H, Lagrèze WA, Schlötzer-Schrehardt U, Ueffing M, Cursiefen C, das DOG Forschungslandkartenteam
Ophthalmologie, 119(6):582-590, 23 May 2022
Cited by: 2 articles | PMID: 35925367
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Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.
Solaki M, Baumann B, Reuter P, Andreasson S, Audo I, Ayuso C, Balousha G, Benedicenti F, Birch D, Bitoun P, Blain D, Bocquet B, Branham K, Català-Mora J, De Baere E, Dollfus H, Falana M, Giorda R, Golovleva I, [...] Kohl S
Hum Mutat, 43(7):832-858, 14 Apr 2022
Cited by: 8 articles | PMID: 35332618
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[Diagnosis of inherited retinal dystrophies. Relevance of molecular genetic testing from the patient's perspective].
Kellner U, Jansen S, Bucher F, Stingl K
Ophthalmologie, 119(8):820-826, 21 Mar 2022
Cited by: 2 articles | PMID: 35312834
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Digital 3D "Heads-up" Cataract Surgery: Safety Profile and Comparison with the Conventional Microscope System.
Bedar MS, Kellner U
Klin Monbl Augenheilkd, 239(8):991-995, 18 Feb 2022
Cited by: 3 articles | PMID: 35180783
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[Retinopathy of Prematurity - Update on Classification, Screening, and Therapy].
Li JQ, Kellner U, Lorenz B, Stahl A, Krohne TU
Klin Monbl Augenheilkd, 239(3):346-363, 04 Mar 2022
Cited by: 1 article | PMID: 35253129
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DNAJC30 disease-causing gene variants in a large Central European cohort of patients with suspected Leber's hereditary optic neuropathy and optic atrophy.
Kieninger S, Xiao T, Weisschuh N, Kohl S, Rüther K, Kroisel PM, Brockmann T, Knappe S, Kellner U, Lagrèze W, Mazzola P, Haack TB, Wissinger B, Tonagel F
J Med Genet, 59(10):1027-1034, 28 Jan 2022
Cited by: 10 articles | PMID: 35091433 | PMCID: PMC9554085
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Optical coherence tomography angiography (OCT-A) in retinitis pigmentosa and macular dystrophy patients: a retrospective study.
Deutsch S, Lommatzsch A, Weinitz S, Farmand G, Kellner U
Graefes Arch Clin Exp Ophthalmol, 260(6):1923-1931, 04 Jan 2022
Cited by: 1 article | PMID: 34982219 | PMCID: PMC9061664
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Subtyping non-small cell lung cancer by histology-guided spatial metabolomics.
Neumann JM, Freitag H, Hartmann JS, Niehaus K, Galanis M, Griesshammer M, Kellner U, Bednarz H
J Cancer Res Clin Oncol, 148(2):351-360, 28 Nov 2021
Cited by: 19 articles | PMID: 34839410 | PMCID: PMC8800912
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Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-controlled trial.
Mercuri E, Deconinck N, Mazzone ES, Nascimento A, Oskoui M, Saito K, Vuillerot C, Baranello G, Boespflug-Tanguy O, Goemans N, Kirschner J, Kostera-Pruszczyk A, Servais L, Gerber M, Gorni K, Khwaja O, Kletzl H, Scalco RS, Staunton H, [...] SUNFISH Study Group
Lancet Neurol, 21(1):42-52, 01 Jan 2022
Cited by: 64 articles | PMID: 34942136
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[Collaboration with clinical research organizations : Introduction of a questionnaire for clinical study centers].
Adorf A, Lorenz K, Feltgen N, Wilhelm B, die AG DOG Klinische Studienzentren
Ophthalmologie, 119(6):577-581, 18 Dec 2021
Cited by: 0 articles | PMID: 34923599
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Search life-sciences literature (45,103,589 articles, preprints and more)

Suggested authors matching "AUTH:Kellner U" with an ORCID

Search results

Aflibercept Biosimilar MYL-1701P vs Reference Aflibercept in Diabetic Macular Edema: The INSIGHT Randomized Clinical Trial.

18-Years of single-centre DNA testing in over 7000 index cases with inherited retinal dystrophies and optic neuropathies.

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

[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].

[Less Frequent Vascular Disorders of the Retina - Part 1].

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

Blood taken immediately after fatal resuscitation attempts yields higher quality DNA for genetic studies as compared to autopsy samples.

[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].

[Exogenously induced retinopathies].

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

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

Impact of left atrial appendage fibrosis on atrial fibrillation in patients following coronary bypass surgery.

The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy.

[Near-infrared Fundus Autofluorescence: Clinical Application and Diagnostic Relevance].

[Scientific performance of ophthalmological research institutions in Germany 2018-2020 : Studies, publications, third-party funding and more-The research map of the German Ophthalmological Society (DOG)].

Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.

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

Digital 3D "Heads-up" Cataract Surgery: Safety Profile and Comparison with the Conventional Microscope System.

[Retinopathy of Prematurity - Update on Classification, Screening, and Therapy].

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

Optical coherence tomography angiography (OCT-A) in retinitis pigmentosa and macular dystrophy patients: a retrospective study.

Subtyping non-small cell lung cancer by histology-guided spatial metabolomics.

Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-controlled trial.

[Collaboration with clinical research organizations : Introduction of a questionnaire for clinical study centers].

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