Nicolas Feltgen
Overview
Explore the profile of Nicolas Feltgen including associated specialties, affiliations and a list of published articles.
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Articles
146
Citations
1823
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Recent Articles
1.
Kaminska K, Cancellieri F, Quinodoz M, Moye A, Bauwens M, Lin S, et al.
Am J Hum Genet
. 2025 Mar;
PMID: 40081374
Inherited retinal diseases (IRDs) are a genetically heterogeneous group of Mendelian disorders that often lead to progressive vision loss and involve approximately 300 distinct genes. Although variants in these loci...
2.
Schikora J, Dort A, Wolf H, Jozsi M, Pouw R, Bertelmann T, et al.
J Transl Med
. 2025 Mar;
23(1):317.
PMID: 40075380
Background: The development of age-related macular degeneration (AMD) is influenced by risk factors that contribute to inflammatory processes, cellular stress responses, and a dysregulation of the complement system. Given the...
3.
Chatzimichail E, Steinemann-Inauen A, Gugleta K, Feltgen N, Gatzioufas Z
Klin Monbl Augenheilkd
. 2025 Feb;
PMID: 40015306
No abstract available.
4.
Pfau K, Ansari G, Michels S, Dysli C, Liakopoulos S, Burghaus-Zhang J, et al.
Invest Ophthalmol Vis Sci
. 2025 Feb;
66(2):17.
PMID: 39913163
Purpose: To determine the prevalence and spatial pattern of rod and cone dysfunction in patients with pseudoxanthoma elasticum (PXE) and to correlate these with Bruch's membrane (BrM) calcification. PXE is...
5.
Chatzimichail E, Steinemann-Inauen A, Habra O, Meyer P, Feltgen N, Gatzioufas Z
Klin Monbl Augenheilkd
. 2025 Jan;
PMID: 39870089
No abstract available.
6.
Pfau K, Callizo J, Rossouw P, Gabrani C, Holz F, Charbel Issa P, et al.
Klin Monbl Augenheilkd
. 2025 Jan;
PMID: 39864434
No abstract available.
7.
Bemme S, Buchel S, Hoerauf H, Feltgen N, van Oterendorp C
Curr Eye Res
. 2025 Jan;
1-11.
PMID: 39844471
Purpose: To validate the quantification of the prominent middle limiting membrane (PMLM) sign, a marker of mild-to-moderate acute ischemic damage on optical coherence tomography (OCT), by measuring middle limiting membrane...
8.
Quinodoz M, Rodenburg K, Cvackova Z, Kaminska K, de Bruijn S, Iglesias-Romero A, et al.
medRxiv
. 2025 Jan;
PMID: 39830270
The U4 small nuclear RNA (snRNA) forms a duplex with the U6 snRNA and, together with U5 and ~30 proteins, is part of the U4/U6.U5 tri-snRNP complex, located at the...
9.
Torra R, Lipska-Zietkiewicz B, Acke F, Antignac C, Becker J, Cornec-Le Gall E, et al.
Nephrol Dial Transplant
. 2024 Dec;
PMID: 39673454
Glomerular nephropathy resulting from the genetic defects in COL4A3/4/5 genes including the classical Alport syndrome (AS) is the second commonest hereditary kidney disease characterized by persistent haematuria progressing to the...
10.
Feltgen N, Pfau K, Callizo J
Klin Monbl Augenheilkd
. 2024 Dec;
242(1):71-86.
PMID: 39642927
As retinal vein occlusion is such a complex systemic disease, its underlying risk profile should be narrowed down individually. Ophthalmologists should always rule out glaucoma or ocular hypertension while also...