L Ingeborgh van den Born
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Explore the profile of L Ingeborgh van den Born including associated specialties, affiliations and a list of published articles.
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114
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Recent Articles
1.
Moekotte L, de Boer J, Hiddingh S, de Ligt A, Nguyen X, Hoyng C, et al.
Invest Ophthalmol Vis Sci
. 2025 Feb;
66(2):55.
PMID: 39982393
Purpose: To determine the profile of inflammation-related proteins and complement system factors in the plasma of CRB1-associated inherited retinal dystrophies (CRB1-IRDs). Methods: We used the Olink Explore 384 Inflammation II...
2.
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...
3.
Heutinck P, van den Born L, Vermeer M, Iglesias Gonzales A, Hoyng C, Pott J, et al.
Invest Ophthalmol Vis Sci
. 2024 Aug;
65(10):40.
PMID: 39189993
Purpose: Gene-based therapies for inherited retinal dystrophies (IRDs) are upcoming. Treatment before substantial vision loss will optimize outcomes. It is crucial to identify common phenotypes and causative genes in children....
4.
Heutinck P, van den Born L, van Laar J, van Hagen P, Smailhodzic D, Meester-Smoor M, et al.
BMJ Open Ophthalmol
. 2024 Aug;
9(1).
PMID: 39134323
Aims: This study aimed to evaluate the effectiveness of somatostatin analogues (SA) for cystoid maculopathy (CM) in retinitis pigmentosa (RP) patients. Materials And Methods: In this retrospective case series, clinical...
5.
Testa F, Carreno E, van den Born L, Melillo P, Perea-Romero I, Di Iorio V, et al.
Invest Ophthalmol Vis Sci
. 2024 Jun;
65(6):25.
PMID: 38884554
Purpose: We investigated the natural history of retinal dystrophy owing to variants in the MYO7A gene. Methods: Fifty-three patients (mean age, 33.6 ± 16.7 years) with Usher syndrome owing to...
6.
Balfoort B, Van den Broeck F, Brands M, van Karnebeek C, Bergen A, van den Born L, et al.
Graefes Arch Clin Exp Ophthalmol
. 2024 Jun;
262(11):3589-3596.
PMID: 38847892
Purpose: Gyrate atrophy of the choroid and retina (GACR) is an autosomal recessive inherited metabolic disorder (IMD) characterised by progressive retinal degeneration, leading to severe visual impairment. The rapid developments...
7.
Cornelis S, IntHout J, Runhart E, Grunewald O, Lin S, Corradi Z, et al.
JAMA Ophthalmol
. 2024 Apr;
142(5):463-471.
PMID: 38602673
Importance: Previous studies indicated that female sex might be a modifier in Stargardt disease, which is an ABCA4-associated retinopathy. Objective: To investigate whether women are overrepresented among individuals with ABCA4-associated...
8.
Hitti-Malin R, Panneman D, Corradi Z, Boonen E, Astuti G, Dhaenens C, et al.
Biomolecules
. 2024 Mar;
14(3).
PMID: 38540785
Inherited macular dystrophies (iMDs) are a group of genetic disorders, which affect the central region of the retina. To investigate the genetic basis of iMDs, we used single-molecule Molecular Inversion...
9.
Han J, Rodenburg K, Hayman T, Calzetti G, Kaminska K, Quinodoz M, et al.
Genet Med
. 2024 Feb;
26(6):101106.
PMID: 38420906
Purpose: Inherited retinal diseases (IRDs) are a group of monogenic conditions that can lead to progressive blindness. Their missing heritability is still considerable, due in part to the presence of...
10.
Hensman J, Hahn L, van Schooneveld M, Diederen R, Ten Brink J, Florijn R, et al.
Ophthalmol Retina
. 2023 Dec;
8(6):600-606.
PMID: 38104928
Purpose: To date, there is no standard treatment regimen for carbonic anhydrase inhibitors (CAIs) in X-linked retinoschisis (XLRS) patients. This retrospective study aims to evaluate the efficacy of CAIs on...