Alina C Hilger
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Explore the profile of Alina C Hilger including associated specialties, affiliations and a list of published articles.
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42
Citations
518
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Recent Articles
1.
Mulzer L, Felger T, Munoz L, Engl G, Reutter H, Schiffer M, et al.
Cell Commun Signal
. 2025 Feb;
23(1):60.
PMID: 39901276
Extracellular Vesicles (EVs) play a crucial role in cell differentiation. Despite its role as a well-established vertebrate model, little is known about EVs during zebrafish embryogenesis. This study investigates EVs...
2.
Schwarz S, Denis L, Nedoschill E, Buehler A, Danko V, Hilger A, et al.
Adv Sci (Weinh)
. 2025 Feb;
:e2415235.
PMID: 39899647
During the first days of neonatal growth, the central nervous system (CNS) develops self-regulatory mechanisms to ensure constant cerebral perfusion. However, this vascular neogenesis takes place at a microscopic scale...
3.
Kalanithy J, Mingardo E, Stegmann J, Dhakar R, Dakal T, Rosenfeld J, et al.
J Med Genet
. 2024 Dec;
62(2):126-137.
PMID: 39715634
Background: Previous studies in mouse, and zebrafish embryos show strong expression in progenitor cells of neuronal and neural crest tissues suggesting its involvement in neural crest specification. However, the role...
4.
Almasi-Sperling V, Gall C, Haney B, Latzel N, Knieling F, Hilger A, et al.
J Clin Med
. 2024 Jun;
13(12).
PMID: 38930106
: Arterio-venous fistulas (AVF) are used as first-line access for hemodialysis (HD) in the pediatric population. The aim of this investigation was to describe a single-center experience in the creation...
5.
Ebach F, Wagner P, Stein R, Dolscheid-Pommerich R, Reutter H, Hilger A
Health Sci Rep
. 2024 Mar;
7(3):e1935.
PMID: 38524771
Background: Congenital lower urinary tract obstruction (LUTO) describes a heterogeneous group of congenital malformations. Posterior urethral valves (PUV) represent the most common entity. Familial occurrence has been described, suggestive of...
6.
Stegmann J, Kalanithy J, Dworschak G, Ishorst N, Mingardo E, Lopes F, et al.
NPJ Genom Med
. 2024 Mar;
9(1):18.
PMID: 38429302
CELSR3 codes for a planar cell polarity protein. We describe twelve affected individuals from eleven independent families with bi-allelic variants in CELSR3. Affected individuals presented with an overlapping phenotypic spectrum...
7.
Whitchurch J, Schneider S, Hilger A, Kollges R, Stegmann J, Waffenschmidt L, et al.
Cells
. 2024 Jan;
13(2).
PMID: 38247840
Besides visceral heterotaxia, null mouse embryos exhibit general edema and perinatal lethality. In humans, congenital chylothorax (CCT) is a frequent cause of fetal hydrops. In 2021, Correa and colleagues reported...
8.
Kollges R, Stegmann J, Schneider S, Waffenschmidt L, Fazaal J, Breuer K, et al.
Biomolecules
. 2023 Jul;
13(7).
PMID: 37509153
Background: The bladder exstrophy-epispadias complex (BEEC) is a spectrum of congenital abnormalities that involves the abdominal wall, the bony pelvis, the urinary tract, the external genitalia, and, in severe cases,...
9.
Kolvenbach C, Dworschak G, Rieke J, Woolf A, Reutter H, Odermatt B, et al.
Mol Cell Pediatr
. 2023 Mar;
10(1):2.
PMID: 36977792
Advances in molecular biology are improving our understanding of the genetic causes underlying human congenital lower urinary tract (i.e., bladder and urethral) malformations. This has recently led to the identification...
10.
Kolvenbach C, Felger T, Schierbaum L, Thiffault I, Pastinen T, Szczepanska M, et al.
J Med Genet
. 2022 Nov;
60(6):587-596.
PMID: 36379543
Background: is thought to play an important role in cytoskeletal modification and development of the early nervous system. Previously, single-nucleotide variants (SNVs) or copy number variations (CNVs) in have been...