Georgios Makris
Overview
Explore the profile of Georgios Makris including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
23
Citations
103
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Diep T, Zhou W, Reyes R, Nitzahn M, Day I, Makris G, et al.
Mol Ther Nucleic Acids
. 2025 Mar;
36(1):102470.
PMID: 40083646
Carbamoyl phosphate synthetase 1 (CPS1) deficiency, a urea-cycle disorder, results in hyperammonemia initiating a sequence of adverse events that can lead to coma and death if not treated rapidly. There...
2.
Vukovic T, Kuek L, Yu B, Makris G, Haberle J
J Inherit Metab Dis
. 2024 Jul;
47(6):1157-1174.
PMID: 39021261
Citrin deficiency (CD) is a recessive, liver disease caused by sequence variants in the SLC25A13 gene encoding a mitochondrial aspartate-glutamate transporter. CD manifests as different age-dependent phenotypes and affects crucial...
3.
Ferreira da Cunha Neto J, da Silva Rocha W, Makris G, Sandoval-Denis M, Hagen F, Crous P, et al.
PLoS Negl Trop Dis
. 2024 Jun;
18(6):e0012247.
PMID: 38885283
Background: Fusarium and allied genera (fusarioid) species are common colonizers of roots and aerial plant parts, or act as phytopathogens in forestry and horticultural or grain crops. However, they can...
4.
Matter A, Kaufman C, Zurcher N, Lenggenhager D, Grehten P, Bartholdi D, et al.
Aging Cell
. 2024 May;
23(8):e14189.
PMID: 38757373
Nuclear envelopathies are rare genetic diseases that compromise the integrity of the nuclear envelope. Patients with a defect in LEM domain nuclear envelope protein 2 (LEMD2) leading to LEMD2-associated progeroid...
5.
Kido J, Makris G, Santra S, Haberle J
J Inherit Metab Dis
. 2024 Mar;
47(6):1144-1156.
PMID: 38503330
Citrin deficiency is an autosomal recessive disorder caused by a defect of citrin resulting from mutations in SLC25A13. The clinical manifestation is very variable and comprises three types: neonatal intrahepatic...
6.
Makris G, Veit L, Rufenacht V, Klassa S, Zurcher N, Matsumoto S, et al.
J Inherit Metab Dis
. 2024 Jan;
47(6):1228-1238.
PMID: 38192032
The group of rare metabolic defects termed urea cycle disorders (UCDs) occur within the ammonia elimination pathway and lead to significant neurocognitive sequelae for patients surviving decompensation episodes. Besides orthotopic...
7.
Makris G, Kayhan S, Kreuzer M, Rufenacht V, Faccin E, Underhaug J, et al.
Cancer Commun (Lond)
. 2023 Jan;
43(4):508-512.
PMID: 36708276
No abstract available.
8.
Samarentsis A, Makris G, Spinthaki S, Christodoulakis G, Tsiknakis M, Pantazis A
Sensors (Basel)
. 2022 Dec;
22(24).
PMID: 36560095
Gait analysis refers to the systematic study of human locomotion and finds numerous applications in the fields of clinical monitoring, rehabilitation, sports science and robotics. Wearable sensors for real-time gait...
9.
Kanetis L, Taliadoros D, Makris G, Christoforou M
Plants (Basel)
. 2022 Oct;
11(20).
PMID: 36297757
Besides well-known grapevine trunk disease (GTD)-related pathogens, there is an increased interest in wood-colonizing fungi that infect grapevines. During 2017-2018, a survey was conducted in Cyprus and wood samples were...
10.
Soria L, Makris G, DAlessio A, De Angelis A, Boffa I, Pravata V, et al.
Nat Commun
. 2022 Sep;
13(1):5212.
PMID: 36064721
Life-threatening hyperammonemia occurs in both inherited and acquired liver diseases affecting ureagenesis, the main pathway for detoxification of neurotoxic ammonia in mammals. Protein O-GlcNAcylation is a reversible and nutrient-sensitive post-translational...