Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
6 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.
Clin Genet. 2017 Nov;92(5):517-527. doi: 10.1111/cge.13077. Epub 2017 Sep 25.
Clin Genet. 2017.
PMID: 28632965
Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlife.
Żurowska AM, Bielska O, Daca-Roszak P, Jankowski M, Szczepańska M, Roszkowska-Bjanid D, Kuźma-Mroczkowska E, Pańczyk-Tomaszewska M, Moczulska A, Drożdż D, Hadjipanagi D, Deltas C, Ostalska-Nowicka D, Rabiega A, Taraszkiewicz J, Taranta-Janusz K, Wieczorkiewicz-Plaza A, Jobs K, Mews J, Musiał K, Jakubowska A, Nosek H, Jander AE, Koutsofti C, Stanisławska-Sachadyn A, Kuleszo D, Ziętkiewicz E, Lipska-Ziętkiewicz BS.
Żurowska AM, et al. Among authors: koutsofti c.
Kidney Int. 2021 Jun;99(6):1451-1458. doi: 10.1016/j.kint.2020.10.040. Epub 2020 Dec 10.
Kidney Int. 2021.
PMID: 33309955
Free article.
Item in Clipboard
TP53 Mutant Versus Wild-Type Zebrafish Larvae Under Starvation Stress: Larvae Can Live Up to 17 Days Post-Fertilization Without Food.
Voskarides K, Koutsofti C, Pozova M.
Voskarides K, et al. Among authors: koutsofti c.
Zebrafish. 2022 Apr;19(2):49-55. doi: 10.1089/zeb.2022.0003. Epub 2022 Apr 12.
Zebrafish. 2022.
PMID: 35417275
Item in Clipboard
Novel and Founder Pathogenic Variants in X-Linked Alport Syndrome Families in Greece.
Hadjipanagi D, Papagregoriou G, Koutsofti C, Polydorou C, Alivanis P, Andrikos A, Christodoulidou S, Dardamanis M, Diamantopoulos AA, Fountoglou A, Frangou E, Georgaki E, Giannikouris I, Gkinis V, Goudas PC, Kalaitzidis RG, Kaperonis N, Koutroumpas G, Makrydimas G, Myserlis G, Mitsioni A, Paliouras C, Papachristou F, Papadopoulou D, Papagalanis N, Papagianni A, Perysinaki G, Siomou E, Sombolos K, Tzanakis I, Vergoulas GV, Printza N, Deltas C.
Hadjipanagi D, et al. Among authors: koutsofti c.
Genes (Basel). 2022 Nov 24;13(12):2203. doi: 10.3390/genes13122203.
Genes (Basel). 2022.
PMID: 36553470
Free PMC article.
Item in Clipboard
Case report: Aborted sudden cardiac death as a first presentation of severe mitral annulus disjunction-a case series and review of the literature.
Apostolou F, Ioannides M, Mitsis A, Koutsofti C, Deltas C, Avraamides P.
Apostolou F, et al. Among authors: koutsofti c.
Front Cardiovasc Med. 2023 Jul 20;10:1171226. doi: 10.3389/fcvm.2023.1171226. eCollection 2023.
Front Cardiovasc Med. 2023.
PMID: 37547253
Free PMC article.
Item in Clipboard
Massive Parallel DNA Sequencing of Patients with Inherited Cardiomyopathies in Cyprus and Suggestion of Digenic or Oligogenic Inheritance.
Koutsofti C, Ioannides M, Polydorou C, Papagregoriou G, Malatras A, Michael G, Hadjiioannou I, Pieri S, Loizidou EM, Eftychiou C, Papasavvas E, Christophides T, Alkelai A, Kapoor M, Shuldiner AR, Avraamides P, Deltas C.
Koutsofti C, et al.
Genes (Basel). 2024 Feb 28;15(3):319. doi: 10.3390/genes15030319.
Genes (Basel). 2024.
PMID: 38540378
Free PMC article.
Item in Clipboard
Cite
Cite