Mollaki V - Search Results

1

Polymorphisms and haplotypes in MyD88 are associated with the development of sarcoidosis: a candidate-gene association study.

Daniil Z, Mollaki V, Malli F, Koutsokera A, Antoniou KM, Rodopoulou P, Gourgoulianis K, Zintzaras E, Vassilopoulos G. Daniil Z, et al. Among authors: mollaki v. Mol Biol Rep. 2013 Jul;40(7):4281-6. doi: 10.1007/s11033-013-2513-7. Epub 2013 May 11. Mol Biol Rep. 2013. PMID: 23666053

2

Polymorphisms and haplotypes in TLR9 and MYD88 are associated with the development of Hodgkin's lymphoma: a candidate-gene association study.

Mollaki V, Georgiadis T, Tassidou A, Ioannou M, Daniil Z, Koutsokera A, Papathanassiou AA, Zintzaras E, Vassilopoulos G. Mollaki V, et al. J Hum Genet. 2009 Nov;54(11):655-9. doi: 10.1038/jhg.2009.90. Epub 2009 Sep 11. J Hum Genet. 2009. PMID: 19745833

3

The -938C>A Polymorphism in MYD88 Is Associated with Susceptibility to Tuberculosis: A Pilot Study.

Aggelou K, Siapati EK, Gerogianni I, Daniil Z, Gourgoulianis K, Ntanos I, Simantirakis E, Zintzaras E, Mollaki V, Vassilopoulos G. Aggelou K, et al. Among authors: mollaki v. Dis Markers. 2016;2016:4961086. doi: 10.1155/2016/4961086. Epub 2016 Dec 29. Dis Markers. 2016. PMID: 28127112 Free PMC article.

4

Programmed Death Ligand 1: Unveiling its Impact on Endometrial Carcinogenesis.

Koutras A, Fasoulakis Z, Mollaki V, Perros P, Theodoulidis V, Syllaios A, Garmpis N, Kontomanolis EN. Koutras A, et al. Among authors: mollaki v. Cancer Diagn Progn. 2024 Jan 3;4(2):91-96. doi: 10.21873/cdp.10292. eCollection 2024 Mar-Apr. Cancer Diagn Progn. 2024. PMID: 38434913 Free PMC article. Review.

5

Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study.

European Atherosclerosis Society Familial Hypercholesterolaemia Studies Collaboration. European Atherosclerosis Society Familial Hypercholesterolaemia Studies Collaboration. Lancet. 2024 Jan 6;403(10421):55-66. doi: 10.1016/S0140-6736(23)01842-1. Epub 2023 Dec 12. Lancet. 2024. PMID: 38101429 Free article.

6

Ethical Challenges in Organoid Use.

Mollaki V. Mollaki V. BioTech (Basel). 2021 Jun 28;10(3):12. doi: 10.3390/biotech10030012. BioTech (Basel). 2021. PMID: 35822766 Free PMC article.

7

Comparison of the mutation spectrum and association with pre and post treatment lipid measures of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries.

Futema M, Ramaswami U, Tichy L, Bogsrud MP, Holven KB, Roeters van Lennep J, Wiegman A, Descamps OS, De Leener A, Fastre E, Vrablik M, Freiberger T, Esterbauer H, Dieplinger H, Greber-Platzer S, Medeiros AM, Bourbon M, Mollaki V, Drogari E, Humphries SE. Futema M, et al. Among authors: mollaki v. Atherosclerosis. 2021 Feb;319:108-117. doi: 10.1016/j.atherosclerosis.2021.01.008. Epub 2021 Jan 13. Atherosclerosis. 2021. PMID: 33508743

8

Characterization and prevalence of two novel CHEK2 large deletions in Greek breast cancer patients.

Apostolou P, Fostira F, Mollaki V, Delimitsou A, Vlassi M, Pentheroudakis G, Faliakou E, Kollia P, Fountzilas G, Yannoukakos D, Konstantopoulou I. Apostolou P, et al. Among authors: mollaki v. J Hum Genet. 2018 Jul;63(8):877-886. doi: 10.1038/s10038-018-0466-3. Epub 2018 May 22. J Hum Genet. 2018. PMID: 29785007

9

Public and physician's expectations and ethical concerns about electronic health record: Benefits outweigh risks except for information security.

Entzeridou E, Markopoulou E, Mollaki V. Entzeridou E, et al. Among authors: mollaki v. Int J Med Inform. 2018 Feb;110:98-107. doi: 10.1016/j.ijmedinf.2017.12.004. Epub 2017 Dec 12. Int J Med Inform. 2018. PMID: 29331259

10

Genetic analysis and clinical description of Greek patients with Peutz-Jeghers syndrome: Creation of a National Registry.

Fostira F, Mollaki V, Lypas G, Alexandrakis G, Christianakis E, Tzouvala M, Zacharopoulou E, Kalfakakou D, Konstantopoulou I, Yannoukakos D. Fostira F, et al. Among authors: mollaki v. Cancer Genet. 2018 Jan;220:19-23. doi: 10.1016/j.cancergen.2017.11.004. Epub 2017 Nov 20. Cancer Genet. 2018. PMID: 29310834

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