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Sex Differences under Vitamin D Supplementation in an Animal Model of Progressive Multiple Sclerosis.
Nutrients. 2024 Feb 17;16(4):554. doi: 10.3390/nu16040554.
Nutrients. 2024.
PMID: 38398879
Free PMC article.
Serum neurofilament light as a potential marker of illness duration in bipolar disorder.
Queissner R, Buchmann A, Demjaha R, Tafrali C, Benkert P, Kuhle J, Jerkovic A, Dalkner N, Fellendorf F, Birner A, Platzer M, Tmava-Berisha A, Maget A, Stross T, Lenger M, Häussl A, Khalil M, Reininghaus E.
Queissner R, et al. Among authors: tafrali c.
J Affect Disord. 2024 Apr 1;350:366-371. doi: 10.1016/j.jad.2024.01.088. Epub 2024 Jan 10.
J Affect Disord. 2024.
PMID: 38215991
Free article.
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Elevated serum neurofilament light chain protein in patients with essential tremor.
Franthal S, Khalil M, Kern D, Gattermeyer L, Buchmann A, Katschnig-Winter P, Kögl M, Demjaha R, Tafrali C, Hofer E, Schmidt R, Schwingenschuh P.
Franthal S, et al. Among authors: tafrali c.
Eur J Neurol. 2024 Feb;31(2):e16143. doi: 10.1111/ene.16143. Epub 2023 Nov 17.
Eur J Neurol. 2024.
PMID: 37975778
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Social foraging extends associative odor-food memory expression in an automated learning assay for Drosophila melanogaster.
Sehdev A, Mohammed YG, Tafrali C, Szyszka P.
Sehdev A, et al. Among authors: tafrali c.
J Exp Biol. 2019 Oct 8;222(Pt 19):jeb207241. doi: 10.1242/jeb.207241.
J Exp Biol. 2019.
PMID: 31527181
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Genomic variation in the MAP3K5 gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacy.
Tafrali C, Paizi A, Borg J, Radmilovic M, Bartsakoulia M, Giannopoulou E, Giannakopoulou O, Stojiljkovic-Petrovic M, Zukic B, Poulas K, Stavrou EF, Lambropoulou P, Kourakli A, Felice AE, Papachatzopoulou A, Philipsen S, Pavlovic S, Georgitsi M, Patrinos GP.
Tafrali C, et al.
Pharmacogenomics. 2013 Apr;14(5):469-83. doi: 10.2217/pgs.13.31.
Pharmacogenomics. 2013.
PMID: 23556445
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KLF10 gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patients.
Borg J, Phylactides M, Bartsakoulia M, Tafrali C, Lederer C, Felice AE, Papachatzopoulou A, Kourakli A, Stavrou EF, Christou S, Hou J, Karkabouna S, Lappa-Manakou C, Ozgur Z, van Ijcken W, von Lindern M, Grosveld FG, Georgitsi M, Kleanthous M, Philipsen S, Patrinos GP.
Borg J, et al. Among authors: tafrali c.
Pharmacogenomics. 2012 Oct;13(13):1487-500. doi: 10.2217/pgs.12.125.
Pharmacogenomics. 2012.
PMID: 23057549
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A single nucleotide polymorphism in the HBBP1 gene in the human β-globin locus is associated with a mild β-thalassemia disease phenotype.
Giannopoulou E, Bartsakoulia M, Tafrali C, Kourakli A, Poulas K, Stavrou EF, Papachatzopoulou A, Georgitsi M, Patrinos GP.
Giannopoulou E, et al. Among authors: tafrali c.
Hemoglobin. 2012;36(5):433-45. doi: 10.3109/03630269.2012.717515.
Hemoglobin. 2012.
PMID: 22943111
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Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase.
Georgitsi M, Viennas E, Gkantouna V, Christodoulopoulou E, Zagoriti Z, Tafrali C, Ntellos F, Giannakopoulou O, Boulakou A, Vlahopoulou P, Kyriacou E, Tsaknakis J, Tsakalidis A, Poulas K, Tzimas G, Patrinos GP.
Georgitsi M, et al. Among authors: tafrali c.
Pharmacogenomics. 2011 Jan;12(1):49-58. doi: 10.2217/pgs.10.169.
Pharmacogenomics. 2011.
PMID: 21174622
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