Δημοσιεύσεις

Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.

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Συντάκτης Τίτλος Τύπος [ Έτος(Asc)]
Φίλτρα: Keyword is Phenotype  [Clear All Filters]
2018
Papakonstantinou, A., Ioannides D., Vakirlis E., Savvoulidis C., Lallas A., Apalla Z., et al. (2018).  Dermoscopic features of melanocytic skin lesions in Greek children and adolescents and their association with environmental factors and skin types.. J Eur Acad Dermatol Venereol. 32(12), 2142-2148.
Kotsis, V., Jamthikar A. D., Araki T., Gupta D., Laird J. R., Giannopoulos A. A., et al. (2018).  Echolucency-based phenotype in carotid atherosclerosis disease for risk stratification of diabetes patients.. Diabetes Res Clin Pract. 143, 322-331.
Liakopoulos, V., Jeron A., Shah A., Bruder D., Mertens P. R., & Gorny X. (2018).  Hemodialysis-related changes in phenotypical features of monocytes.. Sci Rep. 8(1), 13964.
Bouziana, S. D., Tziomalos K., Goulas A., Vyzantiadis T-A., Panderi A., & Ηatzitolios A. Ι. (2018).  Major Adipokines and the -420C>G Resistin Gene Polymorphism as Predictors of Acute Ischemic Stroke Severity and In-Hospital Outcome.. J Stroke Cerebrovasc Dis. 27(4), 963-970.
Christodoulou, I., Goulielmaki M., Devetzi M., Panagiotidis M., Koliakos G., & Zoumpourlis V. (2018).  Mesenchymal stem cells in preclinical cancer cytotherapy: a systematic review.. Stem Cell Res Ther. 9(1), 336.
Papadopoulou, A., Dinopoulos A., Koutsodontis G., Pons R., Vorgia P., Koute V., et al. (2018).  Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome.. Eur J Paediatr Neurol. 22(3), 419-426.
Fastré, E., Lanteigne L-E., Helaers R., Giacalone G., Revencu N., Dionyssiou D., et al. (2018).  Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedema.. Clin Genet. 94(1), 179-181.
Patas, K., Willing A., Demiralay C., Engler J. Broder, Lupu A., Ramien C., et al. (2018).  T Cell Phenotype and T Cell Receptor Repertoire in Patients with Major Depressive Disorder.. Front Immunol. 9, 291.
2017
Tsitlakidis, D., Katopodi T., Goulis D. G., Papadimas I., & Kritis A. (2017).  Association of follicle-stimulating hormone receptor single nucleotide polymorphisms with fertility in Greek men.. J Endocrinol Invest. 40(7), 721-726.
Cohen, S. A., Yu M., Baker K., Redman M., Wu C., Heinzerling T. J., et al. (2017).  The CpG island methylator phenotype is concordant between primary colorectal carcinoma and matched distant metastases.. Clin Epigenetics. 9, 46.
Ribero, S., Argenziano G., Lallas A., Moscarella E., Benati E., Raucci M., et al. (2017).  Dermoscopic features predicting the presence of mitoses in thin melanoma.. J Dermatol Sci. 86(2), 158-161.
Mendrinou, E., Patsatsi A., Zafiriou E., Papadopoulou D., Aggelou L., Sarri C., et al. (2017).  FCGR3A-V158F polymorphism is a disease-specific pharmacogenetic marker for the treatment of psoriasis with Fc-containing TNFα inhibitors.. Pharmacogenomics J. 17(3), 237-241.
Bougea, A., Koros C., Stamelou M., Simitsi A., Papagiannakis N., Antonelou R., et al. (2017).  Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene.. Parkinsonism Relat Disord. 35, 82-87.
Sarri, C. A., Roussaki-Schulze A., Vasilopoulos Y., Zafiriou E., Patsatsi A., Stamatis C., et al. (2017).  Netherton Syndrome: A Genotype-Phenotype Review.. Mol Diagn Ther. 21(2), 137-152.
Pavlidou, E., Ramachandran V., Govender V., Wilson C., Das R., Vlachou V., et al. (2017).  A novel PLP1 mutation associated with optic nerve enlargement in two siblings with Pelizaeus-Merzbacher disease: A new MRI finding.. Brain Dev. 39(3), 271-274.
Wollstein, A., Walsh S., Liu F., Chakravarthy U., Rahu M., Seland J. H., et al. (2017).  Novel quantitative pigmentation phenotyping enhances genetic association, epistasis, and prediction of human eye colour.. Sci Rep. 7, 43359.
Forés, M., Papagianni A., Rodríguez-Muñoz L., & Jiménez G. (2017).  Using CRISPR-Cas9 to Study ERK Signaling in Drosophila.. Methods Mol Biol. 1487, 353-365.

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Τμήμα Ιατρικής, Πανεπιστημιούπολη ΑΠΘ, T.K. 54124, Θεσσαλονίκη
 

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