Δημοσιεύσεις

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

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Bakkum, M., Loobeek B., Richir M., & Papaioannidou P. (2022).  Novel teaching resources for the European Open Platform for Prescribing Education (EurOP2E) – a nominal group technique study. European Journal of Clinical Pharmacology .
Samanidou, V., Kovatsi L., Fragou D., & Rentifis K. (2011).  Novel strategies for sample preparation in forensic toxicology.. Bioanalysis. 3(17), 2019-46.
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.
Doumas, A., Zegkos T., Parcharidou D., Gossios T., Ntelios D., Chatzileontiadou S., et al. (2022).  A novel quantitative method for assessing the therapeutic response to Tafamidis therapy in patients with cardiac TTR amyloidosis. A preliminary report.. Hell J Nucl Med. 25(2), 216-219.
Galli-Tsinopoulou, A., Hiort O., Schuster T., Messer G., & Kuhnle U. (2003).  A novel point mutation in the hormone binding domain of the androgen receptor associated with partial and minimal androgen insensitivity syndrome.. J Pediatr Endocrinol Metab. 16(2), 149-54.
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.
Paraskevas, G. P., Yapijakis C., Bougea A., Constantinides V., Bourbouli M., Stamboulis E., et al. (2017).  Novel PANK2 mutation in the first Greek compound heterozygote patient with pantothenate-kinase-associated neurodegeneration.. SAGE Open Med Case Rep. 5, 2050313X17720101.
Vassilikos, V., Dakos G., Chatzizisis Y. S., Chouvarda I., Karvounis C., Maynard C., et al. (2011).  Novel non-invasive P wave analysis for the prediction of paroxysmal atrial fibrillation recurrences in patients without structural heart disease: a prospective pilot study.. Int J Cardiol. 153(2), 165-72.
Polyzos, S. A., Kountouras J., Slavakis A., Zafeiriadou E., Patsiaoura K., Katsiki E., et al. (2013).  A novel noninvasive index for nonalcoholic steatohepatitis: a pilot study.. Biomarkers. 18(7), 607-13.
Agakidou, E., Agakidis C., Kambouris M., Printza N., Farini M., Vourda E., et al. (2020).  A Novel Mutation of 33 Gene Associated with Incomplete Arthrogryposis-Renal Dysfunction-Cholestasis Phenotype.. Case Rep Genet. 2020, 8872294.
Ash, D. B., Papadimitriou D., Hays A. P., Dimauro S., & Hirano M. (2012).  A novel mutation in PNPLA2 leading to neutral lipid storage disease with myopathy.. Arch Neurol. 69(9), 1190-2.
Tsiambas, E., Fotiades P. P., Sioka C., Kotrotsios D., Gkika E., Fotopoulos A., et al. (2017).  Novel molecular and metabolic aspects in osteosarcoma.. J BUON. 22(6), 1595-1598.
Christoforidis, A., Skordis N., Fanis P., Dimitriadou M., Sevastidou M., Phelan M. M., et al. (2017).  A novel MKRN3 nonsense mutation causing familial central precocious puberty.. Endocrine. 56(2), 446-449.
Pentheroudakis, G., Pavlidis N., Fountzilas G., Krikelis D., Goussia A., Stoyianni A., et al. (2013).  Novel microRNA-based assay demonstrates 92% agreement with diagnosis based on clinicopathologic and management data in a cohort of patients with carcinoma of unknown primary.. Mol Cancer. 12, 57.
Sivaji, N., Arshad F. A., & Karkos P. D. (2011).  A novel method of draining a peritonsillar abscess.. Clin Otolaryngol. 36(2), 189-90.
Kopsachilis, N., Tsaousis K. T., Tsinopoulos I. T., Kruse F. E., & Welge-Luessen U. (2013).  A novel mechanism of UV-A and riboflavin-mediated corneal cross-linking through induction of tissue transglutaminases.. Cornea. 32(7), 1034-9.
Vrochides, D., Kardassis D., Ntinas A., Miliaras D., Papalois A., Magnissalis E., et al. (2014).  A novel liver parenchyma transection technique using locking straight rigid ties. An experimental study in pigs.. J Invest Surg. 27(2), 106-13.
Deuteraiou, K., Kitas G., Garyfallos A., & Dimitroulas T. (2018).  Novel insights into the role of inflammasomes in autoimmune and metabolic rheumatic diseases.. Rheumatol Int. 38(8), 1345-1354.
Chatzikyriakidou, A., Kollios K. D., & Georgiou I. (2009).  Novel human pathological mutations. Gene symbol: SLC3A1. Disease: Cystinuria.. Hum Genet. 126(2), 335.
Pells, S., Koutsouraki E., Morfopoulou S., Valencia-Cadavid S., Tomlinson S. R., Kalathur R., et al. (2015).  Novel Human Embryonic Stem Cell Regulators Identified by Conserved and Distinct CpG Island Methylation State.. PLoS One. 10(7), e0131102.
Chefetz, I., Heller R., Galli-Tsinopoulou A., Richard G., Wollnik B., Indelman M., et al. (2005).  A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification.. Hum Genet. 118(2), 261-6.
Kilintzis, V., Pappas T., Chouvarda I., Salonikiou A., Maglaveras N., Dimitrakos S., et al. (2011).  Novel Heidelberg retina tomograph-based morphological parameters derived from optic disc cupping surface processing.. Invest Ophthalmol Vis Sci. 52(2), 947-51.
Hibar, D. P., Adams H. H. H., Jahanshad N., Chauhan G., Stein J. L., Hofer E., et al. (2017).  Novel genetic loci associated with hippocampal volume.. Nat Commun. 8, 13624.
Yu, Y. P., Ding Y., Chen Z., Liu S., Michalopoulos A., Chen R., et al. (2014).  Novel fusion transcripts associate with progressive prostate cancer.. Am J Pathol. 184(10), 2840-9.
Stamou, M. I., Plummer L., Koika V., Galli-Tsinopoulou A., & Georgopoulos N. A. (2019).  A novel FGF8 mutation in a female patient with isolated congenital anosmia.. Hormones (Athens). 18(2), 241-244.

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