Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
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Συντάκτης Τίτλος [ Τύπος] Έτος Φίλτρα: Συντάκτης is Gioula, Georgia [Clear All Filters]
Absence of human bocavirus in atherosclerotic plaques of carotid arteries by real-time polymerase chain reaction..
Scand J Infect Dis. 42(8), 623-5.
(2010). Association Between Upper Respiratory Tract Viral Load, Comorbidities, Disease Severity, and Outcome of Patients With SARS-CoV-2 Infection..
J Infect Dis. 223(7), 1132-1138.
(2021). Bloodstream Infection by in Two COVID-19 Patients after Receiving Supplementation of in the ICU..
J Fungi (Basel). 6(3),
(2020). Challenges in antigenic characterization of circulating influenza A(H3N2) viruses during the 2011-2012 influenza season: an ongoing problem?.
J Clin Microbiol. 53(5), 1493-9.
(2015). Genetic analysis of post-pandemic 2010-2011 influenza A(H1N1)pdm09 hemagglutinin virus variants that caused mild, severe, and fatal infections in Northern Greece..
J Med Virol. 87(1), 57-67.
(2015). Identification of complement-related host genetic risk factors associated with influenza A(H1N1)pdm09 outcome: challenges ahead..
Med Microbiol Immunol. 208(5), 631-640.
(2019). Influenza vaccine effectiveness against laboratory confirmed influenza in Greece during the 2013-2014 season: a test-negative study..
Vaccine. 33(2), 367-73.
(2015). Influenza vaccine effectiveness in preventing hospitalizations with laboratory-confirmed influenza in Greece during the 2014-2015 season: A test-negative study..
J Med Virol. 88(11), 1896-904.
(2016). Molecular and phylogenetic analysis and vaccine strain match of human influenza A(H3N2) viruses isolated in Northern Greece between 2004 and 2008..
Virus Res. 145(2), 220-6.
(2009). Molecular and phylogenetic analysis of the haemagglutinin gene of pandemic influenza H1N1 2009 viruses associated with severe and fatal infections..
Virus Res. 151(2), 192-9.
(2010). Multiple Coronary Artery Microfistulas in a Girl with Kleefstra Syndrome..
Case Rep Genet. 2016, 3056053.
(2016). Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome..
Am J Med Genet A. 164A(3), 764-8.
(2014).
(2020).