Δημοσιεύσεις

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

Export 11032 results:
[ Συντάκτης(Asc)] Τίτλος Τύπος Έτος
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
S
Spyratos, D., Chloros D., Haidich B., Dagdilelis L., Markou S., & Sichletidis L. (2012).  Chest imaging and lung function impairment after long-term occupational exposure to low concentrations of chrysotile.. Arch Environ Occup Health. 67(2), 84-90.
Spyratos, D., & Sichletidis L. (2015).  Umeclidinium bromide/vilanterol combination in the treatment of chronic obstructive pulmonary disease: a review.. Ther Clin Risk Manag. 11, 481-7.
Spyratos, D., Kalpakidis V., Giouleka P., Chloros D., & Sichletidis L. (2011).  An unusual cause of spontaneous pneumothorax.. BMJ Case Rep. 2011,
Spyratos, D., Sichletidis L., Manika A., Kontakiotis T., Chloros D., & Patakas D. (2007).  Expiratory Flow Limitation in Patients with Pleural Effusion. Respiration. 74(5), 572 - 578.
Spulber, G., Simmons A., Muehlboeck J-S., Mecocci P., Vellas B., Tsolaki M., et al. (2013).  An MRI-based index to measure the severity of Alzheimer's disease-like structural pattern in subjects with mild cognitive impairment.. J Intern Med. 273(4), 396-409.
Spoto, B., Ntounousi E., Testa A., Liakopoulos V., D'Arrigo G., Tripepi G., et al. (2018).  The sirtuin1 gene associates with left ventricular myocardial hypertrophy and remodeling in two chronic kidney disease cohorts: a longitudinal study.. J Hypertens. 36(8), 1705-1711.
Sponholz, C., Kramer M., Schöneweck F., Menzel U., Rahatloo K. Inanloo, Giamarellos-Bourboulis E. J., et al. (2015).  Polymorphisms of cystathionine beta-synthase gene are associated with susceptibility to sepsis.. Eur J Hum Genet.
Spiroglou, K., Xinias I., Karatzas N., Karatza E., Arsos G., & Panteliadis C. (2004).  Gastric emptying in children with cerebral palsy and gastroesophageal reflux.. Pediatr Neurol. 31(3), 177-82.
Spiridis, C., Kambaroudis A., Ntinas A., Papadopoulos S., Papanicolaou A., & Gerasimidis T. (2011).  Intussusception of the small bowel secondary to malignant metastases in two 80-year-old people: a case series.. J Med Case Rep. 5, 176.
Spilioti, M., Evangeliou A. E., Tramma D., Theodoridou Z., Metaxas S., Michailidi E., et al. (2013).  Evidence for treatable inborn errors of metabolism in a cohort of 187 Greek patients with autism spectrum disorder (ASD).. Front Hum Neurosci. 7, 858.
Spilioti, M., Pavlou E., Gogou M., Katsanika I., Papadopoulou-Alataki E., Grafakou O., et al. (2016).  Valproate effect on ketosis in children under ketogenic diet.. Eur J Paediatr Neurol. 20(4), 555-9.
Spengler, E. K., O'Leary J. G., Te H. S., Rogal S., Pillai A. A., Al-Osaimi A., et al. (2017).  Liver Transplantation in the Obese Cirrhotic Patient.. Transplantation. 101(10), 2288-2296.
Spellberg, B., Ibrahim A., Roilides E., Lewis R. E., Lortholary O., Petrikkos G., et al. (2012).  Combination therapy for mucormycosis: why, what, and how?. Clin Infect Dis. 54 Suppl 1, S73-8.
Speletas, M., Mamara A., Papadopoulou-Alataki E., Iordanakis G., Liadaki K., Bardaka F., et al. (2011).  TNFRSF13B/TACI alterations in Greek patients with antibody deficiencies.. J Clin Immunol. 31(4), 550-9.
Speletas, M., Argentou N., Germanidis G., Vasiliadis T., Mantzoukis K., Patsiaoura K., et al. (2011).  Foxp3 expression in liver correlates with the degree but not the cause of inflammation.. Mediators Inflamm. 2011, 827565.
Speletas, M., Argentou N., Karanikas V., Gramoustianou E. S., Mandala E., Braimi M., et al. (2011).  Survivin isoform expression patterns in CML patients correlate with resistance to imatinib and progression, but do not trigger cytolytic responses.. Clin Immunol. 139(2), 155-63.
Speletas, M., Boukas K., Papadopoulou-Alataki E., Tsitsami E., & Germenis A. E. (2009).  Hereditary angioedema in Greek families caused by novel and recurrent mutations.. Hum Immunol. 70(11), 925-9.
Speletas, M., Kanariou M., Kanakoudi-Tsakalidou F., Papadopoulou-Alataki E., Arvanitidis K., Pardali E., et al. (2001).  Analysis of Btk mutations in patients with X-linked agammaglobulinaemia (XLA) and determination of carrier status in normal female relatives: a nationwide study of Btk deficiency in Greece.. Scand J Immunol. 54(3), 321-7.
Speletas, M., Kioumi A., Loules G., Hytiroglou P., Tsitouridis J., Christakis J., et al. (2008).  Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV.. Blood Cells Mol Dis. 40(3), 353-9.
Specchio, F., Argenziano G., Tiodorovic-Zivkovic D., Moscarella E., Lallas A., Zalaudek I., et al. (2015).  Dermoscopic clues to diagnose acantholytic dyskeratosis.. Dermatol Pract Concept. 5(1), 59-60.
Specchio, F., Argenziano G., Zalaudek I., Guardoli D., Longo C., Moscarella E., et al. (2014).  Photoletter to the editor: Collision tumor of melanoma and atypical fibroxanthoma of the scalp.. J Dermatol Case Rep. 8(3), 84-5.
Spartalis, M., & Papagianni A. (2016).  Receptor activator of nuclear factor κB ligand/osteoprotegerin axis and vascular calcifications in patients with chronic kidney disease.. World J Nephrol. 5(1), 1-5.
Spanoudaki, A., Oikonomou A., Dimitrova K., & Prassopoulos P. (2008).  Pedunculated uterine leiomyoma mimicking abdominal mass: a case report.. Cases J. 1(1), 315.
Spanos, K., Georgiou E., Saleptsis V., Athanasoulas A., Sakkas L., & Giannoukas A. D. (2015).  Effectiveness of intravenous ilomedin infusion and smoking cessation in the treatment of acutely symptomatic Buerger disease.. Angiology. 66(2), 114-7.
Spanos, K., Athanasoulas A., Argyriou C., Vassilopoulos I., & Giannoukas A. D. (2015).  Acute limb ischemia and anticoagulation in patients with history of atrial fibrillation.. Int Angiol.

Σελίδες

Επικοινωνία

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

Συνδεθείτε

Το τμήμα Ιατρικής στα κοινωνικά δίκτυα.
Ακολουθήστε μας ή συνδεθείτε μαζί μας.

           

Σύνδεσμοι

 

Το πανεπιστήμιο

 
 

Προσωπικό & Φοιτητές