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Curriculum Vitae

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Konstantinos Kollios

Associate Professor, School of Medicine

Personal Information

Portrait de kkollios

- 2310992891
kkollios@auth.gr

Course Work

Courses of Winter semester of 2016–17 academic year

	TMĪMA IATRIKĪS
ΙΑ0323	Paediatrics

Courses of Spring semester of 2016–17 academic year

	TMĪMA IATRIKĪS
ΙΑ0323	Paediatrics
ΙΑ0325	Paediatrics I

Theses Supervised

Student Theses within AUTh

In progress

. Επίδραση του δείκτη μάζας σώματος και της μεταβλητότητας της αρτηριακής πίεσης στην αριστερή κοιλία και στην αρτηριακή σκληρία σε παιδιά και εφήβους

Publications

2014

Tratselas A, Simitsopoulou Maria, Giannakopoulou Alexandra, Dori Ioanna, Saoulidis S, Kollios Konstantinos, Papaioannidou Paraskevi, Pournaras S, Roilides Emmanuel (2014). Effect of Ceftriaxone on the Outcome of Murine Pyelonephritis Caused by Extended-Spectrum- -Lactamase-Producing Escherichia coli. Antimicrobial Agents and Chemotherapy. vol.58 no.12 p.7102-7111.

2013

Xinias Ioannis, Mavroudi Antigoni, Sapountzi Evi, Thomaidou Agathi, Fotoulaki Maria, Kalambakas Athansios, Karypidou Elina, Kollios Konstantinos, Pardalos Grigorios, Imvrios George (2013). Primary Intestinal Lymphangiectasia: Is It Always Bad? Two Cases with Different Outcome. Case Reports in Gastroenterology.

2011

Christoforidis A, Printza N, Gkogka C, Siomou E, Challa A, Kazantzidou E, Kollios K, Papachristou F (2011). Comparative study of quantitative ultrasonography and dual-energy X-ray absorptiometry for evaluating renal osteodystrophy in children with chronic kidney disease. J Bone Miner Metab. vol.29 no.3 p.321-327.
Kollios Konstantinos, Tsolaki A, Antachopoulos Charalampos, Moix I, Morris M. A, Papadopoulou Maria, Roilides Emmanuel (2011). Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl. Journal of Pediatric Endocrinology and Metabolism. vol.24 no.7-8 p.599-601.
Printza Nikoleta, Bosdou J, Pantzaki A, Badouraki M, Kollios Konstantinos, Ghogha C, Papachristou Fotios (2011). Percutaneous ultrasound-guided renal biopsy in children: a single centre experience. Hippokratia. vol.15 no.3 p.258-261.
Tratselas A, Iosifidis E, Ioannidou M, Saoulidis S, Kollios Konstantinos, Antachopoulos Charalampos, Sofianou D, Roilides Emmanuel (2011). Outcome of urinary tract infections caused by extended spectrum β-lactamase-producing Enterobacteriaceae in children. Pediatric Infectious Disease Journal. vol.30 no.8 p.707-710.

2010

Kefala-Agoropoulou K, Protonotariou E, Vitti D, Sarafidou S, Anastasiou A, Kollios Konstantinos, Roilides Emmanuel (2010). Life-threatening infection due to community-acquired methicillin-resistant Staphylococcus aureus: case report and review. European Journal of Pediatrics. vol.169 no.1 p.47-53.

2009

Chatzikyriakidou A, Kollios K. D, Georgiou I (2009). Novel human pathological mutations. Gene symbol: SLC3A1. Disease: Cystinuria. Hum Genet. vol.126 no.2 p.335.
Platnaris A, Hatzimichael A, Ktenidou-Kartali S, Kontoyiannides K, Kollios Konstantinos, Anagnostopoulos Ioannis, Roilides Emmanuel (2009). A case of Listeria meningoencephalitis complicated by hydrocephalus in an immunocompetent infant. European Journal of Pediatrics. vol.168 no.3 p.343-346.
Xinias I, Demertzidou V, Mavroudi A, Kollios K, Kardaras P, Papachristou F, Arsos G, Tsiouris I (2009). Bilirubin levels predict renal cortical changes in jaundiced neonates with urinary tract infection. World J Pediatr. vol.5 no.1 p.42-45.

2007

Kollios K. D, Skiadopoulou E, Siondi I, Papadopoulou Z. L (2007). Coxsackie virus B1 infection in a child, complicated by severe oliguric renal failure. Clin Nephrol. vol.67 no.4 p.260-262.
Siomou E, Bouba I, Kollios K. D, Papadopoulou F, Syrrou M, Georgiou I, Siamopoulou A (2007). Angiotensin II type 2 receptor gene polymorphism in Caucasian children with a wide spectrum of congenital anomalies of the kidney and urinary tract. Pediatr Res. vol.62 no.1 p.83-87.

1998

Andronikou S, Kollios Konstantinos, Dimou S, Kamina S, Bourantas K, Papadopoulou ZL (1998). Hemolytic uremic syndrome and thymic dysplasia in an infant. Pediatric nephrol. vol.12 p.231-233.

Mis à jour: 2017-07-30