Emmanouil Kanavakis
Overview
Explore the profile of Emmanouil Kanavakis including associated specialties, affiliations and a list of published articles.
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Articles
11
Citations
176
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0
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Recent Articles
1.
Bourousis E, Xatzipsalti M, Polychroni I, Kanavakis E, Stamoyannou L
Hormones (Athens)
. 2024 May;
23(3):591-593.
PMID: 38789914
Silver-Russell syndrome 5 (SRS5) is characterized by asymmetric intrauterine growth restriction (IUGR), poor postnatal growth, macrocephaly at birth, and feeding difficulties. Other possible features include triangular shaped face, prominent forehead,...
2.
Zachou A, Palaiologou D, Kanavakis E, Anagnostou E
Brain Dev
. 2022 Feb;
44(5):347-352.
PMID: 35148930
Background: ITPR1 gene encodes inositol 1,4,5-trisphosphate-receptor-type 1, a Ca2+ channel highly expressed in cerebellar Purkinje cells. ITPR1 gene variants, through a loss-of-function mechanism, have been found to be related with...
3.
Kallinikou D, Tsentidis C, Kekou K, Katsalouli M, Louraki M, Kanaka-Gantenbein C, et al.
Pediatr Diabetes
. 2021 Nov;
23(1):104-114.
PMID: 34773353
Background: Diabetic neuropathy (DN) is the least recognized complication of diabetes mellitus and may start early in the course of the disease. Aldose reductase (AKR1B1) gene promoter Z-2/Z-2 polymorphism increases...
4.
Kallinikou D, Soldatou A, Tsentidis C, Louraki M, Kanaka-Gantenbein C, Kanavakis E, et al.
Diabetes Metab Res Rev
. 2019 May;
35(7):e3178.
PMID: 31083769
Diabetic neuropathy (DN) is a common long-term complication of type 1 (T1D) and type 2 (T2D) diabetes mellitus, with significant morbidity and mortality. DN is defined as impaired function of...
5.
Rampias T, Karagiannis D, Avgeris M, Polyzos A, Kokkalis A, Kanaki Z, et al.
EMBO Rep
. 2019 Jan;
20(3).
PMID: 30665945
Genome-wide studies in tumor cells have indicated that chromatin-modifying proteins are commonly mutated in human cancers. The lysine-specific methyltransferase 2C (KMT2C/MLL3) is a putative tumor suppressor in several epithelia and...
6.
Tsoutsou E, Tzetis M, Giannikou K, Braoudaki M, Mitrakos A, Amenta S, et al.
Pediatr Res
. 2017 Apr;
82(2):253-260.
PMID: 28422950
BackroundMicrocephaly can either be isolated or it may coexist with other neurological entities and/or multiple congenital anomalies, known as syndromic microcephaly. Although many syndromic cases can be classified based on...
7.
Makrythanasis P, Nelis M, Santoni F, Guipponi M, Vannier A, Bena F, et al.
Hum Mutat
. 2014 Jul;
35(10):1203-10.
PMID: 25044680
Rare, atypical, and undiagnosed autosomal-recessive disorders frequently occur in the offspring of consanguineous couples. Current routine diagnostic genetic tests fail to establish a diagnosis in many cases. We employed exome...
8.
Lepetsos P, Pampanos A, Kanavakis E, Tzetis M, Korres D, Papavassiliou A, et al.
J Orthop Res
. 2014 May;
32(9):1155-60.
PMID: 24838892
Osteoarthritis is the most common form of arthritis with still unknown pathogenic etiology and considerable contribution of genetic factors. One of the mechanisms of cartilage degradation in osteoarthritis is enzymatic...
9.
Lepetsos P, Pampanos A, Lallos S, Kanavakis E, Korres D, Papavassiliou A, et al.
Mol Biol Rep
. 2013 Aug;
40(9):5491-9.
PMID: 23922196
Osteoarthritis (OA) is the most common form of arthritis with still unknown pathogenic etiology and considerable contribution of genetic factors. Recently, a new emerging role of oxidative stress in the...
10.
Karamanou M, Kanavakis E, Mavrou A, Petridou E, Androutsos G
Acta Med Hist Adriat
. 2013 Apr;
10(2):311-6.
PMID: 23560757
Jérôme Lejeune's greatest achievement was the discovery of the genetic basis of Down's syndrome, which he named trisomy 21. His important research in human genetics, as well as his humanitarian...