Emmanouil Kanavakis
Athens, ESYE31, Greece
Last Updated: 09/26/2026
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Found 9 publications
A variant of uncertain significance of the HMGA2 gene in a child with Silver-Russell syndrome-like phenotype: a case report.
Journal: Hormones (Athens, Greece)
Published: September 16, 2023
Retrocollis as the cardinal feature in a de novo ITRP1 variant.
Journal: Brain & development
Published: October 21, 2021
Homozygosity of the Z-2 polymorphic variant in the aldose reductase gene promoter confers increased risk for neuropathy in children and adolescents with Type 1 diabetes.
Journal: Pediatric diabetes
Published: May 11, 2021
The lysine-specific methyltransferase KMT2C/MLL3 regulates DNA repair components in cancer.
Journal: EMBO reports
Published: July 27, 2018
Diabetic neuropathy in children and adolescents with type 1 diabetes mellitus: Diagnosis, pathogenesis, and associated genetic markers.
Journal: Diabetes/metabolism research and reviews
Published: January 08, 2018
Association of MMP-1 -1607 1G/2G (rs1799750) polymorphism with primary knee osteoarthritis in the Greek population.
Journal: Journal of orthopaedic research : official publication of the Orthopaedic Research Society
Published: March 09, 2014
Association of NADPH oxidase p22phox gene C242T, A640G and -930A/G polymorphisms with primary knee osteoarthritis in the Greek population.
Journal: Molecular biology reports
Published: March 18, 2013
Jérôme Lejeune (1926-1994): father of modern genetics.
Journal: Acta medico-historica adriatica : AMHA
Published: January 01, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026