Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases

por Tsipi, Maria, Tzetis, Maria, Kosma, Konstantina, Moschos, Marilita, Braoudaki, Maria, Poulou, Myrto, Kanavakis, Emmanuel, Kitsiou-Tzeli, Sofia
Publicado 2016

BTNL2 gene SNPs as a contributing factor to sarcoidosis pathogenesis in a cohort of Greek patients

por Delaveri, Aikaterini, Rapti, Aggeliki, Poulou, Myrto, Fylaktou, Eirini, Tsipi, Maria, Roussos, Charis, Makrythanasis, Periklis, Kanavakis, Emmanuel, Tzetis, Maria
Publicado 2014

Characteristics of Café-au-lait Macules and their Association with the Neurofibromatosis type I Genotype in a Cohort of Greek Children

por NASI, Lamprini, ALEXOPOULOS, Alexios, KOKKINOU, Eleftheria, ROKA, Kleoniki, TZETIS, Maria, TSIPI, Maria, KAKOUROU, Talia, KANAKA-GANTENBEIN, Christina, CHROUSOS, George, KATTAMIS, Antonis, PONS, Roser
Publicado 2023