Myrto Poulou
Athens, ESYE31 11527, Greece
Last Updated: 09/26/2026
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Found 16 publications
Wiedemann-Steiner Syndrome (WSS): A Neonatal Case Report Expanding the Phenotypic Spectrum of a Previously Reported Missense Variant.
Journal: International journal of molecular sciences
Published: March 16, 2026
Differential and Common Signatures of miRNA Expression and Methylation in Childhood Central Nervous System Malignancies: An Experimental and Computational Approach.
Journal: Cancers
Published: October 20, 2021
Frequencies of pathogenic CFTR variants in Greek cystic fibrosis patients with allergic bronchopulmonary aspergillosis and Aspergillus fumigatus chronic colonization: A retrospective cohort study.
Journal: Journal de mycologie medicale
Published: May 13, 2021
Reprogramming of bone marrow derived mesenchymal stromal cells to human induced pluripotent stem cells from pediatric patients with hematological diseases using a commercial mRNA kit.
Journal: Blood cells, molecules & diseases
Published: November 11, 2018
Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA.
Journal: Journal of the neurological sciences
Published: January 29, 2018
Serum microRNA array analysis identifies miR-140-3p, miR-33b-3p and miR-671-3p as potential osteoarthritis biomarkers involved in metabolic processes.
Journal: Clinical epigenetics
Published: August 21, 2017
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Syndrome: Additional Clinical Features.
Journal: Pediatric neurology
Published: October 28, 2016
Complex preimplantation genetic diagnosis for beta-thalassaemia, sideroblastic anaemia, and human leukocyte antigen (HLA)-typing.
Journal: Systems biology in reproductive medicine
Published: December 05, 2015
Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases.
Journal: Meta gene
Published: September 21, 2015
Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD).
Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: April 23, 2015
Multi-allele genotyping platform for the simultaneous detection of mutations in the Wilson disease related ATP7B gene.
Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
Published: March 09, 2015
Last Updated: 09/26/2026