Eleftheria Kokkinou

Athens, ESYE31 11527, Greece

Last Updated: 09/26/2026

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Found 10 publications

Rare-ID: Genomic Diagnosis in Symptomatic Neonates and Young Infants with Complex Clinical Phenotypes: A Descriptive Cohort Study.

Rare-ID: Genomic Diagnosis in Symptomatic Neonates and Young Infants with Complex Clinical Phenotypes: A Descriptive Cohort Study.

Journal: Genes

Published: May 19, 2026

"Tuberous sclerosis in Greece: A national cohort study on clinical features and rare manifestations".

"Tuberous sclerosis in Greece: A national cohort study on clinical features and rare manifestations".

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: March 29, 2025

Development and Preliminary Validation of a Parkinsonism-Dystonia Scale for Infants and Young Children.

Development and Preliminary Validation of a Parkinsonism-Dystonia Scale for Infants and Young Children.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: September 16, 2024

Motor phenotyping in a Greek cohort of patients with neonatal and infantile onset developmental and epileptic encephalopathy.

Motor phenotyping in a Greek cohort of patients with neonatal and infantile onset developmental and epileptic encephalopathy.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: July 06, 2024

Ischemic stroke in a pediatric patient with very rare coexistence of sickle-cell/β-thalassemia and neurofibromatosis type 1.

Ischemic stroke in a pediatric patient with very rare coexistence of sickle-cell/β-thalassemia and neurofibromatosis type 1.

Journal: Pediatric blood & cancer

Published: March 07, 2023

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

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

Journal: Acta dermato-venereologica

Published: December 11, 2022

Cerebrospinal Fluid Concentrations of Neurotransmitters in a Greek Pediatric Reference Population.

Cerebrospinal Fluid Concentrations of Neurotransmitters in a Greek Pediatric Reference Population.

Journal: Neuropediatrics

Published: November 28, 2022

Development of a multidisciplinary clinic of neurofibromatosis type 1 and other neurocutaneous disorders in Greece. A 3-year experience.

Development of a multidisciplinary clinic of neurofibromatosis type 1 and other neurocutaneous disorders in Greece. A 3-year experience.

Journal: Postgraduate medicine

Published: August 25, 2019

The genetic etiology in cerebral palsy mimics: The results from a Greek tertiary care center.

The genetic etiology in cerebral palsy mimics: The results from a Greek tertiary care center.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: September 26, 2018

Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA.

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

Showing 1-10 of 10

Last Updated: 09/26/2026