Eleftheria Kokkinou

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

K. Anagnostopoulou, F. Santorelli, R. Artuch, 2019, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

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

S. Kitsiou‐Tzeli, M. Tzetis, H. Fryssira, 2018, Journal of the Neurological Sciences.

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

M. Tzetis, A. Kattamis, K. Kosma, 2019, Postgraduate medicine.

Cerebrospinal Fluid Concentrations of Neurotransmitters in a Greek Pediatric Reference Population

E. Paramera, R. Pons, E. Papakonstantinou, 2022, Neuropediatrics.

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

E. Rigatou, A. Kattamis, R. Pons, 2023, Pediatric blood & cancer.

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

M. Tzetis, C. Kanaka-Gantenbein, A. Kattamis, 2023, Acta dermato-venereologica.