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  • Home
  • The Department
    • Chair's Greetings
    • Description
    • Administration
    • Εσωτερικός Κανονισμός Λειτουργίας
      Τμήματος Λογοθεραπείας
    • Quality Policy
    • Internal and external registries
    • Video presentation
    • Facilities
  • Studies
    • Undergraduate Studies
    • Postgraduate studies
    • Doctoral studies
    • Postdoctoral studies
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    • Ακαδημαϊκό Ημερολόγιο 2025-2026
    • Study guide
    • Qualification Exams
    • Erasmus+
    • Document Request Forms
    • Alumni
  • Research
    • Research Labs
      • Laboratory of Audiology, Neurootology and Neurosciences
      • Laboratory of New Approaches in Communication Disorders
    • Educational Labs
      • Learning Difficulties Lab
      • Computer Based SLP Lab
      • Computer Lab
  • Staff
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Faculty

Efterpi Pavlidou

Assistant Professor

Dr. Pavlidou Efterpi is a Pediatrician-Pediatric Neurologist and a graduate of the Medical School of the Democritus University of Thrace, she completed postgraduate studies at the Hellenic Open University and the British Academy of Pediatric Neurology, while she received her Doctorate Thesis from the Medical School of the Aristotle University of Thessaloniki. She retrained in Pediatric Neurology in London. She also served in the National Health System as a Consultant Pediatric Neurologist for 11 years. She has participated in International research protocols and has over 40 publications in foreign language and Greek scientific journals of recognized prestige, while she has held numerous lectures on Pediatric Neurological topics at Greek and International conferences.

Contact details
  • -
  • efterpipavlidou@uoi.gr
  • Department of Speech & Language Therapy
    University of Ioannina
    Ioannina University Campus B,
    4o km National road Ioannina-Athens
    GR 45500 Ioannina, Greece
Teaching Courses
  • (slt-56) - Paediatrics
  • (slt-69) - Principles Of Paediatric Neurology and Developmental Paediatrics
  • (slt-610) - Genetic Syndromes that Define Neuro-Developmental Diseases
  • (slt-78) - Cerebral Palsy in Children

Academic Information

Domain of interest/Discipline

Pediatrics

Education
  • 2007 - PhD at School of Medicine (Aristotle University of Thessaloniki)
  • 2018 - MSc “Management of Health Services” at Hellenic Open University
  • 1999 - Degree of Medical School of Democritus, University of Thrace, Greece
Scientific/Research Interests

Elaboration of research protocols related to Pediatric Neurology (neuromuscular diseases in children, pediatric epilepsy, neurodevelopmental diseases, etc.)

Indicative Papers
  • Frasca A, Pavlidou E, Bizzotto M, Gao Y, Balestra D, Pinotti M, Dahl HA, Mazarakis ND, Landsberger N, Kinali M.
    Not Just Loss-of-Function Variations: Identification of a Hypermorphic Variant in a Patient With a CDKL5 Missense Substitution.
    Neurol Genet. 2022 Mar 9;8(2):e666. doi: 10.1212/NXG.0000000000000666. eCollection 2022 Apr.
  • Zimmels S, Balfour-Lynn IM, Christodoulou L, Pantazi M, Pavlidou E, Pitt M, Kinali M, Ismayilova N.
    Isolated bulbar palsy and dysphagia in children with respiratory symptoms.
    Dev Med Child Neurol. 2022 Apr;64(4):518-522. doi: 10.1111/dmcn.15074. Epub 2021 Oct 2.
  • Vrachnis N, Papoulidis I, Vrachnis D, Siomou E, Antonakopoulos N, Oikonomou S, Zygouris D, Loukas N, Iliodromiti Z, Pavlidou E, Thomaidis L, Manolakos E.
    Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search.
    Mol Cytogenet. 2021 Jul 24;14(1):39. doi: 10.1186/s13039-021-00557-y.
  • Gogou M, Pavlou E, Kimiskidis V, Kouskouras K, Pavlidou E, Papadopoulos T, Haidopoulou K, Fidani L.
    Novel Mutations Involved in Charcot-Marie-Tooth 4C and Intrafamilial Variability: Let’s Not Miss the Forest for the Trees.
    J Pediatr Genet. 2021 Jun;10(2):147-151. doi: 10.1055/s-0040-1709695. Epub 2020 Apr 29.
  • Gogou M, Pavlidou E, Pavlou E, Papageorgiou T, Tragiannidis A, Giannopoulos A, Hatzipantelis E.
    Charcot-Marie-Tooth 1A concurrent with anaplastic ependymoma in a toddler: when an acute event unmasks a chronic condition.
    Turk J Pediatr. 2019;61(3):428-430. doi: 10.24953/turkjped.2019.03.017.
  • Vlachou V, Larsen L, Pavlidou E, Ismayilova N, Mazarakis ND, Scala M, Pantazi M, Mankad K, Kinali M.
    SCN2A mutation in an infant with Ohtahara syndrome and neuroimaging findings: expanding the phenotype of neuronal migration disorders.
    J Genet. 2019 Jun;98(2):54.
  • Vlachou V, Chu V, Pavlidou E, Ismayilova N, Kshitij M, Kinali M.
    Benign Infantile Epilepsy Mimicking Reflex Anoxic Seizures in an Infant with PRRT2 Gene Mutation.
    Indian J Pediatr. 2018 Aug;85(8):690. doi: 10.1007/s12098-017-2568-x. Epub 2017 Dec 18.
  • Alexopoulos H, Akrivou S, Mastroyanni S, Antonopoulou M, Dinopoulos A, Giorgi M, Konstantinou K, Kouremenos E, Lariou M, Naoumis D, Pavlidou E, Pavlou E, Voudris K, Vlachoyiannopoulos P, Dalakas MC.
    Postherpes simplex encephalitis: a case series of viral-triggered autoimmunity, synaptic autoantibodies and response to therapy.
    Ther Adv Neurol Disord. 2018 Apr 23;11:1756286418768778. doi: 10.1177/1756286418768778. eCollection 2018.
  • Pavlidou E, Ramachandran V, Govender V, Wilson C, Das R, Vlachou V, Pavlou E, Saggar A, Mankad K, Kinali M.
    A novel PLP1 mutation associated with optic nerve enlargement in two siblings with Pelizaeus-Merzbacher disease: A new MRI finding.
    Brain Dev. 2017 Mar;39(3):271-274. doi: 10.1016/j.braindev.2016.09.012. Epub 2016 Oct 25
Student's collaboration hours

…

ORCID:

0000-0002-1542-0070

Full CV in Greek

Efterpi Pevlidou (CV in greeks)

Full CV in English

Efterpi Pavlidou (CV in english)

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