Dr Maria Kinali, Consultant Paediatric Neurologist

Dr Maria Kinali MD, FRCPCH FAAN

Consultant Paediatric Neurologist

MD, FRCPCH FAAN

Areas of expertise

  • Paiediatric epilepsy
  • Progressive neurodegenerative
  • Childhood neuromuscular diseases
  • Neurogenetics
  • Neurorehabilitation

Recommendations for Dr Kinali

These recommendations are for information purposes only. Doctors providing recommendations do so in good faith and are not responsible for clinical outcomes.

Recommended by:

  • byDr Anand Saggar, Clinical Genetic Specialist

    Excellent comprehensive review and thoughtful opinion

  • byDr Olga Kapellou, Paediatrician

    Recommended paediatrician

  • byDr Anand Saggar, Clinical Genetic Specialist

    Excellent comprehensive review and thoughtful opinion

  • byDr Olga Kapellou, Paediatrician

    Recommended paediatrician

  • Address

    • The Portland Hospital

      205-209 Great Portland St, London, W1W 5AH

    • Chiswick Medical Centre

      Bond House, 347-353 Chiswick High Road, London, W4 4HS

    • Urgent Care Centre for Children

      234, Great Portland Street, London, W1W 5QT

    • Telephone or video consultation

      Virtual

  • Chelsea And Westminster Hospital NHS Foundation Trust

    Chelsea & Westminster Hospital, 369 Fulham Road, London, Greater London, SW10 9NH

  • About Dr Maria Kinali

    GMC number: 4077471

    Year qualified: 1992

    Place of primary qualification: University of Patras

    Areas of expertise

    • Epilepsy
    • Paediatric neurology
    • Neuromuscular diseases

    Professional memberships

    Royal College of Paediatrics and Child Health copy
    British Paediatric Neurology Association
    European Paediatric Neurology Society
    World Muscle Society
    Medical Defence Union
    British Medical Association (BMA)
    General Medical Council

    Articles by Dr Maria Kinali

    The interaction of genetic mutations in park2 and fa2h causes a novel phenotype in a case of childhood-onset movement disordervideo_1.mp4

    Scn2a mutation in an infant with ohtahara syndrome and neuroimaging findings: expanding the phenotype of neuronal migration disorders

    A novel plp1 mutation associated with optic nerve enlargement in two siblings with pelizaeus–merzbacher disease: a new mri finding

    A microrna-328 binding site in pax6 is associated with centrotemporal spikes of rolandic epilepsy

    Benign infantile epilepsy mimicking reflex anoxic seizures in an infant with prrt2 gene mutation

    Use of the ketogenic diet to treat intractable epilepsy in mitochondrial disorders

    Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures

    Metaphyseal dysplasia associated with chronic facial nerve palsy

    Zellweger syndrome and secondary mitochondrial myopathy