İlknur Erol

Akademik Profiller

1. 1
   Single gene, two diseases, and multiple clinical presentations: Biotin-thiamine-responsive basal ganglia diseaseBrain and Development
   2020
2. 2
   Expanding the phenotype of phospholipid remodelling disease due to MBOAT7 gene defectJournal of Inherited Metabolic Disease
   2019
3. 3
   Neuroblastoma and Opsomyoclonus Syndrome: Experience of 6 Cases at a Single CenterPediatric Blood and Cancer
   2019
4. 4
   Clinical presentation of anti-N-methyl-D-aspartate receptor and anti-voltage-gated potassium channel complex antibodies in children: A series of 24 casesEuropean Journal of Paediatric Neurology
   2018
5. 5
   Electroencephalographic findings in anti-N-methyl-D-aspartate receptor encephalitis in children: A series of 12 patientsEpilepsy & Behavior
   2018
6. 6
   Endovascular Treatment of a Patient with Moyamoya Disease and Seckel Syndrome: A Case ReportJournal of Pediatric Neurosciences
   2018
7. 7
   Overview of therapeutic plasma exchange in pediatric neurology: a single-center experienceActa Neurologica Belgica
   2018
8. 8
   Overview of therapeutic plasma exchange in pediatric neurology: a single-center experience (vol 118, pg 451, 2018)Acta Neurologica Belgica
   2018
9. 9
   Serum Magnesium and Calcium Levels in Children With Breath-holding SpellsErciyes Tıp Dergisi/Erciyes Medical Journal
   2018
10. 10
    The mutation spectrum of DHCR7 gene and two novel mutationsEuropean Journal of Human Genetics
    2018

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