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The International Child Neurology Congresses
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  3. Presenters/Mehmet Canpolat
  • 368. Mitochondrial Complex 1 Deficiency Nuclear Type 4 in a Toddler: A Case Report of NDUFV1 Gene Mutation

  • 375. Presentation of the Second Case in the World of “Cortıcal Myoclonıc Tremor with Epilepsy, Familial 7”

  • 376. The Importance of Examination in Febrile Convulsions: Hypotonic Infant Case with Coenzyme Q10 Deficiency

  • 405. A Unique Case of Subclinical Becker Muscular Dystrophy Due to a Single Exon 48 Deletion in the Dystrophin Gene