1 Ocak 2020 Dergi makalesi Açık Erişim

Paketci, C.; Edem, P.; Hiz, S.; Sonmezler, E.; Soydemir, D.; Uzan, G. Sarikaya; Oktay, Y.; O'Heir, E.; Beltran, S.; Laurie, S.; Topf, A.; Lochmuller, H.; Horvath, R.; Yis, U.

JSON-LD (schema.org)

{
  "@context": "https://schema.org/", 
  "@id": 5909, 
  "@type": "ScholarlyArticle", 
  "creator": [
    {
      "@type": "Person", 
      "affiliation": "Dokuz Eylul Univ, Sch Med, Dept Paediat Neurol, Izmir, Turkey", 
      "name": "Paketci, C."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Dokuz Eylul Univ, Sch Med, Dept Paediat Neurol, Izmir, Turkey", 
      "name": "Edem, P."
    }, 
    {
      "@type": "Person", 
      "name": "Hiz, S."
    }, 
    {
      "@type": "Person", 
      "name": "Sonmezler, E."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Dokuz Eylul Univ, Sch Med, Dept Paediat Neurol, Izmir, Turkey", 
      "name": "Soydemir, D."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Dokuz Eylul Univ, Sch Med, Dept Paediat Neurol, Izmir, Turkey", 
      "name": "Uzan, G. Sarikaya"
    }, 
    {
      "@type": "Person", 
      "name": "Oktay, Y."
    }, 
    {
      "@type": "Person", 
      "name": "O'Heir, E."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Barcelona Inst Sci & Technol, Ctr Genom Regulat, CNAG CRG, Barcelona, Spain", 
      "name": "Beltran, S."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Barcelona Inst Sci & Technol, Ctr Genom Regulat, CNAG CRG, Barcelona, Spain", 
      "name": "Laurie, S."
    }, 
    {
      "@type": "Person", 
      "name": "Topf, A."
    }, 
    {
      "@type": "Person", 
      "name": "Lochmuller, H."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Univ Cambridge, Dept Clin Neurosci, Cambridge, England", 
      "name": "Horvath, R."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Dokuz Eylul Univ, Sch Med, Dept Paediat Neurol, Izmir, Turkey", 
      "name": "Yis, U."
    }
  ], 
  "datePublished": "2020-01-01", 
  "description": "Background: Congenital disorders of glycosylation (CDG) is a heterogeneous group of congenital metabolic diseases with multisystem clinical involvement. ALG3-CDG is a very rare subtype with only 24 cases reported so far.", 
  "headline": "Successful treatment of intractable epilepsy with ketogenic diet therapy in twins with ALG3-CDG", 
  "identifier": 5909, 
  "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", 
  "license": "http://www.opendefinition.org/licenses/cc-by", 
  "name": "Successful treatment of intractable epilepsy with ketogenic diet therapy in twins with ALG3-CDG", 
  "url": "https://aperta.ulakbim.gov.tr/record/5909"
}