Meral Karadağ

ORCID: 0000-0003-4490-387X
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About
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Research Areas
  • Multiple Sclerosis Research Studies
  • Autism Spectrum Disorder Research
  • Dermatoglyphics and Human Traits
  • Cerebral Palsy and Movement Disorders
  • Herpesvirus Infections and Treatments
  • Genetics and Neurodevelopmental Disorders
  • Pharmacological Effects and Toxicity Studies
  • Peripheral Neuropathies and Disorders
  • Ocular Diseases and Behçet’s Syndrome
  • Genomics and Rare Diseases
  • Child Nutrition and Water Access
  • Bacterial Infections and Vaccines

Turgut Özal University
2025

Inonu University
2021-2023

Objectives To evaluate the demographic, clinical, laboratory, and prognostic data of children with acute disseminated encephalomyelitis respect to anti-myelin oligodendrocyte glycoprotein (MOG) antibody status. Methods Acute patients (n = 245) from 24 centers followed up between 2010 2022 were evaluated retrospectively. The short- long-term outcome characteristics (disease severity course, clinical relapse, recovery rates) assessed. Incomplete was defined as modified Rankin Score ≥1 or...

10.1177/08830738251334219 article EN Journal of Child Neurology 2025-05-08

Abstract Background Many studies evaluating the nutritional status of children with cerebral palsy (CP) have focused on energy requirements and protein intake. The present work aimed to assess micronutrient levels (CP). Methods This multicenter, cross‐sectional observational study was conducted in 10 different cities Turkey. Data were available for 398 participants. Anthropometric measurements, feeding mode, status, evaluated. Results participants (303 patients 95 healthy controls)....

10.1111/ped.15005 article EN Pediatrics International 2021-09-29

Abstract Background Although the underlying genetic causes of intellectual disability (ID) continue to be rapidly identified, biological pathways and processes that could targets for a potential molecular therapy are not yet known. This study aimed identify ID-related shared utilizing enrichment analyses. Methods In this multicenter study, causative genes patients with ID were used as input Disease Ontology (DO), Gene (GO), Kyoto Encyclopedia Genes Genomes analysis. Results Genetic test...

10.1055/a-2034-8528 article EN Neuropediatrics 2023-02-14
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