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akaturk Academic measurement

Academician profile · PROFESÖR

BÜLENT KARA

KOCAELİ ÜNİVERSİTESİ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Çocuk Nörolojisi (Çocuk Sağlığı ve Hastalıkları)
  • TIP FAKÜLTESİ
  • DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
Articles YÖKSİS 105
Projects 0
Books 27
Proceedings 51
Patents 0
Artistic 0
Scopus (SJR)
Q1 43 Q2 23 Q3 14 Q4 9
WoS (JCR)
Q1 21 Q2 27 Q3 19 Q4 21
TR Index 10 articles

Scopus (SJR)

Q1 43 Q2 23 Q3 14 Q4 9

WoS (JCR)

Q1 21 Q2 27 Q3 19 Q4 21

TR Index

10 articles

105 publications total

Articles

  1. 2025 Profiles of paediatric patients experiencing stroke-like episodes associated with mitochondrial disease Frontiers in Neurology DOI 10.3389/fneur.2025.1657852
  2. 2025 Genetic Etiology of Developmental and Epileptic Encephalopathyin a Turkish Cohort: A Single-Center Study with Targeted Gene Panel and Whole Exome Sequencing Genes DOI 10.390/genes16101152
  3. 2025 Corrigendum: Neonatal Rhabdomyolysis: A Case Report and Review of the Literature Neuropediatrics DOI 10.1055/a-2678-0792
  4. 2025 Nusinersen for children with type I spinal muscular atrophy: 4 yeras' clinical experience in Turkey Frontiers in Neurology DOI 10.3389/fneurol.2025.154107
  5. 2025 Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder The American Journal of Human Genetics DOI 10.1016/j.ajhg.2025.03.015
  6. 2025 Phenotypic variability in cases with CACNA1A mutation European Journal of Pediatrics DOI 10.1007/s00431-025-06062-3
  7. 2025 Apparent efficacy of NMDAR antagonist use as a targeted therapy for status epilepticus in an infant with ATP1A2-related developmental epileptic encephalopathy Seizure: European Journal of Epilepsy DOI 10.1016/j.seizure.2025.02.002
  8. 2025 Phenotypic similarities and differences between SLC6A1-related neurodevelopmental disorder and GLUT1 deficiency syndrome Seizure: European Journal of Epilepsy DOI 10.1016/j.seizure.2025.04.010
  9. 2025 Diagnosis of Congenital Cytomegalovirus in a 14-Month-Old Patient Presenting with Sensorineural Hearing Loss: Storing Dry Blood Samples Turkish Archives of Pediatrics DOI 10.5152/TurkArchPediatr.2025.2498
  10. 2025 The contribution of de novo coding mutations to meningomyelocele Nature DOI 10.1038/s41586-025-08676-x
  11. 2024 Evaluation of mental performance and cognitive functions of children and adolescents diagnosed with radiologically isolated syndrome Multiple Sclerosis and Related Disorders DOI 10.1016/j.msard.2024.105735
  12. 2024 Genotype-Phenotype Correlation in Lipoid Proteinosis: 15 Cases from Turkiye Molecular Syndromology DOI 10.1159/000542675
  13. 2024 Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study Seizure DOI 10.1016/j.seizure.2024.09.021
  14. 2024 Retinal and Choroidal Vascularity Evaluation in Pediatric Radiologically Isolated Syndrome and Multiple Sclerosis Pediatric Neurology DOI 10.1016/j.pediatrneurol.2024.01.013.
  15. 2024 NEONATAL RHABDOMYOLYSIS: A CASE REPORT AND REVIEW OF THE LITERATURE Neuropediatrics DOI 10.1055/a-2505-8378
  16. 2024 Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study Cerebellum DOI 10.1007/s12311-024-01690-1.
  17. 2024 A Retrospective Review of 18 Patients With Childhood-Onset Hereditary Spastic Paraplegia, Nine With Novel Variants Pediatric Neurology DOI 10.1016/j.pediatrneurol.2024.01.005
  18. 2024 Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes Nature Neuroscience DOI 10.1038/s41593-024-01747-8.
  19. 2024 The effect of ruminative thoughts on sexuality in obese women Pakistan Journal of Medical Sciences DOI 10.12669/pjms.40.1.8625
  20. 2024 Risk of meningomyelocele mediated by the common 22q11.2 deletion Science DOI 10.1126/science.adl1624

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