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Akademisyen

DİDEM ARDIÇLI

DOÇENT

ANKARA YILDIRIM BEYAZIT ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Çocuk Nörolojisi (Çocuk Sağlığı ve Hastalıkları)

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 29
  • Proje 0
  • Kitap 11
  • Bildiri 41
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 10 Q2 7 Q3 2 Q4 1
WoS (JCR) Q1 5 Q2 7 Q3 4 Q4 4
TR Index 7 makale

Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.

Üst %1 makale 2
Üst %10 makale 5
Ort. yüzdelik 62.7%
Üst %1 payı 7.1%
Üst %10 payı 17.9%

Makaleler

YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.

Dizin filtreleri

Toplam 29 yayın

Makale listesi

  1. 2026 Effects of newborn screening and nusinersen on survival and functional outcomes in spinal muscular atrophy with two SMN2 copies: A nationwide multicentre real-world study from Turkey European Journal of Paediatric Neurology DOI 10.1016/j.ejpn.2026.08.003 YÖKSİS SJR Q1 JCR Q1 OpenAlex 78.1%
  2. 2026 Association between thoracic ultrasound findings and respiratory function in children with Duchenne muscular dystrophy EUROPEAN JOURNAL OF PEDIATRICS DOI 10.1007/s00431-026-06879-6 YÖKSİS SJR Q1 JCR Q1 OpenAlex 23.7%
  3. 2025 Nusinersen for children with type I spinal muscular atrophy: 4 years’ clinical experience in Turkish cohort Frontiers in Neurology DOI 10.3389/fneur.2025.1541507 YÖKSİS SJR Q2 JCR Q2 OpenAlex üst %10 OpenAlex 92.5%
  4. 2025 Genetic and clinical spectrum of PIEZO2-related disorders: insights from a multicenter study of 26 patients Neuromuscular Disorders DOI 10.1016/j.nmd.2025.105423 YÖKSİS SJR Q1 JCR Q2 OpenAlex 88.8%
  5. 2025 Thick Corpus Callosum: An Unusual Finding of TUBGCP2‐Related Tubulinopathy American Journal of Medical Genetics Part A DOI 10.1002/ajmg.a.64134 YÖKSİS SJR Q2 JCR Q4 OpenAlex üst %10 OpenAlex 92.3%
  6. 2023 An Oxidative Stress Marker in Pediatric Migraine Patients: Dynamic Thiol-Disulfide Homeostasis Turkish Journal of Pediatric Disease DOI 10.12956/tchd.1041332 YÖKSİS TR Index OpenAlex 42.2%
  7. 2023 Clinical Characteristics and Possible Risk Factors of Epilepsy in Children with Cerebral Palsy: A Tertiary-Center Experience Turkish Journal of Pediatric Disease DOI 10.12956/tchd.1213912 YÖKSİS TR Index OpenAlex 0.2%
  8. 2022 High diagnostic yield of targeted next‐generation sequencing panel as a first‐tier molecular test for the patients with myopathy or muscular dystrophy Annals of Human Genetics DOI 10.1111/ahg.12492 YÖKSİS SJR Q3 JCR Q4 OpenAlex 69.2%
  9. 2022 FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum Journal of Medical Genetics DOI 10.1136/jmedgenet-2021-108341 YÖKSİS SJR Q1 JCR Q2 OpenAlex 71.5%
  10. 2022 Etiology and prognosis of childhood pseudotumor cerebri syndrome: A retrospective single center study from Turkey Neurology Asia DOI 10.54029/2022jsi YÖKSİS SJR Q4 JCR Q4 OpenAlex 52.4%
  11. 2022 Clinical and laboratory features of children with tremor: a single-center experience Acta Neurologica Belgica DOI 10.1007/s13760-021-01804-0 YÖKSİS SJR Q2 JCR Q3 OpenAlex 47.1%
  12. 2022 Etiology, Diagnosis, and Management of Childhood Microcephaly: A single-center retrospective study Malang Neurology Journal DOI 10.21776/ub.mnj.2022.008.02.3 YÖKSİS OpenAlex 16.1%
  13. 2022 Evaluation and management of the first unprovoked seizure in children: Single-center experience first unprovoked seizure in children Annals of Medical Research DOI 10.5455/annalsmedres.2022.05.162 YÖKSİS TR Index OpenAlex 48.6%
  14. 2022 Clinical Profile of Late-Infantile and Juvenile Metachromatic Leukodystrophy: A Retrospective Study Ankara Üniversitesi Tıp Fakültesi Mecmuası DOI 10.4274/atfm.galenos.2022.87004 YÖKSİS TR Index OpenAlex 0.7%
  15. 2021 Unraveling neuronal ceroid lipofuscinosis type 2 (CLN2) disease: A tertiary center experience for determinants of diagnostic delay European Journal of Paediatric Neurology DOI 10.1016/j.ejpn.2021.05.015 YÖKSİS SJR Q1 JCR Q2 OpenAlex 59.5%
  16. 2020 Long-term effects of vagus nerve stimulation in refractory pediatric epilepsy: A single-center experience Epilepsy&Behavior DOI 10.1016/j.yebeh.2020.107147 YÖKSİS SJR Q2 JCR Q2 OpenAlex 76.8%
  17. 2020 Selenoprotein N-related myopathy: a retrospective natural history study to guide clinical trials Annals of Clinical and Translational Neurology DOI 10.1002/acn3.51218 YÖKSİS SJR Q1 JCR Q2 OpenAlex 84.9%
  18. 2019 Diagnostic Pathway to Nonsense Mutation Dystrophinopathy: A Tertiary-Center, Retrospective Experience Neuropediatrics DOI 10.1055/s-0038-1675626 YÖKSİS SJR Q2 JCR Q3 OpenAlex 57.1%
  19. 2019 A novel case of MSTO1 gene related congenital muscular dystrophy with progressive neurological involvement Neuromuscular Disorders DOI 10.1016/j.nmd.2019.03.011 YÖKSİS SJR Q1 JCR Q2 OpenAlex 71.1%
  20. 2019 Clinical outcomes of two patients with a novel pathogenic variant in ASNS: response to asparagine supplementation and review of the literature Human Genome Variation DOI 10.1038/s41439-019-0055-9 YÖKSİS SJR Q3 JCR Q4 OpenAlex 81.6%

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