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.
Makale listesi
- 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 YÖKSİS SJR Q1 JCR Q1 OpenAlex 78.1%
- 2026 Association between thoracic ultrasound findings and respiratory function in children with Duchenne muscular dystrophy YÖKSİS SJR Q1 JCR Q1 OpenAlex 23.7%
- 2025 Nusinersen for children with type I spinal muscular atrophy: 4 years’ clinical experience in Turkish cohort YÖKSİS SJR Q2 JCR Q2 OpenAlex üst %10 OpenAlex 92.5%
- 2025 Genetic and clinical spectrum of PIEZO2-related disorders: insights from a multicenter study of 26 patients YÖKSİS SJR Q1 JCR Q2 OpenAlex 88.8%
- 2025 Thick Corpus Callosum: An Unusual Finding of TUBGCP2‐Related Tubulinopathy YÖKSİS SJR Q2 JCR Q4 OpenAlex üst %10 OpenAlex 92.3%
- 2023 An Oxidative Stress Marker in Pediatric Migraine Patients: Dynamic Thiol-Disulfide Homeostasis YÖKSİS TR Index OpenAlex 42.2%
- 2023 Clinical Characteristics and Possible Risk Factors of Epilepsy in Children with Cerebral Palsy: A Tertiary-Center Experience YÖKSİS TR Index OpenAlex 0.2%
- 2022 High diagnostic yield of targeted next‐generation sequencing panel as a first‐tier molecular test for the patients with myopathy or muscular dystrophy YÖKSİS SJR Q3 JCR Q4 OpenAlex 69.2%
- 2022 FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum YÖKSİS SJR Q1 JCR Q2 OpenAlex 71.5%
- 2022 Etiology and prognosis of childhood pseudotumor cerebri syndrome: A retrospective single center study from Turkey YÖKSİS SJR Q4 JCR Q4 OpenAlex 52.4%
- 2022 Clinical and laboratory features of children with tremor: a single-center experience YÖKSİS SJR Q2 JCR Q3 OpenAlex 47.1%
- 2022 Etiology, Diagnosis, and Management of Childhood Microcephaly: A single-center retrospective study YÖKSİS OpenAlex 16.1%
- 2022 Evaluation and management of the first unprovoked seizure in children: Single-center experience first unprovoked seizure in children YÖKSİS TR Index OpenAlex 48.6%
- 2022 Clinical Profile of Late-Infantile and Juvenile Metachromatic Leukodystrophy: A Retrospective Study YÖKSİS TR Index OpenAlex 0.7%
- 2021 Unraveling neuronal ceroid lipofuscinosis type 2 (CLN2) disease: A tertiary center experience for determinants of diagnostic delay YÖKSİS SJR Q1 JCR Q2 OpenAlex 59.5%
- 2020 Long-term effects of vagus nerve stimulation in refractory pediatric epilepsy: A single-center experience YÖKSİS SJR Q2 JCR Q2 OpenAlex 76.8%
- 2020 Selenoprotein N-related myopathy: a retrospective natural history study to guide clinical trials YÖKSİS SJR Q1 JCR Q2 OpenAlex 84.9%
- 2019 Diagnostic Pathway to Nonsense Mutation Dystrophinopathy: A Tertiary-Center, Retrospective Experience YÖKSİS SJR Q2 JCR Q3 OpenAlex 57.1%
- 2019 A novel case of MSTO1 gene related congenital muscular dystrophy with progressive neurological involvement YÖKSİS SJR Q1 JCR Q2 OpenAlex 71.1%
- 2019 Clinical outcomes of two patients with a novel pathogenic variant in ASNS: response to asparagine supplementation and review of the literature YÖKSİS SJR Q3 JCR Q4 OpenAlex 81.6%