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Neslihan Özcan

Observed names: N. Ozcan, Neslihan Ozcan, Neslihan ÖZCAN, Özcan, Neslihan
ORCID: 0000-0003-4352-1685
Observed ORCID: 0000-0003-4352-1685
OpenAlex ID: A5101700741
Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients
2019 · Gülen Gül Mert, Neslihan Özcan, et al. · Acta Neurologica Belgica · 21
Factors affecting epilepsy prognosis in patients with tuberous sclerosis
2019 · Gülen Gül Mert, Şakir Altunbaşak, et al. · Child s Nervous System · 13
Optic Nerve Sheath Diameter and Retinal Artery Resistive Index Measurements with Bedside Ophthalmic Ultrasound in Pediatric Patients with Pseudotumor Cerebri Syndrome
2020 · Nagehan Aslan, Dincer Yildizdas, et al. · Journal of Pediatric Intensive Care · 10
Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study
2021 · Sema Bozkaya-Yilmaz, Eda Karadag-Oncel, et al. · European Journal of Pediatrics · 8
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The outcome of 41 Late-Diagnosed Turkish GA-1 Patients: A Candidate for the Turkish NBS
2021 · Sebile Kılavuz, Derya Bulut, et al. · Neuropediatrics · 7
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The effect of thrombocytopenia on outcome in critically ill children
2013 · Sema Yılmaz, Dinçer Yıldızdaş, et al. · 6
A Novel Adverse Event of Nusinersen Treatment: Thrombocytosis
2019 · Nagehan Aslan, Dincer Yildizdas, et al. · The Indian Journal of Pediatrics · 2
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Acetazolamide-Induced agranulocytosis in a patient with pseudotumor cerebri
2019 · Faruk Incecik, Neslihan Ozcan, et al. · Annals of Indian Academy of Neurology · 2
Atypic subacute sclerosing panensefalitis in a six-year-old male
2022 · Serap Bilge, Neslihan Özcan, et al. · Journal of Advanced Pediatrics and Child Health · 1
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2.05P Clinical and genetic spectrum of congenital muscular dystrophy in Turkey: a large multicenter cohort
2026 · Mustafa Kömür, Ezgi Caglar, et al. · Neuromuscular Disorders
1.15eP Beyond limb-girdile weakness: a single center experience with calpainopathy
2026 · Serdar Pekuz, Neslihan Özcan, et al. · Neuromuscular Disorders
1.14eP A retrospective analysis of patients with sarcoglycanopathy from a single tertiary center
2026 · Neslihan Ozcan, Serdar Pekuz, et al. · Neuromuscular Disorders
Clinical, demographic and genetic features of pediatric limb-girdle muscular dystrophy in the Çukurova region
2026 · Duygu Güner Özcanyüz, Gülen GüL Mert, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics
5-Oxoprolinase Deficiency and Epilepsy: A Report of Four Cases with New Clinical Findings and Clinical Diversity Even in the Same Family
2025 · Burcu Koseci, Esra Kara, et al. · Molecular Syndromology
Reçete Örnekleri ile Aile Hekimleri İçin Pediatrik
2022 · Pınar Bilgili, Deniz Kör, et al. · Akademisyen Kitabevi eBooks
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Ketoliz defekti tanısıyla izlenen 16 hastanın klinik ve moleküler özelliklerinin incelenmesi: Tek merkez deneyimi
2020 · Fatma Derya BULUT, Deniz KOR, et al. · Mersin üniversitesi sağlık bilimleri dergisi/Mersin üniversitesi sağlık bilimleri dergisi
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EP.123Selenoprotein-related congenital myopathy in two siblings
2019 · O. Herguner, S. Bilge, et al. · Neuromuscular Disorders
Çocuklarda psödotümör serebri: etyoloji, klinik bulgular, prognoz
2019 · Gülen Gül Mert, Neslihan Özcan, et al. · Çukurova medical journal (Online)/Çukurova medical journal
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Works count: 20
Citation count: 70
H-index: 6
I10-index: 3
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