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Nezir Özgün

Observed names: N Özgün, Nezir Ozgun, Nezir ÖZGÜN, ÖZGÜN, NEZİR
ORCID: 0000-0002-0866-2004
Observed ORCID: 0000-0002-0866-2004
OpenAlex ID: A5000328985
Short-term results of continuous venovenous haemodiafiltration versus peritoneal dialysis in 40 neonates with inborn errors of metabolism
2019 · Muhittin Celik, Osman Akdeniz, et al. · European Journal of Pediatrics · 18
Insomnia, parasomnia, and predisposing factors in Turkish school children
2016 · Nezir Ozgun, F Mujgan Sonmez, et al. · Pediatrics International · 16
Congenital myotonia: a review of twenty cases and a new splice-site mutation in the CLCN1 gene
2020 · Nezir Özgün, Hasan Taşlıdere · The Turkish Journal of Pediatrics · 9
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Evaluation of Children and Adolescents with Thalassemia Major in Terms of Osteoporosis: A Single-Centre Experience
2025 · Özhan Orhan, Hasan Demir, et al. · Journal of Clinical Medicine · 7
Clinical and Genetic Spectrum of Myotonia Congenita in Turkish Children
2023 · Gökçen Öz Tunçer, Aslıhan Sanri, et al. · Journal of Neuromuscular Diseases · 7
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A Case of Wernicke Encephalopathy Developing After Ileal Bypass Surgery
2018 · Tülay Kamaşak, Sibel Kul, et al. · Pediatric Emergency Care · 7
Efficacy of peritoneal dialysis in neonates presenting with hyperammonaemia due to urea cycle defects and organic acidaemia
2018 · Muhittin Celik, Osman Akdeniz, et al. · Nephrology · 7
Neurological Involvement in Pediatric Hemolytic Uremic Syndrome: A Symptom-Oriented Analysis
2017 · Elif Özdoğan, Gülay Kaya, et al. · Neuropediatrics · 7
Early neurological complications in children with classical galactosemia and p.gln188arg mutation
2019 · Nezir Özgün, Muhittin Celik, et al. · International Journal of Developmental Neuroscience · 6
Effectiveness of Valproic Acid in the Treatment of Sydenham’s Chorea and a Literature Review
2023 · Nezir Özgün, Osman Akdeniz · Clinical Pediatrics · 5
A case with congenital disorder of glycosylation with defective fucosylation 2 and new mutation in FUK gene
2021 · Nezir Özgün, Yavuz Şahin · Brain and Development · 5
Folate deficiency in patients with classical galactosemia: A novel finding that needs to be considered for dietary treatments
2018 · Muhittin Çelik, Nezir Özgün, et al. · The Turkish Journal of Pediatrics · 3
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Rafiq Syndrome: Old Variant in MAN1B1 Gene and Some New Phenotypic Features.
2025 · Nezir Özgün, Merve Saka Güvenç · Iranian journal of child neurology. · 2
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Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study
2023 · Çağatay Günay, Duygu Aykol, et al. · Neuropediatrics · 2
Clinical Diagnosis, Biochemical Findings, Genetics and Incidence of Zellweger Syndrome
2017 · Muhittin Celik, Mehmet Sah Ipek, et al. · Iranian Journal of Pediatrics · 2
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Thirteen-year surveillance results of acute flaccid paralysis cases in Southeast Turkey and the effect of refugee movements on surveillance results
2024 · Nezir Özgün, Gülnaz Kubat, et al. · Central European Journal of Public Health · 1
The Efficacy of Iron and Piracetam in Breath Holding Spells and Levetiracetam in Anoxic Epileptic Seizures
2023 · Nezir ÖZGÜN, Osman AKDENİZ, et al. · Artuklu International Journal of Health Sciences · 1
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The role of metabolic diseases in neonatal convulsions.
2023 · S Samanci, M Celik, et al. · PubMed · 1
A rare cause of epileptic encephalopathy: a beta-propeller protein associated neurodegeneration case with a new mutation and literature review
2020 · Nezir Özgün, Leyla Özer, et al. · The Turkish Journal of Pediatrics · 1
The Importance of Neurological Examination For Computerized Brain Tomography Indication In Pediatric Emergency Room
2018 · Nezir Özgün · SiSli Etfal Hastanesi Tip Bulteni / The Medical Bulletin of Sisli Hospital · 1
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Prenatal Clues of Cerebral Palsy: A Retrospective Case–Control Study Based on Mid-Trimester Fetal Ultrasonography
2026 · Hümeyra Akbaş, Nezir Özgün, et al. · Bratislavské lekárske listy/Bratislava medical journal
Artificial intelligence in the physician’s seat: a scenario-based evaluation of scientific accuracy, quality, and readability
2026 · Humeyra Akbas, Nezir Ozgun · Archives of Gynecology and Obstetrics
2.06P Clinical and genetic profile of children with LAMA2-related dystrophies in Turkey
2026 · Didem Ardıçlı, Busranur Cavdarli, et al. · Neuromuscular Disorders
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
2026 · Mustafa Komur, Ezgi Çağlar, et al. · European Journal of Paediatric Neurology
Not Just for Adults: Transient Global Amnesia is Rare—But Possible—in Children
2026 · Nezir Özgün · Cognitive and Behavioral Neurology
Works count: 34
Citation count: 108
H-index: 7
I10-index: 2
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