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Şeyda Beşen

Observed names: BEŞEN, ŞEYDA, Besen, Şeyda, Beşen, Şeyda, S. Besen, Seyda Besen, Şeyda Besen
Institution: Başkent University
ORCID: 0000-0002-6276-8133
Observed ORCID: 0000-0002-6276-8133
OpenAlex ID: A5021886897
Late-onset Leigh syndrome due to NDUFV1 mutation in a 10-year-old boy initially presenting with ataxia
2018 · Faruk Incecik, OzlemM Herguner, et al. · Journal of Pediatric Neurosciences · 19
Acute rhabdomyolysis associated with levetiracetam therapy in a child
2015 · Faruk Incecik, Ozlem M. Herguner, et al. · Acta Neurologica Belgica · 18
Limbic encephalitis with antibodies to glutamic acid decarboxylase presenting with brainstem symptoms
2015 · Faruk Incecik, OzlemM Hergüner, et al. · Annals of Indian Academy of Neurology · 13
Autoimmune encephalitis associated with glutamic acid decarboxylase antibodies: a case series
2018 · Faruk Incecik, Ozlem M. Herguner, et al. · Acta Neurologica Belgica · 12
A presentation of Lyme disease: pseudotumor cerebri
2015 · Burcu Şahin, Faruk İncecik, et al. · The Turkish Journal of Pediatrics · 10
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First pediatric case with primary familial brain calcification due to a novel variant on the MYORG gene and review of the literature
2021 · Leman Tekin Orgun, Şeyda Besen, et al. · Brain and Development · 9
Hereditary spastic paraplegia type 35 with a novel mutation in fatty acid 2-hydroxylase gene and literature review of the clinical features
2018 · Faruk Incecik, Seyda Besen, et al. · Annals of Indian Academy of Neurology · 9
Guillain–Barré syndrome with hyperreflexia and bilateral papillitis in a child
2016 · Faruk Incecik, OzlemM Herguner, et al. · Journal of Pediatric Neurosciences · 8
Urinary and fecal incontinence during levetiracetam therapy
2015 · Faruk Incecik, OzlemM Herguner, et al. · Annals of Indian Academy of Neurology · 8
Phenotypic variability in cases with CACNA1A mutation
2025 · Sema Bozkaya-Yilmaz, Nihal Olgac-Dundar, et al. · European Journal of Pediatrics · 7
Clinical and laboratory findings and etiologies of genetic homocystinemia: a single-center experience
2023 · Seyda Besen, Yasemin Ozkale, et al. · Acta Neurologica Belgica · 7
Intravenous levetiracetam in critically ill children
2015 · Faruk Incecik, OzdenO Horoz, et al. · Annals of Indian Academy of Neurology · 7
Optic neuritis in Turkish children and adolescents: A multicenter retrospective study
2023 · Meltem Çobanoğulları Direk, Şeyda Besen, et al. · Multiple Sclerosis and Related Disorders · 5
Effect of levetiracetam usage on serum creatine phosphokinase concentration in patients with epilepsy
2020 · Faruk Incecik, OzlemM Herguner, et al. · Journal of Pediatric Neurosciences · 5
Limbic encephalitis associated with anti-leucine-rich glioma-inactivated-1 protein antibodies in a child
2016 · Faruk Incecik, OzlemM Hergüner, et al. · Neurology India · 5
Evaluation of seizure semiology, genetics, magnetic resonance imaging, and electroencephalogram findings in children with Rett syndrome: A multicenter retrospective study
2024 · Nihal Yıldız, Esra Serdaroğlu, et al. · Epilepsy Research · 4
Dynamic thiol/disulphide homeostasis in children with neurofibromatosis type 1 and tuberous sclerosis
2019 · Faruk Incecik, Gamze Avcıoğlu, et al. · Acta Neurologica Belgica · 4
Finger drop sign in a child with acute motor and sensory axonal neuropathy form of Guillain–Barré syndrome
2016 · Faruk Incecik, Ozlem M. Herguner, et al. · Acta Neurologica Belgica · 4
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study
2023 · Çağatay Günay, Duygu Aykol, et al. · Neuropediatrics · 2
Acute rhabdomyolysis associated with levetiracetam therapy in a child
2017 · Faruk Incecik, Ozlem M. Herguner, et al. · European Journal of Paediatric Neurology · 2
Risk factors for epilepsy after ischemic stroke in children
2017 · Faruk İncecik, Ozlem M Hergüner, et al. · Journal of Dr Behcet Uz Children s Hospital · 2
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Mitochondrial membrane protein-associated neurodegeneration in a Turkish patient
2016 · Faruk Incecik, OzlemM Hergüner, et al. · Journal of Pediatric Neurosciences · 2
Congenital myasthenic syndromes in Türkiye: genetic and clinical spectrum revisited in a nationwide pediatric cohort
2026 · Canan Üstün, İpek Polat, et al. · Neuromuscular Disorders · 1
The genetic landscape of childhood-onset dystonia in a nationwide Turkish cohort: Clinical spectrum, molecular diagnostics, and therapeutic implications
2026 · Sanem Yilmaz, Esra Serdaroglu, et al. · European Journal of Paediatric Neurology · 1
Hospitalized Versus Outpatient Benign Acute Childhood Myositis: A 10-Year Single-Center Experience
2026 · Yasemin Özkale, Murat Özkale, et al. · Medicina · 1
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Works count: 62
Citation count: 167
H-index: 8
I10-index: 5
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