Doç. Dr. Safiye Güneş Sağer
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Claim profilePerson ↔ Disease
Which diseases does this doctor work on?
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Epilepsy 6 publicationsSource: OpenAlex / PubMed MeSHView publications
- Intellectual Disability 4 publications
- Spasms, Infantile 3 publications
- Status Epilepticus 3 publications
- Pseudotumor Cerebri 2 publications
- Papilledema 2 publications
- Epilepsy, Generalized 2 publications
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- SpecialtyPaediatric Neurologysaglik.gov.trFrom source
- Department name at the sourceÇocuk Nörolojisaglik.gov.trFrom source
- InstitutionKartal Dr. Lütfi Kırdar Şehir Hastanesisaglik.gov.trFrom source
- Area of workEpilepsyExtracted from 6 publications · Model version —From source
- Publications45 publicationsEurope PMC, OpenAlexFrom source
- ORCID0000-0002-9876-2454ORCIDFrom source
- Last synchronised5 November 2026 08:56https://lutfikirdareah.saglik.gov.tr/TR-1480031/doktorlarimiz.html#safiye-gunes-sagersaglik.gov.tr
Scientific work
Publications on Epilepsy
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The clinical spectrum of MECP2 variants in males: a multicenter Turkish cohort of 22 probands, with implications for diagnosis and variant interpretation
BMC pediatrics, 2026
DOI 10.1186/s12887-026-07905-0 PMID 42920114 Open-access full textSource: Europe PMC
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ESAM Loss of Function and Congenital Neurovascular Injury: Strengthening the Case for a Recognizable Clinical Phenotype
Clinical Genetics, 2026
DOI 10.1111/cge.70140 PMID 41525715 1 citation (OpenAlex) Open-access full textSource: OpenAlex
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Clinical, electrophysiological, and neuroimaging characterization of childhood-onset non-5q spinal muscular atrophies: a retrospective pediatric case series
Neurogenetics, 2026
DOI 10.1007/s10048-026-00913-3 PMID 42230463 Open-access full textSource: OpenAlex
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The Angelman Mimic: Navigating Diagnostic Uncertainty in a Genetically Diverse Landscape
Research Square, 2026
DOI 10.21203/rs.3.rs-10974080/v1 Open-access full textSource: OpenAlex
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Additional file 2 of The clinical spectrum of MECP2 variants in males: a multicenter Turkish cohort of 22 probands, with implications for diagnosis and variant interpretation
Figshare, 2026
DOI 10.6084/m9.figshare.34762223 Open-access full textSource: OpenAlex
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Fatal Late-Onset Presentation of Ornithine Transcarbamylase (OTC) Deficiency: A Case Report Highlighting Diagnostic Challenges and Cerebral Complications
Indian Journal of Clinical Biochemistry, 2025
DOI 10.1007/s12291-025-01307-2 Source: OpenAlex
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P462: Exploring genotypic diversity in Angelman-like syndromes: Clinical implications
Genetics in Medicine Open, 2025
DOI 10.1016/j.gimo.2025.103329 Open-access full textSource: OpenAlex
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The Effect of Levetiracetam and Valproic Acid Treatment on Anger and Attention Deficit Hyperactivity Disorder Clinical Features in Children and Adolescents with Epilepsy: A Prospective Study
Paediatric drugs, 2024
DOI 10.1007/s40272-024-00652-8 PMID 39331340 6 citations (Europe PMC) Source: Europe PMC
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Analysis of TSC1 and TSC2 genes and evaluation of phenotypic correlations with tuberous sclerosis
Molecular genetics and genomics : MGG, 2024
DOI 10.1007/s00438-024-02210-w PMID 39722056 5 citations (Europe PMC) Source: Europe PMC
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A case of ocular flutter associated with sole anti-sulphatide antibody positivity: successful treatment with intravenous immunoglobulin in a pediatric patient
Acta neurologica Belgica, 2024
DOI 10.1007/s13760-024-02645-3 PMID 39342054 Source: Europe PMC