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Integrated D4Z4 structural, epigenetic and exome-based evaluation of facioscapulohumeral muscular dystrophy in a tertiary referral cohort from Türkiye. J Med Genet. 2026 Jul 24.
Avci S, Eraslan S, Eren I, Kaptan M, Yavuzcan B, Ozdag Acarli AN, Kaysin MC, Yunisova G, Arduç Akçay A, Demirhan M, Oflazer ZP, Kayserili H. PMID: 42498520.
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Impaired nucleocytoplasmic transport in SOD1-mediated ALS. Mol Neurodegener. 2026 Feb 14; 21(1):14.
Argueti-Ostrovsky S, Lim SM, Arogundade OA, Diaz-Garcia S, Yunisova G, Meng A, Hermann A, Ong K, Eremenko E, Bravo-Hernandez M, Driscoll SP, Lee CZ, Jiang X, Stavsky A, Barel S, Shani T, Kahn J, Pfaff SL, Monsonego A, Marsala M, Ravits J, Lagier-Tourenne C, Israelson A. PMID: 41691309; PMCID: PMC12922372.
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HumansAnimalsCells
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Myasthenia-Like Presentations Following PD-1 Inhibitors: CD8+ Myositis, Myasthenia, or Both? Cureus. 2026 Feb; 18(2):e103430.
Ucem S, Yunisova G, Bulus E, Lacin S, Oflazer P. PMID: 41835655; PMCID: PMC12988698.
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Congenital Myasthenic Syndrome: Long-Term Outcomes up to 60 Years, Molecular Characterization, and Eight Novel Variants. Clin Genet. 2026 May; 109(5):889-903.
Akçay AA, Yunisova G, Avci S, Acarli ANÖ, Kayserili H, Oflazer P. PMID: 41451794.
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Humans
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Enteral topiramate treatment in refractory status epilepticus. Epilepsy Res. 2025 Jul; 213:107551.
Keskin-Güler S, Karadas Ö, Atmaca MM, Özek SÜ, Yunisova G, Bulus E, Eren F, Atmaca MC, Reyhani A, Gürses C. PMID: 40187217.
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The clinical use of impulse oscillometry in neuromuscular diseases. Respir Med. 2022 Aug-Sep; 200:106931.
Iliaz S, Yunisova G, Cakmak OO, Celebi O, Bulus E, Duman A, Bayraktaroglu M, Oflazer P. PMID: 35858508.
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4 Fields:
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Humans
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Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up study. Neuromuscul Disord. 2022 09; 32(9):718-727.
Yunisova G, Ceylaner S, Oflazer P, Deymeer F, Parman YG, Durmus H. PMID: 35922275.
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2 Fields:
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Humans
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Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort. Neurol Genet. 2021 Oct; 7(5):e621.
Candayan A, Çakar A, Yunisova G, Özdag Acarli AN, Atkinson D, Topaloglu P, Durmus H, Yapici Z, Jordanova A, Parman Y, Battaloglu E. PMID: 34476298; PMCID: PMC8409130.
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6
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Patients with Lately Diagnosed Cerebrotendinous Xanthomatosis. Neurodegener Dis. 2019; 19(5-6):218-224.
Yunisova G, Tufekcioglu Z, Dogu O, Bilgic B, Kaleagasi H, Akca Kalem S, Lohmann E, Gurvit HI, Emre M, Hanagasi HA. PMID: 32349000.
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8 Fields:
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Humans
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The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype. Neurogenetics. 2020 01; 21(1):73-78.
Candayan A, Yunisova G, Çakar A, Durmus H, Basak AN, Parman Y, Battaloglu E. PMID: 31673878.
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13 Fields:
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Humans
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Stabbing Headache as the Presenting Symptom of Idiopathic Intracranial Hypertension. Headache. 2017 07; 57(7):1152-1153.
Yunisova G, Güngör I, Kocasoy Orhan E, Baykan B. PMID: 28699330.
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1 Fields:
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Humans