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Neurocirugia (English Edition)|April 8, 2024
Combined thalamic and pallidal deep brain stimulation in diabetic hemiballism/hemichoreaOnur Ozturk, Nihan Hande Akcakaya, Mehmet Osman Akcakaya
Neurologia I Neurochirurgia Polska|November 21, 2017
A case with CMTX1 disease showing transient ischemic-attack-like episodesZehra Aktan, Nihan Hande Akcakaya, Pinar Tekturk, et al.
Brain & Development|May 18, 2016
A novel gene mutation in PANK2 in a patient with severe jaw-opening dystoniaZuhal Yapici, Nihan Hande Akcakaya, Pinar Tekturk, et al.
Neurocase|February 21, 2022
Two cases with mitochondrial membrane protein-associated neurodegeneration: genetic features and long-term clinical follow-upSevcan Mercan, Sibel Aylin Ugur Iseri, Remzi Yigiter, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|May 24, 2017
De novo 8p23.1 deletion in a patient with absence epilepsyNihan Hande Akcakaya, Özlem Yalcin Capan, Herbert Schulz, et al.
Genes & Genomics|November 13, 2022
Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinitySevcan Mercan, Nihan Hande Akcakaya, Baris Salman, et al.
Parkinsonism & Related Disorders|February 28, 2026
Essential tremor: Family-based sequencing suggests involvement of neuronal and metabolic pathwaysAgharza Aghayev, Melda Erdoğdu, Duygu Aydemir, et al.
Neurotoxicology|January 25, 2026
From Clinical Observation to Experimental Validation: Investigating the Neurotoxic Impact of DimethylacetamideHizir Asliyuksek, Nihan Hande Akcakaya, Rumeysa Hekimoglu, et al.
Clinical Neurology and Neurosurgery|January 24, 2017
Clinical and genetic features of PKAN patients in a tertiary centre in TurkeyNihan Hande Akcakaya, Sibel Ugur Iseri, Birdal Bilir, et al.
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