| Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study D Adams, M Polydefkis, A González-Duarte, J Wixner, AV Kristen, ... The Lancet Neurology 20 (1), 49-59, 2021 | 133 | 2021 |
| Coronavirus disease 2019 (COVID-19) from the point of view of neurologists: observation of neurological findings and symptoms during the combat against a pandemic ANÖ Acarli, B Samanci, E Ekizoğlu, A Çakar, NG Şirin, T Gündüz, ... Archives of Neuropsychiatry 57 (2), 154, 2020 | 52 | 2020 |
| CD4+ T Cells of Myasthenia Gravis Patients Are Characterized by Increased IL-21, IL-4, and IL-17A Productions and Higher Presence of PD-1 and ICOS M Çebi, H Durmus, F Aysal, B Özkan, GE Gül, A Çakar, M Hocaoglu, ... Frontiers in Immunology 11, 809, 2020 | 41 | 2020 |
| Familial amyloid polyneuropathy A Cakar, H Durmuş-Tekçe, Y Parman Archives of Neuropsychiatry 56 (2), 150, 2019 | 36 | 2019 |
| Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey H Durmuş-Tekçe, Z Matur, MM Atmaca, M Poda, A Çakar, ÜH Ulaş, ... Neuromuscular Disorders 26 (7), 441-446, 2016 | 34 | 2016 |
| Genetic pain loss disorders A Lischka, P Lassuthova, A Çakar, CJ Record, J Van Lent, J Baets, ... Nature Reviews Disease Primers 8 (1), 41, 2022 | 28 | 2022 |
| The COVID-19 from neurological overview T Acar, E Demirel, N Afsar, A Akcali, G Demir, A ALAGÖZ, T Mengi, ... Turkish Journal of Neurology 26 (2), 2020 | 24 | 2020 |
| Nörolojik bakış açısından COVID-19 T Acar, EA Demirel, N Afşar, A Akçalı, GA Demir, AN Alagöz, TA Mengi, ... Turk J Neurol 26 (2), 56-106, 2020 | 18 | 2020 |
| The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype A Candayan, G Yunisova, A Çakar, H Durmuş, AN Başak, Y Parman, ... neurogenetics 21, 73-78, 2020 | 17 | 2020 |
| Adult-onset phenylketonuria with rapidly progressive dementia and parkinsonism Z Tufekcioglu, A Cakar, B Bilgic, H Hanagasi, H Gurvit, M Emre Neurocase 22 (3), 273-275, 2016 | 17 | 2016 |
| A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID F Akçimen, A Vural, H Durmuş, A Çakar, H Houlden, YG Parman, ... Journal of human genetics 64 (11), 1141-1144, 2019 | 15 | 2019 |
| Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database C Tunca, T Şeker, F Akcimen, C Coşkun, E Bayraktar, R Palvadeau, S Zor, ... Human mutation 41 (8), e7-e45, 2020 | 14 | 2020 |
| İşçi sağlığı ve iş güvenliğinde günümüz gelişmelerine çok yönlü bakış AE Çakar Mühendis ve Makina, 12-16, 0 | 14 | |
| The complex genetic landscape of hereditary ataxias in Turkey and implications in clinical practice A Vural, G Şimşir, Ş Tekgül, C Koçoğlu, F Akcimen, E Kartal, NE Şen, ... Movement Disorders 36 (7), 1676-1688, 2021 | 12 | 2021 |
| Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies A Lischka, K Eggermann, CJ Record, MF Dohrn, P Laššuthová, F Kraft, ... Brain 146 (12), 4880-4890, 2023 | 9 | 2023 |
| Thymoma patients with or without myasthenia gravis have increased Th17 cells, IL-17 production and ICOS expression M Cebi, A Cakar, E Erdogdu, H Durmus-Tekce, G Yegen, B Ozkan, ... Journal of Neuroimmunology 381, 578129, 2023 | 5 | 2023 |
| Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features A Çakar, E Şahin, S Tezel, A Candayan, B Samancı, E Battaloğlu, ... Acta Neurologica Belgica 122 (4), 939-945, 2022 | 5 | 2022 |
| Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder A Çakar, M İnci, AN Özdağ Acarlı, S Çomu, A Candayan, E Battaloğlu, ... Acta Neurologica Scandinavica 145 (5), 619-626, 2022 | 5 | 2022 |
| Genetic survey of autosomal recessive peripheral neuropathy cases unravels high genetic heterogeneity in a Turkish cohort A Candayan, A Çakar, G Yunisova, AN Özdağ Acarlı, D Atkinson, ... Neurology: Genetics 7 (5), e621, 2021 | 5 | 2021 |
| Clinical features of the patients with neuromyelitis optica spectrum disorder A Cakar, C Ulusoy, T Gündüz, Cİ Küçükali, M Kürtüncü Archives of Neuropsychiatry 58 (1), 21, 2021 | 5 | 2021 |
