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Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia.
Cells. 2022 Sep 8;11(18):2804. doi: 10.3390/cells11182804.
Cells. 2022.
PMID: 36139378
Free PMC article.
Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort.
Candayan A, Çakar A, Yunisova G, Özdağ Acarlı AN, Atkinson D, Topaloğlu P, Durmuş H, Yapıcı Z, Jordanova A, Parman Y, Battaloğlu E.
Candayan A, et al.
Neurol Genet. 2021 Aug 31;7(5):e621. doi: 10.1212/NXG.0000000000000621. eCollection 2021 Oct.
Neurol Genet. 2021.
PMID: 34476298
Free PMC article.
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MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability.
Ylikallio E, Woldegebriel R, Tumiati M, Isohanni P, Ryan MM, Stark Z, Walsh M, Sawyer SL, Bell KM, Oshlack A, Lockhart PJ, Shcherbii M, Estrada-Cuzcano A, Atkinson D, Hartley T, Tetreault M, Cuppen I, van der Pol WL, Candayan A, Battaloglu E, Parman Y, van Gassen KLI, van den Boogaard MH, Boycott KM, Kauppi L, Jordanova A, Lönnqvist T, Tyynismaa H.
Ylikallio E, et al. Among authors: candayan a.
Brain. 2017 Aug 1;140(8):2093-2103. doi: 10.1093/brain/awx138.
Brain. 2017.
PMID: 28633435
Free article.
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Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity.
Kurolap A, Kreuder F, Gonzaga-Jauregui C, Duvdevani MP, Harel T, Tammer L, Xin B, Bakhtiari S, Rice J, van Eyk CL, Gecz J, Mah JK, Atkinson D, Cope H, Sullivan JA, Douek AM, Colquhoun D, Henry J, Wlodkowic D, Parman Y, Candayan A, Kocasoy-Orhan E, Ilivitzki A, Soudry S, Leibu R, Glaser F, Sency V; Undiagnosed Diseases Network; Ast G, Shashi V, Fahey MC, Battaloğlu E, Jordanova A, Meiner V, Innes AM, Wang H, Elpeleg O, Kruer MC, Kaslin J, Baris Feldman H.
Kurolap A, et al. Among authors: candayan a.
Am J Hum Genet. 2022 Mar 3;109(3):518-532. doi: 10.1016/j.ajhg.2022.01.004. Epub 2022 Feb 1.
Am J Hum Genet. 2022.
PMID: 35108495
Free PMC article.
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Clinical and Genetic Survey for Charcot-Marie-Tooth Neuropathy Based on the Findings in Turkey, a Country with a High Rate of Consanguineous Marriages.
Candayan A, Parman Y, Battaloğlu E.
Candayan A, et al.
Balkan Med J. 2022 Jan 25;39(1):3-11. doi: 10.4274/balkanmedj.galenos.2021.2021-11-13.
Balkan Med J. 2022.
PMID: 35325986
Free PMC article.
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The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype.
Candayan A, Yunisova G, Çakar A, Durmuş H, Başak AN, Parman Y, Battaloğlu E.
Candayan A, et al.
Neurogenetics. 2020 Jan;21(1):73-78. doi: 10.1007/s10048-019-00594-1. Epub 2019 Oct 31.
Neurogenetics. 2020.
PMID: 31673878
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Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder.
Çakar A, İnci M, Özdağ Acarlı AN, Çomu S, Candayan A, Battaloğlu E, Tekgül Ş, Başak AN, Durmuş H, Parman Y.
Çakar A, et al. Among authors: candayan a.
Acta Neurol Scand. 2022 May;145(5):619-626. doi: 10.1111/ane.13592. Epub 2022 Feb 7.
Acta Neurol Scand. 2022.
PMID: 35130357
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Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features.
Çakar A, Şahin E, Tezel S, Candayan A, Samancı B, Battaloğlu E, Başak AN, Bilgiç B, Hanağası H, Durmuş H, Parman Y.
Çakar A, et al. Among authors: candayan a.
Acta Neurol Belg. 2022 Aug;122(4):939-945. doi: 10.1007/s13760-021-01721-2. Epub 2021 Jun 8.
Acta Neurol Belg. 2022.
PMID: 34101140
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