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ANO10 Function in Health and Disease.
Chrysanthou A, Ververis A, Christodoulou K. Chrysanthou A, et al. Among authors: christodoulou k. Cerebellum. 2023 Jun;22(3):447-467. doi: 10.1007/s12311-022-01395-3. Epub 2022 Jun 1. Cerebellum. 2023. PMID: 35648332 Free PMC article. Review.
Distal hereditary motor neuronopathy of the Jerash type is caused by a novel SIGMAR1 c.500A>T missense mutation.
Ververis A, Dajani R, Koutsou P, Aloqaily A, Nelson-Williams C, Loring E, Arafat A, Mubaidin AF, Horany K, Bader MB, Al-Baho Y, Ali B, Muhtaseb A, DeSpenza T Jr, Al-Qudah AA, Middleton LT, Zamba-Papanicolaou E, Lifton R, Christodoulou K. Ververis A, et al. Among authors: christodoulou k. J Med Genet. 2020 Mar;57(3):178-186. doi: 10.1136/jmedgenet-2019-106108. Epub 2019 Sep 11. J Med Genet. 2020. PMID: 31511340 Free PMC article.
Greek Sage Exhibits Neuroprotective Activity against Amyloid Beta-Induced Toxicity.
Ververis A, Savvidou G, Ioannou K, Nicolaou P, Christodoulou K, Plioukas M. Ververis A, et al. Among authors: christodoulou k. Evid Based Complement Alternat Med. 2020 Dec 7;2020:2975284. doi: 10.1155/2020/2975284. eCollection 2020. Evid Based Complement Alternat Med. 2020. PMID: 33505483 Free PMC article.
A novel GBA2 gene missense mutation in spastic ataxia.
Votsi C, Zamba-Papanicolaou E, Middleton LT, Pantzaris M, Christodoulou K. Votsi C, et al. Among authors: christodoulou k. Ann Hum Genet. 2014 Jan;78(1):13-22. doi: 10.1111/ahg.12045. Epub 2013 Nov 20. Ann Hum Genet. 2014. PMID: 24252062
134 results