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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 1
2007 1
2008 2
2009 4
2010 3
2011 4
2012 1
2013 1
2014 5
2015 4
2016 6
2017 3
2018 4
2019 4
2020 3
2021 2
2022 1
2023 3
2024 1

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45 results

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Page 1
Genetic landscape of early-onset dementia in Hungary.
Csaban D, Illes A, Renata TB, Balicza P, Pentelenyi K, Molnar V, Gezsi A, Grosz Z, Gal A, Kovacs T, Klivenyi P, Molnar MJ. Csaban D, et al. Among authors: gal a. Neurol Sci. 2022 Sep;43(9):5289-5300. doi: 10.1007/s10072-022-06168-8. Epub 2022 Jun 25. Neurol Sci. 2022. PMID: 35752680 Free PMC article.
Wernicke-Korsakoff syndrome associated with mtDNA disease.
Jimoh IJ, Sebe B, Balicza P, Fedor M, Pataky I, Rudas G, Gal A, Inczedy-Farkas G, Nemeth G, Molnar MJ. Jimoh IJ, et al. Among authors: gal a. Ther Adv Neurol Disord. 2020 Jul 30;13:1756286420938972. doi: 10.1177/1756286420938972. eCollection 2020. Ther Adv Neurol Disord. 2020. PMID: 32821290 Free PMC article.
Mitochondrial DNA mutations and cognition: a case-series report.
Inczedy-Farkas G, Trampush JW, Perczel Forintos D, Beech D, Andrejkovics M, Varga Z, Remenyi V, Bereznai B, Gal A, Molnar MJ. Inczedy-Farkas G, et al. Among authors: gal a. Arch Clin Neuropsychol. 2014 Jun;29(4):315-21. doi: 10.1093/arclin/acu016. Epub 2014 Apr 28. Arch Clin Neuropsychol. 2014. PMID: 24777554
Broadening the phenotype of the TWNK gene associated Perrault syndrome.
Fekete B, Pentelényi K, Rudas G, Gál A, Grosz Z, Illés A, Idris J, Csukly G, Domonkos A, Molnar MJ. Fekete B, et al. Among authors: gal a. BMC Med Genet. 2019 Dec 18;20(1):198. doi: 10.1186/s12881-019-0934-4. BMC Med Genet. 2019. PMID: 31852434 Free PMC article.
Exclusive neuronal expression of SUCLA2 in the human brain.
Dobolyi A, Ostergaard E, Bagó AG, Dóczi T, Palkovits M, Gál A, Molnár MJ, Adam-Vizi V, Chinopoulos C. Dobolyi A, et al. Among authors: gal a. Brain Struct Funct. 2015 Jan;220(1):135-51. doi: 10.1007/s00429-013-0643-2. Epub 2013 Oct 2. Brain Struct Funct. 2015. PMID: 24085565
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia.
Nasca A, Scotton C, Zaharieva I, Neri M, Selvatici R, Magnusson OT, Gal A, Weaver D, Rossi R, Armaroli A, Pane M, Phadke R, Sarkozy A, Muntoni F, Hughes I, Cecconi A, Hajnóczky G, Donati A, Mercuri E, Zeviani M, Ferlini A, Ghezzi D. Nasca A, et al. Among authors: gal a. Hum Mutat. 2017 Aug;38(8):970-977. doi: 10.1002/humu.23262. Epub 2017 Jun 6. Hum Mutat. 2017. PMID: 28544275 Free PMC article.
45 results