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

Year Number of Results
1968 1
1976 1
1977 1
1991 1
2004 1
2007 1
2010 1
2011 1
2013 2
2014 2
2015 3
2016 5
2017 7
2018 6
2019 10
2020 14
2021 15
2022 8
2023 1
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70 results
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Page 1
Spastic paraplegia preceding PSEN1-related familial Alzheimer's disease.
Chelban V, Breza M, Szaruga M, Vandrovcova J, Murphy D, Lee CJ, Alikhwan S, Bourinaris T, Vavougios G, Ilyas M, Halim SA, Al-Harrasi A, Kartanou C, Ronald C, Blumcke I, Alexoudi A, Gatzonis S, Stefanis L, Karadima G, Wood NW, Chávez-Gutiérrez L, Hardy J, Houlden H, Koutsis G. Chelban V, et al. Among authors: breza m. Alzheimers Dement (Amst). 2021 May 2;13(1):e12186. doi: 10.1002/dad2.12186. eCollection 2021. Alzheimers Dement (Amst). 2021. PMID: 33969176 Free PMC article.
HINT1-related neuropathy in Greek patients with Charcot-Marie-Tooth disease.
Kontogeorgiou Z, Voudommatis C, Kartanou C, Pandis D, Breza M, Zambelis T, Stefanis L, Panas M, Koutsis G, Karadima G. Kontogeorgiou Z, et al. Among authors: breza m. J Peripher Nerv Syst. 2021 Dec;26(4):444-448. doi: 10.1111/jns.12473. Epub 2021 Oct 29. J Peripher Nerv Syst. 2021. PMID: 34694653
Current advances in the management of cluster headaches.
Mavridis T, Breza M, Deligianni C, Mitsikostas DD. Mavridis T, et al. Among authors: breza m. Expert Opin Pharmacother. 2021 Oct;22(14):1931-1943. doi: 10.1080/14656566.2021.1924148. Epub 2021 May 14. Expert Opin Pharmacother. 2021. PMID: 33989098
Evidence for Cognitive Deficits in X-Linked Charcot-Marie-Tooth Disease.
Kasselimis D, Karadima G, Angelopoulou G, Breza M, Tsolakopoulos D, Potagas C, Panas M, Koutsis G. Kasselimis D, et al. Among authors: breza m. J Int Neuropsychol Soc. 2020 Mar;26(3):294-302. doi: 10.1017/S1355617719001188. Epub 2020 Jan 17. J Int Neuropsychol Soc. 2020. PMID: 31948496
Genotype-Phenotype Correlations for ATX-TBP (SCA17): MDSGene Systematic Review.
Rossi M, Hamed M, Rodríguez-Antigüedad J, Cornejo-Olivas M, Breza M, Lohmann K, Klein C, Rajalingam R, Marras C, van de Warrenburg BP. Rossi M, et al. Among authors: breza m. Mov Disord. 2023 Mar;38(3):368-377. doi: 10.1002/mds.29278. Epub 2022 Nov 14. Mov Disord. 2023. PMID: 36374860 Review.
α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism.
Sokratous M, Breza M, Senkevich K, Gan-Or Z, Kalampokini S, Spanaki C, Provatas A, Zaunmuktane Z, Valotassiou V, Georgoulias P, Efthymiou S, Hadjigeorgiou GM, Houlden H, Xiromerisiou G. Sokratous M, et al. Among authors: breza m. Mov Disord. 2021 Sep;36(9):2209-2212. doi: 10.1002/mds.28735. Mov Disord. 2021. PMID: 34543462 No abstract available.
70 results