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Year Number of Results
2002 1
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2004 4
2005 4
2006 3
2009 1
2010 1
2011 3
2012 3
2013 7
2014 4
2015 4
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2017 2
2018 6
2019 5
2020 3
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Page 1
Recommendations for the predictive genetic test in Huntington's disease.
MacLeod R, Tibben A, Frontali M, Evers-Kiebooms G, Jones A, Martinez-Descales A, Roos RA; Editorial Committee and Working Group ‘Genetic Testing Counselling’ of the European Huntington Disease Network. MacLeod R, et al. Clin Genet. 2013 Mar;83(3):221-31. doi: 10.1111/j.1399-0004.2012.01900.x. Epub 2012 Jul 30. Clin Genet. 2013. PMID: 22642570 No abstract available.
Spinocerebellar ataxia type 3 (Machado-Joseph disease).
Dulski J, Al-Shaikh RH, Sulek A, Kasprzak J, Sławek J, Wszolek ZK. Dulski J, et al. Among authors: sulek a. Pol Arch Intern Med. 2022 Oct 21;132(10):16322. doi: 10.20452/pamw.16322. Epub 2022 Aug 22. Pol Arch Intern Med. 2022. PMID: 35997122 Free article. No abstract available.
The needle EMG findings in myotonia congenita.
Nojszewska M, Lusakowska A, Gawel M, Sierdzinski J, Sulek A, Krysa W, Elert-Dobkowska E, Seroka A, Kaminska AM, Kostera-Pruszczyk A. Nojszewska M, et al. Among authors: sulek a. J Electromyogr Kinesiol. 2019 Dec;49:102362. doi: 10.1016/j.jelekin.2019.102362. Epub 2019 Oct 3. J Electromyogr Kinesiol. 2019. PMID: 31610484 Free article.
SCAview: an Intuitive Visual Approach to the Integrative Analysis of Clinical Data in Spinocerebellar Ataxias.
Uebachs M, Wegner P, Schaaf S, Kugai S, Jacobi H, Kuo SH, Ashizawa T, Fluck J; EUROSCA study group; ESMI study group; RISCA study group; CRC-SCA study group; SCA Registry study group; Klockgether T, Faber J. Uebachs M, et al. Cerebellum. 2024 Jun;23(3):887-895. doi: 10.1007/s12311-023-01546-0. Epub 2023 Mar 31. Cerebellum. 2024. PMID: 37002505 Free PMC article.
65 results