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EMQN Best Practice Guidelines for molecular genetic testing of SCAs.
Sequeiros J, Martindale J, Seneca S, Giunti P, Kämäräinen O, Volpini V, Weirich H, Christodoulou K, Bazak N, Sinke R, Sulek-Piatkowska A, Garcia-Planells J, Davis M, Frontali M, Hämäläinen P, Wieczorek S, Zühlke C, Saraiva-Pereira ML, Warner J, Leguern E, Thonney F, Quintáns Castro B, Jonasson J, Storm K, Andersson A, Ravani A, Correia L, Silveira I, Alonso I, Martins C, Pinto Basto J, Coutinho P, Perdigão A, Barton D, Davis M; European Molecular Quality Genetics Network. Sequeiros J, et al. Among authors: sulek piatkowska a. Eur J Hum Genet. 2010 Nov;18(11):1173-6. doi: 10.1038/ejhg.2010.8. Epub 2010 Feb 24. Eur J Hum Genet. 2010. PMID: 20179742 Free PMC article.
[Familial occurrence of FXTAS caused by premutation in the FMR1 gene].
Koziorowski D, Rajkiewicz M, Sułek-Piątkowska A, Zaremba J, Kaca-Oryńska M, Mandat T, Friedman A. Koziorowski D, et al. Among authors: sulek piatkowska a. Neurol Neurochir Pol. 2011 Jul-Aug;45(4):391-8. doi: 10.1016/s0028-3843(14)60111-0. Neurol Neurochir Pol. 2011. PMID: 22102001 Polish.
[Myotonic dystrophy - a new insight into a well-known disease].
Lusakowska A, Sułek-Piatkowska A. Lusakowska A, et al. Among authors: sulek piatkowska a. Neurol Neurochir Pol. 2010 May-Jun;44(3):264-76. doi: 10.1016/s0028-3843(14)60041-4. Neurol Neurochir Pol. 2010. PMID: 20625963 Review. Polish.
Familial distal monosomy 3p26.3-pter with trisomy 4q32.2-qter, presenting with progressive ataxia, intellectual disability, and dysmorphic features.
Petriczko E, Biczysko-Mokosa A, Bogdanowicz J, Constantinou M, Zdziennicka E, Horodnicka-Jozwa A, Barg E, Gawlik-Zawislak S, Sulek-Piatkowska A, Dawid G, Walczak M, Pesz K, Kedzia A, Zajaczek S. Petriczko E, et al. Among authors: sulek piatkowska a. Am J Med Genet A. 2012 Jun;158A(6):1442-6. doi: 10.1002/ajmg.a.35345. Epub 2012 May 11. Am J Med Genet A. 2012. PMID: 22581569 Review.