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

Year Number of Results
2005 1
2008 2
2010 1
2011 4
2012 2
2013 3
2014 2
2015 2
2016 1
2018 2
2019 2
2022 1
2024 0

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21 results

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Page 1
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: krysa w. 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.
Does quantitative EMG differ myotonic dystrophy type 2 and type 1?
Szmidt-Salkowska E, Gawel M, Lusakowska A, Nojszewska M, Lipowska M, Sulek A, Krysa W, Rajkiewicz M, Seroka A, Kaminska AM. Szmidt-Salkowska E, et al. Among authors: krysa w. J Electromyogr Kinesiol. 2014 Oct;24(5):755-61. doi: 10.1016/j.jelekin.2014.05.012. Epub 2014 Jun 25. J Electromyogr Kinesiol. 2014. PMID: 25052913
Value of short exercise and short exercise with cooling tests in diagnosis of recessive form of myotonia congenita (Becker disease) - are sex differences important?
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: krysa w. Neurol Neurochir Pol. 2022;56(5):399-403. doi: 10.5603/PJNNS.a2022.0051. Epub 2022 Jul 6. Neurol Neurochir Pol. 2022. PMID: 35792560 Free article.
Hereditary form of prion disease in Poland.
Zimowski J, Kulczycki J, Lojkowska W, Szpak G, Krysa W, Szirkowiec W, Limon-Sztencel A, Zaremba J. Zimowski J, et al. Among authors: krysa w. Neurol Neurochir Pol. 2012 Nov-Dec;46(6):509-18. doi: 10.5114/ninp.2012.32353. Neurol Neurochir Pol. 2012. PMID: 23319218
Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.
Sulek A, Lusakowska A, Krysa W, Rajkiewicz M, Kaminska A, Nojszewska M, Kostera-Pruszczyk A, Zdzienicka E, Kubalska J, Rakowicz M, Szirkowiec W, Kwiecinski H, Zaremba J. Sulek A, et al. Among authors: krysa w. Neurol Neurochir Pol. 2018 Nov-Dec;52(6):736-742. doi: 10.1016/j.pjnns.2018.02.008. Epub 2018 Mar 7. Neurol Neurochir Pol. 2018. PMID: 29588063
WITHDRAWN: Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients.
Sulek A, Lusakowska A, Krysa W, Rajkiewicz M, Kaminska A, Nojszewska M, Kostera-Pruszczyk A, Zdzienicka E, Kubalska J, Rakowicz M, Szirkowiec W, Kwiecinski H, Zaremba J. Sulek A, et al. Among authors: krysa w. Neurol Neurochir Pol. 2018 May 17:S0028-3843(18)30152-X. doi: 10.1016/j.pjnns.2018.04.004. Online ahead of print. Neurol Neurochir Pol. 2018. PMID: 29880430 Free article.
The personal experience of parenting a child with juvenile Huntington's disease: perceptions across Europe.
Eatough V, Santini H, Eiser C, Goller ML, Krysa W, de Nicola ', Paduanello M, Petrollini M, Rakowicz M, Squitieri F, Tibben A, Weille KL, Landwehrmeyer B, Quarrell O, Smith JA. Eatough V, et al. Among authors: krysa w. Eur J Hum Genet. 2013 Oct;21(10):1042-8. doi: 10.1038/ejhg.2013.15. Epub 2013 Feb 27. Eur J Hum Genet. 2013. PMID: 23443023 Free PMC article.
21 results