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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: elert dobkowska e. 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.
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: elert dobkowska e. 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.
Germline SMARCE1 mutations predispose to both spinal and cranial clear cell meningiomas.
Smith MJ, Wallace AJ, Bennett C, Hasselblatt M, Elert-Dobkowska E, Evans LT, Hickey WF, van Hoff J, Bauer D, Lee A, Hevner RF, Beetz C, du Plessis D, Kilday JP, Newman WG, Evans DG. Smith MJ, et al. Among authors: elert dobkowska e. J Pathol. 2014 Dec;234(4):436-40. doi: 10.1002/path.4427. Epub 2014 Oct 6. J Pathol. 2014. PMID: 25143307
Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients.
Elert-Dobkowska E, Stepniak I, Krysa W, Rajkiewicz M, Rakowicz M, Sobanska A, Rudzinska M, Wasielewska A, Pilch J, Kubalska J, Lipczynska-Lojkowska W, Kulczycki J, Kurdziel K, Sikorska A, Beetz C, Zaremba J, Sulek A. Elert-Dobkowska E, et al. J Neurol Sci. 2015 Dec 15;359(1-2):35-9. doi: 10.1016/j.jns.2015.10.030. Epub 2015 Oct 17. J Neurol Sci. 2015. PMID: 26671083
13 results