Zobrazeno 1 - 10
of 317
pro vyhledávání: '"Potulska, A."'
Autor:
Anna Łusakowska, Adrianna Wójcik, Anna Frączek, Karolina Aragon-Gawińska, Anna Potulska-Chromik, Paweł Baranowski, Ryszard Nowak, Grzegorz Rosiak, Krzysztof Milczarek, Dariusz Konecki, Zuzanna Gierlak-Wójcicka, Małgorzata Burlewicz, Anna Kostera-Pruszczyk
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-13 (2023)
Abstract Background Spinal muscular atrophy (SMA) is an autosomal recessive disorder caused by a biallelic mutation in the SMN1 gene, resulting in progressive muscle weakness and atrophy. Nusinersen is the first disease-modifying drug for all SMA typ
Externí odkaz:
https://doaj.org/article/caba915b35344630ab47436ccc08a777
Akademický článek
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Autor:
Jacek Jakubowski, Anna Potulska-Chromik, Jolanta Chmielińska, Monika Nojszewska, Anna Kostera-Pruszczyk
Publikováno v:
Bulletin of the Polish Academy of Sciences: Technical Sciences, Vol 71, Iss 2 (2023)
Finger tapping is one of the standard tests for Parkinson's disease diagnosis performed to assess the motor function of patients' upper limbs. In clinical practice, the assessment of the patient's ability to perform the test is carried out visually a
Externí odkaz:
https://doaj.org/article/ad3957b8f1354bf6a8428fc78b595ae7
Autor:
Białek, Kamila, Potulska-Chromik, Anna, Jakubowski, Jacek, Nojszewska, Monika, Kostera-Pruszczyk, Anna
Publikováno v:
Electronics (2079-9292); Oct2024, Vol. 13 Issue 19, p3962, 17p
Autor:
Behin, Anthony, Boentert, Matthias, Carvalho, Gerson, Chahin, Nizar, Charrow, Joel, Deegan, Patrick, Durmus Tekce, Hacer, Duval, Fanny, Genge, Angela, Gutmann, Ludwig, Henderson, Robert D, Hennermann, Julia B, Hiwot, Tarekegn, Hughes, Derralynn, Karaa, Amel, Karam, Chafic, Kautzky-Willer, Alexandra, Komaki, Hirofumi, Laforet, Pascal, Longo, Nicola, Malinova, Vera, Maré, Ricardo, Maxit, Clarisa, Mengel, Eugen, Moggio, Maurizio Gualtiero, Molnár, Mária Judit, Mongini, Tiziana Enrica, Nadaj-Pakleza, Aleksandra, Nascimento Osorio, Andres, Noury, Jean-Baptiste, Oliveira, Acary Souza Bulle, Parman, Yesim, Pena, Loren, Remiche, Gauthier, Sciacco, Monica, Shieh, Perry B, Smith, Cheryl, Stulnig, Thomas, Taithe, Frederic, Tard, Céline, Tarnopolsky, Mark, Vorgerd, Matthias, Whitley, Chester, Young, Peter, Alonso-Pérez, Jorge, Altemus, Patricia, Aubé-Nathier, Anne-Catherine, Avelar, Jennifer B, Bailey, Carrie, Bekircan-Kurt, Can Ebru, Billy, Jenny, Boschi, Silvia, Brown, Kathryn E, Carrera Garcia, Laura, Chase, Lauren, Cirne, Hamilton, Danjoux, Loïc, Davion, Jean-Baptiste, DeArmey, Stephanie, Fedotova, Ekaterina, Gandolfo, Eve, Grosz, Zoltan, Guellec, Dewi, Guettsches, Anne-Katrin, Guglieri, Michela, Hatcher, Erin, Helms, Sina, Hufgard-Leitner, Miriam, Klyushnikov, Sergey A., Langton, Jacqui, Linková, Lenka, Mavroudakis, Nicolas, Mazurová, Stella, Mori, Madoka, Müller-Miny, Louisa, Musumeci, Olimpia, Nance, Christopher S, Natera-de Benito, Daniel, Neel, Robert, Niizawa, Gabriela A, Noll, Lauren, Ortega, Erik, Pasnoor, Mamatha, Pautot, Vivien, Potulska-Chromik, Anna, Pugliese, Alessia, Questienne, Claire, Ramos Lopes, Margarida, Reyes-Leiva, David, Riedl, Michaela, Rugiero, Marcelo Francisco, Salort-Campana, Emmanuelle, Sgobbi Souza, Paulo Victor, Sole, Guilhem, Solera, Luca, Souto Lopes, Suzara, Specht, Sabine, Statland, Jeffrey, Swenson, Andrea, Tan, Chong Yew, Tizon, Sónia, van der Beek, N A M E, van Kooten, Harmke A., Wencel, Marie, Wenninger, Stephan, Zagnoli, Fabien, Diaz-Manera, Jordi *, *, Kishnani, Priya S *, Kushlaf, Hani, Ladha, Shafeeq, Mozaffar, Tahseen, Straub, Volker, Toscano, Antonio, van der Ploeg, Ans T, Berger, Kenneth I, Clemens, Paula R, Chien, Yin-Hsiu, Day, John W, Illarioshkin, Sergey, Roberts, Mark, Attarian, Shahram, Borges, Joao Lindolfo, Bouhour, Francoise, Choi, Young Chul, Erdem-Ozdamar, Sevim, Goker-Alpan, Ozlem, Kostera-Pruszczyk, Anna, Haack, Kristina An, Hug, Christopher, Huynh-Ba, Olivier, Johnson, Judith, Thibault, Nathan, Zhou, Tianyue, Dimachkie, Mazen M †, Schoser, Benedikt †
Publikováno v:
In The Lancet Neurology December 2021 20(12):1012-1026
Autor:
Jędrzejowska, Maria, Potulska-Chromik, Anna, Gos, Monika, Gambin, Tomasz, Dębek, Emilia, Rosiak, Edyta, Stępień, Agnieszka, Szymańczak, Robert, Wojtaś, Bartosz, Gielniewski, Bartłomiej, Ciara, Elżbieta, Sobczyńska, Agnieszka, Chrzanowska, Krystyna, Kostera-Pruszczyk, Anna, Madej-Pilarczyk, Agnieszka
Publikováno v:
In European Journal of Paediatric Neurology May 2021 32:115-121
Autor:
JAKUBOWSKI, Jacek1 jacek.jakubowski@wat.edu.pl, POTULSKA-CHROMIK, Anna2, CHMIELIŃSKA, Jolanta1, NOJSZEWSKA, Monika2, KOSTERA-PRUSZCZYK, Anna2
Publikováno v:
Bulletin of the Polish Academy of Sciences: Technical Sciences. 2023, Vol. 71 Issue 2, p1-9. 9p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Małgorzata Łukawska, Anna Potulska-Chromik, Marta Lipowska, Dorota Hoffman-Zacharska, Beata Olchowik, Magdalena Figlerowicz, Karolina Kanabus, Edyta Rosiak, Anna Kostera-Pruszczyk
Publikováno v:
Frontiers in Neurology, Vol 12 (2022)
Externí odkaz:
https://doaj.org/article/155442a6133a4994bb511fc4f017b414
Autor:
Kalina Andrysiak, Alicja Martyniak, Anna Potulska-Chromik, Anna Kostera-Pruszczyk, Jacek Stępniewski, Józef Dulak
Publikováno v:
Stem Cell Research, Vol 57, Iss , Pp 102563- (2021)
Spinal Muscular Atrophy (SMA) is a genetic neuromuscular disease caused by mutations inSMN1 gene encoding survival motor neuron (SMN) protein. Lack of this protein leads to progressive loss of motor neurons and therefore to gradual loss of signal tra
Externí odkaz:
https://doaj.org/article/7bc2e014b8df4854b25bfcb570300c17