Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Andrzej, Seroka"'
Autor:
Monika Nojszewska, Anna Lusakowska, Malgorzata Gawel, Janusz Sierdzinski, Anna Sulek, Wioletta Krysa, Ewelina Elert-Dobkowska, Andrzej Seroka, Anna M. Kaminska, Anna Kostera-Pruszczyk
Publikováno v:
Neurologia i neurochirurgia polska. 56(5)
In myotonia congenita (MC), activation with exercise or cooling can induce transient changes in compound motor action potential (CMAP) parameters, thus providing a guide to genetic analysis.We performed the short exercise test (SET) and the short exe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d1f1923a5a7e3108b22317dd05f87c2
https://pubmed.ncbi.nlm.nih.gov/35792560
https://pubmed.ncbi.nlm.nih.gov/35792560
Autor:
Marta Lipowska, Damian Gawel, Elzbieta Szmidt-Salkowska, Anna Potulska-Chromik, Anna Kamińska, Anna Kostera-Pruszczyk, Anna Lusakowska, Anna Macias, Biruta Kierdaszuk, Monika Nojszewska, Malgorzata Gawel, Andrzej Seroka
Publikováno v:
Muscle & Nerve. 56:427-432
Introduction Reproducible non-insertional spontaneous activity (SA), with the exception of endplate activity, is an unequivocal sign of abnormality and is one of the most useful findings obtained on electromyography. Methods In this retrospective stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb019ec4f3bc017b3f0fe3d67de05ae0
https://doi.org/10.1002/mus.25521
https://doi.org/10.1002/mus.25521
Autor:
Wioletta Krysa, Anna Sulek, Anna Kamińska, Monika Nojszewska, Malgorzata Gawel, Andrzej Seroka, Janusz Sierdziński, Anna Lusakowska, Anna Kostera-Pruszczyk, Ewelina Elert-Dobkowska
Publikováno v:
Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology. 49
Introduction Myotonia congenita (MC) is caused by pathogenic variants in the CLCN1 gene coding the chloride channel protein. Methods To test the hypothesis that needle EMG could be helpful in distinguishing between the recessive and dominant MC, we p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3a983a6f54832569373e5a885ca64b7
https://pubmed.ncbi.nlm.nih.gov/31610484
https://pubmed.ncbi.nlm.nih.gov/31610484
Autor:
Andrzej Seroka, Anna Kostera-Pruszczyk, Anna Potulska-Chromik, Anna Kamińska, Dagmara Kabzińska, Karolina Aragon-Gawinska, Marta Lipowska, Barbara Ryniewicz
Publikováno v:
Journal of the Peripheral Nervous System. 21:22-26
Childhood chronic inflammatory demyelinating polyneuropathy (CIDP) needs to be differentiated from hereditary neuropathy. We aimed to validate existing CIDP nerve conduction study (NCS) criteria in a group of children with demyelinating neuropathies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7c72c0b730fc32c02e7082e7d63ad7e
https://doi.org/10.1111/jns.12152
https://doi.org/10.1111/jns.12152
Autor:
Monika Nojszewska, Malgorzata Gawel, Elzbieta Szmidt-Salkowska, Anna Kostera-Pruszczyk, Biruta Kierdaszuk, Janusz Sierdziński, Andrzej Seroka, Anna Kamińska
Publikováno v:
Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology. 39
Introduction Clinically oriented diagnostic criteria can be as specific for diagnosis of sporadic inclusion body myositis (sIBM) as pathological criteria, especially at the time of presentation. EMG may provide an convincing proof that a muscle biops
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63a4cda540f94a31a5dc8ddba618b9fe
https://pubmed.ncbi.nlm.nih.gov/29482084
https://pubmed.ncbi.nlm.nih.gov/29482084
Publikováno v:
Clinical Neurophysiology. 130:e99
Background Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare type of neuropathy in childhood as the majority of polyneuropathies occurring in children, about 85%, is hereditary. Material and methods Retrospective analysis of clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b227103cd8a65287dc5a672d9f87372
https://doi.org/10.1016/j.clinph.2019.04.555
https://doi.org/10.1016/j.clinph.2019.04.555
Autor:
Ewelina Elert-Dobkowska, Anna Kamińska, Marta Lipowska, Wioletta Krysa, Monika Nojszewska, Anna Łusakowska, Malgorzata Gawel, Anna Sulek, Anna Kostera-Pruszczyk, Janusz Sierdziński, Andrzej Seroka
Publikováno v:
Clinical Neurophysiology. 130:e53
Background In myotonia congenita provocative tests may induce transient or persistent changes in compound motor action potential (CMAP) parameters. These changes are variable and correspond to partial inexcitability of the myotonic muscle membrane. S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be4652d9a1fdac0b6a38524c50b2414c
https://doi.org/10.1016/j.clinph.2019.04.411
https://doi.org/10.1016/j.clinph.2019.04.411
Autor:
Anna Kamińska, Anna Sulek, Andrzej Seroka, Anna Łusakowska, Woiletta Krysa, Malgorzata Gawel, Monika Nojszewska, Ewelina Elert-Dobkowska, Anna Kostera-Pruszczyk, Janusz Sierdziński
Publikováno v:
Clinical Neurophysiology. 130:e52
Background Myotonia congenita (MC) is the most common nondystrophic myotonia caused by loss of function mutations in the CLCN-1 chloride channel. Aims: The purpose of this study was to describe detailed EMG characteristics of patients with MC as well
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38ceb385f12d9e5cbef2e62cce91fea9
https://doi.org/10.1016/j.clinph.2019.04.410
https://doi.org/10.1016/j.clinph.2019.04.410
Autor:
Andrzej Seroka, Anna Kostera-Pruszczyk, Dagmara Kabzińska, Malgorzata Gawel, Malgorzata Lukawska, Anna Potulska-Chromik, Andrzej Kochański
Publikováno v:
Clinical Neurophysiology. 130:e32
Background The differentiation between hereditary neuropathy and chronic inflammatory demyelinating polyneuropathy (CIDP) in children is especially significant because of completely different treatment possibilities and prognosis in these conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7675e043497159f8cfd2421a1493465f
https://doi.org/10.1016/j.clinph.2019.04.350
https://doi.org/10.1016/j.clinph.2019.04.350
Autor:
Andrzej Seroka, Anna Sulek, Elzbieta Szmidt-Salkowska, Malgorzata Gawel, Wioletta Krysa, Marta Rajkiewicz, Monika Nojszewska, Anna Kamińska, Anna Lusakowska
Publikováno v:
Muscle & Nerve. 49:277-283
Introduction: Standard electromyography (EMG) is useful in the diagnosis of myotonic dystrophy type 1 (DM1) and type 2 (DM2), but it does not differentiate between them. The aim of this study was to estimate the utility of the short exercise test (SE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::faafd933277d651b6d576accc03ffd7c
https://doi.org/10.1002/mus.23908
https://doi.org/10.1002/mus.23908