Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Anna M. Kaminska"'
Autor:
Anna Macias, Jakub Piotr Fichna, Malgorzata Topolewska, Maria J. Rȩdowicz, Anna M. Kaminska, Anna Kostera-Pruszczyk
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Limb–girdle muscular dystrophy type R1 (LGMDR1) is caused by mutations in CAPN3 and is the most common type of recessive LGMD. Even with the use of whole-exome sequencing (WES), only one mutant allele of CAPN3 is found in a significant number of LG
Externí odkaz:
https://doaj.org/article/337ad31ac4cd4a9d8166ab21a5852521
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
Autor:
Jakub P, Fichna, Anna, Potulska-Chromik, Przemysław, Miszta, Maria Jolanta, Redowicz, Anna M, Kaminska, Cezary, Zekanowski, Sławomir, Filipek
Publikováno v:
BBA Clinical
Myofibrillar myopathy (MFM) is a group of inherited muscular disorders characterized by myofibrils dissolution and abnormal accumulation of degradation products. So far causative mutations have been identified in nine genes encoding Z-disk proteins,
Autor:
Monika, Nojszewska, Malgorzata, Gawel, Elzbieta, Szmidt-Salkowska, Anna, Kostera-Pruszczyk, Anna, Potulska-Chromik, Anna, Lusakowska, Biruta, Kierdaszuk, Marta, Lipowska, Anna, Macias, Damian, Gawel, Andrzej, Seroka, Anna M, Kaminska
Publikováno v:
Musclenerve. 56(3)
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.In this retrospective study we analyzed occurre
Autor:
Anna, Potulska-Chromik, Barbara, Ryniewicz, Karolina, Aragon-Gawinska, Dagmara, Kabzinska, Andrzej, Seroka, Marta, Lipowska, Anna M, Kaminska, Anna, Kostera-Pruszczyk
Publikováno v:
Journal of the peripheral nervous system : JPNS. 21(1)
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
Autor:
Malgorzata, Gawel, Elzbieta, Szmidt-Salkowska, Anna, Lusakowska, Monika, Nojszewska, Anna, Sulek, Wioletta, Krysa, Marta, Rajkiewicz, Andrzej, Seroka, Anna M, Kaminska
Publikováno v:
Musclenerve. 49(2)
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 (SET) and short e
Autor:
Marek Guziewicz, Anna M. Kaminska
Publikováno v:
Thin Solid Films. 254:194-199
In this paper we describe the application of ellipsometry to study (100)GaAs surfaces. Investigations concern the surfaces after polishing, cleaning, wet and dry etching of GaAs substrates and the surfaces of liquid phase epitaxy- and molecular beam
Publikováno v:
Journal of the Neurological Sciences. 76:165-172
The alkaline phosphatase (AP) reaction was carried out on muscle sections from a large series of rats under various experimental neuromuscular disorders. Only denervated and non-innervated muscle fibers stained positively with the AP reaction. In oth
Publikováno v:
Aktualności Neurologiczne, Vol 13, Iss 4, Pp 275-278 (2013)
Tętnica Percherona jest rzadkim wariantem anatomicznym unaczynienia, w którym przyśrodkowe części obu wzgórz i przyśrodkowa część śródmózgowia zaopatrywane są przez odgałęzienia pojedynczego naczynia krwionośnego odchodzącego od j
Externí odkaz:
https://doaj.org/article/7250614398cf45ee9e1d4bdb6618040a
Publikováno v:
Annals of Neurology. 9:605-607
Intracellular polyamine levels were measured in 17 patients with neuromuscular diseases and 13 normal controls and were correlated with morphological changes in muscle biopsies. Elevated polyamine levels were found in muscles with marked morphologica