Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ewa Naganska"'
Autor:
Michał Sobstyl, Ewa Nagańska, Piotr Glinka, Teresa Wierzba-Bobrowicz, Albert Acewicz, Aleksandra Kuls-Oszmaniec
Publikováno v:
Folia Neuropathologica, Vol 61, Iss 4, Pp 433-441 (2023)
Intracranial collision tumours are rare pathologies in which two distinct neoplasms are found in the same location. We present an unusual case of an intracranial collision tumour composed of meningothelial meningioma (CNS WHO G1) and glioblastoma (ID
Externí odkaz:
https://doaj.org/article/90bd57b1cd944a4ab739611881968665
Autor:
Michał Sobstyl, Magdalena Kowalska, Magdalena Konopko, Aleksandra Wierzbicka, Karol Karamon, Ewa Nagańska
Publikováno v:
Epilepsy & Behavior Reports, Vol 27, Iss , Pp 100677- (2024)
Temporal lobe epilepsy (TLE) is the most common form of drug-resistant epilepsy. The main pathological changes primarily involve hippocampal sclerosis (HS). Early resective surgery of the sclerotic hippocampus is typically associated with favorable c
Externí odkaz:
https://doaj.org/article/20f9b68a1ecc4c118af05b42c0b49098
Autor:
Anna Raczkiewicz, Artur Bachta, Ewa Nagańska, Marian Sułek, Aleksandra Juszkiewicz, Małgorzata Tłustochowicz
Publikováno v:
Rheumatology, Vol 48, Iss 5, Pp 320-329 (2010)
Wstęp: Zmiany zapalne w kręgosłupie szyjnym występują u 25–80% chorych na reumatoidalne zapalenie stawów (RZS). W większościbadań podkreśla się brak związku między zgłaszanymi dolegliwościamia zmianami radiologicznymi w kręgosłupie
Externí odkaz:
https://doaj.org/article/61ce363fb2a54ee5bfcfa0fd57b9b6b8
Publikováno v:
Folia Neuropathologica, Vol 54, Iss 3, Pp 197-211 (2016)
Pilocytic astrocytomas (PAs) are the most frequent primary astroglial tumours affecting children and adolescents. They occur sporadically or in association with a genetically determined syndrome – neurofibromatosis type 1. Classic PA usually manife
Externí odkaz:
https://doaj.org/article/af966e024881484988590a89d290bef6
Autor:
Ewa, Naganska, Ewa, Matyja
Publikováno v:
Folia neuropathologica. 49(1)
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease characterized by loss of motor neurons in the spinal cord, brain stem and motor cortex which dramatically reduces life expectancy. ALS occurs either in familial or, more f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8d0464b00bba834bd195e4b970f581d0
https://pubmed.ncbi.nlm.nih.gov/21455838
https://pubmed.ncbi.nlm.nih.gov/21455838
Autor:
Anna, Karaszewska, Ewa, Nagańska, Ewa, Matyja, Jolanta, Gębarowska, Elżbieta, Grzywaczewska, Paweł, Grieb, Janina, Rafałowska
Publikováno v:
In Pharmacological Reports November-December 2009 61(6):1247-1247