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Congenital glioblastoma coexisting with vascular developmental anomaly.
Laure-Kamionowska M, Szymanska K, Biekiesinska-Figatowska M, Gierowska-Bogusz B, Michalak E, Klepacka T. Laure-Kamionowska M, et al. Folia Neuropathol. 2013;51(4):333-9. doi: 10.5114/fn.2013.39724. Folia Neuropathol. 2013. PMID: 24374962 Free article.
POLG gene mutation. Clinico-neuropathological study.
Tarka S, Laure-Kamionowska M, Wierzba-Bobrowicz T, Witulska K, Ciara E, Szymańska K, Krajewski P, Stępień T, Acewicz A, Felczak P. Tarka S, et al. Among authors: laure kamionowska m. Folia Neuropathol. 2020;58(4):386-392. doi: 10.5114/fn.2020.102441. Folia Neuropathol. 2020. PMID: 33480243 Free article.
Clinico-pathological correlation in case of BRAT1 mutation.
Szymańska K, Laure-Kamionowska M, Szczałuba K, Koppolu A, Furmanek M, Kuśmierska K, Boniel S, Płoski R, Rydzanicz M. Szymańska K, et al. Among authors: laure kamionowska m. Folia Neuropathol. 2018;56(4):362-371. doi: 10.5114/fn.2018.80870. Folia Neuropathol. 2018. PMID: 30786674 Free article.
A de novo loss-of-function DYNC1H1 mutation in a patient with parkinsonian features and a favourable response to levodopa.
Szczałuba K, Szymańska K, Rydzanicz M, Ciara E, Walczak A, Piekutowska-Abramczuk D, Kosińska J, Jacoszek A, Czerska K, Biernacka A, Laure-Kamionowska M, Gasperowicz P, Pronicka E, Płoski R. Szczałuba K, et al. Among authors: laure kamionowska m. Clin Genet. 2018 May;93(5):1107-1108. doi: 10.1111/cge.13133. Epub 2017 Dec 15. Clin Genet. 2018. PMID: 29243232
59 results