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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 1
1973 1
1974 2
1975 2
1977 2
1978 1
1979 3
1980 1
1982 1
1983 5
1984 4
1985 2
1986 1
1987 1
1989 3
1990 5
1991 2
1992 2
1993 1
1994 1
1995 4
1996 7
1997 1
1999 2
2000 1
2001 3
2002 2
2003 1
2004 4
2005 5
2006 11
2007 5
2008 5
2009 4
2010 2
2011 2
2012 5
2013 4
2014 1
2016 3
2019 1
2021 1
2023 2
2024 1

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115 results

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Page 1
Dravet Syndrome-The Polish Family's Perspective Study.
Paprocka J, Lewandowska A, Zieliński P, Kurczab B, Emich-Widera E, Mazurczak T. Paprocka J, et al. Among authors: mazurczak t. J Clin Med. 2021 Apr 28;10(9):1903. doi: 10.3390/jcm10091903. J Clin Med. 2021. PMID: 33924914 Free PMC article.
The Generation of Human iPSC Lines from Three Individuals with Dravet Syndrome and Characterization of Neural Differentiation Markers in iPSC-Derived Ventral Forebrain Organoid Model.
Zayat V, Kuczynska Z, Liput M, Metin E, Rzonca-Niewczas S, Smyk M, Mazurczak T, Goszczanska-Ciuchta A, Leszczynski P, Hoffman-Zacharska D, Buzanska L. Zayat V, et al. Among authors: mazurczak t. Cells. 2023 Jan 16;12(2):339. doi: 10.3390/cells12020339. Cells. 2023. PMID: 36672274 Free PMC article.
The spectrum of intermediate SCN8A-related epilepsy.
Johannesen KM, Gardella E, Encinas AC, Lehesjoki AE, Linnankivi T, Petersen MB, Lund ICB, Blichfeldt S, Miranda MJ, Pal DK, Lascelles K, Procopis P, Orsini A, Bonuccelli A, Giacomini T, Helbig I, Fenger CD, Sisodiya SM, Hernandez-Hernandez L, Krithika S, Rumple M, Masnada S, Valente M, Cereda C, Giordano L, Accorsi P, Bürki SE, Mancardi M, Korff C, Guerrini R, von Spiczak S, Hoffman-Zacharska D, Mazurczak T, Coppola A, Buono S, Vecchi M, Hammer MF, Varesio C, Veggiotti P, Lal D, Brünger T, Zara F, Striano P, Rubboli G, Møller RS. Johannesen KM, et al. Among authors: mazurczak t. Epilepsia. 2019 May;60(5):830-844. doi: 10.1111/epi.14705. Epub 2019 Apr 10. Epilepsia. 2019. PMID: 30968951
ADCY5-related dyskinesia - case series with literature review.
Kozon K, Łysikowska W, Olszewski J, Milanowski Ł, Figura M, Mazurczak T, Hoffman-Zacharska D, Koziorowski D. Kozon K, et al. Among authors: mazurczak t. Neurol Neurochir Pol. 2024 Jan 17. doi: 10.5603/pjnns.97024. Online ahead of print. Neurol Neurochir Pol. 2024. PMID: 38230756 Free article.
Genetic Risk Factors for Neurological Disorders in Children with Adverse Events Following Immunization: A Descriptive Study of a Polish Case Series.
Charzewska A, Terczyńska I, Lipiec A, Mazurczak T, Górka-Skoczylas P, Szlendak R, Kanabus K, Tataj R, Dawidziuk M, Wojtaś B, Gielniewski B, Bal J, Stawicka E, Hoffman-Zacharska D. Charzewska A, et al. Among authors: mazurczak t. Int J Mol Sci. 2023 Jan 6;24(2):1117. doi: 10.3390/ijms24021117. Int J Mol Sci. 2023. PMID: 36674629 Free PMC article.
High rate of mosaicism in tuberous sclerosis complex.
Verhoef S, Bakker L, Tempelaars AM, Hesseling-Janssen AL, Mazurczak T, Jozwiak S, Fois A, Bartalini G, Zonnenberg BA, van Essen AJ, Lindhout D, Halley DJ, van den Ouweland AM. Verhoef S, et al. Among authors: mazurczak t. Am J Hum Genet. 1999 Jun;64(6):1632-7. doi: 10.1086/302412. Am J Hum Genet. 1999. PMID: 10330349 Free PMC article.
Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability.
Bartnik M, Nowakowska B, Derwińska K, Wiśniowiecka-Kowalnik B, Kędzior M, Bernaciak J, Ziemkiewicz K, Gambin T, Sykulski M, Bezniakow N, Korniszewski L, Kutkowska-Kaźmierczak A, Klapecki J, Szczałuba K, Shaw CA, Mazurczak T, Gambin A, Obersztyn E, Bocian E, Stankiewicz P. Bartnik M, et al. Among authors: mazurczak t. J Appl Genet. 2014 Feb;55(1):125-44. doi: 10.1007/s13353-013-0181-x. Epub 2013 Dec 3. J Appl Genet. 2014. PMID: 24297458 Free PMC article.
115 results