Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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
2022 0
Text availability
Article attribute
Article type
Publication date

Search Results

112 results
Results by year
Filters applied: . Clear all
Page 1
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
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.
[Mutations causing hereditary hyperphenylalaninemia].
Zekanowski C, Nowacka M, Cabalska B, Sendecka E, Słowik M, Gizewska M, Filipowicz J, Mazurczak T, Bal J. Zekanowski C, et al. Among authors: mazurczak t. Med Wieku Rozwoj. 1999 Jan-Mar;3(1):55-66. Med Wieku Rozwoj. 1999. PMID: 10910639 Review. Polish.
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.
112 results