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

Year Number of Results
1989 6
1990 2
1991 2
1993 7
1994 7
1995 6
1996 9
1997 7
1998 3
1999 5
2000 4
2001 6
2002 7
2003 2
2004 2
2005 4
2006 5
2007 3
2009 5
2010 5
2011 4
2012 2
2013 1
2014 4
2015 3
2016 6
2017 5
2018 1
2019 2
2020 2
2021 2
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123 results
Results by year
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Page 1
Natural history of genetically proven autosomal recessive Alport syndrome.
Oka M, Nozu K, Kaito H, Fu XJ, Nakanishi K, Hashimura Y, Morisada N, Yan K, Matsuo M, Yoshikawa N, Vorechovsky I, Iijima K. Oka M, et al. Among authors: vorechovsky i. Pediatr Nephrol. 2014 Sep;29(9):1535-44. doi: 10.1007/s00467-014-2797-4. Epub 2014 Mar 15. Pediatr Nephrol. 2014. PMID: 24633401
Transposon clusters as substrates for aberrant splice-site activation.
Alvarez MEV, Chivers M, Borovska I, Monger S, Giannoulatou E, Kralovicova J, Vorechovsky I. Alvarez MEV, et al. Among authors: vorechovsky i. RNA Biol. 2021 Mar;18(3):354-367. doi: 10.1080/15476286.2020.1805909. Epub 2020 Sep 23. RNA Biol. 2021. PMID: 32965162 Free PMC article.
Genetics of IgA deficiency.
Truedsson L, Baskin B, Pan Q, Rabbani H, Vorĕchovský I, Smith CI, Hammarström L. Truedsson L, et al. Among authors: vorechovsky i. APMIS. 1995 Dec;103(12):833-42. doi: 10.1111/j.1699-0463.1995.tb01442.x. APMIS. 1995. PMID: 8562023 Review.
A birth of bipartite exon by intragenic deletion.
Nozu K, Iijima K, Igarashi T, Yamada S, Kralovicova J, Nozu Y, Yamamura T, Minamikawa S, Morioka I, Ninchoji T, Kaito H, Nakanishi K, Vorechovsky I. Nozu K, et al. Among authors: vorechovsky i. Mol Genet Genomic Med. 2017 Mar 1;5(3):287-294. doi: 10.1002/mgg3.277. eCollection 2017 May. Mol Genet Genomic Med. 2017. PMID: 28546999 Free PMC article.
X-linked agammaglobulinemia and other immunoglobulin deficiencies.
Smith CI, Islam KB, Vorechovský I, Olerup O, Wallin E, Rabbani H, Baskin B, Hammarström L. Smith CI, et al. Among authors: vorechovsky i. Immunol Rev. 1994 Apr;138:159-83. doi: 10.1111/j.1600-065x.1994.tb00851.x. Immunol Rev. 1994. PMID: 8070814 Review. No abstract available.
BTKbase: XLA-mutation registry.
Vihinen M, Brooimans RA, Kwan SP, Lehväslaiho H, Litman GW, Ochs HD, Resnick I, Schwaber JH, Vorĕchovsky I, Smith CI. Vihinen M, et al. Among authors: vorechovsky i. Immunol Today. 1996 Nov;17(11):502-6. doi: 10.1016/0167-5699(96)30058-3. Immunol Today. 1996. PMID: 8961625 No abstract available.
123 results
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