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

Year Number of Results
1970 1
1982 2
1983 2
1984 3
1985 3
1986 4
1987 6
1988 6
1989 8
1990 8
1991 4
1992 9
1993 11
1994 8
1995 16
1996 13
1997 12
1998 12
1999 10
2000 5
2001 12
2002 16
2003 28
2004 12
2005 20
2006 17
2007 14
2008 20
2009 18
2010 16
2011 15
2012 18
2013 8
2014 11
2015 14
2016 9
2017 8
2018 3
2019 1
2020 3
2021 2
2022 0
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382 results
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Page 1
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Burgmaier K, Brinker L, Erger F, Beck BB, Benz MR, Bergmann C, Boyer O, Collard L, Dafinger C, Fila M, Kowalewska C, Lange-Sperandio B, Massella L, Mastrangelo A, Mekahli D, Miklaszewska M, Ortiz-Bruechle N, Patzer L, Prikhodina L, Ranchin B, Ranguelov N, Schild R, Seeman T, Sever L, Sikora P, Szczepanska M, Teixeira A, Thumfart J, Uetz B, Weber LT, Wühl E, Zerres K; ESCAPE Study group; GPN study group, Dötsch J, Schaefer F, Liebau MC; ARegPKD consortium. Burgmaier K, et al. Among authors: zerres k. Kidney Int. 2021 Sep;100(3):650-659. doi: 10.1016/j.kint.2021.04.019. Epub 2021 Apr 30. Kidney Int. 2021. PMID: 33940108
Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD).
Bergmann C, Senderek J, Windelen E, Küpper F, Middeldorf I, Schneider F, Dornia C, Rudnik-Schöneborn S, Konrad M, Schmitt CP, Seeman T, Neuhaus TJ, Vester U, Kirfel J, Büttner R, Zerres K; APN (Arbeitsgemeinschaft für Pädiatrische Nephrologie). Bergmann C, et al. Among authors: zerres k. Kidney Int. 2005 Mar;67(3):829-48. doi: 10.1111/j.1523-1755.2005.00148.x. Kidney Int. 2005. PMID: 15698423 Free article.
Pontocerebellar hypoplasia.
Rudnik-Schöneborn S, Barth PG, Zerres K. Rudnik-Schöneborn S, et al. Among authors: zerres k. Am J Med Genet C Semin Med Genet. 2014 Jun;166C(2):173-83. doi: 10.1002/ajmg.c.31403. Epub 2014 Jun 12. Am J Med Genet C Semin Med Genet. 2014. PMID: 24924738 Review.
[Genetically-induced kidney diseases].
Zerres K, Rudnik-Schöneborn S. Zerres K, et al. Internist (Berl). 1999 May;40(5):534-42. doi: 10.1007/s001080050367. Internist (Berl). 1999. PMID: 10407763 Review. German. No abstract available.
Genes and the preeclampsia syndrome.
Mütze S, Rudnik-Schöneborn S, Zerres K, Rath W. Mütze S, et al. Among authors: zerres k. J Perinat Med. 2008;36(1):38-58. doi: 10.1515/JPM.2008.004. J Perinat Med. 2008. PMID: 18184097 Review.
[Johanson-Blizzard syndrome].
Rudnik-Schöneborn S, Keller B, Beemer FA, Pistor K, Swanenburg de Veye HF, Zerres K. Rudnik-Schöneborn S, et al. Among authors: zerres k. Klin Padiatr. 1991 Jan-Feb;203(1):33-8. doi: 10.1055/s-2007-1025396. Klin Padiatr. 1991. PMID: 2027265 German.
Cystinuria: an inborn cause of urolithiasis.
Eggermann T, Venghaus A, Zerres K. Eggermann T, et al. Among authors: zerres k. Orphanet J Rare Dis. 2012 Apr 5;7:19. doi: 10.1186/1750-1172-7-19. Orphanet J Rare Dis. 2012. PMID: 22480232 Free PMC article. Review.
[Cystic kidney diseases].
Zerres K, Ortiz Brüchle N. Zerres K, et al. Internist (Berl). 2012 Apr;53(4):419-21, 423-5, 427-8. doi: 10.1007/s00108-011-2985-2. Internist (Berl). 2012. PMID: 22410941 German.
Autosomal recessive polycystic kidney disease.
Zerres K, Rudnik-Schöneborn S, Steinkamm C, Becker J, Mücher G. Zerres K, et al. J Mol Med (Berl). 1998 Apr;76(5):303-9. doi: 10.1007/s001090050221. J Mol Med (Berl). 1998. PMID: 9587064 Review.
382 results