Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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 21
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
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

383 results

Results by year

Filters applied: . Clear all
Page 1
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.
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
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.
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.
Autosomal recessive polycystic kidney disease.
Zerres K, Rudnik-Schöneborn S, Steinkamm C, Mücher G. Zerres K, et al. Nephrol Dial Transplant. 1996;11 Suppl 6:29-33. doi: 10.1093/ndt/11.supp6.29. Nephrol Dial Transplant. 1996. PMID: 9044325 Review.
Pregnancy and spinal muscular atrophy.
Rudnik-Schöneborn S, Zerres K, Ignatius J, Rietschel M. Rudnik-Schöneborn S, et al. Among authors: zerres k. J Neurol. 1992 Jan;239(1):26-30. doi: 10.1007/BF00839207. J Neurol. 1992. PMID: 1541965 Review.
383 results