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

Year Number of Results
1985 1
1986 1
1989 1
1991 1
1993 2
1994 1
1995 3
1996 6
1997 1
1998 8
1999 7
2000 5
2001 7
2002 4
2003 5
2004 3
2005 4
2006 3
2007 4
2008 7
2009 2
2010 4
2011 7
2012 7
2013 8
2014 2
2015 2
2016 8
2017 4
2018 2
2019 6
2020 4
2021 3
2022 5
2023 2
2024 0

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Similar articles for PMID: 10603123

126 results

Results by year

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Page 1
Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations.
Schumacher V, Schärer K, Wühl E, Altrogge H, Bonzel KE, Guschmann M, Neuhaus TJ, Pollastro RM, Kuwertz-Bröking E, Bulla M, Tondera AM, Mundel P, Helmchen U, Waldherr R, Weirich A, Royer-Pokora B. Schumacher V, et al. Kidney Int. 1998 Jun;53(6):1594-600. doi: 10.1046/j.1523-1755.1998.00948.x. Kidney Int. 1998. PMID: 9607189 Free article.
WT1 and glomerular diseases.
Niaudet P, Gubler MC. Niaudet P, et al. Pediatr Nephrol. 2006 Nov;21(11):1653-60. doi: 10.1007/s00467-006-0208-1. Epub 2006 Aug 23. Pediatr Nephrol. 2006. PMID: 16927106 Review.
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.
Jeanpierre C, Denamur E, Henry I, Cabanis MO, Luce S, Cécille A, Elion J, Peuchmaur M, Loirat C, Niaudet P, Gubler MC, Junien C. Jeanpierre C, et al. Am J Hum Genet. 1998 Apr;62(4):824-33. doi: 10.1086/301806. Am J Hum Genet. 1998. PMID: 9529364 Free PMC article.
126 results