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

Year Number of Results
1985 1
1987 1
1990 1
1993 1
1994 4
1995 4
1996 4
1997 7
1998 3
1999 5
2000 6
2001 3
2002 3
2003 5
2004 3
2006 4
2007 4
2008 3
2009 6
2010 3
2011 6
2012 2
2013 2
2014 5
2015 4
2016 4
2017 7
2018 5
2019 4
2020 3
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Similar Articles for PMID: 12819251

98 results
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Page 1
Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p.
Ruf RG, Fuchshuber A, Karle SM, Lemainque A, Huck K, Wienker T, Otto E, Hildebrandt F. Ruf RG, et al. J Am Soc Nephrol. 2003 Jul;14(7):1897-900. doi: 10.1097/01.asn.0000070070.03811.02. J Am Soc Nephrol. 2003. PMID: 12819251 Free article.
A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2.
Ruf RG, Wolf MT, Hennies HC, Lucke B, Zinn C, Varnholt V, Lichtenberger A, Pasch A, Imm A, Briese S, Lennert T, Fuchshuber A, Nurnberg P, Hildebrandt F. Ruf RG, et al. J Am Soc Nephrol. 2003 Jun;14(6):1519-22. doi: 10.1097/01.asn.0000066141.55735.8d. J Am Soc Nephrol. 2003. PMID: 12761252 Free article.
Association of HLA-DR/DQ alleles and haplotypes with nephrotic syndrome.
Ramanathan AS, Senguttuvan P, Chinniah R, Vijayan M, Thirunavukkarasu M, Raju K, Mani D, Ravi PM, Rajendran P, Krishnan JI, Karuppiah B. Ramanathan AS, et al. Nephrology (Carlton). 2016 Sep;21(9):745-52. doi: 10.1111/nep.12669. Nephrology (Carlton). 2016. PMID: 26566811
HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.
Adeyemo A, Esezobor C, Solarin A, Abeyagunawardena A, Kari JA, El Desoky S, Greenbaum LA, Kamel M, Kallash M, Silva C, Young A, Hunley TE, de Jesus-Gonzalez N, Srivastava T, Gbadegesin R. Adeyemo A, et al. Am J Kidney Dis. 2018 Mar;71(3):399-406. doi: 10.1053/j.ajkd.2017.10.013. Epub 2017 Dec 23. Am J Kidney Dis. 2018. PMID: 29277510 Free PMC article.
Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations.
Landau D, Oved T, Geiger D, Abizov L, Shalev H, Parvari R. Landau D, et al. Pediatr Nephrol. 2007 May;22(5):661-9. doi: 10.1007/s00467-006-0409-7. Epub 2007 Jan 12. Pediatr Nephrol. 2007. PMID: 17219184
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14.
Bejaoui K, Hirabayashi K, Hentati F, Haines JL, Ben Hamida C, Belal S, Miller RG, McKenna-Yasek D, Weissenbach J, Rowland LP, et al. Bejaoui K, et al. Neurology. 1995 Apr;45(4):768-72. doi: 10.1212/wnl.45.4.768. Neurology. 1995. PMID: 7723968
A new locus for familial FSGS on chromosome 2p.
Gbadegesin R, Lavin P, Janssens L, Bartkowiak B, Homstad A, Wu G, Bowling B, Eckel J, Potocky C, Abbott D, Conlon P, Scott WK, Howell D, Hauser E, Winn MP. Gbadegesin R, et al. J Am Soc Nephrol. 2010 Aug;21(8):1390-7. doi: 10.1681/ASN.2009101046. Epub 2010 Jul 8. J Am Soc Nephrol. 2010. PMID: 20616172 Free PMC article.
Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome.
Gbadegesin R, Hinkes B, Vlangos C, Mucha B, Liu J, Hopcian J, Hildebrandt F. Gbadegesin R, et al. Pediatr Nephrol. 2007 Apr;22(4):509-13. doi: 10.1007/s00467-006-0377-y. Epub 2007 Jan 10. Pediatr Nephrol. 2007. PMID: 17216259
Mutations in EMP2 cause childhood-onset nephrotic syndrome.
Gee HY, Ashraf S, Wan X, Vega-Warner V, Esteve-Rudd J, Lovric S, Fang H, Hurd TW, Sadowski CE, Allen SJ, Otto EA, Korkmaz E, Washburn J, Levy S, Williams DS, Bakkaloglu SA, Zolotnitskaya A, Ozaltin F, Zhou W, Hildebrandt F. Gee HY, et al. Am J Hum Genet. 2014 Jun 5;94(6):884-90. doi: 10.1016/j.ajhg.2014.04.010. Epub 2014 May 8. Am J Hum Genet. 2014. PMID: 24814193 Free PMC article.
Human leukocyte antigen association with familial steroid-sensitive nephrotic syndrome.
Korsgaard T, Joshi S, Andersen RF, Moeller K, Seeman T, Podrack√° L, Eiberg H, Rittig S. Korsgaard T, et al. Eur J Pediatr. 2020 Sep;179(9):1481-1486. doi: 10.1007/s00431-020-03634-3. Epub 2020 Mar 20. Eur J Pediatr. 2020. PMID: 32198629
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