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Journal Abstract Search

312 related items for PubMed ID: 26156092

  • 1. Focal segmental glomerulosclerosis: molecular genetics and targeted therapies.
    Chen YM, Liapis H.
    BMC Nephrol; 2015 Jul 09; 16():101. PubMed ID: 26156092
    [Abstract] [Full Text] [Related]

  • 2. TRPC6 and FSGS: the latest TRP channelopathy.
    Mukerji N, Damodaran TV, Winn MP.
    Biochim Biophys Acta; 2007 Aug 09; 1772(8):859-68. PubMed ID: 17459670
    [Abstract] [Full Text] [Related]

  • 3. Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis.
    Barua M, Brown EJ, Charoonratana VT, Genovese G, Sun H, Pollak MR.
    Kidney Int; 2013 Feb 09; 83(2):316-22. PubMed ID: 23014460
    [Abstract] [Full Text] [Related]

  • 4. [The genetic basis of familial focal segmental glomerulosclerosis and related nephrotic syndrome].
    Tsukaguchi H, Kitamura A.
    Nihon Jinzo Gakkai Shi; 2007 Feb 09; 49(2):88-97. PubMed ID: 17375615
    [No Abstract] [Full Text] [Related]

  • 5. Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa.
    Nandlal L, Winkler CA, Bhimma R, Cho S, Nelson GW, Haripershad S, Naicker T.
    Eur J Pediatr; 2022 Oct 09; 181(10):3595-3606. PubMed ID: 35920919
    [Abstract] [Full Text] [Related]

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    [No Abstract] [Full Text] [Related]

  • 7. Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
    Santín S, Bullich G, Tazón-Vega B, García-Maset R, Giménez I, Silva I, Ruíz P, Ballarín J, Torra R, Ars E.
    Clin J Am Soc Nephrol; 2011 May 09; 6(5):1139-48. PubMed ID: 21415313
    [Abstract] [Full Text] [Related]

  • 8. Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.
    Bińczak-Kuleta A, Rubik J, Litwin M, Ryder M, Lewandowska K, Taryma-Leśniak O, Clark JS, Grenda R, Ciechanowicz A.
    Bosn J Basic Med Sci; 2014 May 09; 14(2):89-93. PubMed ID: 24856380
    [Abstract] [Full Text] [Related]

  • 9. Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis.
    Löwik M, Levtchenko E, Westra D, Groenen P, Steenbergen E, Weening J, Lilien M, Monnens L, van den Heuvel L.
    Nephrol Dial Transplant; 2008 Oct 09; 23(10):3146-51. PubMed ID: 18443213
    [Abstract] [Full Text] [Related]

  • 10. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.
    Bullich G, Trujillano D, Santín S, Ossowski S, Mendizábal S, Fraga G, Madrid Á, Ariceta G, Ballarín J, Torra R, Estivill X, Ars E.
    Eur J Hum Genet; 2015 Sep 09; 23(9):1192-9. PubMed ID: 25407002
    [Abstract] [Full Text] [Related]

  • 11. [Focal segmental glomerulosclerosis].
    Yuzawa Y, Matsuo S.
    Nihon Rinsho; 2004 Oct 09; 62(10):1837-41. PubMed ID: 15500127
    [Abstract] [Full Text] [Related]

  • 12. Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis.
    Büscher AK, Celebi N, Hoyer PF, Klein HG, Weber S, Hoefele J.
    Pediatr Nephrol; 2018 Mar 09; 33(3):433-437. PubMed ID: 29038887
    [Abstract] [Full Text] [Related]

  • 13. Screening of ACTN4 and TRPC6 mutations in a Chinese cohort of patients with adult-onset familial focal segmental glomerulosclerosis.
    Zhang Q, Ma J, Xie J, Wang Z, Zhu B, Hao X, Yang L, Ren H, Chen N.
    Contrib Nephrol; 2013 Mar 09; 181():91-100. PubMed ID: 23689571
    [Abstract] [Full Text] [Related]

  • 14. Molecular analysis of NPHS2 and ACTN4 genes in a series of 33 Italian patients affected by adult-onset nonfamilial focal segmental glomerulosclerosis.
    Aucella F, De Bonis P, Gatta G, Muscarella LA, Vigilante M, di Giorgio G, D'Errico M, Zelante L, Stallone C, Bisceglia L.
    Nephron Clin Pract; 2005 Mar 09; 99(2):c31-6. PubMed ID: 15627790
    [Abstract] [Full Text] [Related]

  • 15. Genetics of focal segmental glomerulosclerosis.
    Woroniecki RP, Kopp JB.
    Pediatr Nephrol; 2007 May 09; 22(5):638-44. PubMed ID: 17347836
    [Abstract] [Full Text] [Related]

  • 16. Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin.
    Bertelli R, Ginevri F, Caridi G, Dagnino M, Sandrini S, Di Duca M, Emma F, Sanna-Cherchi S, Scolari F, Neri TM, Murer L, Massella L, Basile G, Rizzoni G, Perfumo F, Ghiggeri GM.
    Am J Kidney Dis; 2003 Jun 09; 41(6):1314-21. PubMed ID: 12776285
    [Abstract] [Full Text] [Related]

  • 17. [Steroid-resistant focal segmental glomerulosclerosis treated with cascade plasmafiltration and rituximab].
    Tatangelo P, Londrino F, Di Vasta G, Guido G, Centi A, Dominijanni S, Bernabei E, Caramiello MS, Di Franco D, Palumbo R.
    G Ital Nefrol; 2018 May 09; 35(3):. PubMed ID: 29786187
    [Abstract] [Full Text] [Related]

  • 18. Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis.
    Komatsuda A, Wakui H, Maki N, Kigawa A, Goto H, Ohtani H, Hamai K, Oyama Y, Makoto H, Sawada K, Imai H.
    Ren Fail; 2003 Jan 09; 25(1):87-93. PubMed ID: 12617336
    [Abstract] [Full Text] [Related]

  • 19. Familial focal segmental glomerulosclerosis (FSGS) in a Nigerian family and exclusion of mutations in NPHS2,WT1 and APOL1.
    Anochie IC, Eke FU, Okpere AN.
    West Afr J Med; 2012 Jan 09; 31(4):273-6. PubMed ID: 23468032
    [Abstract] [Full Text] [Related]

  • 20. A case of familial kidney disease.
    Pollak MR, Alexander MP, Henderson JM.
    Clin J Am Soc Nephrol; 2007 Nov 09; 2(6):1367-74. PubMed ID: 17942774
    [No Abstract] [Full Text] [Related]

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