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Journal Abstract Search

229 related items for PubMed ID: 27733133

  • 1. Diagnosing FSGS without kidney biopsy - a novel INF2-mutation in a family with ESRD of unknown origin.
    Münch J, Grohmann M, Lindner TH, Bergmann C, Halbritter J.
    BMC Med Genet; 2016 Oct 12; 17(1):73. PubMed ID: 27733133
    [Abstract] [Full Text] [Related]

  • 2. 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 12; 33(3):433-437. PubMed ID: 29038887
    [Abstract] [Full Text] [Related]

  • 3. Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic.
    Safarikova M, Stekrova J, Honsova E, Horinova V, Tesar V, Reiterova J.
    BMC Med Genet; 2018 Aug 20; 19(1):147. PubMed ID: 30126379
    [Abstract] [Full Text] [Related]

  • 4. Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
    Büscher AK, Konrad M, Nagel M, Witzke O, Kribben A, Hoyer PF, Weber S.
    Clin Nephrol; 2012 Jul 20; 78(1):47-53. PubMed ID: 22732337
    [Abstract] [Full Text] [Related]

  • 5. Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy.
    Caridi G, Lugani F, Dagnino M, Gigante M, Iolascon A, Falco M, Graziano C, Benetti E, Dugo M, Del Prete D, Granata A, Borracelli D, Moggia E, Quaglia M, Rinaldi R, Gesualdo L, Ghiggeri GM.
    Nephrol Dial Transplant; 2014 Sep 20; 29 Suppl 4():iv80-6. PubMed ID: 25165188
    [Abstract] [Full Text] [Related]

  • 6. Variable renal phenotype in a family with an INF2 mutation.
    Lee HK, Han KH, Jung YH, Kang HG, Moon KC, Ha IS, Choi Y, Cheong HI.
    Pediatr Nephrol; 2011 Jan 20; 26(1):73-6. PubMed ID: 20803156
    [Abstract] [Full Text] [Related]

  • 7. Focal segmental glomerulosclerosis after renal transplantation.
    Shimizu A, Higo S, Fujita E, Mii A, Kaneko T.
    Clin Transplant; 2011 Jul 20; 25 Suppl 23():6-14. PubMed ID: 21623907
    [Abstract] [Full Text] [Related]

  • 8. Spectrum of disease in familial focal and segmental glomerulosclerosis.
    Conlon PJ, Lynn K, Winn MP, Quarles LD, Bembe ML, Pericak-Vance M, Speer M, Howell DN.
    Kidney Int; 1999 Nov 20; 56(5):1863-71. PubMed ID: 10571795
    [Abstract] [Full Text] [Related]

  • 9. [Not Available].
    Helmuth A, Huynh-Do U.
    Ther Umsch; 2015 Mar 20; 72(3):189-93. PubMed ID: 25722312
    [Abstract] [Full Text] [Related]

  • 10. INF2 p.Arg214Cys mutation in a Chinese family with rapidly progressive renal failure and follow-up of renal transplantation: case report and literature review.
    Zhao W, Ma X, Zhang X, Luo D, Zhang J, Li M, Ye Z, Peng H.
    BMC Nephrol; 2021 Feb 04; 22(1):51. PubMed ID: 33541266
    [Abstract] [Full Text] [Related]

  • 11. INF2 and ROBO2 gene mutation in an Indian family with end stage renal failure and follow-up of renal transplantation.
    Shah V, Singh JK, Srivastava SK, Konnur A, Gang S, Pandey SN.
    Nephrology (Carlton); 2024 Jan 04; 29(1):48-54. PubMed ID: 37772439
    [Abstract] [Full Text] [Related]

  • 12. Focal segmental glomerulosclerosis is not a sufficient predictor of renal outcome in patients with membranous nephropathy.
    Heeringa SF, Branten AJ, Deegens JK, Steenbergen E, Wetzels JF.
    Nephrol Dial Transplant; 2007 Aug 04; 22(8):2201-7. PubMed ID: 17442739
    [Abstract] [Full Text] [Related]

  • 13. INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy.
    Boyer O, Nevo F, Plaisier E, Funalot B, Gribouval O, Benoit G, Huynh Cong E, Arrondel C, Tête MJ, Montjean R, Richard L, Karras A, Pouteil-Noble C, Balafrej L, Bonnardeaux A, Canaud G, Charasse C, Dantal J, Deschenes G, Deteix P, Dubourg O, Petiot P, Pouthier D, Leguern E, Guiochon-Mantel A, Broutin I, Gubler MC, Saunier S, Ronco P, Vallat JM, Alonso MA, Antignac C, Mollet G.
    N Engl J Med; 2011 Dec 22; 365(25):2377-88. PubMed ID: 22187985
    [Abstract] [Full Text] [Related]

  • 14. Clinical and histological findings of autosomal dominant renal-limited disease with LMX1B mutation.
    Konomoto T, Imamura H, Orita M, Tanaka E, Moritake H, Sato Y, Fujimoto S, Harita Y, Hisano S, Yoshiura K, Nunoi H.
    Nephrology (Carlton); 2016 Sep 22; 21(9):765-73. PubMed ID: 26560070
    [Abstract] [Full Text] [Related]

  • 15. A novel heterozygous variant of the COL4A4 gene in a Chinese family with hematuria and proteinuria leads to focal segmental glomerulosclerosis and chronic kidney disease.
    Fan LL, Liu L, Luo FM, Du R, Wang CY, Dong Y, Liu JS.
    Mol Genet Genomic Med; 2020 Dec 22; 8(12):e1545. PubMed ID: 33159707
    [Abstract] [Full Text] [Related]

  • 16. INF2 mutations associated with dominant inherited intermediate Charcot-Marie-Tooth neuropathy with focal segmental glomerulosclerosis in two Chinese patients.
    Jin S, Wang W, Wang R, Lv H, Zhang W, Wang Z, Jiao J, Yuan Y.
    Clin Neuropathol; 2015 Dec 22; 34(5):275-81. PubMed ID: 25943269
    [Abstract] [Full Text] [Related]

  • 17. Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis.
    Gbadegesin RA, Lavin PJ, Hall G, Bartkowiak B, Homstad A, Jiang R, Wu G, Byrd A, Lynn K, Wolfish N, Ottati C, Stevens P, Howell D, Conlon P, Winn MP.
    Kidney Int; 2012 Jan 22; 81(1):94-9. PubMed ID: 21866090
    [Abstract] [Full Text] [Related]

  • 18. Reduced INF2 expression in nephrotic syndrome is possibly related to clinical severity of steroid resistance in children.
    Tamura H, Nakazato H, Kuraoka S, Yoneda K, Takahashi W, Endo F.
    Nephrology (Carlton); 2016 Jun 22; 21(6):467-75. PubMed ID: 26383224
    [Abstract] [Full Text] [Related]

  • 19. A novel mutation, outside of the candidate region for diagnosis, in the inverted formin 2 gene can cause focal segmental glomerulosclerosis.
    Sanchez-Ares M, Garcia-Vidal M, Antucho EE, Julio P, Eduardo VM, Lens XM, Garcia-Gonzalez MA.
    Kidney Int; 2013 Jan 22; 83(1):153-9. PubMed ID: 22971997
    [Abstract] [Full Text] [Related]

  • 20. Secondary Focal Segmental Glomerulosclerosis: From Podocyte Injury to Glomerulosclerosis.
    Kim JS, Han BG, Choi SO, Cha SK.
    Biomed Res Int; 2016 Jan 22; 2016():1630365. PubMed ID: 27088082
    [Abstract] [Full Text] [Related]

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