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Journal Abstract Search

229 related items for PubMed ID: 27733133

  • 21. 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; 181():91-100. PubMed ID: 23689571
    [Abstract] [Full Text] [Related]

  • 22. NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis.
    Kerti A, Csohány R, Wagner L, Jávorszky E, Maka E, Tory K.
    Pediatr Nephrol; 2013 Oct; 28(10):2061-4. PubMed ID: 23800802
    [Abstract] [Full Text] [Related]

  • 23.
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  • 24. Increased risk of treatment failure and end-stage renal disease in familial focal segmental glomerular sclerosis.
    Hao X, Xie J, Ma J, Wang Z, Zhou Q, Yang L, Pan X, Ren H, Chen N.
    Contrib Nephrol; 2013 Oct; 181():101-8. PubMed ID: 23689572
    [Abstract] [Full Text] [Related]

  • 25. MCP1 2518 A/G polymorphism affects progression of childhood focal segmental glomerulosclerosis.
    Besbas N, Kalyoncu M, Cil O, Ozgul RK, Bakkaloglu A, Ozaltin F.
    Ren Fail; 2015 Oct; 37(9):1435-9. PubMed ID: 26335292
    [Abstract] [Full Text] [Related]

  • 26. Familial focal segmental glomerulosclerosis: mutation in inverted formin 2 mimicking Alport syndrome.
    Rood IM, Bongers EM, Lugtenberg D, Klein IH, Steenbergen EJ, Wetzels JF, Deegens JK.
    Neth J Med; 2016 Feb; 74(2):82-5. PubMed ID: 26951353
    [Abstract] [Full Text] [Related]

  • 27.
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  • 28. NPHS2 gene polymorphism aggravates renal damage caused by focal segmental glomerulosclerosis with COL4A3 mutation.
    Sun L, Zhang X, Wang Z.
    Biosci Rep; 2021 Jan 29; 41(1):. PubMed ID: 33305316
    [Abstract] [Full Text] [Related]

  • 29. C1q nephropathy: a variant of focal segmental glomerulosclerosis.
    Markowitz GS, Schwimmer JA, Stokes MB, Nasr S, Seigle RL, Valeri AM, D'Agati VD.
    Kidney Int; 2003 Oct 29; 64(4):1232-40. PubMed ID: 12969141
    [Abstract] [Full Text] [Related]

  • 30. Inverted formin 2-related Charcot-Marie-Tooth disease: extension of the mutational spectrum and pathological findings in Schwann cells and axons.
    Roos A, Weis J, Korinthenberg R, Fehrenbach H, Häusler M, Züchner S, Mache C, Hubmann H, Auer-Grumbach M, Senderek J.
    J Peripher Nerv Syst; 2015 Mar 29; 20(1):52-9. PubMed ID: 25676889
    [Abstract] [Full Text] [Related]

  • 31. Uptake of next-generation sequencing in children with end-stage renal disease secondary to focal segmental glomerulosclerosis and parental decision for kidney transplantation-Experience from a low resource setting: A Retrospective Cohort Study.
    Sinha R, Sarkar S, Mandal K, Tse Y.
    Pediatr Transplant; 2021 Aug 29; 25(5):e13960. PubMed ID: 33368894
    [Abstract] [Full Text] [Related]

  • 32. Idiopathic focal segmental glomerulosclerosis: a favourable prognosis in untreated patients?
    Deegens JK, Assmann KJ, Steenbergen EJ, Hilbrands LB, Gerlag PG, Jansen JL, Wetzels JF.
    Neth J Med; 2005 Nov 29; 63(10):393-8. PubMed ID: 16301760
    [Abstract] [Full Text] [Related]

  • 33. 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 29; 23(9):1192-9. PubMed ID: 25407002
    [Abstract] [Full Text] [Related]

  • 34. A novel truncating PAX2 mutation in a boy with renal coloboma syndrome with focal segmental glomerulosclerosis causing rapid progression to end-stage kidney disease.
    Saida K, Kamei K, Morisada N, Ogura M, Ogata K, Matsuoka K, Nozu K, Iijima K, Ito S.
    CEN Case Rep; 2020 Feb 29; 9(1):19-23. PubMed ID: 31538321
    [Abstract] [Full Text] [Related]

  • 35. Exome analysis resolves differential diagnosis of familial kidney disease and uncovers a potential confounding variant.
    Gibson J, Gilbert RD, Bunyan DJ, Angus EM, Fowler DJ, Ennis S.
    Genet Res (Camb); 2013 Dec 29; 95(6):165-73. PubMed ID: 24472419
    [Abstract] [Full Text] [Related]

  • 36. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 29; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 37. Cosegregation of focal segmental glomerulosclerosis in a family with familial partial lipodystrophy due to a mutation in LMNA.
    Thong KM, Xu Y, Cook J, Takou A, Wagner B, Kawar B, Ong AC.
    Nephron Clin Pract; 2013 Aug 29; 124(1-2):31-7. PubMed ID: 24080738
    [Abstract] [Full Text] [Related]

  • 38. Significance of genetic analysis in adult patients with inherited chronic kidney disease.
    Maity I, Barwad AW, Bhowmik D, Bagchi S.
    BMJ Case Rep; 2024 Mar 05; 17(3):. PubMed ID: 38442966
    [Abstract] [Full Text] [Related]

  • 39. A prospective study of collapsing focal segmental glomerulosclerosis.
    Raja R, Nada R, Yadav AK, Kumar A, Goyal A, Kumar V, Rathi M, Kohli HS, Gupta KL, Sakhuja V, Jha V.
    Ren Fail; 2016 Jul 05; 38(6):894-8. PubMed ID: 27266801
    [Abstract] [Full Text] [Related]

  • 40. A 19-year-old man with hypertension, proteinuria, and renal insufficiency.
    Broumand V, Paueksakon P, Lewis JB, Nadeau J, Fogo A.
    Am J Kidney Dis; 1999 Oct 05; 34(4):768-74. PubMed ID: 10516364
    [No Abstract] [Full Text] [Related]

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