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239 related items for PubMed ID: 23886564

  • 1. A patient with nephrotic-range proteinuria and focal global glomerulosclerosis.
    Fervenza FC.
    Clin J Am Soc Nephrol; 2013 Nov; 8(11):1979-87. PubMed ID: 23886564
    [Abstract] [Full Text] [Related]

  • 2. [Clinical features and genetic variants of Dent disease in 10 children].
    Zhao SL, Zhao F, Sha YG, Chen QX, Cheng XQ, Huang SM.
    Zhonghua Er Ke Za Zhi; 2018 Apr 02; 56(4):289-293. PubMed ID: 29614570
    [Abstract] [Full Text] [Related]

  • 3. A boy with proteinuria and focal global glomerulosclerosis: Question and Answers.
    Sethi SK, Otto EA, Ma S, Duggal R, Vega-Warner V, Kher V.
    Pediatr Nephrol; 2015 Nov 02; 30(11):1945-9. PubMed ID: 25245502
    [No Abstract] [Full Text] [Related]

  • 4. Expanding the phenotype of proteinuria in Dent disease. A case series.
    Cramer MT, Charlton JR, Fogo AB, Fathallah-Shaykh SA, Askenazi DJ, Guay-Woodford LM.
    Pediatr Nephrol; 2014 Oct 02; 29(10):2051-4. PubMed ID: 24810952
    [Abstract] [Full Text] [Related]

  • 5. Dent disease in Poland: what we have learned so far?
    Zaniew M, Mizerska-Wasiak M, Załuska-Leśniewska I, Adamczyk P, Kiliś-Pstrusińska K, Haliński A, Zawadzki J, Lipska-Ziętkiewicz BS, Pawlaczyk K, Sikora P, Ludwig M, Szczepańska M.
    Int Urol Nephrol; 2017 Nov 02; 49(11):2005-2017. PubMed ID: 28815356
    [Abstract] [Full Text] [Related]

  • 6. Does Dent disease remain an underrecognized cause for young boys with focal glomerulosclerosis?
    Kubo K, Aizawa T, Watanabe S, Tsugawa K, Tsuruga K, Ito E, Joh K, Tanaka H.
    Pediatr Int; 2016 Aug 02; 58(8):747-9. PubMed ID: 27324082
    [Abstract] [Full Text] [Related]

  • 7. Proteinuria in Dent disease: a review of the literature.
    van Berkel Y, Ludwig M, van Wijk JAE, Bökenkamp A.
    Pediatr Nephrol; 2017 Oct 02; 32(10):1851-1859. PubMed ID: 27757584
    [Abstract] [Full Text] [Related]

  • 8. Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene.
    Drosataki E, Maragkou S, Dermitzaki K, Stavrakaki I, Lygerou D, Latsoudis H, Pleros C, Petrakis I, Zaganas I, Stylianou K.
    BMC Nephrol; 2022 May 12; 23(1):182. PubMed ID: 35549682
    [Abstract] [Full Text] [Related]

  • 9. Clinical features and genetic analysis of 15 Chinese children with dent disease.
    Li Q, Yang Z, Zang R, Liu S, Yu L, Wang J, Wang C, Wang X, Sun S.
    Ren Fail; 2024 Dec 12; 46(1):2349133. PubMed ID: 38726999
    [Abstract] [Full Text] [Related]

  • 10. Nephrotic-range proteinuria in the obese patient.
    Lim AK.
    Med J Aust; 2006 Oct 02; 185(7):405-6. PubMed ID: 17014414
    [No Abstract] [Full Text] [Related]

  • 11. Primary focal segmental glomerulosclerosis in nephrotic patients: common complications and risk factors.
    Zhang Q, Zeng C, Cheng Z, Xie K, Zhang J, Liu Z.
    J Nephrol; 2012 Oct 02; 25(5):679-88. PubMed ID: 22009935
    [Abstract] [Full Text] [Related]

  • 12. [Clinical characteristics and molecular genetics of Dent's disease: an update].
    Zhang J, Xia ZK.
    Zhonghua Er Ke Za Zhi; 2012 Dec 02; 50(12):909-12. PubMed ID: 23324147
    [No Abstract] [Full Text] [Related]

  • 13. [Clinical and genetic analysis of Dent' s disease in 6 Chinese children with low molecular weight proteinuria].
    Zhu BZ, Li P, Huang JP.
    Zhonghua Er Ke Za Zhi; 2010 May 02; 48(5):329-33. PubMed ID: 20654030
    [Abstract] [Full Text] [Related]

  • 14. Absence of hypoalbuminemia despite massive proteinuria in focal segmental glomerulosclerosis secondary to hyperfiltration.
    Praga M, Morales E, Herrero JC, Pérez Campos A, Domínguez-Gil B, Alegre R, Vara J, Martínez MA.
    Am J Kidney Dis; 1999 Jan 02; 33(1):52-8. PubMed ID: 9915267
    [Abstract] [Full Text] [Related]

  • 15. A novel CLCN5 mutation in a boy with asymptomatic proteinuria and focal global glomerulosclerosis.
    Valina MR, Larsen CP, Kanosky S, Suchy SF, Nield LS, Onder AM.
    Clin Nephrol; 2013 Nov 02; 80(5):377-84. PubMed ID: 22735364
    [Abstract] [Full Text] [Related]

  • 16. A big boy with proteinuria. Focal and segmental glomerulosclerosis.
    Quinlan C, Dorman T, Gill D.
    Pediatr Nephrol; 2008 Dec 02; 23(12):2175-8. PubMed ID: 18704510
    [No Abstract] [Full Text] [Related]

  • 17. Galactose therapy reduces proteinuria in patients with recurrent focal segmental glomerulosclerosis after kidney transplantation.
    Robson K, Hill P, Langsford D, Dwyer K, Goodman D, Langham R.
    Nephrology (Carlton); 2015 Mar 02; 20 Suppl 1():13-6. PubMed ID: 25807852
    [Abstract] [Full Text] [Related]

  • 18. Japanese Dent disease has a wider clinical spectrum than Dent disease in Europe/USA: genetic and clinical studies of 86 unrelated patients with low-molecular-weight proteinuria.
    Sekine T, Komoda F, Miura K, Takita J, Shimadzu M, Matsuyama T, Ashida A, Igarashi T.
    Nephrol Dial Transplant; 2014 Feb 02; 29(2):376-84. PubMed ID: 24081861
    [Abstract] [Full Text] [Related]

  • 19. Clinical features and long-term outcome of obesity-associated focal segmental glomerulosclerosis.
    Praga M, Hernández E, Morales E, Campos AP, Valero MA, Martínez MA, León M.
    Nephrol Dial Transplant; 2001 Sep 02; 16(9):1790-8. PubMed ID: 11522860
    [Abstract] [Full Text] [Related]

  • 20. Meclofenamate treatment of recurrent idiopathic nephrotic syndrome with focal segmental glomerulosclerosis after renal transplantation.
    Torres VE, Velosa JA, Holley KE, Frohnert PP, Zincke H, Sterioff S.
    Mayo Clin Proc; 1984 Mar 02; 59(3):146-52. PubMed ID: 6369011
    [Abstract] [Full Text] [Related]

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