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Journal Abstract Search

282 related items for PubMed ID: 24969201

  • 21. 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; 41(6):1314-21. PubMed ID: 12776285
    [Abstract] [Full Text] [Related]

  • 22. NPHS2 mutation analysis and primary nephrotic syndrome in southern Indians.
    Jaffer A, Unnisa W, Raju DS, Jahan P.
    Nephrology (Carlton); 2014 Jul; 19(7):398-403. PubMed ID: 24674236
    [Abstract] [Full Text] [Related]

  • 23. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.
    Trautmann A, Bodria M, Ozaltin F, Gheisari A, Melk A, Azocar M, Anarat A, Caliskan S, Emma F, Gellermann J, Oh J, Baskin E, Ksiazek J, Remuzzi G, Erdogan O, Akman S, Dusek J, Davitaia T, Özkaya O, Papachristou F, Firszt-Adamczyk A, Urasinski T, Testa S, Krmar RT, Hyla-Klekot L, Pasini A, Özcakar ZB, Sallay P, Cakar N, Galanti M, Terzic J, Aoun B, Caldas Afonso A, Szymanik-Grzelak H, Lipska BS, Schnaidt S, Schaefer F, PodoNet Consortium.
    Clin J Am Soc Nephrol; 2015 Apr 07; 10(4):592-600. PubMed ID: 25635037
    [Abstract] [Full Text] [Related]

  • 24. Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
    Chernin G, Heeringa SF, Gbadegesin R, Liu J, Hinkes BG, Vlangos CN, Vega-Warner V, Hildebrandt F.
    Pediatr Nephrol; 2008 Sep 07; 23(9):1455-60. PubMed ID: 18543005
    [Abstract] [Full Text] [Related]

  • 25. A novel mutation of NPHS2 identified in a Chinese family.
    Yu Z, Ding J, Guan N, Shi Y, Zhang J, Huang J, Yao Y, Yang J.
    Pediatr Nephrol; 2004 Nov 07; 19(11):1285-9. PubMed ID: 15322893
    [Abstract] [Full Text] [Related]

  • 26. 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 07; 28(10):2061-4. PubMed ID: 23800802
    [Abstract] [Full Text] [Related]

  • 27. Genetic basis of nephrotic syndrome--review.
    Obeidová H, Merta M, Reiterová J, Maixnerová D, Stekrová J, Rysavá R, Tesar V.
    Prague Med Rep; 2006 Oct 07; 107(1):5-16. PubMed ID: 16752799
    [Abstract] [Full Text] [Related]

  • 28. NPHS2 variation in Chinese southern infants with late steroid-resistant nephrotic syndrome.
    Dai Y, Yang H, Gao P, Liu WD.
    Ren Fail; 2014 Oct 07; 36(9):1395-8. PubMed ID: 25112471
    [Abstract] [Full Text] [Related]

  • 29. TRPC6 and NPHS2 gene variants in adult patients with steroid-resistant nephrotic syndrome in North-West of Iran.
    Zununi Vahed S, Moghaddas Sani H, Haghi M, Mohajel Shoja M, Ardalan M.
    Mol Biol Rep; 2019 Dec 07; 46(6):6339-6344. PubMed ID: 31529341
    [Abstract] [Full Text] [Related]

  • 30. Novel NPHS2 variant in patients with familial steroid-resistant nephrotic syndrome with early onset, slow progression and dominant inheritance pattern.
    Suvanto M, Patrakka J, Jahnukainen T, Sjöström PM, Nuutinen M, Arikoski P, Kataja J, Kestilä M, Jalanko H.
    Clin Exp Nephrol; 2017 Aug 07; 21(4):677-684. PubMed ID: 27573339
    [Abstract] [Full Text] [Related]

  • 31. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
    Weber S, Gribouval O, Esquivel EL, Morinière V, Tête MJ, Legendre C, Niaudet P, Antignac C.
    Kidney Int; 2004 Aug 07; 66(2):571-9. PubMed ID: 15253708
    [Abstract] [Full Text] [Related]

  • 32. Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome.
    Oleggini R, Bertelli R, Di Donato A, Di Duca M, Caridi G, Sanna-Cherchi S, Scolari F, Murer L, Allegri L, Coppo R, Emma F, Camussi G, Perfumo F, Ghiggeri GM.
    Gene Expr; 2006 Aug 07; 13(1):59-66. PubMed ID: 16572591
    [Abstract] [Full Text] [Related]

  • 33. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review.
    Franceschini N, North KE, Kopp JB, McKenzie L, Winkler C.
    Genet Med; 2006 Feb 07; 8(2):63-75. PubMed ID: 16481888
    [Abstract] [Full Text] [Related]

  • 34. WT-1 and NPHS2 mutation analysis in patients with non-familial steroid-resistant focal-segmental glomerulosclerosis.
    Löwik MM, Levtchenko EN, Monnens LA, van den Heuvel LP.
    Clin Nephrol; 2003 Feb 07; 59(2):143-6. PubMed ID: 12608558
    [Abstract] [Full Text] [Related]

  • 35. Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management.
    Bierzynska A, McCarthy HJ, Soderquest K, Sen ES, Colby E, Ding WY, Nabhan MM, Kerecuk L, Hegde S, Hughes D, Marks S, Feather S, Jones C, Webb NJ, Ognjanovic M, Christian M, Gilbert RD, Sinha MD, Lord GM, Simpson M, Koziell AB, Welsh GI, Saleem MA.
    Kidney Int; 2017 Apr 07; 91(4):937-947. PubMed ID: 28117080
    [Abstract] [Full Text] [Related]

  • 36. Clinical features and mutational survey of NPHS2 (podocin) in Japanese children with focal segmental glomerulosclerosis who underwent renal transplantation.
    Furue T, Hattori M, Tsukaguchi H, Kitamura A, Oomori T, Ogino D, Nakakura H, Ashida A, Miura K, Hisano M, Takahashi K, Chikamoto H, Akioka Y, Sakano T.
    Pediatr Transplant; 2008 May 07; 12(3):341-6. PubMed ID: 18208440
    [Abstract] [Full Text] [Related]

  • 37. Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome.
    Carraro M, Caridi G, Bruschi M, Artero M, Bertelli R, Zennaro C, Musante L, Candiano G, Perfumo F, Ghiggeri GM.
    J Am Soc Nephrol; 2002 Jul 07; 13(7):1946-52. PubMed ID: 12089392
    [Abstract] [Full Text] [Related]

  • 38. 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 Jul 07; 99(2):c31-6. PubMed ID: 15627790
    [Abstract] [Full Text] [Related]

  • 39. Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.
    Koziell A, Grech V, Hussain S, Lee G, Lenkkeri U, Tryggvason K, Scambler P.
    Hum Mol Genet; 2002 Feb 15; 11(4):379-88. PubMed ID: 11854170
    [Abstract] [Full Text] [Related]

  • 40. Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect.
    Thomas MM, Ahmed HM, El-Dessouky SH, Ramadan A, Botrous OE, Abdel-Hamid MS.
    Mol Genet Genomics; 2022 May 15; 297(3):689-698. PubMed ID: 35278126
    [Abstract] [Full Text] [Related]

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