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Journal Abstract Search

201 related items for PubMed ID: 31754646

  • 21. APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses.
    Watanabe A, Guaragna MS, Belangero VMS, Casimiro FMS, Pesquero JB, de Santis Feltran L, Palma LMP, Varela P, de Menezes Neves PDM, Lerario AM, de Souza ML, de Mello MP, de Brito Lutaif ACG, Ferrari CR, Sampson MG, Onuchic LF, Nogueira PCK.
    Pediatr Nephrol; 2021 Aug; 36(8):2327-2336. PubMed ID: 33585978
    [Abstract] [Full Text] [Related]

  • 22. The p.R229Q variant of the NPHS2 (podocin) gene in focal segmental glomerulosclerosis and steroid-resistant nephrotic syndrome: a meta-analysis.
    Lu L, Wan H, Yin Y, Feng WJ, Wang M, Zou YC, Huang B, Wang DT, Shi Y, Zhao Y, Wei LB.
    Int Urol Nephrol; 2014 Jul; 46(7):1383-93. PubMed ID: 24715228
    [Abstract] [Full Text] [Related]

  • 23. 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; 297(3):689-698. PubMed ID: 35278126
    [Abstract] [Full Text] [Related]

  • 24. 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; 66(2):571-9. PubMed ID: 15253708
    [Abstract] [Full Text] [Related]

  • 25. NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.
    Berdeli A, Mir S, Yavascan O, Serdaroglu E, Bak M, Aksu N, Oner A, Anarat A, Donmez O, Yildiz N, Sever L, Tabel Y, Dusunsel R, Sonmez F, Cakar N.
    Pediatr Nephrol; 2007 Dec; 22(12):2031-40. PubMed ID: 17899208
    [Abstract] [Full Text] [Related]

  • 26. 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; 19(11):1285-9. PubMed ID: 15322893
    [Abstract] [Full Text] [Related]

  • 27. Advances in molecular diagnosis and therapeutics in nephrotic syndrome and focal and segmental glomerulosclerosis.
    Sharif B, Barua M.
    Curr Opin Nephrol Hypertens; 2018 May; 27(3):194-200. PubMed ID: 29465426
    [Abstract] [Full Text] [Related]

  • 28. TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.
    Gigante M, Caridi G, Montemurno E, Soccio M, d'Apolito M, Cerullo G, Aucella F, Schirinzi A, Emma F, Massella L, Messina G, De Palo T, Ranieri E, Ghiggeri GM, Gesualdo L.
    Clin J Am Soc Nephrol; 2011 Jul; 6(7):1626-34. PubMed ID: 21734084
    [Abstract] [Full Text] [Related]

  • 29. [A novel mutation of NPHS2 identified in a Chinese family with steroid-resistant nephrotic syndrome].
    Yu ZH, Ding J, Guan N, Shi Y, Zhang JJ, Huang JP, Yao Y, Yang JY.
    Zhonghua Er Ke Za Zhi; 2004 Feb; 42(2):108-12. PubMed ID: 15059485
    [Abstract] [Full Text] [Related]

  • 30. 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; 14(2):89-93. PubMed ID: 24856380
    [Abstract] [Full Text] [Related]

  • 31. [Mutations in NPHS2 in familial steroid-resistant nephrotic syndrome in Southern Chinese Han ethnic group].
    Fu R, Chen XM, Wang QH, Chen SP, Yu ZH, Ye LY, Ren RN, Huang J, Wang CF.
    Zhonghua Er Ke Za Zhi; 2008 Aug; 46(8):591-6. PubMed ID: 19099831
    [Abstract] [Full Text] [Related]

  • 32. Glomerular Transcriptome Profiles in Focal Glomerulosclerosis: New Genes and Pathways for Steroid Resistance.
    Tong J, Jin Y, Weng Q, Yu S, Jafar Hussain HM, Ren H, Xu J, Zhang W, Li X, Wang W, Xie J, Chen N.
    Am J Nephrol; 2020 Aug; 51(6):442-452. PubMed ID: 32348995
    [Abstract] [Full Text] [Related]

  • 33. Mutational spectrum and novel candidate genes in Chinese children with sporadic steroid-resistant nephrotic syndrome.
    Li J, Wang L, Wan L, Lin T, Zhao W, Cui H, Li H, Cao L, Wu J, Zhang T.
    Pediatr Res; 2019 May; 85(6):816-821. PubMed ID: 30712057
    [Abstract] [Full Text] [Related]

  • 34. Shared genetic risk across different presentations of gene test-negative idiopathic nephrotic syndrome.
    Downie ML, Gupta S, Chan MMY, Sadeghi-Alavijeh O, Cao J, Parekh RS, Diz CB, Bierzynska A, Levine AP, Pepper RJ, Stanescu H, Saleem MA, Kleta R, Bockenhauer D, Koziell AB, Gale DP.
    Pediatr Nephrol; 2023 Jun; 38(6):1793-1800. PubMed ID: 36357634
    [Abstract] [Full Text] [Related]

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

  • 36. A novel mutation in NPHS2 gene identified in a Chinese pedigree with autosomal recessive steroid-resistant nephrotic syndrome.
    Sun H, Zhou W, Wang J, Yin L, Lu Y, Fu Q.
    Pathology; 2009 Oct; 41(7):661-5. PubMed ID: 20001346
    [Abstract] [Full Text] [Related]

  • 37. Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis.
    Laurin LP, Lu M, Mottl AK, Blyth ER, Poulton CJ, Weck KE.
    Nephrol Dial Transplant; 2014 Nov; 29(11):2062-9. PubMed ID: 24500309
    [Abstract] [Full Text] [Related]

  • 38. The genetic basis of FSGS and steroid-resistant nephrosis.
    Pollak MR.
    Semin Nephrol; 2003 Mar; 23(2):141-6. PubMed ID: 12704574
    [Abstract] [Full Text] [Related]

  • 39. 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 Mar; 13(1):59-66. PubMed ID: 16572591
    [Abstract] [Full Text] [Related]

  • 40. 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; 13(7):1946-52. PubMed ID: 12089392
    [Abstract] [Full Text] [Related]

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