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Journal Abstract Search

205 related items for PubMed ID: 27882743

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  • 2. Two Korean infants with genetically confirmed congenital nephrotic syndrome of Finnish type.
    Lee BH, Ahn YH, Choi HJ, Kang HK, Kim SD, Cho BS, Moon KC, Ha IS, Cheong HI, Choi Y.
    J Korean Med Sci; 2009 Jan; 24 Suppl(Suppl 1):S210-4. PubMed ID: 19194555
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  • 3. Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approach.
    Gigante M, Monno F, Roberto R, Laforgia N, Assael MB, Livolti S, Caringella A, La Manna A, Masella L, Iolascon A.
    J Nephrol; 2002 Jan; 15(6):696-702. PubMed ID: 12495287
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  • 4. Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.
    Beltcheva O, Martin P, Lenkkeri U, Tryggvason K.
    Hum Mutat; 2001 May; 17(5):368-73. PubMed ID: 11317351
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  • 6. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome.
    Sako M, Nakanishi K, Obana M, Yata N, Hoshii S, Takahashi S, Wada N, Takahashi Y, Kaku Y, Satomura K, Ikeda M, Honda M, Iijima K, Yoshikawa N.
    Kidney Int; 2005 Apr; 67(4):1248-55. PubMed ID: 15780077
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  • 8. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.
    Heeringa SF, Vlangos CN, Chernin G, Hinkes B, Gbadegesin R, Liu J, Hoskins BE, Ozaltin F, Hildebrandt F, Members of the APN Study Group.
    Nephrol Dial Transplant; 2008 Nov; 23(11):3527-33. PubMed ID: 18503012
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  • 9. 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
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  • 11. [A Case of Congenital Nephrotic Syndrome of the Finnish Type].
    Zhou Y, Chen Q, Huang X, Yang LM, Chen J.
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2020 Nov 15; 51(6):881-884. PubMed ID: 33236617
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  • 12. Three Novel Heterozygous Mutations of NPHS1 Gene Causing Infants with Congenital Nephrotic Syndrome: Two Chinese (Han) Cases.
    Lv H, Liu F, Wang Q, Dong Z, Ren P, Zhang H, Yan X, Li L.
    Clin Lab; 2023 Aug 01; 69(8):. PubMed ID: 37560858
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