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Journal Abstract Search

213 related items for PubMed ID: 26882358

  • 1. Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash Syndrome.
    Hillen LM, Kamsteeg EJ, Schoots J, Tiebosch AT, Speel EJ, Roemen GM, Peutz-Koostra CJ, Stumpel CT.
    Fetal Pediatr Pathol; 2016; 35(2):112-9. PubMed ID: 26882358
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  • 2. Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene.
    Furtado LV, Pysher T, Opitz J, Lamb R, Comstock J, Batish S, Mauch T, Nelson R, Zhou H.
    Fetal Pediatr Pathol; 2011; 30(4):266-72. PubMed ID: 21434831
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  • 3. Renal failure from birth-AKI or CKD? Answers.
    Carter S, Dixit A, Lunn A, Deorukhkar A, Christian M.
    Pediatr Nephrol; 2016 Dec; 31(12):2259-2262. PubMed ID: 26891727
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  • 4. Case report: WT1 exon 6 truncation mutation and ambiguous genitalia in a patient with Denys-Drash syndrome.
    Chiang PW, Aliaga S, Travers S, Spector E, Tsai AC.
    Curr Opin Pediatr; 2008 Feb; 20(1):103-6. PubMed ID: 18197048
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  • 5. A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndrome.
    Hakan N, Aydin M, Erdogan O, Cavusoglu YH, Aycan Z, Ozaltin F, Zenciroglu A, Apaydin S, Gunes R, Sahin G, Cinar G, Okumus N.
    Genet Couns; 2012 Feb; 23(2):255-61. PubMed ID: 22876585
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  • 6. Denys-Drash syndrome and congenital diaphragmatic hernia: another case with the 1097G > A(Arg366His) mutation.
    Antonius T, van Bon B, Eggink A, van der Burgt I, Noordam K, van Heijst A.
    Am J Med Genet A; 2008 Feb 15; 146A(4):496-9. PubMed ID: 18203154
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  • 7. A novel WT1 gene mutation in a chinese girl with denys-drash syndrome.
    Wang F, Cai J, Wang J, He M, Mao J, Zhu K, Zhao M, Guan Z, Li L, Jin H, Shu Q.
    J Clin Lab Anal; 2021 May 15; 35(5):e23769. PubMed ID: 33942367
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  • 12. [Clinical and pathological features of Denys-Drash syndrome: report of 3 cases].
    Wang HY, Sun LZ, Yue ZH, Yang J, Jiang XY, Mo Y.
    Zhonghua Er Ke Za Zhi; 2012 Nov 15; 50(11):855-8. PubMed ID: 23302619
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  • 13. Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect.
    Cho HY, Lee BS, Kang CH, Kim WH, Ha IS, Cheong HI, Choi Y.
    Pediatr Nephrol; 2006 Dec 15; 21(12):1909-12. PubMed ID: 16932893
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  • 15. Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome.
    Swiatecka-Urban A, Mokrzycki MH, Kaskel F, Da Silva F, Denamur E.
    Pediatr Nephrol; 2001 Aug 15; 16(8):627-30. PubMed ID: 11519891
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  • 16. A familial WT1 mutation associated with incomplete Denys-Drash syndrome.
    Zhu C, Zhao F, Zhang W, Wu H, Chen Y, Ding G, Zhang A, Huang S.
    Eur J Pediatr; 2013 Oct 15; 172(10):1357-62. PubMed ID: 23715653
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  • 20. WT1-related disorders: more than Denys-Drash syndrome.
    Lopez-Gonzalez M, Ariceta G.
    Pediatr Nephrol; 2024 Sep 15; 39(9):2601-2609. PubMed ID: 38326647
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