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Journal Abstract Search

156 related items for PubMed ID: 35304980

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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; 23(2):255-61. PubMed ID: 22876585
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  • 6. Effects of Denys-Drash syndrome point mutations on the DNA binding activity of the Wilms' tumor suppressor protein WT1.
    Borel F, Barilla KC, Hamilton TB, Iskandar M, Romaniuk PJ.
    Biochemistry; 1996 Sep 17; 35(37):12070-6. PubMed ID: 8810912
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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 17; 35(5):e23769. PubMed ID: 33942367
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  • 8. Prophylactic bilateral nephrectomy and preemptive kidney transplantation for Denys-Drash syndrome prior to development of kidney failure.
    Hosokawa C, Hotta K, Okamoto T, Cho Y, Hirose T, Iwahara N, Manabe A, Shinohara N.
    Pediatr Nephrol; 2024 Mar 17; 39(3):905-909. PubMed ID: 37572117
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  • 10. Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children.
    Yue Z, Pei Y, Sun L, Huang W, Huang H, Hu B, Yang J, Jiang X, Mo Y, Chen S, Lai KN, Wang Y.
    Ren Fail; 2011 Mar 17; 33(9):910-4. PubMed ID: 21851196
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  • 11. Focal Segmental Membranoproliferative Glomerulonephritis: A Histological Variant of Denys-Drash Syndrome.
    Karmila AB, Yap YC, Appadurai M, Oh L, Fazarina M, Abd Ghani F, Ariffin H.
    Fetal Pediatr Pathol; 2021 Apr 17; 40(2):113-120. PubMed ID: 31707902
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  • 13. [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 17; 50(11):855-8. PubMed ID: 23302619
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  • 14. 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 17; 20(1):103-6. PubMed ID: 18197048
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  • 16. A novel WT1 gene mutation in a patient with Wilms' tumor and 46, XY gonadal dysgenesis.
    Lee DG, Han DH, Park KH, Baek M.
    Eur J Pediatr; 2011 Aug 17; 170(8):1079-82. PubMed ID: 21384108
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  • 17. A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome.
    Little S, Hanks S, King-Underwood L, Picton S, Cullinane C, Rapley E, Rahman N, Pritchard-Jones K.
    Pediatr Nephrol; 2005 Jan 17; 20(1):81-5. PubMed ID: 15503171
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  • 18. 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 Jan 17; 30(4):266-72. PubMed ID: 21434831
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  • 19. [A case of Denys-Drash syndrome with prophylactic bilateral nephrectomy].
    Yamamoto K, Santo Y, Satomura K.
    Nihon Jinzo Gakkai Shi; 2003 Jan 17; 45(1):42-6. PubMed ID: 12680320
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