BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 36800604)

  • 1. A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report.
    Xie D; Wu J; Zhang W; Jin T; Wu P; An B; Huang S
    Medicine (Baltimore); 2023 Feb; 102(7):e32970. PubMed ID: 36800604
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [NPHS1 mutations in a Chinese family with congenital nephrotic syndrome].
    Shi Y; Ding J; Liu JC; Wang H; Bu DF
    Zhonghua Er Ke Za Zhi; 2005 Nov; 43(11):805-9. PubMed ID: 16316524
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel NPHS1 splice site mutations in a Chinese child with congenital nephrotic syndrome.
    Fu R; Gou MF; Ma WH; He JJ; Luan Y; Liu J
    Genet Mol Res; 2015 Jan; 14(1):433-9. PubMed ID: 25729976
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 69(8):. PubMed ID: 37560858
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome.
    Li GM; Cao Q; Shen Q; Sun L; Zhai YH; Liu HM; An Y; Xu H
    BMC Nephrol; 2018 Dec; 19(1):382. PubMed ID: 30594156
    [TBL] [Abstract][Full Text] [Related]  

  • 6. NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
    Guaragna MS; Cleto TL; Souza ML; Lutaif AC; de Castro LC; Penido MG; Maciel-Guerra AT; Belangero VM; Guerra-Junior G; De Mello MP
    Nephrology (Carlton); 2016 Sep; 21(9):753-7. PubMed ID: 26560236
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation analysis of NPHS1 in a worldwide cohort of congenital nephrotic syndrome patients.
    Ovunc B; Ashraf S; Vega-Warner V; Bockenhauer D; Elshakhs NA; Joseph M; Hildebrandt F;
    Nephron Clin Pract; 2012; 120(3):c139-46. PubMed ID: 22584503
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in NPHS1 in a Chinese child with congenital nephrotic syndrome.
    Yu ZH; Wang DJ; Meng DC; Huang J; Nie XJ
    Genet Mol Res; 2012 May; 11(2):1460-4. PubMed ID: 22653594
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Congenital nephrotic syndrome with a novel NPHS1 mutation.
    Yoshizawa C; Kobayashi Y; Ikeuchi Y; Tashiro M; Kakegawa S; Watanabe T; Goto Y; Nakanishi K; Yoshikawa N; Arakawa H
    Pediatr Int; 2016 Nov; 58(11):1211-1215. PubMed ID: 27882743
    [TBL] [Abstract][Full Text] [Related]  

  • 10. NPHS1 gene mutation in Japanese patients with congenital nephrotic syndrome.
    Aya K; Shimizu J; Ohtomo Y; Satomura K; Suzuki H; Yan K; Sado Y; Morishima T; Tanaka H
    Nephrol Dial Transplant; 2009 Aug; 24(8):2411-4. PubMed ID: 19321760
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
    Schoeb DS; Chernin G; Heeringa SF; Matejas V; Held S; Vega-Warner V; Bockenhauer D; Vlangos CN; Moorani KN; Neuhaus TJ; Kari JA; MacDonald J; Saisawat P; Ashraf S; Ovunc B; Zenker M; Hildebrandt F;
    Nephrol Dial Transplant; 2010 Sep; 25(9):2970-6. PubMed ID: 20172850
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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;
    Nephrol Dial Transplant; 2008 Nov; 23(11):3527-33. PubMed ID: 18503012
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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; 51(6):881-884. PubMed ID: 33236617
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel mutation of congenital nephrotic syndrome in a Slovenian child eventually receiving a renal transplant.
    Golob V; Nosan G; Bertok S; Frelih M; Boštjanči E; Rus R
    Croat Med J; 2021 Apr; 62(2):187-191. PubMed ID: 33938658
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital nephrotic syndrome associated with 22q11.2 duplication syndrome in a Chinese family and functional analysis of the intronic NPHS1 c. 3286 + 5G > A mutation.
    Li L; Yi Z; Xi H; Ma L; Shao H; Wang W; Pan H; Li M; Jiang H
    Ital J Pediatr; 2019 Aug; 45(1):109. PubMed ID: 31443662
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital nephrotic syndrome of NPHS1 associated with cardiac malformation.
    Uysal B; Dönmez O; Uysal F; Akacı O; Vuruşkan BA; Berdeli A
    Pediatr Int; 2015; 57(1):177-9. PubMed ID: 25711261
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Simultaneous mutations of LAMB2 and NPHP1genes in a Chinese girl with isolated congenital nephrotic syndrome: a case report.
    Qiu L; Zhou J
    BMC Pediatr; 2016 Mar; 16():44. PubMed ID: 27004562
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cyclosporine A responsive congenital nephrotic syndrome with single heterozygous variants in NPHS1, NPHS2, and PLCE1.
    Eichinger A; Ponsel S; Bergmann C; Günthner R; Hoefele J; Amann K; Lange-Sperandio B
    Pediatr Nephrol; 2018 Jul; 33(7):1269-1272. PubMed ID: 29663071
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetics of congenital and infantile nephrotic syndrome.
    Sharief SN; Hefni NA; Alzahrani WA; Nazer II; Bayazeed MA; Alhasan KA; Safdar OY; El-Desoky SM; Kari JA
    World J Pediatr; 2019 Apr; 15(2):198-203. PubMed ID: 30721404
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.