These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 32231453)

  • 1. A case of Type 1 Dent disease presenting with isolated persistent proteinuria.
    Güngör T; Eroğlu FK; Yazılıtaş F; Gür G; Çakıcı EK; Ludwig M; Bülbül M
    Turk Pediatri Ars; 2020; 55(1):72-75. PubMed ID: 32231453
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Clinical features and genetic variants of Dent disease in 10 children].
    Zhao SL; Zhao F; Sha YG; Chen QX; Cheng XQ; Huang SM
    Zhonghua Er Ke Za Zhi; 2018 Apr; 56(4):289-293. PubMed ID: 29614570
    [No Abstract]   [Full Text] [Related]  

  • 3. Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene.
    Drosataki E; Maragkou S; Dermitzaki K; Stavrakaki I; Lygerou D; Latsoudis H; Pleros C; Petrakis I; Zaganas I; Stylianou K
    BMC Nephrol; 2022 May; 23(1):182. PubMed ID: 35549682
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical features and genetic analysis of 15 Chinese children with dent disease.
    Li Q; Yang Z; Zang R; Liu S; Yu L; Wang J; Wang C; Wang X; Sun S
    Ren Fail; 2024 Dec; 46(1):2349133. PubMed ID: 38726999
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Nephrolithiasis, kidney failure and bone disorders in Dent disease patients with and without CLCN5 mutations.
    Anglani F; D'Angelo A; Bertizzolo LM; Tosetto E; Ceol M; Cremasco D; Bonfante L; Addis MA; Del Prete D;
    Springerplus; 2015; 4():492. PubMed ID: 26389017
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dent Disease Type 2 as a Cause of Focal Segmental Glomerulosclerosis in a 6-Year-Old Boy: A Case Report.
    Bezdíčka M; Langer J; Háček J; Zieg J
    Front Pediatr; 2020; 8():583230. PubMed ID: 33194915
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dent disease manifesting as nephrotic syndrome.
    Chen Q; Li Y; Wu X
    Intractable Rare Dis Res; 2023 Feb; 12(1):67-70. PubMed ID: 36873671
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The first Sri Lankan family with Dent disease-1 due to a pathogenic variant in the CLCN5 gene: a case report.
    Ranawaka R; Sirisena ND; Dayasiri KC; Cogal AG; Lieske JC; Gamage MP; Dissanayake VHW
    BMC Res Notes; 2017 Oct; 10(1):539. PubMed ID: 29084614
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expanding the phenotype of proteinuria in Dent disease. A case series.
    Cramer MT; Charlton JR; Fogo AB; Fathallah-Shaykh SA; Askenazi DJ; Guay-Woodford LM
    Pediatr Nephrol; 2014 Oct; 29(10):2051-4. PubMed ID: 24810952
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A Novel
    Bitsori M; Vergadi E; Galanakis E
    J Pediatr Genet; 2019 Dec; 8(4):235-239. PubMed ID: 31687264
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nephrotic-range Albuminuria as the presenting symptom of Dent-2 disease.
    De Mutiis C; Pasini A; La Scola C; Pugliese F; Montini G
    Ital J Pediatr; 2015 Jun; 41():46. PubMed ID: 26108450
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Next-Generation Sequencing in Early Diagnosis of Dent Disease 1: Two Case Reports.
    Wen M; Shen T; Wang Y; Li Y; Shi X; Dang X
    Front Med (Lausanne); 2018; 5():347. PubMed ID: 30581818
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Proteinuria in Dent disease: a review of the literature.
    van Berkel Y; Ludwig M; van Wijk JAE; Bökenkamp A
    Pediatr Nephrol; 2017 Oct; 32(10):1851-1859. PubMed ID: 27757584
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical manifestation and genetic findings in three boys with low molecular Weight Proteinuria - three case reports for exploring Dent Disease and Fanconi syndrome.
    Duan N; Huang C; Pang L; Jiang S; Yang W; Li H
    BMC Nephrol; 2021 Jan; 22(1):24. PubMed ID: 33430795
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel CLCN5 mutation in a boy with asymptomatic proteinuria and focal global glomerulosclerosis.
    Valina MR; Larsen CP; Kanosky S; Suchy SF; Nield LS; Onder AM
    Clin Nephrol; 2013 Nov; 80(5):377-84. PubMed ID: 22735364
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dent disease in Poland: what we have learned so far?
    Zaniew M; Mizerska-Wasiak M; Załuska-Leśniewska I; Adamczyk P; Kiliś-Pstrusińska K; Haliński A; Zawadzki J; Lipska-Ziętkiewicz BS; Pawlaczyk K; Sikora P; Ludwig M; Szczepańska M
    Int Urol Nephrol; 2017 Nov; 49(11):2005-2017. PubMed ID: 28815356
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of pre-mRNA Splicing Defects Caused by
    Mura-Escorche G; Perdomo-Ramírez A; Ramos-Trujillo E; Trujillo-Frías CJ; Claverie-Martín F;
    Biomedicines; 2023 Nov; 11(11):. PubMed ID: 38002082
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hypercalciuria in patients with CLCN5 mutations.
    Ludwig M; Utsch B; Balluch B; Fründ S; Kuwertz-Bröking E; Bökenkamp A
    Pediatr Nephrol; 2006 Sep; 21(9):1241-50. PubMed ID: 16807762
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dent disease: Same
    Zhang H; Wang F; Xiao H; Yao Y
    Intractable Rare Dis Res; 2017 May; 6(2):114-118. PubMed ID: 28580211
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.