180 related articles for article (PubMed ID: 27174143)
1. Dent Disease in Chinese Children and Findings from Heterozygous Mothers: Phenotypic Heterogeneity, Fetal Growth, and 10 Novel Mutations.
Li F; Yue Z; Xu T; Chen M; Zhong L; Liu T; Jing X; Deng J; Hu B; Liu Y; Wang H; Lai KN; Sun L; Liu J; Maxwell PH; Wang Y
J Pediatr; 2016 Jul; 174():204-210.e1. PubMed ID: 27174143
[TBL] [Abstract][Full Text] [Related]
2. Japanese Dent disease has a wider clinical spectrum than Dent disease in Europe/USA: genetic and clinical studies of 86 unrelated patients with low-molecular-weight proteinuria.
Sekine T; Komoda F; Miura K; Takita J; Shimadzu M; Matsuyama T; Ashida A; Igarashi T
Nephrol Dial Transplant; 2014 Feb; 29(2):376-84. PubMed ID: 24081861
[TBL] [Abstract][Full Text] [Related]
3. Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease.
Ye Q; Shen Q; Rao J; Zhang A; Zheng B; Liu X; Shen Y; Chen Z; Wu Y; Hou L; Jian S; Wei M; Ma M; Sun S; Li Q; Dang X; Wang Y; Xu H; Mao J;
Clin Genet; 2020 Mar; 97(3):407-417. PubMed ID: 31674016
[TBL] [Abstract][Full Text] [Related]
4. A novel CLCN5 mutation in a Chinese boy with Dent's disease.
Ji LN; Chen CY; Wang JJ; Cao L
World J Pediatr; 2014 Aug; 10(3):275-7. PubMed ID: 25124980
[TBL] [Abstract][Full Text] [Related]
5. Dent's disease.
Devuyst O; Thakker RV
Orphanet J Rare Dis; 2010 Oct; 5():28. PubMed ID: 20946626
[TBL] [Abstract][Full Text] [Related]
6. Genetic Analysis of Dent's Disease and Functional Research of CLCN5 Mutations.
Zhang Y; Fang X; Xu H; Shen Q
DNA Cell Biol; 2017 Dec; 36(12):1151-1158. PubMed ID: 29058463
[TBL] [Abstract][Full Text] [Related]
7. [Clinical and genetic analysis of Dent disease in 4 Chinese children].
Jian S; Wei M; He YY; Wang W; Kang YL; Sun ZX
Zhongguo Dang Dai Er Ke Za Zhi; 2015 Dec; 17(12):1261-6. PubMed ID: 26695661
[TBL] [Abstract][Full Text] [Related]
8. Phenotype of Dent Disease in a Cohort of Indian Children.
Bhardwaj S; Thergaonkar R; Sinha A; Hari P; Hi C; Bagga A
Indian Pediatr; 2016 Nov; 53(11):977-982. PubMed ID: 27889724
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease.
Deng H; Zhang Y; Xiao H; Yao Y; Zhang H; Liu X; Su B; Guan N; Zhong X; Wang S; Ding J; Wang F
Mol Genet Genomic Med; 2020 Aug; 8(8):e1306. PubMed ID: 32495484
[TBL] [Abstract][Full Text] [Related]
11. Genetics and phenotypic heterogeneity of Dent disease: the dark side of the moon.
Gianesello L; Del Prete D; Anglani F; Calò LA
Hum Genet; 2021 Mar; 140(3):401-421. PubMed ID: 32860533
[TBL] [Abstract][Full Text] [Related]
12. Renal manifestations of Dent disease and Lowe syndrome.
Cho HY; Lee BH; Choi HJ; Ha IS; Choi Y; Cheong HI
Pediatr Nephrol; 2008 Feb; 23(2):243-9. PubMed ID: 18038239
[TBL] [Abstract][Full Text] [Related]
13. OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variability.
Shrimpton AE; Hoopes RR; Knohl SJ; Hueber P; Reed AA; Christie PT; Igarashi T; Lee P; Lehman A; White C; Milford DV; Sanchez MR; Unwin R; Wrong OM; Thakker RV; Scheinman SJ
Nephron Physiol; 2009; 112(2):p27-36. PubMed ID: 19390221
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A Study on the CLCN5 Gene in Iranian Patients: A Report of Novel and Recurrent Mutations.
Mollataheri A; Mojbafan M; Hosseini R; Houman N; Mousavi M; Otoukesh H
Nephron; 2023; 147(8):470-477. PubMed ID: 36646056
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Novel OCRL1 mutations in patients with the phenotype of Dent disease.
Utsch B; Bökenkamp A; Benz MR; Besbas N; Dötsch J; Franke I; Fründ S; Gok F; Hoppe B; Karle S; Kuwertz-Bröking E; Laube G; Neb M; Nuutinen M; Ozaltin F; Rascher W; Ring T; Tasic V; van Wijk JA; Ludwig M
Am J Kidney Dis; 2006 Dec; 48(6):942.e1-14. PubMed ID: 17162149
[TBL] [Abstract][Full Text] [Related]
18. Update on Dent Disease.
Ehlayel AM; Copelovitch L
Pediatr Clin North Am; 2019 Feb; 66(1):169-178. PubMed ID: 30454742
[TBL] [Abstract][Full Text] [Related]
19. Dent's disease: clinical features and molecular basis.
Claverie-Martín F; Ramos-Trujillo E; García-Nieto V
Pediatr Nephrol; 2011 May; 26(5):693-704. PubMed ID: 20936522
[TBL] [Abstract][Full Text] [Related]
20. [Clinical and genetic analysis of Dent' s disease in 6 Chinese children with low molecular weight proteinuria].
Zhu BZ; Li P; Huang JP
Zhonghua Er Ke Za Zhi; 2010 May; 48(5):329-33. PubMed ID: 20654030
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]