536 related articles for article (PubMed ID: 20798957)
1. Genetics of congenital anomalies of the kidney and urinary tract.
Song R; Yosypiv IV
Pediatr Nephrol; 2011 Mar; 26(3):353-64. PubMed ID: 20798957
[TBL] [Abstract][Full Text] [Related]
2. Congenital anomalies of the kidney and urinary tract: an embryogenetic review.
dos Santos Junior AC; de Miranda DM; Simões e Silva AC
Birth Defects Res C Embryo Today; 2014 Dec; 102(4):374-81. PubMed ID: 25420794
[TBL] [Abstract][Full Text] [Related]
3. Disease mechanisms of monogenic congenital anomalies of the kidney and urinary tract American Journal of Medical Genetics Part C.
Connaughton DM; Hildebrandt F
Am J Med Genet C Semin Med Genet; 2022 Sep; 190(3):325-343. PubMed ID: 36208064
[TBL] [Abstract][Full Text] [Related]
4. Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.
Capone VP; Morello W; Taroni F; Montini G
Int J Mol Sci; 2017 Apr; 18(4):. PubMed ID: 28398236
[TBL] [Abstract][Full Text] [Related]
5. Congenital anomalies of the kidney and urinary tract (CAKUT) associated with Hirschsprung's disease: a systematic review.
Hofmann AD; Duess JW; Puri P
Pediatr Surg Int; 2014 Aug; 30(8):757-61. PubMed ID: 24974188
[TBL] [Abstract][Full Text] [Related]
6. [Genetics of congenital anomalies of the kidney and urinary tract].
Zwolińska D; Polak-Jonkisz D; Makulska I
Postepy Hig Med Dosw (Online); 2011 Dec; 65():829-37. PubMed ID: 22173447
[TBL] [Abstract][Full Text] [Related]
7. Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
van der Ven AT; Connaughton DM; Ityel H; Mann N; Nakayama M; Chen J; Vivante A; Hwang DY; Schulz J; Braun DA; Schmidt JM; Schapiro D; Schneider R; Warejko JK; Daga A; Majmundar AJ; Tan W; Jobst-Schwan T; Hermle T; Widmeier E; Ashraf S; Amar A; Hoogstraaten CA; Hugo H; Kitzler TM; Kause F; Kolvenbach CM; Dai R; Spaneas L; Amann K; Stein DR; Baum MA; Somers MJG; Rodig NM; Ferguson MA; Traum AZ; Daouk GH; Bogdanović R; Stajić N; Soliman NA; Kari JA; El Desoky S; Fathy HM; Milosevic D; Al-Saffar M; Awad HS; Eid LA; Selvin A; Senguttuvan P; Sanna-Cherchi S; Rehm HL; MacArthur DG; Lek M; Laricchia KM; Wilson MW; Mane SM; Lifton RP; Lee RS; Bauer SB; Lu W; Reutter HM; Tasic V; Shril S; Hildebrandt F
J Am Soc Nephrol; 2018 Sep; 29(9):2348-2361. PubMed ID: 30143558
[TBL] [Abstract][Full Text] [Related]
8. Anatomy and embryology of congenital surgical anomalies: Congenital Anomalies of the Kidney and Urinary Tract.
Costigan CS; Rosenblum ND
Semin Pediatr Surg; 2022 Dec; 31(6):151232. PubMed ID: 36423515
[TBL] [Abstract][Full Text] [Related]
9. Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract.
Kohl S; Chen J; Vivante A; Hwang DY; Shril S; Dworschak GC; Van Der Ven A; Sanna-Cherchi S; Bauer SB; Lee RS; Soliman NA; Kehinde EO; Reutter HM; Tasic V; Hildebrandt F
Nephrol Dial Transplant; 2016 Aug; 31(8):1280-3. PubMed ID: 26908769
[TBL] [Abstract][Full Text] [Related]
10. Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Connaughton DM; Dai R; Owen DJ; Marquez J; Mann N; Graham-Paquin AL; Nakayama M; Coyaud E; Laurent EMN; St-Germain JR; Blok LS; Vino A; Klämbt V; Deutsch K; Wu CW; Kolvenbach CM; Kause F; Ottlewski I; Schneider R; Kitzler TM; Majmundar AJ; Buerger F; Onuchic-Whitford AC; Youying M; Kolb A; Salmanullah D; Chen E; van der Ven AT; Rao J; Ityel H; Seltzsam S; Rieke JM; Chen J; Vivante A; Hwang DY; Kohl S; Dworschak GC; Hermle T; Alders M; Bartolomaeus T; Bauer SB; Baum MA; Brilstra EH; Challman TD; Zyskind J; Costin CE; Dipple KM; Duijkers FA; Ferguson M; Fitzpatrick DR; Fick R; Glass IA; Hulick PJ; Kline AD; Krey I; Kumar S; Lu W; Marco EJ; Wentzensen IM; Mefford HC; Platzer K; Povolotskaya IS; Savatt JM; Shcherbakova NV; Senguttuvan P; Squire AE; Stein DR; Thiffault I; Voinova VY; Somers MJG; Ferguson MA; Traum AZ; Daouk GH; Daga A; Rodig NM; Terhal PA; van Binsbergen E; Eid LA; Tasic V; Rasouly HM; Lim TY; Ahram DF; Gharavi AG; Reutter HM; Rehm HL; MacArthur DG; Lek M; Laricchia KM; Lifton RP; Xu H; Mane SM; Sanna-Cherchi S; Sharrocks AD; Raught B; Fisher SE; Bouchard M; Khokha MK; Shril S; Hildebrandt F
Am J Hum Genet; 2020 Oct; 107(4):727-742. PubMed ID: 32891193
[TBL] [Abstract][Full Text] [Related]
11. Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT).
Neirijnck Y; Reginensi A; Renkema KY; Massa F; Kozlov VM; Dhib H; Bongers EMHF; Feitz WF; van Eerde AM; Lefebvre V; Knoers NVAM; Tabatabaei M; Schulz H; McNeill H; Schaefer F; Wegner M; Sock E; Schedl A
Kidney Int; 2018 May; 93(5):1142-1153. PubMed ID: 29459093
[TBL] [Abstract][Full Text] [Related]
12. Maternal risk factors for congenital anomalies of the kidney and urinary tract: A case-control study.
Boato RT; Aguiar MB; Mak RH; Colosimo EA; Simões E Silva AC; Oliveira EA
J Pediatr Urol; 2023 Apr; 19(2):199.e1-199.e11. PubMed ID: 36535837
[TBL] [Abstract][Full Text] [Related]
13. Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience.
Riedhammer KM; Ćomić J; Tasic V; Putnik J; Abazi-Emini N; Paripovic A; Stajic N; Meitinger T; Nushi-Stavileci V; Berutti R; Braunisch MC; Hoefele J
Eur J Hum Genet; 2023 Jun; 31(6):674-680. PubMed ID: 36922632
[TBL] [Abstract][Full Text] [Related]
14. Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans.
Vivante A; Kohl S; Hwang DY; Dworschak GC; Hildebrandt F
Pediatr Nephrol; 2014 Apr; 29(4):695-704. PubMed ID: 24398540
[TBL] [Abstract][Full Text] [Related]
15. GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tract.
Du X; Wang C; Liu J; Yu M; Ju H; Xue S; Li Y; Liu J; Dai R; Chen J; Zhai Y; Rao J; Wang X; Sun Y; Sun L; Wu X; Xu H; Shen Q
Hum Genomics; 2024 Apr; 18(1):41. PubMed ID: 38654324
[TBL] [Abstract][Full Text] [Related]
16. Spectrum of congenital anomalies of the kidney and urinary tract (CAKUT) including renal parenchymal malformations during fetal life and the implementation of prenatal exome sequencing (WES).
Koenigbauer JT; Fangmann L; Reinhardt C; Weichert A; Henrich W; Saskia B; Gabriel HP
Arch Gynecol Obstet; 2024 Jun; 309(6):2613-2622. PubMed ID: 37535131
[TBL] [Abstract][Full Text] [Related]
17. Congenital anomalies of the kidney and urinary tract: defining risk factors of disease progression and determinants of outcomes.
Walawender L; Becknell B; Matsell DG
Pediatr Nephrol; 2023 Dec; 38(12):3963-3973. PubMed ID: 36867265
[TBL] [Abstract][Full Text] [Related]
18. Novel Insights into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary Tract.
van der Ven AT; Vivante A; Hildebrandt F
J Am Soc Nephrol; 2018 Jan; 29(1):36-50. PubMed ID: 29079659
[TBL] [Abstract][Full Text] [Related]
19. Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
Kohl S; Hwang DY; Dworschak GC; Hilger AC; Saisawat P; Vivante A; Stajic N; Bogdanovic R; Reutter HM; Kehinde EO; Tasic V; Hildebrandt F
J Am Soc Nephrol; 2014 Sep; 25(9):1917-22. PubMed ID: 24700879
[TBL] [Abstract][Full Text] [Related]
20. Ocular manifestations of congenital anomalies of the kidney and urinary tract (CAKUT).
Virth J; Mack HG; Colville D; Crockett E; Savige J
Pediatr Nephrol; 2024 Feb; 39(2):357-369. PubMed ID: 37468646
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]