263 related articles for article (PubMed ID: 32188635)
1. A Primer on Congenital Anomalies of the Kidneys and Urinary Tracts (CAKUT).
Murugapoopathy V; Gupta IR
Clin J Am Soc Nephrol; 2020 May; 15(5):723-731. PubMed ID: 32188635
[TBL] [Abstract][Full Text] [Related]
2. Congenital Anomalies of the Kidney and Urinary Tract in Children Born Small for Gestational Age.
Janchevska A; Gucev Z; Tasevska-Rmus L; Tasic V
Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2017 Mar; 38(1):53-57. PubMed ID: 28593895
[TBL] [Abstract][Full Text] [Related]
3. Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).
Ristoska-Bojkovska N
Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2017 Mar; 38(1):59-62. PubMed ID: 28593883
[TBL] [Abstract][Full Text] [Related]
4. Clinical Integration of Genome Diagnostics for Congenital Anomalies of the Kidney and Urinary Tract.
Westland R; Renkema KY; Knoers NVAM
Clin J Am Soc Nephrol; 2020 Dec; 16(1):128-137. PubMed ID: 32312792
[TBL] [Abstract][Full Text] [Related]
5. Association between the clinical presentation of congenital anomalies of the kidney and urinary tract (CAKUT) and gene mutations: an analysis of 66 patients at a single institution.
Ishiwa S; Sato M; Morisada N; Nishi K; Kanamori T; Okutsu M; Ogura M; Sako M; Kosuga M; Kamei K; Ito S; Nozu K; Iijima K; Ishikura K
Pediatr Nephrol; 2019 Aug; 34(8):1457-1464. PubMed ID: 30937553
[TBL] [Abstract][Full Text] [Related]
6. The genetics and pathogenesis of CAKUT.
Kolvenbach CM; Shril S; Hildebrandt F
Nat Rev Nephrol; 2023 Nov; 19(11):709-720. PubMed ID: 37524861
[TBL] [Abstract][Full Text] [Related]
7.
Le Tanno P; Breton J; Bidart M; Satre V; Harbuz R; Ray PF; Bosson C; Dieterich K; Jaillard S; Odent S; Poke G; Beddow R; Digilio MC; Novelli A; Bernardini L; Pisanti MA; Mackenroth L; Hackmann K; Vogel I; Christensen R; Fokstuen S; Béna F; Amblard F; Devillard F; Vieville G; Apostolou A; Jouk PS; Guebre-Egziabher F; Sartelet H; Coutton C
J Med Genet; 2017 Jul; 54(7):502-510. PubMed ID: 28270404
[TBL] [Abstract][Full Text] [Related]
8. Pattern of clinical presentation of congenital anomalies of the kidney and urinary tract among infants and children.
Soliman NA; Ali RI; Ghobrial EE; Habib EI; Ziada AM
Nephrology (Carlton); 2015 Jun; 20(6):413-8. PubMed ID: 25645028
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Congenital Anomalies of the Kidneys and Urinary Tract.
Stein D; McNamara E
Clin Perinatol; 2022 Sep; 49(3):791-798. PubMed ID: 36113935
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract.
Saygili S; Atayar E; Canpolat N; Elicevik M; Kurugoglu S; Sever L; Caliskan S; Ozaltin F
Clin Genet; 2020 Oct; 98(4):390-395. PubMed ID: 32666543
[TBL] [Abstract][Full Text] [Related]
13. SIX1 gene: absence of mutations in children with isolated congenital anomalies of kidney and urinary tract.
Negrisolo S; Centi S; Benetti E; Ghirardo G; Della Vella M; Murer L; Artifoni L
J Nephrol; 2014 Dec; 27(6):667-71. PubMed ID: 24899122
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Whole genome sequencing and novel candidate genes for CAKUT and altered nephrogenesis in the HSRA rat.
Showmaker KC; Cobb MB; Johnson AC; Yang W; Garrett MR
Physiol Genomics; 2020 Jan; 52(1):56-70. PubMed ID: 31841396
[TBL] [Abstract][Full Text] [Related]
16. Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT).
Kosfeld A; Kreuzer M; Daniel C; Brand F; Schäfer AK; Chadt A; Weiss AC; Riehmer V; Jeanpierre C; Klintschar M; Bräsen JH; Amann K; Pape L; Kispert A; Al-Hasani H; Haffner D; Weber RG
Hum Genet; 2016 Jan; 135(1):69-87. PubMed ID: 26572137
[TBL] [Abstract][Full Text] [Related]
17. Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract.
Dong S; Wang C; Li X; Shen Q; Fu X; Wu M; Song C; Yang N; Wu Y; Wang H; Jin L; Xu H; Zhang F
Mol Genet Genomics; 2019 Apr; 294(2):493-500. PubMed ID: 30604070
[TBL] [Abstract][Full Text] [Related]
18. The genetic basis of congenital anomalies of the kidney and urinary tract.
Kagan M; Pleniceanu O; Vivante A
Pediatr Nephrol; 2022 Oct; 37(10):2231-2243. PubMed ID: 35122119
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract.
Zheng B; Wang C; Seltzsam S; Schneider S; Schierbaum L; Wu W; Dai R; Connaughton DM; Nakayama M; Mann N; Bauer SB; Awad HS; Eid LA; Tasic V; Shril S; Hildebrandt F
Am J Med Genet A; 2022 Jan; 188(1):310-313. PubMed ID: 34525250
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
