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Items: 1 to 20 of 140

1.

Study of the association between the BMP4 gene and congenital anomalies of the kidney and urinary tract.

Reis GS, Simões E Silva AC, Freitas IS, Heilbuth TR, Marco LA, Oliveira EA, Miranda DM.

J Pediatr (Rio J). 2014 Jan-Feb;90(1):58-64. doi: 10.1016/j.jped.2013.06.004. Epub 2013 Oct 13.

2.

PAX2 polymorphisms and congenital abnormalities of the kidney and urinary tract in a Brazilian pediatric population: evidence for a role in vesicoureteral reflux.

de Miranda DM, Dos Santos Júnior AC, Dos Reis GS, Freitas IS, Carvalho TG, de Marco LA, Oliveira EA, Simões E Silva AC.

Mol Diagn Ther. 2014 Aug;18(4):451-7. doi: 10.1007/s40291-014-0096-1.

PMID:
24633556
3.

Association of angiotensin type 2 receptor gene polymorphisms with ureteropelvic junction obstruction in Brazilian patients.

Miranda DM, Dos Santos AC Jr, Sarubi HC, Bastos-Rodrigues L, Rosa DV, Freitas IS, De Marco LA, Oliveira EA, Simões e Silva AC.

Nephrology (Carlton). 2014 Nov;19(11):714-20. doi: 10.1111/nep.12308.

PMID:
24995698
4.

Screening for mutations in BMP4 and FOXC1 genes in congenital anomalies of the kidney and urinary tract in humans.

Nakano T, Niimura F, Hohenfellner K, Miyakita E, Ichikawa I.

Tokai J Exp Clin Med. 2003 Oct;28(3):121-6.

PMID:
15055404
5.

Hirschsprung disease and congenital anomalies of the kidney and urinary tract (CAKUT): a novel syndromic association.

Pini Prato A, Musso M, Ceccherini I, Mattioli G, Giunta C, Ghiggeri GM, Jasonni V.

Medicine (Baltimore). 2009 Mar;88(2):83-90. doi: 10.1097/MD.0b013e31819cf5da.

6.

High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT.

Bulum B, Ozçakar ZB, Ustüner E, Düşünceli E, Kavaz A, Duman D, Walz K, Fitoz S, Tekin M, Yalçınkaya F.

Pediatr Nephrol. 2013 Nov;28(11):2143-7. doi: 10.1007/s00467-013-2530-8. Epub 2013 Jun 28.

PMID:
23812353
7.

Assessing urinary tract defects in mice: methods to detect the presence of vesicoureteric reflux and urinary tract obstruction.

Murawski IJ, Watt CL, Gupta IR.

Methods Mol Biol. 2012;886:351-62. doi: 10.1007/978-1-61779-851-1_31.

PMID:
22639276
8.

MMP-1 and -3 haplotype is associated with congenital anomalies of the kidney and urinary tract.

Djuric T, Zivkovic M, Milosevic B, Andjelevski M, Cvetkovic M, Kostic M, Stankovic A.

Pediatr Nephrol. 2014 May;29(5):879-84. doi: 10.1007/s00467-013-2699-x. Epub 2014 Jan 12.

PMID:
24414606
9.

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. doi: 10.1111/nep.12414.

PMID:
25645028
10.

[Multicystic dysplastic kidney. In defense of a conservative experience].

Caldeira F, Juvandes C, Pinto M, Braga M, Calhau P.

Acta Med Port. 2011 Dec;24 Suppl 2:549-56. Epub 2011 Dec 31. Portuguese.

11.

A locus for renal malformations including vesico-ureteric reflux on chromosome 13q33-34.

Vats KR, Ishwad C, Singla I, Vats A, Ferrell R, Ellis D, Moritz M, Surti U, Jayakar P, Frederick DR, Vats AN.

J Am Soc Nephrol. 2006 Apr;17(4):1158-67.

12.

Conditional loss of kidney microRNAs results in congenital anomalies of the kidney and urinary tract (CAKUT).

Bartram MP, Höhne M, Dafinger C, Völker LA, Albersmeyer M, Heiss J, Göbel H, Brönneke H, Burst V, Liebau MC, Benzing T, Schermer B, Müller RU.

J Mol Med (Berl). 2013 Jun;91(6):739-48. doi: 10.1007/s00109-013-1000-x. Epub 2013 Jan 24.

PMID:
23344677
13.

[Genetic basis for malformation-associated uropathy and renal dysplasia].

Oppezzo C, Barberis V, Edefonti A, Cusi D, Marra G.

G Ital Nefrol. 2003 Mar-Apr;20(2):120-6. Review. Italian.

PMID:
12746796
14.

Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathies.

Rigoli L, Chimenz R, di Bella C, Cavallaro E, Caruso R, Briuglia S, Fede C, Salpietro CD.

Pediatr Res. 2004 Dec;56(6):988-93. Epub 2004 Oct 6.

PMID:
15470205
15.

Ontogeny of congenital anomalies of the kidney and urinary tract, CAKUT.

Miyazaki Y, Ichikawa I.

Pediatr Int. 2003 Oct;45(5):598-604.

PMID:
14521544
16.

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. doi: 10.1007/s00383-014-3529-3. Epub 2014 Jun 29. Review.

PMID:
24974188
17.

Changing concepts in urological management of the congenital anomalies of kidney and urinary tract, CAKUT.

Nakai H, Asanuma H, Shishido S, Kitahara S, Yasuda K.

Pediatr Int. 2003 Oct;45(5):634-41. Review.

PMID:
14521549
18.

Functional analysis of BMP4 mutations identified in pediatric CAKUT patients.

Tabatabaeifar M, Schlingmann KP, Litwin M, Emre S, Bakkaloglu A, Mehls O, Antignac C, Schaefer F, Weber S; ESCAPE Trial Group.

Pediatr Nephrol. 2009 Dec;24(12):2361-8. doi: 10.1007/s00467-009-1287-6. Epub 2009 Aug 14.

PMID:
19685083
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. doi: 10.1681/ASN.2013101103. Epub 2014 Apr 3.

20.

Vesicoureteral reflux and other urinary tract malformations in mice compound heterozygous for Pax2 and Emx2.

Boualia SK, Gaitan Y, Murawski I, Nadon R, Gupta IR, Bouchard M.

PLoS One. 2011;6(6):e21529. doi: 10.1371/journal.pone.0021529. Epub 2011 Jun 24.

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