(Q62937752)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

7

Katherina Walz

1 reference

4 March 2020

Burcu Bulum

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Ebru Düşünceli

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Aslı Kavaz

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Duygu Duman

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Suat Fitoz

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Fatoş Yalçınkaya

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Z Birsin Ozçakar

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

Evren Ustüner

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

publication date

28 June 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

volume

28

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

page(s)

2143-2147

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23812353%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00467-013-2530-8

4 March 2020

exact match

0 references

cites work

Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis

1 reference

12 December 2020

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

1 reference

12 December 2020

A family study and the natural history of prenatally detected unilateral multicystic dysplastic kidney

1 reference

12 December 2020

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

1 reference

12 December 2020

Congenital anomalies of the kidney and urinary tract: a genetic disorder?

1 reference

12 December 2020

Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT)

1 reference

12 December 2020

Clinical characteristics and outcomes of children with stage 3-5 chronic kidney disease

1 reference

12 December 2020

Malformations in newborn: results based on 30,940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998)

1 reference

12 December 2020

Chronic kidney disease in children in Turkey.

1 reference

12 December 2020

A molecular and genetic view of human renal and urinary tract malformations.

1 reference

12 December 2020

Genetics of congenital anomalies of the kidney and urinary tract

1 reference

12 December 2020

SIX2 and BMP4 mutations associate with anomalous kidney development

1 reference

12 December 2020

Renal duplication and fusion anomalies

1 reference

12 December 2020

Organotypic specificity of key RET adaptor-docking sites in the pathogenesis of neurocristopathies and renal malformations in mice

1 reference

12 December 2020

Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study

1 reference

12 December 2020

Renal anomalies in families of individuals with congenital solitary kidney

1 reference

12 December 2020

Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709,030 births in 12 European countries

1 reference

12 December 2020

Renal aplasia in humans is associated with RET mutations

1 reference

12 December 2020

Traditional and targeted exome sequencing reveals common, rare and novel functional deleterious variants in RET-signaling complex in a cohort of living US patients with urinary tract malformations

1 reference

12 December 2020

Epidemiology of chronic renal failure in children: data from the ItalKid project

1 reference

12 December 2020

Renal anomalies in family members of infants with bilateral renal agenesis/adysplasia

1 reference

12 December 2020

Familial nature of congenital absence and severe dysgenesis of both kidneys

1 reference

12 December 2020

A study of the inheritance of duplication of the kidneys and ureters

1 reference

12 December 2020

Renal revision: from lobulation to duplication--what is normal?

1 reference

12 December 2020

Maternal risk factors for congenital urinary anomalies: results of a population-based case-control study

1 reference

12 December 2020

Toward an etiological classification of developmental disorders of the kidney and upper urinary tract

1 reference

12 December 2020

Renal multicystic dysplasia: an occasional manifestation of the hereditary renal adysplasia syndrome

1 reference

12 December 2020

UK Renal Registry 12th Annual Report (December 2009): chapter 14: demography of the UK paediatric renal replacement therapy population in 2008

1 reference

12 December 2020