(Q36586925)

15 August 2017

1 reference

title

Unilateral renal agenesis and the congenital solitary functioning kidney: developmental, genetic and clinical perspectives (English)

1 reference

15 August 2017

0 references

1 reference

Adrian S Woolf

1

1 reference

15 August 2017

Katherine A Hillman

series ordinal

2

1 reference

15 August 2017

publication date

6 September 2006

1 reference

15 August 2017

number of pages

5

1 reference

based on heuristic

inferred from page(s)

published in

BJU International

1 reference

15 August 2017

volume

99

1 reference

15 August 2017

issue

1

1 reference

15 August 2017

page(s)

17-21

1 reference

Embryology of the adrenal glands and its relevance to diagnostic imaging

15 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Sonographic findings of fetuses with an empty renal fossa and normal amniotic fluid volume

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Perinatal renal venous thrombosis: presenting renal length predicts outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Clinical and genetic features of patients with congenital unilateral absence of the vas deferens

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Associated anomalies in children with congenital solitary functioning kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

A family with the branchio-oto-renal syndrome: clinical and genetic correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Proteinuria, hypertension and chronic renal failure in X-linked Kallmann's syndrome, a defined genetic cause of solitary functioning kidney.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: implications for the developmental anomalies of X chromosome-linked Kallmann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Mayer-Rokitansky-Küster-Hauser anomaly and its associated malformations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Poland syndrome associated with renal agenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Townes-Brocks syndrome and renal dysplasia: a novel mutation in the SALL1 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Renal tract ultrasonography and calcium homeostasis in Williams-Beuren syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Familial unilateral renal agenesis and focal and segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Teratogenicity with angiotensin II receptor antagonists in pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Risk of specific congenital abnormalities in offspring of women with diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Implication of Wt1 in the pathogenesis of nephrogenic failure in a mouse model of retinoic acid-induced caudal regression syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Fetal compensatory renal hypertrophy with a unilateral functioning kidney.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Nephron number in patients with primary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Sonographic assessment of renal length in normal children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Kidney dimensions at sonography: correlation with age, sex, and habitus in 665 adult volunteers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Associated urologic anomalies in children with solitary kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Ambulatory blood pressure monitoring in children with a solitary kidney - a comparison between unilateral renal agenesis and uninephrectomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Prognosis of patients with unilateral renal agenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Factors influencing the progression of renal damage in patients with unilateral renal agenesis and remnant kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

Dominantly inherited renal adysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2006.06504.X

10.1111/J.1464-410X.2006.06504.X

21 January 2018

Identifiers

DOI

1 reference

15 August 2017

1 reference