(Q38204264)

31 August 2017

Familial haematuria: when to consider genetic testing (English)

1 reference

31 August 2017

Judy Taylor

1

1 reference

PubMed ID

24728446

31 August 2017

Frances Flinter

series ordinal

2

1 reference

PubMed ID

24728446

31 August 2017

language of work or name

English

0 references

publication date

12 April 2014

1 reference

Archives of Disease in Childhood

31 August 2017

1 reference

31 August 2017

99

1 reference

31 August 2017

9

1 reference

31 August 2017

857-861

1 reference

Urinary screening of elementary and junior high-school children over a 13-year period in Tokyo.

31 August 2017

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

Genetics of classic Alport's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

Clinical and genetic features in autosomal recessive and X-linked Alport syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

The value of clinical criteria in identifying patients with X-linked Alport syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

Molecular genetics of familial hematuric diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

Persistent glomerular hematuria in living kidney donors confers a risk of progressive kidney disease in donors after heminephrectomy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

Living donor kidney transplantation from relatives with mild urinary abnormalities in Alport syndrome: long-term risk, benefit and outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FARCHDISCHILD-2013-304827

10.1136/ARCHDISCHILD-2013-304827

21 January 2018

Identifiers

DOI

1 reference

31 August 2017

1 reference

PubMed ID

24728446