(Q83195367)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

Pierson syndrome in an adolescent girl with nephrotic range proteinuria but a normal GFR (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

5

Martin Zenker

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author name string

Anja Lehnhardt

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Albert Lama

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Kerstin Amann

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Verena Matejas

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Markus J Kemper

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

8 January 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

27

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

865-868

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22228401%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00467-011-2088-2

19 January 2020

exact match

0 references

cites work

Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

1 reference

12 December 2020

Variable phenotype of Pierson syndrome

1 reference

12 December 2020

Laminins: structure and genetic regulation

1 reference

12 December 2020

A missense LAMB2 mutation causes congenital nephrotic syndrome by impairing laminin secretion

1 reference

12 December 2020

Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum

1 reference

12 December 2020

A milder variant of Pierson syndrome.

1 reference

12 December 2020

A simple estimate of glomerular filtration rate in adolescent boys.

1 reference

12 December 2020

A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2

1 reference

12 December 2020

[AN UNUSUAL CONGENITAL AND FAMILIAL CONGENITAL MALFORMATIVE COMBINATION INVOLVING THE EYE AND KIDNEY.]

1 reference

12 December 2020

Ophthalmological aspects of Pierson syndrome

1 reference

12 December 2020

Neurodevelopmental deficits in Pierson (microcoria-congenital nephrosis) syndrome

1 reference

12 December 2020