(Q52582863)

English

A milder variant of Pierson syndrome.

scientific article published on 18 October 2007

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scholarly article

1 reference

Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

A milder variant of Pierson syndrome. (English)

1 reference

Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

1

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Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

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object named as

Martin Zenker

1 reference

Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

author name string

Arthur H Cohen

2

1 reference

Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

Verena Matejas

3

1 reference

Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

Christopher Vlangos

4

1 reference

Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

publication date

18 October 2007

1 reference

Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

Pediatric Nephrology

1 reference

Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

23

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Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

2

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Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

323-327

1 reference

Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

https://scigraph.springernature.com/pub.10.1007/s00467-007-0624-x

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome in the 1st year of life

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Laminins: structure and genetic regulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The renal glomerulus of mice lacking s-laminin/laminin beta 2: nephrosis despite molecular compensation by laminin beta 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kidney in Galloway-Mowat syndrome: clinical spectrum with description of pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pierson syndrome: a novel cause of congenital nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LAMB2 gene mutation as a cause of congenital nephrotic syndrome with distinct eye abnormalities and hypotonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of laminin terminal globular domains in basement membrane assembly

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A laminin-like adhesive protein concentrated in the synaptic cleft of the neuromuscular junction

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurodevelopmental deficits in Pierson (microcoria-congenital nephrosis) syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17943323

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-007-0624-X

1 reference

Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

1 reference

Europe PubMed Central

3 May 2018

http://europepmc.org/abstract/MED/17943323

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