Similar articles for PMID: 21236492

Year	Number of Results
1999	2
2002	1
2003	1
2004	3
2005	2
2006	7
2007	5
2008	6
2009	4
2010	4
2011	9
2012	3
2013	6
2014	4
2015	5
2016	10
2017	12
2018	9
2019	1
2020	10
2021	8
2022	1
2023	2
2024	0

1

A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.

Mohney BG, Pulido JS, Lindor NM, Hogan MC, Consugar MB, Peters J, Pankratz VS, Nasr SH, Smith SJ, Gloor J, Kubly V, Spencer D, Nielson R, Puffenberger EG, Strauss KA, Morton DH, Eldahdah L, Harris PC. Mohney BG, et al. Ophthalmology. 2011 Jun;118(6):1137-44. doi: 10.1016/j.ophtha.2010.10.009. Epub 2011 Jan 13. Ophthalmology. 2011. PMID: 21236492 Free PMC article.

2

A novel LAMB2 gene mutation associated with a severe phenotype in a neonate with Pierson syndrome.

Zemrani B, Cachat F, Bonny O, Giannoni E, Durig J, Fellmann F, Chehade H. Zemrani B, et al. Eur J Med Res. 2016 Apr 30;21:19. doi: 10.1186/s40001-016-0215-z. Eur J Med Res. 2016. PMID: 27130041 Free PMC article.

3

First Japanese case of Pierson syndrome with mutations in LAMB2.

Togawa H, Nakanishi K, Mukaiyama H, Hama T, Shima Y, Nakano M, Fujita N, Iijima K, Yoshikawa N. Togawa H, et al. Pediatr Int. 2013 Apr;55(2):229-31. doi: 10.1111/j.1442-200X.2012.03629.x. Pediatr Int. 2013. PMID: 23679161

4

A novel mutation of laminin β2 (LAMB2) in two siblings with renal failure.

Falix FA, Bennebroek CA, van der Zwaag B, Lapid-Gortzak R, Florquin S, Oosterveld MJ. Falix FA, et al. Eur J Pediatr. 2017 Apr;176(4):515-519. doi: 10.1007/s00431-017-2871-6. Epub 2017 Feb 10. Eur J Pediatr. 2017. PMID: 28188379 Free PMC article.

5

LAMB2 mutation with different phenotypes in China .

Zhang H, Cui J, Wang F, Xiao H, Ding J, Yao Y. Zhang H, et al. Clin Nephrol. 2017 Jan;87 (2017)(1):33-38. doi: 10.5414/CN108979. Clin Nephrol. 2017. PMID: 27925579

6

Laminin β2 gene missense mutation produces endoplasmic reticulum stress in podocytes.

Chen YM, Zhou Y, Go G, Marmerstein JT, Kikkawa Y, Miner JH. Chen YM, et al. J Am Soc Nephrol. 2013 Jul;24(8):1223-33. doi: 10.1681/ASN.2012121149. Epub 2013 May 30. J Am Soc Nephrol. 2013. PMID: 23723427 Free PMC article.

7

Skeletal impairment in Pierson syndrome: Is there a role for lamininβ2 in bone physiology?

Beaufils C, Farlay D, Machuca-Gayet I, Fassier A, Zenker M, Freychet C, Bonnelye E, Bertholet-Thomas A, Ranchin B, Bacchetta J. Beaufils C, et al. Bone. 2018 Jan;106:187-193. doi: 10.1016/j.bone.2017.10.015. Epub 2017 Oct 16. Bone. 2018. PMID: 29051055

8

A novel mutation of laminin β-2 gene in Pierson syndrome manifested with nephrotic syndrome in the early neonatal period.

Aydin B, Ipek MS, Ozaltin F, Zenciroğlu A, Dilli D, Beken S, Okumuş N, Hoşağasi N, Saygili-Karagöl B, Kundak A, Renda R, Aydog O. Aydin B, et al. Genet Couns. 2013;24(2):141-7. Genet Couns. 2013. PMID: 24032283

9

Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome.

Bull KR, Mason T, Rimmer AJ, Crockford TL, Silver KL, Bouriez-Jones T, Hough TA, Chaudhry S, Roberts IS, Goodnow CC, Cornall RJ. Bull KR, et al. J Pathol. 2014 May;233(1):18-26. doi: 10.1002/path.4308. Epub 2014 Feb 6. J Pathol. 2014. PMID: 24293254 Free PMC article.

10

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

Hasselbacher K, Wiggins RC, Matejas V, Hinkes BG, Mucha B, Hoskins BE, Ozaltin F, Nürnberg G, Becker C, Hangan D, Pohl M, Kuwertz-Bröking E, Griebel M, Schumacher V, Royer-Pokora B, Bakkaloglu A, Nürnberg P, Zenker M, Hildebrandt F. Hasselbacher K, et al. Kidney Int. 2006 Sep;70(6):1008-12. doi: 10.1038/sj.ki.5001679. Epub 2006 Aug 16. Kidney Int. 2006. PMID: 16912710 Free article.

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