Similar articles for PMID: 24225367

Year	Number of Results
1982	1
1995	9
1996	10
1997	12
1998	15
1999	8
2000	6
2001	6
2002	6
2003	4
2004	3
2005	3
2006	5
2007	5
2008	7
2009	2
2010	4
2011	7
2012	3
2013	6
2014	13
2015	13
2016	6
2017	19
2018	12
2019	7
2020	16
2021	13
2022	9
2023	4
2024	0

1

High creatine kinase levels and white matter changes: clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency.

Beytía Mde L, Dekomien G, Hoffjan S, Haug V, Anastasopoulos C, Kirschner J. Beytía Mde L, et al. Mol Cell Probes. 2014 Aug;28(4):118-22. doi: 10.1016/j.mcp.2013.11.002. Epub 2013 Nov 10. Mol Cell Probes. 2014. PMID: 24225367

2

Merosin-deficient congenital muscular dystrophy type 1A.

Buteică E, Roşulescu E, Burada F, Stănoiu B, Zăvăleanu M. Buteică E, et al. Rom J Morphol Embryol. 2008;49(2):229-33. Rom J Morphol Embryol. 2008. PMID: 18516331 Free article.

3

Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy.

Pegoraro E, Mancias P, Swerdlow SH, Raikow RB, Garcia C, Marks H, Crawford T, Carver V, Di Cianno B, Hoffman EP. Pegoraro E, et al. Ann Neurol. 1996 Nov;40(5):782-91. doi: 10.1002/ana.410400515. Ann Neurol. 1996. PMID: 8957020

4

The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review.

Jones KJ, Morgan G, Johnston H, Tobias V, Ouvrier RA, Wilkinson I, North KN. Jones KJ, et al. J Med Genet. 2001 Oct;38(10):649-57. doi: 10.1136/jmg.38.10.649. J Med Genet. 2001. PMID: 11584042 Free PMC article. Review.

5

Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophy.

Sewry CA, D'Alessandro M, Wilson LA, Sorokin LM, Naom I, Bruno S, Ferlini A, Dubowitz V, Muntoni F. Sewry CA, et al. Neuropediatrics. 1997 Aug;28(4):217-22. doi: 10.1055/s-2007-973703. Neuropediatrics. 1997. PMID: 9309712

6

Severe congenital muscular dystrophy in a LAMA2-mutated case.

Di Blasi C, van Alfen N, Colleoni F, ter Laak H, Mora M. Di Blasi C, et al. Pediatr Neurol. 2007 Sep;37(3):212-4. doi: 10.1016/j.pediatrneurol.2007.05.008. Pediatr Neurol. 2007. PMID: 17765811

7

LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients.

Oliveira J, Santos R, Soares-Silva I, Jorge P, Vieira E, Oliveira ME, Moreira A, Coelho T, Ferreira JC, Fonseca MJ, Barbosa C, Prats J, Aríztegui ML, Martins ML, Moreno T, Heinimann K, Barbot C, Pascual-Pascual SI, Cabral A, Fineza I, Santos M, Bronze-da-Rocha E. Oliveira J, et al. Clin Genet. 2008 Dec;74(6):502-12. doi: 10.1111/j.1399-0004.2008.01068.x. Epub 2008 Jun 11. Clin Genet. 2008. PMID: 18700894

8

Severe congenital muscular dystrophy in a Mexican family with a new nonsense mutation (R2578X) in the laminin alpha-2 gene.

Coral-Vazquez RM, Rosas-Vargas H, Meza-Espinosa P, Mendoza I, Huicochea JC, Ramon G, Salamanca F. Coral-Vazquez RM, et al. J Hum Genet. 2003;48(2):91-5. doi: 10.1007/s100380300013. J Hum Genet. 2003. PMID: 12601554

9

Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin).

Allamand V, Guicheney P. Allamand V, et al. Eur J Hum Genet. 2002 Feb;10(2):91-4. doi: 10.1038/sj.ejhg.5200743. Eur J Hum Genet. 2002. PMID: 11938437

10

Merosin and congenital muscular dystrophy.

Miyagoe-Suzuki Y, Nakagawa M, Takeda S. Miyagoe-Suzuki Y, et al. Microsc Res Tech. 2000 Feb 1-15;48(3-4):181-91. doi: 10.1002/(SICI)1097-0029(20000201/15)48:3/4<181::AID-JEMT6>3.0.CO;2-Q. Microsc Res Tech. 2000. PMID: 10679965 Review.

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