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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2007 | 1 |
2008 | 1 |
2010 | 1 |
2011 | 1 |
2013 | 1 |
2014 | 1 |
2015 | 1 |
2024 | 0 |
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Phenotypic clustering of lamin A/C mutations in neuromuscular patients.
Neurology. 2007 Sep 18;69(12):1285-92. doi: 10.1212/01.wnl.0000261254.87181.80. Epub 2007 Mar 21.
Neurology. 2007.
PMID: 17377071
De novo LMNA mutations cause a new form of congenital muscular dystrophy.
Quijano-Roy S, Mbieleu B, Bönnemann CG, Jeannet PY, Colomer J, Clarke NF, Cuisset JM, Roper H, De Meirleir L, D'Amico A, Ben Yaou R, Nascimento A, Barois A, Demay L, Bertini E, Ferreiro A, Sewry CA, Romero NB, Ryan M, Muntoni F, Guicheney P, Richard P, Bonne G, Estournet B.
Quijano-Roy S, et al.
Ann Neurol. 2008 Aug;64(2):177-86. doi: 10.1002/ana.21417.
Ann Neurol. 2008.
PMID: 18551513
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Novel LMNA mutation presenting as severe congenital muscular dystrophy.
Prigogine C, Richard P, Van den Bergh P, Groswasser J, Deconinck N.
Prigogine C, et al.
Pediatr Neurol. 2010 Oct;43(4):283-6. doi: 10.1016/j.pediatrneurol.2010.05.016.
Pediatr Neurol. 2010.
PMID: 20837309
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Inflammatory changes in infantile-onset LMNA-associated myopathy.
Komaki H, Hayashi YK, Tsuburaya R, Sugie K, Kato M, Nagai T, Imataka G, Suzuki S, Saitoh S, Asahina N, Honke K, Higuchi Y, Sakuma H, Saito Y, Nakagawa E, Sugai K, Sasaki M, Nonaka I, Nishino I.
Komaki H, et al.
Neuromuscul Disord. 2011 Aug;21(8):563-8. doi: 10.1016/j.nmd.2011.04.010. Epub 2011 May 31.
Neuromuscul Disord. 2011.
PMID: 21632249
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Congenital muscular dystrophy with dropped head linked to the LMNA gene in a Brazilian cohort.
Pasqualin LM, Reed UC, Costa TV, Quedas E, Albuquerque MA, Resende MB, Rutkowski A, Chadi G, Zanoteli E.
Pasqualin LM, et al.
Pediatr Neurol. 2014 Apr;50(4):400-6. doi: 10.1016/j.pediatrneurol.2013.11.010. Epub 2013 Nov 21.
Pediatr Neurol. 2014.
PMID: 24508248
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Phenotype-Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy.
Tan D, Yang H, Yuan Y, Bonnemann C, Chang X, Wang S, Wu Y, Wu X, Xiong H.
Tan D, et al.
PLoS One. 2015 Jun 22;10(6):e0129699. doi: 10.1371/journal.pone.0129699. eCollection 2015.
PLoS One. 2015.
PMID: 26098624
Free PMC article.
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