Solla E - Search Results

1

Evolution of the phenotype in a family with an LMNA gene mutation presenting with isolated cardiac involvement.

Carboni N, Porcu M, Mura M, Cocco E, Marrosu G, Maioli MA, Solla E, Tranquilli S, Orrù P, Marrosu MG. Carboni N, et al. Among authors: solla e. Muscle Nerve. 2010 Jan;41(1):85-91. doi: 10.1002/mus.21443. Muscle Nerve. 2010. PMID: 19768759

2

A novel mutation in the central rod domain of lamin A/C producing a phenotype resembling the Emery-Dreifuss muscular dystrophy phenotype.

Maioli MA, Marrosu G, Mateddu A, Solla E, Carboni N, Tacconi P, Lai C, Marrosu MG. Maioli MA, et al. Among authors: solla e. Muscle Nerve. 2007 Dec;36(6):828-32. doi: 10.1002/mus.20879. Muscle Nerve. 2007. PMID: 17701980

3

Muscle MRI findings in patients with an apparently exclusive cardiac phenotype due to a novel LMNA gene mutation.

Carboni N, Mura M, Marrosu G, Cocco E, Ahmad M, Solla E, Mateddu A, Maioli MA, Marini S, Nissardi V, Frau J, Mallarini G, Mercuro G, Marrosu MG. Carboni N, et al. Among authors: solla e. Neuromuscul Disord. 2008 Apr;18(4):291-8. doi: 10.1016/j.nmd.2008.01.009. Epub 2008 Mar 11. Neuromuscul Disord. 2008. PMID: 18337098

4

Muscle imaging analogies in a cohort of patients with different clinical phenotypes caused by LMNA gene mutations.

Carboni N, Mura M, Marrosu G, Cocco E, Marini S, Solla E, Mateddu A, Maioli MA, Piras R, Mallarini G, Mercuro G, Porcu M, Marrosu MG. Carboni N, et al. Among authors: solla e. Muscle Nerve. 2010 Apr;41(4):458-63. doi: 10.1002/mus.21514. Muscle Nerve. 2010. PMID: 19882644

5

Aberrant splicing in the LMNA gene caused by a novel mutation on the polypyrimidine tract of intron 5.

Carboni N, Floris M, Mateddu A, Porcu M, Marrosu G, Solla E, Cocco E, Mura M, Marini S, Maioli MA, Piras R, Aste R, Marrosu MG. Carboni N, et al. Among authors: solla e. Muscle Nerve. 2011 May;43(5):688-93. doi: 10.1002/mus.21937. Epub 2011 Apr 1. Muscle Nerve. 2011. PMID: 21462202

6

Dilated cardiomyopathy with conduction defects in a patient with partial merosin deficiency due to mutations in the laminin-α2-chain gene: a chance association or a novel phenotype?

Carboni N, Marrosu G, Porcu M, Mateddu A, Solla E, Cocco E, Maioli MA, Oppo V, Piras R, Marrosu MG. Carboni N, et al. Among authors: solla e. Muscle Nerve. 2011 Nov;44(5):826-8. doi: 10.1002/mus.22228. Muscle Nerve. 2011. PMID: 22006699

7

Cardiac involvement in patients with lamin A/C gene mutations: a cohort observation.

Carboni N, Sardu C, Cocco E, Marrosu G, Manzi RC, Nissardi V, Isola F, Mateddu A, Solla E, Maioli MA, Oppo V, Piras R, Coghe G, Lai C, Marrosu MG. Carboni N, et al. Among authors: solla e. Muscle Nerve. 2012 Aug;46(2):187-92. doi: 10.1002/mus.23294. Muscle Nerve. 2012. PMID: 22806367

8

Partial lipodystrophy associated with muscular dystrophy of unknown genetic origin.

Carboni N, Brancati F, Cocco E, Solla E, D'Apice MR, Mateddu A, McIntyre A, Fadda E, Mura M, Lattanzi G, Piras R, Maioli MA, Marrosu G, Novelli G, Marrosu MG, Hegele RA. Carboni N, et al. Among authors: solla e. Muscle Nerve. 2014 Jun;49(6):928-30. doi: 10.1002/mus.24157. Muscle Nerve. 2014. PMID: 24375490 No abstract available.

9

Overlapping syndromes in laminopathies: a meta-analysis of the reported literature.

Carboni N, Politano L, Floris M, Mateddu A, Solla E, Olla S, Maggi L, Antonietta Maioli M, Piras R, Cocco E, Marrosu G, Giovanna Marrosu M. Carboni N, et al. Among authors: solla e. Acta Myol. 2013 May;32(1):7-17. Acta Myol. 2013. PMID: 23853504 Free PMC article. Review.

10

PTPRC (CD45) C77G mutation does not contribute to multiple sclerosis susceptibility in Sardinian patients.

Cocco E, Murru MR, Melis C, Schirru L, Solla E, Lai M, Rolesu M, Marrosu MG. Cocco E, et al. Among authors: solla e. J Neurol. 2004 Sep;251(9):1085-8. doi: 10.1007/s00415-004-0485-1. J Neurol. 2004. PMID: 15372250

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