Romano A - Search Results

1

Serum neurofilament light chain: a promising early diagnostic biomarker for hereditary transthyretin amyloidosis?

Romano A, Primiano G, Antonini G, Ceccanti M, Fenu S, Forcina F, Gentile L, Inghilleri M, Leonardi L, Manganelli F, Obici L, Sabino A, Sciarrone MA, Tozza S, Vitali F, Luigetti M. Romano A, et al. Eur J Neurol. 2024 Jan;31(1):e16070. doi: 10.1111/ene.16070. Epub 2023 Sep 19. Eur J Neurol. 2024. PMID: 37724995 Free PMC article.

2

Sural nerve pathology in ALS patients: a single-centre experience.

Luigetti M, Conte A, Del Grande A, Bisogni G, Romano A, Sabatelli M. Luigetti M, et al. Among authors: romano a. Neurol Sci. 2012 Oct;33(5):1095-9. doi: 10.1007/s10072-011-0909-5. Epub 2011 Dec 28. Neurol Sci. 2012. PMID: 22203334

3

Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease.

Lattante S, Conte A, Zollino M, Luigetti M, Del Grande A, Marangi G, Romano A, Marcaccio A, Meleo E, Bisogni G, Rossini PM, Sabatelli M. Lattante S, et al. Among authors: romano a. Neurology. 2012 Jul 3;79(1):66-72. doi: 10.1212/WNL.0b013e31825dceca. Epub 2012 Jun 20. Neurology. 2012. PMID: 22722621

4

Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation.

Conte A, Lattante S, Luigetti M, Del Grande A, Romano A, Marcaccio A, Marangi G, Rossini PM, Neri G, Zollino M, Sabatelli M. Conte A, et al. Among authors: romano a. J Neurol Neurosurg Psychiatry. 2012 Dec;83(12):1201-3. doi: 10.1136/jnnp-2012-302897. Epub 2012 Jul 8. J Neurol Neurosurg Psychiatry. 2012. PMID: 22773853

5

Inherited neuropathies and deafness caused by a PMP22 point mutation: a case report and a review of the literature.

Luigetti M, Zollino M, Conti G, Romano A, Sabatelli M. Luigetti M, et al. Among authors: romano a. Neurol Sci. 2013 Sep;34(9):1705-7. doi: 10.1007/s10072-012-1277-5. Epub 2012 Dec 24. Neurol Sci. 2013. PMID: 23263778 Review. No abstract available.

6

Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis.

Sabatelli M, Moncada A, Conte A, Lattante S, Marangi G, Luigetti M, Lucchini M, Mirabella M, Romano A, Del Grande A, Bisogni G, Doronzio PN, Rossini PM, Zollino M. Sabatelli M, et al. Among authors: romano a. Hum Mol Genet. 2013 Dec 1;22(23):4748-55. doi: 10.1093/hmg/ddt328. Epub 2013 Jul 11. Hum Mol Genet. 2013. PMID: 23847048

7

Ultrasound evaluation in transthyretin-related amyloid neuropathy.

Granata G, Luigetti M, Coraci D, Del Grande A, Romano A, Bisogni G, Bramanti P, Rossini PM, Sabatelli M, Padua L. Granata G, et al. Among authors: romano a. Muscle Nerve. 2014 Sep;50(3):372-6. doi: 10.1002/mus.24168. Epub 2014 Jun 16. Muscle Nerve. 2014. PMID: 24395461

8

Clinical, electrophysiological and pathological findings in a patient with Charcot-Marie-Tooth disease 4D caused by the NDRG1 Lom mutation.

Luigetti M, Taroni F, Milani M, Del Grande A, Romano A, Bisogni G, Conte A, Contaldo I, Mercuri E, Sabatelli M. Luigetti M, et al. Among authors: romano a. J Neurol Sci. 2014 Oct 15;345(1-2):271-3. doi: 10.1016/j.jns.2014.07.042. Epub 2014 Jul 30. J Neurol Sci. 2014. PMID: 25108819 No abstract available.

9

Distinct lymphocytes subsets in IgM-related neuropathy: clinical-immunological correlations.

Iorio R, Sabatelli M, Del Grande A, Bisogni G, Damato V, Plantone D, Marti A, Frisullo G, Romano A, Rossini PM, Luigetti M. Iorio R, et al. Among authors: romano a. Neurol Sci. 2015 Feb;36(2):303-8. doi: 10.1007/s10072-014-1935-x. Epub 2014 Sep 6. Neurol Sci. 2015. PMID: 25192662

10

Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience.

Luigetti M, Fabrizi GM, Bisogni G, Romano A, Taioli F, Ferrarini M, Bernardo D, Rossini PM, Sabatelli M. Luigetti M, et al. Among authors: romano a. Clin Neurol Neurosurg. 2016 May;144:67-71. doi: 10.1016/j.clineuro.2016.03.007. Epub 2016 Mar 9. Clin Neurol Neurosurg. 2016. PMID: 26989944

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