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Page 1
Clinical features and outcome of 6 new patients carrying de novo KCNB1 gene mutations.
Marini C, Romoli M, Parrini E, Costa C, Mei D, Mari F, Parmeggiani L, Procopio E, Metitieri T, Cellini E, Virdò S, De Vita D, Gentile M, Prontera P, Calabresi P, Guerrini R. Marini C, et al. Among authors: romoli m. Neurol Genet. 2017 Dec 11;3(6):e206. doi: 10.1212/NXG.0000000000000206. eCollection 2017 Dec. Neurol Genet. 2017. PMID: 29264397 Free PMC article.
Prognostic factors in children with PRES and hematologic diseases.
Tambasco N, Mastrodicasa E, Salvatori C, Mancini G, Romoli M, Caniglia M, Calabresi P, Verrotti A. Tambasco N, et al. Among authors: romoli m. Acta Neurol Scand. 2016 Dec;134(6):474-483. doi: 10.1111/ane.12570. Epub 2016 Feb 15. Acta Neurol Scand. 2016. PMID: 26876986
A53T in a parkinsonian family: a clinical update of the SNCA phenotypes.
Tambasco N, Nigro P, Romoli M, Prontera P, Simoni S, Calabresi P. Tambasco N, et al. Among authors: romoli m. J Neural Transm (Vienna). 2016 Nov;123(11):1301-1307. doi: 10.1007/s00702-016-1578-6. Epub 2016 Jun 1. J Neural Transm (Vienna). 2016. PMID: 27250986 Review.
P066. Migraine with aura in the locker room: 4 case reports.
Bernetti L, Corbelli I, Romoli M, Bedetti C, Brahimi E, Sarchielli P, Calabresi P. Bernetti L, et al. Among authors: romoli m. J Headache Pain. 2015 Dec;16(Suppl 1):A169. doi: 10.1186/1129-2377-16-S1-A169. J Headache Pain. 2015. PMID: 28132219 Free PMC article. No abstract available.
238 results