Vita G - Search Results

1

Does HLA Class II haplotype play a role in adult acute disseminated encephalomyelitis? Preliminary findings from a Southern Italy hospital-based study.

Imbesi D, Calabrò RS, Gervasi G, Casella C, Vita G, Musolino R. Imbesi D, et al. Among authors: vita g. Arch Ital Biol. 2012 Mar;150(1):1-4. doi: 10.4449/aib.v150i1.1384. Arch Ital Biol. 2012. PMID: 22786832

2

Sleep disorders in children with Attention-Deficit/Hyperactivity Disorder (ADHD) recorded overnight by video-polysomnography.

Silvestri R, Gagliano A, Aricò I, Calarese T, Cedro C, Bruni O, Condurso R, Germanò E, Gervasi G, Siracusano R, Vita G, Bramanti P. Silvestri R, et al. Among authors: vita g. Sleep Med. 2009 Dec;10(10):1132-8. doi: 10.1016/j.sleep.2009.04.003. Epub 2009 Jun 13. Sleep Med. 2009. PMID: 19527942

3

Agenesis of the Internal Carotid Artery Associated with Generalized Epilepsy.

La Spina P, Grillo F, Granata F, Casella C, Fazio MC, Colella M, Cotroneo M, Dell'Aera C, Ciacciarelli A, Vita G, Musolino R. La Spina P, et al. Among authors: vita g. J Clin Neurol. 2018 Jul;14(3):417-419. doi: 10.3988/jcn.2018.14.3.417. Epub 2018 May 31. J Clin Neurol. 2018. PMID: 29856165 Free PMC article. No abstract available.

4

Pregnancy after azathioprine therapy for ulcerative colitis in a woman with autoimmune premature ovarian failure and Addison's disease: HLA haplotype characterization.

Ferraù F, Gangemi S, Vita G, Trimarchi F, Cannavò S. Ferraù F, et al. Among authors: vita g. Fertil Steril. 2011 Jun;95(7):2430.e15-7. doi: 10.1016/j.fertnstert.2011.01.170. Epub 2011 Mar 2. Fertil Steril. 2011. PMID: 21367409 Free article.

5

Certain HLA alleles are associated with stress-triggered Graves' disease and influence its course.

Vita R, Lapa D, Trimarchi F, Vita G, Fallahi P, Antonelli A, Benvenga S. Vita R, et al. Among authors: vita g. Endocrine. 2017 Jan;55(1):93-100. doi: 10.1007/s12020-016-0909-6. Epub 2016 Mar 7. Endocrine. 2017. PMID: 26951052

6

Drug-induced TINU syndrome and genetic characterization.

Santoro D, Vita G, Rovito S, Venuto L, Cavallari V, Vita R, Savica V, Bellinghieri G, Gangemi S. Santoro D, et al. Among authors: vita r, vita g. Clin Nephrol. 2012 Sep;78(3):230-6. doi: 10.5414/cn107119. Clin Nephrol. 2012. PMID: 22874112

7

Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements.

D'Amico A, Catteruccia M, Baranello G, Politano L, Govoni A, Previtali SC, Pane M, D'Angelo MG, Bruno C, Messina S, Ricci F, Pegoraro E, Pini A, Berardinelli A, Gorni K, Battini R, Vita G, Trucco F, Scutifero M, Petillo R, D'Ambrosio P, Ardissone A, Pasanisi B, Vita G, Mongini T, Moggio M, Comi GP, Mercuri E, Bertini E. D'Amico A, et al. Among authors: vita g. Neuromuscul Disord. 2017 May;27(5):447-451. doi: 10.1016/j.nmd.2017.02.006. Epub 2017 Feb 14. Neuromuscul Disord. 2017. PMID: 28262469 Free article.

8

Charcot-Marie-Tooth disease: experience from a large Italian tertiary neuromuscular center.

Gentile L, Russo M, Fabrizi GM, Taioli F, Ferrarini M, Testi S, Alfonzo A, Aguennouz M, Toscano A, Vita G, Mazzeo A. Gentile L, et al. Among authors: vita g. Neurol Sci. 2020 May;41(5):1239-1243. doi: 10.1007/s10072-019-04219-1. Epub 2020 Jan 4. Neurol Sci. 2020. PMID: 31902012

9

Immunolocalization and activation of transcription factor nuclear factor kappa B in dysimmune neuropathies and familial amyloidotic polyneuropathy.

Mazzeo A, Aguennouz M, Messina C, Vita G. Mazzeo A, et al. Among authors: vita g. Arch Neurol. 2004 Jul;61(7):1097-102. doi: 10.1001/archneur.61.7.1097. Arch Neurol. 2004. PMID: 15262741

10

Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency.

Musumeci O, Aguennouz M, Comi GP, Rodolico C, Autunno M, Bordoni A, Baratta S, Taroni F, Vita G, Toscano A. Musumeci O, et al. Among authors: vita g. Neuromuscul Disord. 2007 Dec;17(11-12):960-3. doi: 10.1016/j.nmd.2007.05.002. Epub 2007 Jul 24. Neuromuscul Disord. 2007. PMID: 17651973

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