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Early-onset SCA17 with 43 TBP repeats: expanding the phenotype?
Tremolizzo L, Curtò NA, Marzorati L, Lanzani F, Tarantino P, Annesi G, Ferrarese C. Tremolizzo L, et al. Among authors: tarantino p. Neurol Sci. 2011 Oct;32(5):941-3. doi: 10.1007/s10072-011-0662-9. Epub 2011 Jun 28. Neurol Sci. 2011. PMID: 21710129
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.
Mumoli L, Tarantino P, Michelucci R, Bianchi A, Labate A, Franceschetti S, Marini C, Striano P, Gagliardi M, Ferlazzo E, Sofia V, Pennese L, Annesi G, Aguglia U, Guerrini R, Zara F, Gambardella A; Genetic Commission, Italian League Against Epilepsy. Mumoli L, et al. Among authors: tarantino p. Epilepsia. 2015 Apr;56(4):e40-3. doi: 10.1111/epi.12944. Epub 2015 Mar 6. Epilepsia. 2015. PMID: 25752200 Free article.
Marinesco-Sjögren syndrome caused by a new SIL1 frameshift mutation.
Cerami C, Tarantino P, Cupidi C, Annesi G, Lo Re V, Gagliardi M, Piccoli T, Quattrone A. Cerami C, et al. Among authors: tarantino p. J Neurol Sci. 2015 Jul 15;354(1-2):112-3. doi: 10.1016/j.jns.2015.04.026. Epub 2015 Apr 24. J Neurol Sci. 2015. PMID: 25982182 No abstract available.
PCDH19 mutations in female patients from Southern Italy.
Gagliardi M, Annesi G, Sesta M, Tarantino P, Conti P, Labate A, Di Rosa G, Quattrone A, Gambardella A. Gagliardi M, et al. Among authors: tarantino p. Seizure. 2015 Jan;24:118-20. doi: 10.1016/j.seizure.2014.08.010. Epub 2014 Aug 30. Seizure. 2015. PMID: 25218114 Free article.
Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease.
Savettieri G, Annesi G, Civitelli D, Cirò Candiano IC, Salemi G, Ragonese P, Annesi F, Tarantino P, Terruso V, D'Amelio M, Quattrone A. Savettieri G, et al. Among authors: tarantino p. Parkinsonism Relat Disord. 2008 Aug;14(6):509-12. doi: 10.1016/j.parkreldis.2007.10.014. Epub 2008 Mar 7. Parkinsonism Relat Disord. 2008. PMID: 18329316
207 results