Teresa Sprovieri - Search Results

Year	Number of Results
2003	1
2004	3
2005	1
2006	2
2007	2
2008	3
2009	2
2010	4
2011	1
2012	1
2018	2
2019	5
2020	2
2021	1
2024	0

1

A Systems Biology Approach for Personalized Medicine in Refractory Epilepsy.

Naimo GD, Guarnaccia M, Sprovieri T, Ungaro C, Conforti FL, Andò S, Cavallaro S. Naimo GD, et al. Among authors: sprovieri t. Int J Mol Sci. 2019 Jul 30;20(15):3717. doi: 10.3390/ijms20153717. Int J Mol Sci. 2019. PMID: 31366017 Free PMC article. Review.

2

Alternative Splicing of ALS Genes: Misregulation and Potential Therapies.

Perrone B, La Cognata V, Sprovieri T, Ungaro C, Conforti FL, Andò S, Cavallaro S. Perrone B, et al. Among authors: sprovieri t. Cell Mol Neurobiol. 2020 Jan;40(1):1-14. doi: 10.1007/s10571-019-00717-0. Epub 2019 Aug 5. Cell Mol Neurobiol. 2020. PMID: 31385134 Review.

3

Proteomic profiling of cerebrospinal fluid in Creutzfeldt-Jakob disease.

Qualtieri A, Urso E, Le Pera M, Sprovieri T, Bossio S, Gambardella A, Quattrone A. Qualtieri A, et al. Among authors: sprovieri t. Expert Rev Proteomics. 2010 Dec;7(6):907-17. doi: 10.1586/epr.10.80. Expert Rev Proteomics. 2010. PMID: 21142891 Review.

4

Gene symbol: NOTCH3. Disease: CADASIL.

Ungaro C, Sprovieri T, Conforti FL, Consoli D, Citrigno L, Liguori M, Quattrone A, Mazzei R. Ungaro C, et al. Among authors: sprovieri t. Hum Genet. 2008 Jun;123(5):554. Hum Genet. 2008. PMID: 20960662 No abstract available.

5

Genetic investigation of amyotrophic lateral sclerosis patients in south Italy: a two-decade analysis.

Ungaro C, Sprovieri T, Morello G, Perrone B, Spampinato AG, Simone IL, Trojsi F, Monsurrò MR, Spataro R, La Bella V, Andò S, Cavallaro S, Conforti FL. Ungaro C, et al. Among authors: sprovieri t. Neurobiol Aging. 2021 Mar;99:99.e7-99.e14. doi: 10.1016/j.neurobiolaging.2020.08.017. Epub 2020 Aug 27. Neurobiol Aging. 2021. PMID: 32951934

6

Horizontal gaze palsy with progressive scoliosis: is scoliosis linked to ROBO3 mutations?

Ungaro C, Mazzei R, Sprovieri T. Ungaro C, et al. Among authors: sprovieri t. Neurol Sci. 2019 Jan;40(1):207-208. doi: 10.1007/s10072-018-3567-z. Epub 2018 Sep 14. Neurol Sci. 2019. PMID: 30218396 No abstract available.

7

ALS and CHARGE syndrome: a clinical and genetic study.

Ungaro C, Citrigno L, Trojsi F, Sprovieri T, Gentile G, Muglia M, Monsurrò MR, Tedeschi G, Cavallaro S, Conforti FL. Ungaro C, et al. Among authors: sprovieri t. Acta Neurol Belg. 2018 Dec;118(4):629-635. doi: 10.1007/s13760-018-1029-2. Epub 2018 Oct 13. Acta Neurol Belg. 2018. PMID: 30317490 Free PMC article.

8

A novel S379A TARDBP mutation associated to late-onset sporadic ALS.

Sprovieri T, Ungaro C, Perrone B, Naimo GD, Spataro R, Cavallaro S, La Bella V, Conforti FL. Sprovieri T, et al. Neurol Sci. 2019 Oct;40(10):2111-2118. doi: 10.1007/s10072-019-03943-y. Epub 2019 Jun 4. Neurol Sci. 2019. PMID: 31165305

9

Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report.

Sprovieri T, Ungaro C, Sivo S, Quintiliani M, Contaldo I, Veredice C, Citrigno L, Muglia M, Cavalcanti F, Cavallaro S, Mercuri E, Battaglia D. Sprovieri T, et al. BMC Med Genet. 2019 Mar 12;20(1):40. doi: 10.1186/s12881-019-0779-x. BMC Med Genet. 2019. PMID: 30866851 Free PMC article.

10

Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy.

Luisa Conforti F, Sprovieri T, Mazzei R, Patitucci A, Ungaro C, Zoccolella S, Magariello A, Bella VL, Tessitore A, Tedeschi G, Simone IL, Majorana G, Valentino P, Citrigno L, Gabriele A, Bono F, Monsurrò MR, Muglia M, Quattrone A. Luisa Conforti F, et al. Among authors: sprovieri t. Amyotroph Lateral Scler. 2009 Feb;10(1):58-60. doi: 10.1080/17482960802163853. Amyotroph Lateral Scler. 2009. PMID: 18608106

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