Ungaro C - Search Results

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: ungaro c. 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

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. Among authors: ungaro c. Neurol Sci. 2019 Oct;40(10):2111-2118. doi: 10.1007/s10072-019-03943-y. Epub 2019 Jun 4. Neurol Sci. 2019. PMID: 31165305

3

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: ungaro c. 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.

4

A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies.

Muglia M, Patitucci A, Rizzi R, Ungaro C, Conforti FL, Gabriele AL, Magariello A, Mazzei R, Motti L, Sabadini R, Sprovieri T, Marcello N, Quattrone A. Muglia M, et al. Among authors: ungaro c. J Neurol Sci. 2007 Dec 15;263(1-2):194-7. doi: 10.1016/j.jns.2007.05.034. Epub 2007 Aug 20. J Neurol Sci. 2007. PMID: 17707409

5

Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia.

Magariello A, Muglia M, Patitucci A, Ungaro C, Mazzei R, Gabriele AL, Sprovieri T, Citrigno L, Conforti FL, Liguori M, Gambardella A, Bono F, Piccoli T, Patti F, Zappia M, Mancuso M, Iemolo F, Quattrone A. Magariello A, et al. Among authors: ungaro c. J Neurol Sci. 2010 Jan 15;288(1-2):96-100. doi: 10.1016/j.jns.2009.09.025. Epub 2009 Oct 28. J Neurol Sci. 2010. PMID: 19875132

6

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

Ungaro C, Mazzei R, Sprovieri T. Ungaro C, et al. 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

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. 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

8

A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotype.

Sprovieri T, Conforti FL, Fiumara A, Mazzei R, Ungaro C, Citrigno L, Muglia M, Arena A, Quattrone A. Sprovieri T, et al. Among authors: ungaro c. Am J Med Genet A. 2009 Feb 15;149A(4):722-5. doi: 10.1002/ajmg.a.32711. Am J Med Genet A. 2009. PMID: 19253388

9

Clinical, genetic and magnetic resonance findings in an Italian patient affected by L-2-hydroxyglutaric aciduria.

Mazzei R, Ungaro C, Garreffa G, Conforti FL, Mollo A, Sprovieri T, Servillo P, Blasi V, Gallo O, Cerasa A, Lanza PL, Quattrone A. Mazzei R, et al. Among authors: ungaro c. Neurol Sci. 2011 Feb;32(1):95-9. doi: 10.1007/s10072-010-0416-0. Epub 2010 Sep 22. Neurol Sci. 2011. PMID: 20859647

10

Gene symbol: NOTCH3. Disease: CADASIL.

Ungaro C, Conforti FL, Sprovieri T, de Robertis F, Citrigno L, Quattrone A, Mazzei R. Ungaro C, et al. Hum Genet. 2008 Jun;123(5):555. Hum Genet. 2008. PMID: 20960663 No abstract available.

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