Tarantino P - Search Results

1

A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification.

Gagliardi M, Morelli M, Annesi G, Nicoletti G, Perrotta P, Pustorino G, Iannello G, Tarantino P, Gambardella A, Quattrone A. Gagliardi M, et al. Among authors: tarantino p. Gene. 2015 Aug 15;568(1):109-11. doi: 10.1016/j.gene.2015.05.005. Epub 2015 May 7. Gene. 2015. PMID: 25958344

2

Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South Italy.

Gagliardi M, Annesi G, Tarantino P, Nicoletti G, Quattrone A. Gagliardi M, et al. Among authors: tarantino p. Neurobiol Aging. 2014 Oct;35(10):2422.e1-2. doi: 10.1016/j.neurobiolaging.2014.04.020. Epub 2014 Apr 26. Neurobiol Aging. 2014. PMID: 24854799

3

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.

4

DJ-1 is a Parkinson's disease susceptibility gene in southern Italy.

De Marco EV, Annesi G, Tarantino P, Nicoletti G, Civitelli D, Messina D, Annesi F, Arabia G, Salsone M, Condino F, Novellino F, Provenzano G, Rocca FE, Colica C, Morelli M, Scornaienchi V, Greco V, Giofrè L, Quattrone A. De Marco EV, et al. Among authors: tarantino p. Clin Genet. 2010 Feb;77(2):183-8. doi: 10.1111/j.1399-0004.2009.01310.x. Epub 2009 Nov 23. Clin Genet. 2010. PMID: 19968671

5

Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.

De Marco EV, Annesi G, Tarantino P, Rocca FE, Provenzano G, Civitelli D, Cirò Candiano IC, Annesi F, Carrideo S, Condino F, Nicoletti G, Messina D, Novellino F, Morelli M, Quattrone A. De Marco EV, et al. Among authors: tarantino p. Mov Disord. 2008 Feb 15;23(3):460-3. doi: 10.1002/mds.21892. Mov Disord. 2008. PMID: 18074383

6

Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences.

Labate A, Tarantino P, Viri M, Mumoli L, Gagliardi M, Romeo A, Zara F, Annesi G, Gambardella A. Labate A, et al. Among authors: tarantino p. Epilepsia. 2012 Dec;53(12):e196-9. doi: 10.1111/epi.12009. Epub 2012 Nov 5. Epilepsia. 2012. PMID: 23126439 Free article.

7

Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP.

Labate A, Tarantino P, Palamara G, Gagliardi M, Cavalcanti F, Ferlazzo E, Sturniolo M, Incorpora G, Annesi G, Aguglia U, Gambardella A. Labate A, et al. Among authors: tarantino p. Epilepsy Res. 2013 May;104(3):280-4. doi: 10.1016/j.eplepsyres.2012.10.014. Epub 2013 Jan 23. Epilepsy Res. 2013. PMID: 23352743

8

Fahr's disease linked to a novel SLC20A2 gene mutation manifesting with dynamic aphasia.

Brighina L, Saracchi E, Ferri F, Gagliardi M, Tarantino P, Morzenti S, Musarra M, Patassini M, Annesi G, Ferrarese C. Brighina L, et al. Among authors: tarantino p. Neurodegener Dis. 2014;14(3):133-8. doi: 10.1159/000365216. Epub 2014 Sep 25. Neurodegener Dis. 2014. PMID: 25348593

9

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.

10

Role of G-protein coupled receptor kinase 5 gene in cognitive impairment in Parkinson's disease.

Nicoletti G, De Luca V, Tarantino P, Gagliardi M, Iannello G, Novellino F, Morelli M, Annesi G, Quattrone A. Nicoletti G, et al. Among authors: tarantino p. Psychiatry Res. 2015 Dec 30;230(3):975-7. doi: 10.1016/j.psychres.2015.11.026. Epub 2015 Nov 17. Psychiatry Res. 2015. PMID: 26614013

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