Iannello G - 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: iannello g. 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

C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation.

Gagliardi M, Annesi G, Lesca G, Broussolle E, Iannello G, Vaiti V, Gambardella A, Quattrone A. Gagliardi M, et al. Among authors: iannello g. Parkinsonism Relat Disord. 2015 Jul;21(7):813-6. doi: 10.1016/j.parkreldis.2015.04.009. Epub 2015 Apr 23. Parkinsonism Relat Disord. 2015. PMID: 25962551

3

Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria.

Gagliardi M, Iannello G, Colica C, Annesi G, Quattrone A. Gagliardi M, et al. Among authors: iannello g. Neurobiol Aging. 2017 Feb;50:169.e5-169.e6. doi: 10.1016/j.neurobiolaging.2016.10.022. Epub 2016 Oct 21. Neurobiol Aging. 2017. PMID: 27839905

4

A SLC20A2 mutation identified in an asymptomatic patient with brain calcification.

Gagliardi M, Morelli M, Iannello G, Colica C, Annesi G, Quattrone A. Gagliardi M, et al. Among authors: iannello g. J Neurol Sci. 2017 Jan 15;372:70-72. doi: 10.1016/j.jns.2016.11.038. Epub 2016 Nov 17. J Neurol Sci. 2017. PMID: 28017251 No abstract available.

5

A new CHCHD2 mutation identified in a southern italy patient with multiple system atrophy.

Nicoletti G, Gagliardi M, Procopio R, Iannello G, Morelli M, Annesi G, Quattrone A. Nicoletti G, et al. Among authors: iannello g. Parkinsonism Relat Disord. 2018 Feb;47:91-93. doi: 10.1016/j.parkreldis.2017.12.005. Epub 2017 Dec 7. Parkinsonism Relat Disord. 2018. PMID: 29248339 No abstract available.

6

Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria.

Gagliardi M, Arabia G, Nisticò R, Iannello G, Procopio R, Manfredini L, Annesi G, Quattrone A. Gagliardi M, et al. Among authors: iannello g. J Neurol Sci. 2018 Jul 15;390:209-211. doi: 10.1016/j.jns.2018.04.043. Epub 2018 May 1. J Neurol Sci. 2018. PMID: 29801890

7

DNAJC13 mutation screening in patients with Parkinson's disease from South Italy.

Gagliardi M, Annesi G, Procopio R, Morelli M, Iannello G, Bonapace G, Mancini M, Nicoletti G, Quattrone A. Gagliardi M, et al. Among authors: iannello g. Parkinsonism Relat Disord. 2018 Oct;55:134-137. doi: 10.1016/j.parkreldis.2018.06.004. Epub 2018 Jun 4. Parkinsonism Relat Disord. 2018. PMID: 29887357

8

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: iannello g. 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

9

Mutational analysis of COASY in an Italian patient with NBIA.

Annesi G, Gagliardi M, Iannello G, Quattrone A, Iannello G, Quattrone A. Annesi G, et al. Among authors: iannello g. Parkinsonism Relat Disord. 2016 Jul;28:150-1. doi: 10.1016/j.parkreldis.2016.03.011. Epub 2016 Mar 18. Parkinsonism Relat Disord. 2016. PMID: 27021474 No abstract available.

10

A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy.

Iannello G, Graziano C, Cenacchi G, Cordelli DM, Zuntini R, Papa V, Magistà AM, Gagliardi M, Procopio R, Quattrone A, Annesi G. Iannello G, et al. J Neurol Sci. 2017 Oct 15;381:209-212. doi: 10.1016/j.jns.2017.08.3260. Epub 2017 Sep 1. J Neurol Sci. 2017. PMID: 28991683

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