Gulli R - Search Results

1

DRD3 Ser9Gly variant is not associated with essential tremor in a series of Italian patients.

Vitale C, Gulli R, Ciotti P, Scaglione C, Bellone E, Avanzino L, Lantieri F, Abbruzzese G, Martinelli P, Barone P, Mandich P. Vitale C, et al. Among authors: gulli r. Eur J Neurol. 2008 Sep;15(9):985-7. doi: 10.1111/j.1468-1331.2008.02164.x. Epub 2008 May 15. Eur J Neurol. 2008. PMID: 18484990

2

Linkage exclusion in Italian families with hereditary essential tremor.

Novelletto A, Gulli R, Ciotti P, Vitale C, Malaspina P, Blasi P, Pippucci T, Seri M, Cozzolino A, Bilo L, Abbruzzese G, Martinelli P, Bellone E, Barone P, Mandich P. Novelletto A, et al. Among authors: gulli r. Eur J Neurol. 2011 Sep;18(9):e118-20. doi: 10.1111/j.1468-1331.2011.03458.x. Eur J Neurol. 2011. PMID: 21834898 No abstract available.

3

Common mutations in the LRRK2 exon 41 are not responsible for essential tremor in Italian patients.

Vitale C, Ciotti P, Gulli R, Bellone E, Scaglione C, Abbruzzese G, Martinelli P, Barone P, Mandich P. Vitale C, et al. Among authors: gulli r. Parkinsonism Relat Disord. 2009 Feb;15(2):162-3. doi: 10.1016/j.parkreldis.2008.04.035. Epub 2008 Jun 16. Parkinsonism Relat Disord. 2009. PMID: 18556235 No abstract available.

4

Essential tremor is not associated with alpha-synuclein gene haplotypes.

Pigullo S, Di Maria E, Marchese R, Bellone E, Gulli R, Scaglione C, Battaglia S, Barone P, Martinelli P, Abbruzzese G, Ajmar F, Mandich P. Pigullo S, et al. Among authors: gulli r. Mov Disord. 2003 Jul;18(7):823-6. doi: 10.1002/mds.10421. Mov Disord. 2003. PMID: 12815663

5

Contribution of copy number variations in CMT1X: a retrospective study.

Capponi S, Geroldi A, Pezzini I, Gulli R, Ciotti P, Ursino G, Lamp M, Reni L, Schenone A, Grandis M, Mandich P, Bellone E. Capponi S, et al. Among authors: gulli r. Eur J Neurol. 2015 Feb;22(2):406-9. doi: 10.1111/ene.12434. Epub 2014 Apr 12. Eur J Neurol. 2015. PMID: 24724718

6

Germline mutations in the von Hippel-Lindau gene in Italian patients.

Ciotti P, Garuti A, Gulli R, Ballestrero A, Bellone E, Mandich P. Ciotti P, et al. Among authors: gulli r. Eur J Med Genet. 2009 Sep-Oct;52(5):311-4. doi: 10.1016/j.ejmg.2009.05.007. Epub 2009 May 21. Eur J Med Genet. 2009. PMID: 19464396

7

Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease.

Mandich P, Grandis M, Geroldi A, Acquaviva M, Varese A, Gulli R, Ciotti P, Bellone E. Mandich P, et al. Among authors: gulli r. J Hum Genet. 2008;53(6):529-533. doi: 10.1007/s10038-008-0280-4. Epub 2008 Apr 1. J Hum Genet. 2008. PMID: 18379723

8

TNF-α gene polymorphisms: association with disease susceptibility and response to anti-TNF-α treatment in psoriatic arthritis.

Murdaca G, Gulli R, Spanò F, Lantieri F, Burlando M, Parodi A, Mandich P, Puppo F. Murdaca G, et al. Among authors: gulli r. J Invest Dermatol. 2014 Oct;134(10):2503-2509. doi: 10.1038/jid.2014.123. Epub 2014 Mar 4. J Invest Dermatol. 2014. PMID: 24594669 Free article.

9

Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise".

Grandis M, Geroldi A, Gulli R, Manganelli F, Gotta F, Lamp M, Origone P, Trevisan L, Gemelli C, Fabbri S, Schenone A, Tozza S, Santoro L, Bellone E, Mandich P. Grandis M, et al. Among authors: gulli r. Orphanet J Rare Dis. 2018 Oct 4;13(1):177. doi: 10.1186/s13023-018-0917-0. Orphanet J Rare Dis. 2018. PMID: 30286783 Free PMC article.

10

GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course.

Pezzini I, Geroldi A, Capponi S, Gulli R, Schenone A, Grandis M, Doria-Lamba L, La Piana C, Cremonte M, Pisciotta C, Nolano M, Manganelli F, Santoro L, Mandich P, Bellone E. Pezzini I, et al. Among authors: gulli r. Neuromuscul Disord. 2016 Jan;26(1):26-32. doi: 10.1016/j.nmd.2015.09.008. Epub 2015 Sep 16. Neuromuscul Disord. 2016. PMID: 26525999

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