Mandich P - Search Results

1

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: mandich p. 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.

2

Genetic analysis of Huntington disease in Italy.

Ajmar F, Mandich P, Bellone E, Abbruzzese G. Ajmar F, et al. Among authors: mandich p. Am J Med Genet. 1991 May 1;39(2):211-4. doi: 10.1002/ajmg.1320390219. Am J Med Genet. 1991. PMID: 1829583

3

Molecular analysis of the IT15 gene in patients with apparently 'sporadic' Huntington's disease.

Mandich P, Di Maria E, Bellone E, Ajmar F, Abbruzzese G. Mandich P, et al. Eur Neurol. 1996;36(6):348-52. doi: 10.1159/000117292. Eur Neurol. 1996. PMID: 8954302 Clinical Trial.

4

Von Hippel-Lindau (VHL) gene analysis in Italian families with VHL disease.

Montera M, Bellone E, Ajmar F, Mandich P. Montera M, et al. Among authors: mandich p. Contrib Nephrol. 1997;122:109-11. doi: 10.1159/000059877. Contrib Nephrol. 1997. PMID: 9399050 No abstract available.

5

Three novel mutations in the Von Hippel-Lindau tumour suppressor gene in Italian patients.

Mandich P, Montera M, Bellone E, Trojani A, Daniele S, Ajmar F. Mandich P, et al. Hum Mutat. 1998;Suppl 1:S268-70. doi: 10.1002/humu.1380110185. Hum Mutat. 1998. PMID: 9452106 No abstract available.

6

Predictive testing for Huntington's disease: ten years' experience in two Italian centres.

Mandich P, Jacopini G, Di Maria E, Sabbadini G, Abbruzzese G, Chimirri F, Bellone E, Novelletto A, Ajmar F, Frontali M. Mandich P, et al. Ital J Neurol Sci. 1998 Apr;19(2):68-74. doi: 10.1007/BF02427559. Ital J Neurol Sci. 1998. PMID: 10935839

7

No evidence of association between CAG expansions and essential tremor in a large cohort of Italian patients.

Pigullo S, Di Maria E, Marchese R, Assini A, Bellone E, Scaglione C, Vitale C, Bonuccelli U, Barone P, Ajmar F, Martinelli P, Abbruzzese G, Mandich P. Pigullo S, et al. Among authors: mandich p. J Neural Transm (Vienna). 2001;108(3):297-304. doi: 10.1007/s007020170075. J Neural Transm (Vienna). 2001. PMID: 11341481

8

Clinical and genetic study of essential tremor in the Italian population.

Abbruzzese G, Pigullo S, Di Maria E, Martinelli P, Barone P, Marchese R, Scaglione C, Assini A, Lucetti C, Berardelli A, Calzetti S, Bellone E, Ajmar F, Mandich P. Abbruzzese G, et al. Among authors: mandich p. Neurol Sci. 2001 Feb;22(1):39-40. doi: 10.1007/s100720170036. Neurol Sci. 2001. PMID: 11487191

9

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: mandich p. Mov Disord. 2003 Jul;18(7):823-6. doi: 10.1002/mds.10421. Mov Disord. 2003. PMID: 12815663

10

Mutational analysis of parkin gene by denaturing high-performance liquid chromatography (DHPLC) in essential tremor.

Pigullo S, De Luca A, Barone P, Marchese R, Bellone E, Colosimo A, Scaglione C, Martinelli P, Di Maria E, Pizzuti A, Abbruzzese G, Dallapiccola B, Ajmar F, Mandich P. Pigullo S, et al. Among authors: mandich p. Parkinsonism Relat Disord. 2004 Aug;10(6):357-62. doi: 10.1016/j.parkreldis.2004.04.012. Parkinsonism Relat Disord. 2004. PMID: 15261877

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