Sanges G - Search Results

1

Clinical genetic analysis of Parkinson's disease in the Contursi kindred.

Golbe LI, Di Iorio G, Sanges G, Lazzarini AM, La Sala S, Bonavita V, Duvoisin RC. Golbe LI, et al. Among authors: sanges g. Ann Neurol. 1996 Nov;40(5):767-75. doi: 10.1002/ana.410400513. Ann Neurol. 1996. PMID: 8957018

2

Mapping of a gene for Parkinson's disease to chromosome 4q21-q23.

Polymeropoulos MH, Higgins JJ, Golbe LI, Johnson WG, Ide SE, Di Iorio G, Sanges G, Stenroos ES, Pho LT, Schaffer AA, Lazzarini AM, Nussbaum RL, Duvoisin RC. Polymeropoulos MH, et al. Among authors: sanges g. Science. 1996 Nov 15;274(5290):1197-9. doi: 10.1126/science.274.5290.1197. Science. 1996. PMID: 8895469

3

Familial amyloidotic polyneuropathy: description of an Italian kindred.

Di Iorio G, Sanges G, Cerracchio A, Sampaolo S, Sannino V, Bonavita V. Di Iorio G, et al. Among authors: sanges g. Ital J Neurol Sci. 1993 May;14(4):303-9. doi: 10.1007/BF02339296. Ital J Neurol Sci. 1993. PMID: 8325767

4

Lack of sodium channel mutation in an Italian family with paramyotonia congenita.

Sampaolo S, Puca AA, Nigro V, Cappa V, Sannino V, Sanges G, Bonavita V, Di Iorio G. Sampaolo S, et al. Among authors: sanges g. Neurology. 1999 Oct 22;53(7):1549-55. doi: 10.1212/wnl.53.7.1549. Neurology. 1999. PMID: 10534266

5

A comment on: 'Molecular diagnosis of transthyretin Met30 mutation in an Italian family with familial amyloidotic polyneuropathy' by Paola Strocchi et al., FEBS Letters 359 (1995) 203-205.

Di Iorio G, Sanges G, Sampaolo S, Bonavita V. Di Iorio G, et al. Among authors: sanges g. FEBS Lett. 1996 Nov 18;397(2-3):357-8. doi: 10.1016/s0014-5793(96)01161-1. FEBS Lett. 1996. PMID: 8955379 Free article. No abstract available.

6

Craniofacial pain followed by scalp necrosis and stroke. An unusual presentation of the primary antiphospholipid syndrome.

Sanges G, Sampaolo S, Di Iorio G. Sanges G, et al. J Neurol. 1999 Feb;246(2):134-5. doi: 10.1007/s004150050320. J Neurol. 1999. PMID: 10195409 No abstract available.

7

Cognitive impairment in systemic lupus erythematosus: a follow-up study.

Carlomagno S, Migliaresi S, Ambrosone L, Sannino M, Sanges G, Di Iorio G. Carlomagno S, et al. Among authors: sanges g. J Neurol. 2000 Apr;247(4):273-9. doi: 10.1007/s004150050583. J Neurol. 2000. PMID: 10836619

8

A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease.

Di Iorio G, Cappa V, Ciccodicola A, Sampaolo S, Ammendola A, Sanges G, Giugliano R, D'Urso M. Di Iorio G, et al. Among authors: sanges g. Neurol Sci. 2000 Apr;21(2):109-12. doi: 10.1007/s100720070105. Neurol Sci. 2000. PMID: 10938190

9

Peripheral nervous system involvement in Klippel-Trenaunay syndrome.

Di Iorio G, Sanges G, Sannino V, De Cristofaro M, D'Ambrosio MR, Budillon A, Sampaolo S. Di Iorio G, et al. Among authors: sanges g. Clin Neuropathol. 2005 Jan-Feb;24(1):42-7. Clin Neuropathol. 2005. PMID: 15696784

10

[Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia].

Migliaresi S, Di Iorio G, Ammendola A, Ambrosone L, Sanges G, Ugolini G, Sampaolo S, Bravaccio F, Tirri G. Migliaresi S, et al. Among authors: sanges g. Reumatismo. 2001;53(1):26-32. doi: 10.4081/reumatismo.2001.26. Reumatismo. 2001. PMID: 12461575 Free article. Italian.

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