De Michele G - Search Results

1

Brain white matter tracts degeneration in Friedreich ataxia. An in vivo MRI study using tract-based spatial statistics and voxel-based morphometry.

Della Nave R, Ginestroni A, Tessa C, Salvatore E, Bartolomei I, Salvi F, Dotti MT, De Michele G, Piacentini S, Mascalchi M. Della Nave R, et al. Among authors: de michele g. Neuroimage. 2008 Mar 1;40(1):19-25. doi: 10.1016/j.neuroimage.2007.11.050. Epub 2007 Dec 14. Neuroimage. 2008. PMID: 18226551

2

Cerebral blood flow in spinocerebellar degenerations: a single photon emission tomography study in 28 patients.

De Michele G, Mainenti PP, Soricelli A, Di Salle F, Salvatore E, Longobardi MR, Postiglione A, Salvatore M, Filla A. De Michele G, et al. J Neurol. 1998 Sep;245(9):603-8. doi: 10.1007/s004150050253. J Neurol. 1998. PMID: 9758299

3

Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular study.

Coppola G, De Michele G, Cavalcanti F, Pianese L, Perretti A, Santoro L, Vita G, Toscano A, Amboni M, Grimaldi G, Salvatore E, Caruso G, Filla A. Coppola G, et al. Among authors: de michele g. J Neurol. 1999 May;246(5):353-7. doi: 10.1007/s004150050362. J Neurol. 1999. PMID: 10399865

4

Serum transferrin receptor levels in Friedreich's and other degenerative ataxias.

Scarano V, de Cristofaro T, De Michele G, Salvatore E, De Biase I, Monticelli A, Filla A, Cocozza S. Scarano V, et al. Among authors: de biase i, de cristofaro t, de michele g. Neurology. 2001 Jul 10;57(1):159-60. doi: 10.1212/wnl.57.1.159. Neurology. 2001. PMID: 11445653 No abstract available.

5

Stimulation of growth hormone release in multiple system atrophy, Parkinson's disease and idiopathic cerebellar ataxia.

Pellecchia MT, Salvatore E, Pivonello R, Faggiano A, Barone P, De Michele G, Colao AM, Filla A. Pellecchia MT, et al. Among authors: de michele g. Neurol Sci. 2001 Feb;22(1):79-80. doi: 10.1007/s100720170056. Neurol Sci. 2001. PMID: 11487211

6

Possible gluten sensitivity in multiple system atrophy.

Pellecchia MT, Ambrosio G, Salvatore E, Vitale C, De Michele G, Barone P. Pellecchia MT, et al. Among authors: de michele g. Neurology. 2002 Oct 8;59(7):1114-5. doi: 10.1212/wnl.59.7.1114. Neurology. 2002. PMID: 12370481 No abstract available.

7

Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family.

De Michele G, Pocchiari M, Petraroli R, Manfredi M, Caneve G, Coppola G, Casali C, Saccà F, Piccardo P, Salvatore E, Berardelli A, Orio M, Barbieri F, Ghetti B, Filla A. De Michele G, et al. Can J Neurol Sci. 2003 Aug;30(3):233-6. doi: 10.1017/s0317167100002651. Can J Neurol Sci. 2003. PMID: 12945948

8

Reduced striatal [123 I]FP-CIT binding in SCA2 patients without parkinsonism.

Varrone A, Salvatore E, De Michele G, Barone P, Sansone V, Pellecchia MT, Castaldo I, Coppola G, Brunetti A, Salvatore M, Pappatà S, Filla A. Varrone A, et al. Among authors: de michele g. Ann Neurol. 2004 Mar;55(3):426-30. doi: 10.1002/ana.20054. Ann Neurol. 2004. PMID: 14991822

9

Growth hormone response to arginine test distinguishes multiple system atrophy from Parkinson's disease and idiopathic late-onset cerebellar ataxia.

Pellecchia MT, Pivonello R, Salvatore E, Faggiano A, Barone P, De Michele G, Lombardi G, Colao A, Filla A. Pellecchia MT, et al. Among authors: de michele g. Clin Endocrinol (Oxf). 2005 Apr;62(4):428-33. doi: 10.1111/j.1365-2265.2005.02237.x. Clin Endocrinol (Oxf). 2005. PMID: 15807873

10

Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17.

Salvatore E, Varrone A, Sansone V, Nolano M, Bruni AC, De Rosa A, Santoro L, Pappatà S, Filla A, De Michele G. Salvatore E, et al. Among authors: de rosa a, de michele g. Mov Disord. 2006 Jun;21(6):872-5. doi: 10.1002/mds.20827. Mov Disord. 2006. PMID: 16532453

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