Parkinsonism and essential tremor in a family with pseudo-dominant inheritance of PARK2: An FP-CIT SPECT study(96 visite) Pellecchia MT, Varrone A, Annesi G, Amboni M, Cicarelli G, Sansone V, Annesi F, Rocca FE, Vitale C, Pappata S, Quattrone A, Barone P
Mov Disord (ISSN: 0885-3185, 1531-8257), 2007 Mar 15; 22(4): 559-563.
Tipo di articolo: Journal Article, Research Support, Non-U. S. Gov'T,
Impact factor: 3.207, Impact factor a 5 anni: 3.345
*** IBB - CNR *** Department of Neurological Sciences, University Federico II, Napoli, Italy Biostructure and Bioimaging Institute, National Research Council, Napoli, Italy Institute of Neurological Sciences, National Research Council, Mangone, Cosenza, Italy
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Hampe, C., Ardila-Osorio, H., Fournier, M., Brice, A., Corti, O., Biochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin-protein ligase with monoubiquitylation capacity (2006) Hum Mol Genet, 15, pp. 2059-2075
Terreni, L., Calabrese, E., Calella, A.M., Forloni, G., Mariani, C., New mutation (R42P) of the parkin gene in the ubiquitinlike domain associated with parkinsonism (2001) Neurology, 56, pp. 463-466
Louis, E. D., Essential tremor (2005) Lancet Neurol, 4, pp. 100-110
Louis, E. D., Honig, L. S., Vonsattel, J. P. G., Maraganore, D. M., Borden, S., Moskowitz, C. B., Essential tremor associated with focal nonnigral Lewy bodies (2005) Arch Neurol, 62, pp. 1004-1007
Murayama, M. S., Ikeuchi, T., Saito, M., Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism (2000) Ann Neurol, 48, pp. 245-250
Oliveira, S. A., Scott, W. S., Martin, E. R., Parkin mutations and susceptibility alleles in late-onset Parkinson's disease (2003) Ann Neurol, 53, pp. 624-629
Khan, N. L., Brooks, D. J., Pavese, N., Progression of nigrostriatal dysfunction in a parkin kindred: An [18F] dopa PET and clinical study (2002) Brain, 125, pp. 2248-2256
Sriram, S. R., Li, X., Ko, H. S., Familial-associated mutations differentially disrupt the solubility, localization, binding and ubiquitination properties of parkin (2005) Hum Mol Genet, 14, pp. 2571-2586
Antonini A, Vitale C, Barone P, Cilia R, Righini A, Bonuccelli U, Abbruzzese G, Ramat S, Petrone A, Quatrale R, Marconi R, Ceravolo R, Stefani A, Lopiano L, Zappia M, Capus L, Morgante L, Tamma F, Tinazzi M, Colosimo C, Guerra UP, Valzania F, Fagioli G, Distefano A, Bagnato A, Feggi L, Anna S, Maria Teresa Rosaria De Cr, Nobili F, Mazzuca N, Baldari S, Eleopra R, Bestetti A, Benti R, Varrone A, Volterrani D, Massa R, Stocchi F, Schillaci O, Dore F, Zibetti M, Castellano G, Battista SG, Giorgetti G * The relationship between cerebral vascular disease and parkinsonism: The VADO study(154 visite) Parkinsonism Relat Disord (ISSN: 1353-8020, 1873-5126, 1873-5126electronic), 2012; 18(6): 775-780. Impact Factor:3.274 DettagliEsporta in BibTeXEsporta in EndNote
63 Records (54 escludendo Abstract e Conferenze). Impact factor totale: 247.608 (217.334 escludendo Abstract e Conferenze). Impact factor a 5 anni totale: 265.46 (221.712 escludendo Abstract e Conferenze).
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