DJ-1 gene in late-onset recessive Parkinson's Disease

Autor: Tarantino, P, Annesi, G, Annesi, F, Nicoletti, G, Morgante, L, Savettieri, G, Manobianca, G, Logroscino, G, Epifanio, A, Arabia, G, Civitelli, D, DE MARCO EV, CIRO' CANDIANO IC, Carrideo, S, Rocca, Fe, Zappia, Mario, Quattrone, A.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::fa75f8eb80868e2102d3903c9e23b31c
http://hdl.handle.net/10447/24338

Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism

Autor: Scornaienchi V, Civitelli D, De Marco EV, Annesi G, Tarantino P, Rocca FE, Greco V, Provenzano G, Annesi F, Nicoletti G, Colica C, Uncini A, Salsone M, Novellino F, Morelli M, Arabia G, Gambardella A, Quattrone A.

Publikováno v: Parkinsonism & related disorders (2012).
info:cnr-pdr/source/autori:Scornaienchi V, Civitelli D, De Marco EV, Annesi G, Tarantino P, Rocca FE, Greco V, Provenzano G, Annesi F, Nicoletti G, Colica C, Uncini A, Salsone M, Novellino F, Morelli M, Arabia G, Gambardella A, Quattrone A./titolo:Mutation analysis of the PINK1 gene in Southern Italian patients with early-and late-onset parkinsonism./doi:/rivista:Parkinsonism & related disorders/anno:2012/pagina_da:/pagina_a:/intervallo_pagine:/volume

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::5664474ae2bb17bf92a4820793cfc105
https://publications.cnr.it/doc/211400

Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy

Autor: Greco V, De Marco EV, Rocca FE, Annesi F, Civitelli D, Provenzano G, Tarantino P, Scornaienchi V, Pucci F, Salsone M, Novellino F, Morelli M, Paglionico S, Gambardella A, Quattrone A, Annesi G.

Publikováno v: Neurological sciences (Testo stamp.) (2011).
info:cnr-pdr/source/autori:Greco V, De Marco EV, Rocca FE, Annesi F, Civitelli D, Provenzano G, Tarantino P, Scornaienchi V, Pucci F, Salsone M, Novellino F, Morelli M, Paglionico S, Gambardella A, Quattrone A, Annesi G./titolo:Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy./doi:/rivista:Neurological sciences (Testo stamp.)/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volume

Iron overload may lead to neurodegenerative disorders such as Parkinson's disease (PD) and alterations of iron-related genes might be involved in the pathogenesis of this disease. The gene of haemochromatosis (HFE) encodes the HFE protein which inter

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::0dd23973ec5c5f8e1d0fd541032002cd
http://www.cnr.it/prodotto/i/50312

Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy

Autor: Annesi F, Gambardella A, Michelucci R, Bianchi A, Marini C, Canevini MP, Capovilla G, Elia M, Buti D, Chifari R, Striano P, Rocca FE, Castellotti B, Cali F, Labate A, Lepiane E, Besana D, Sofia V, Tabiadon G, Tortorella G, Vigliano P, Vignoli A, Beccaria

Publikováno v: Epilepsia (Cph.) 48 (2007): 1686–1690.
info:cnr-pdr/source/autori:Annesi F, Gambardella A, Michelucci R, Bianchi A, Marini C, Canevini MP, Capovilla G, Elia M, Buti D, Chifari R, Striano P, Rocca FE, Castellotti B, Cali F, Labate A, Lepiane E, Besana D, Sofia V, Tabiadon G, Tortorella G, Vigliano P, Vignoli A, Beccaria/titolo:Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy./doi:/rivista:Epilepsia (Cph.)/anno:2007/pagina_da:1686/pagina_a:1690/intervallo_pagine:1686–1690/volume:48

OBJECTIVES: Mutations in the EFHC1 gene have been reported in six juvenile myoclonic epilepsy (JME) families from Mexico and Belize. In this study, we screened 27 unrelated JME Italian families for mutations in the EFHC1 gene. MATERIALS AND METHODS:

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::0583b1cf863e6d11617cd6552ab6c333
https://publications.cnr.it/doc/50039

Myocardial 123metaiodobenzylguanidine uptake in genetic Parkinson's disease.

Autor: Quattrone A, Bagnato A, Annesi G, Novellino F, Morgante L, Savettieri G, Zappia M, Tarantino P, Candiano IC, Annesi F, Civitelli D, Rocca FE, D'Amelio M, Nicoletti G, Morelli M, Petrone A, Loizzo P, Condino F, Quattrone, Aldo, Bagnato, Antonio

Publikováno v: Movement Disorders; Jan2008, Vol. 23 Issue 1, p21-27, 7p