Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Michele Abbruzzese"'
Autor:
Lucilla Nobbio, Tiziana Vigo, Michele Abbruzzese, Giovanni Levi, Claudio Brancolini, Stefano Mantero, Marina Grandis, Luana Benedetti, Gianluigi Mancardi, Angelo Schenone
Publikováno v:
Neurobiology of Disease, Vol 16, Iss 1, Pp 263-273 (2004)
Charcot-Marie-Tooth type 1A (CMT1A) is a hereditary demyelinating neuropathy due to an increased genetic dosage of the peripheral myelin protein 22 (PMP22). The mechanisms leading from PMP22 overexpression to impairment of myelination are still uncle
Externí odkaz:
https://doaj.org/article/4fab7f8e7277422388a05f8643abd959
Publikováno v:
Europe PubMed Central
Two new components of the human SEP upon stimulation of the contralateral median nerve at the wrist have been identified. Such components have been called N16 and N17, according to their polarity and latency. N16 and N17, as well as the N14-P15 compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdb3d9432a105042345587aed8a1e174
https://doi.org/10.1111/j.1600-0404.1978.tb02896.x
https://doi.org/10.1111/j.1600-0404.1978.tb02896.x
Autor:
Gianfranco Gherardi, Michele Abbruzzese, Tiziana Vigo, Edon Melloni, Gianluigi Mancardi, Mario Passalacqua, Lucilla Nobbio, Angelo Schenone, Klaus-Armin Nave
Publikováno v:
European Journal of Neuroscience. 23:1445-1452
Clinical progression in hereditary and acquired demyelinating disorders of both the central and peripheral nervous system is mainly due to a time-dependent axonal impairment. We established 90-day dorsal root ganglia (DRG) cultures from a rat model o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65919044af7fc4fb704aacbf35df0cbe
https://doi.org/10.1111/j.1460-9568.2006.04666.x
https://doi.org/10.1111/j.1460-9568.2006.04666.x
Autor:
Gianfranco Gherardi, Gianluigi Mancardi, Michael W. Sereda, Tiziana Vigo, Michele Abbruzzese, Klaus-Armin Nave, Lucilla Nobbio, Massimo Leandri, Angelo Schenone, Michele Cilli, Marina Grandis, Luana Benedetti
Publikováno v:
Experimental Neurology. 190:213-223
We investigated early peripheral nervous system impairment in PMP22-transgenic rats ("CMT rat"), an established animal model for Charcot-Marie-Tooth disease 1A, at postnatal day 30 (P30), when the clinical phenotype is not yet apparent. Hemizygous CM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4906d729be4ff0278aaa15ae261cef6
https://doi.org/10.1016/j.expneurol.2004.07.008
https://doi.org/10.1016/j.expneurol.2004.07.008
Autor:
Timmerman, P Van Hummelen, G. L. Mancardi, Tiziana Vigo, Lucilla Nobbio, A Schenone, Michele Abbruzzese
Publikováno v:
Journal of the Peripheral Nervous System. 8:29-58
CMT1A is a hereditary demyelinating neuropathy due to increased genetic dosage of peripheral myelin protein 22 (PMP22). The functions of PMP22 as a structural protein of peripheral myelin and a regulator of the proliferation, differentiation, shaping
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6e1c33cfb398eceea9cd1e32feca63d
https://doi.org/10.1046/j.1529-8027.2003.00033.x
https://doi.org/10.1046/j.1529-8027.2003.00033.x
Publikováno v:
Muscle & Nerve. 21:439-453
Concurrent recordings of (i) the soleus H reflex and (ii) the underlying afferent (P 1 ) and efferent (P 2 ) neural volleys were performed during a protracted, moderate, isometric, voluntary contraction of the soleus (S) muscle, and the subsequent re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f5532bd9ba2906b8888f780ff9e81dd
https://doi.org/10.1002/(sici)1097-4598(199804)21:4<439::aid-mus2>3.0.co
https://doi.org/10.1002/(sici)1097-4598(199804)21:4<439::aid-mus2>3.0.co
Autor:
Emilia Bellone, Anthony J. Windebank, Franco Ajmar, Gianluigi Mancardi, Angelo Schenone, Lucilla Nobbio, Claudia Caponnetto, Gianfranco Gherardi, Paola Mandich, Michele Abbruzzese
Publikováno v:
Annals of Neurology. 42:866-872
Hereditary neuropathy with liability to pressure palsies (HNPP) is associated with a deletion in chromosome 17p 11.2, which includes the gene for the peripheral myelin protein 22 (PMP-22). A “gene dosage” effect is probably the mechanism underlyi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45df6add414d9ecd5b15f3c9ec8a3494
https://doi.org/10.1002/ana.410420607
https://doi.org/10.1002/ana.410420607
Autor:
Carlo Trompetto, Emilio Favale, Claudia Caponnetto, Giovanni Abbruzzese, Michele Abbruzzese, M. Morena
Publikováno v:
Journal of Neurology. 241:63-67
The diagnostic relevance of recording motor evoked potentials (MEPs) after electrical stimulation of the cervical region, as compared with conventional needle electromyography (EMG), was evaluated in 26 patients with brachial plexus (BP) damage of di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7454c01ca9c581575c840c12f08f8074
https://doi.org/10.1007/bf00869765
https://doi.org/10.1007/bf00869765
Publikováno v:
Muscle & Nerve. 15:21-26
Central delay (CD) changes in the soleus H reflex pathway, as demonstrated by variations in the time interval between afferent (P1) and efferent (P2) neurographic volleys underlying the reflex response, were assessed in a group of normal subjects, bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18dc9e5c71278b7f55b211205f40c8fb
https://doi.org/10.1002/mus.880150105
https://doi.org/10.1002/mus.880150105
Autor:
Marina Grandis, Gian Luigi Mancardi, Fulvia Fiorese, Lucilla Nobbio, Michele Abbruzzese, Tiziana Vigo, Angelo Schenone, Gianfranco Gherardi, Roberto Cosimo Melcangi, Michele Cilli
We investigated the contribution of Schwann cell-derived ciliary neurotrophic factor (CNTF) to the pathogenesis of Charcot-Marie-Tooth disease type 1A (CMT1A) and addressed the question as to whether it plays a role in the development of axonal damag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48a048021d26f8875540da0e4c980757
http://hdl.handle.net/11567/267496
http://hdl.handle.net/11567/267496
