المؤلفون: Grandis, M, Obici, L, Luigetti, M, Briani, C, Benedicenti, F, Bisogni, G, Canepa, M, Cappelli, F, Danesino, C, Fabrizi, G M, Fenu, S, Ferrandes, G, Gemelli, C, Manganelli, F, Mazzeo, A, Melchiorri, L, Perfetto, F, Pradotto, L G, Rimessi, P, Tini, G, Tozza, S, Trevisan, L, Pareyson, D, Mandich, P

المساهمون: Grandis, M, Obici, L, Luigetti, M, Briani, C, Benedicenti, F, Bisogni, G, Canepa, M, Cappelli, F, Danesino, C, Fabrizi, G M, Fenu, S, Ferrandes, G, Gemelli, C, Manganelli, F, Mazzeo, A, Melchiorri, L, Perfetto, F, Pradotto, L G, Rimessi, P, Tini, G, Tozza, S, Trevisan, L, Pareyson, D, Mandich, P

مصطلحات موضوعية: ATTRv, Hereditary transthyretin amyloidosis, Pre-symptomatic genetic testing, PST

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33317601; info:eu-repo/semantics/altIdentifier/wos/WOS:000599794300002; volume:15; issue:348; firstpage:1; lastpage:7; numberofpages:7; journal:ORPHANET JOURNAL OF RARE DISEASES; http://hdl.handle.net/11562/1032701Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85097555700; https://doi.org/10.1186/s13023-020-01633-zTest

الإتاحة: https://doi.org/10.1186/s13023-020-01633-zTest
http://hdl.handle.net/11562/1032701Test

المؤلفون: Magliano L., Obici L., Sforzini C., Mazzeo A., Russo M., Cappelli F., Fenu S., Luigetti M., Tagliapietra M., Gemelli C., Leonardi L., Tozza S., Pradotto L. G., Citarelli G., Mauro A., Manganelli F., Antonini G., Grandis M., Fabrizi G. M., Sabatelli M., Pareyson D., Perfetto F., Merlini G., Vita G., Bisogni G., Calabrese D., Cardellini D., Casagrande S., Cavallaro T., DiBuduo E., DiPaolantonio A., Gentile L., Graceffa A., Massucco S., Milesi A., Morino S., Mussinelli R., Saveri P., Severi D.

المساهمون: Magliano L., Obici L., Sforzini C., Mazzeo A., Russo M., Cappelli F., Fenu S., Luigetti M., Tagliapietra M., Gemelli C., Leonardi L., Tozza S., Pradotto L.G., Citarelli G., Mauro A., Manganelli F., Antonini G., Grandis M., Fabrizi G.M., Sabatelli M., Pareyson D., Perfetto F., Merlini G., Vita G., Bisogni G., Calabrese D., Cardellini D., Casagrande S., Cavallaro T., DiBuduo E., DiPaolantonio A., Gentile L., Graceffa A., Massucco S., Milesi A., Morino S., Mussinelli R., Saveri P., Severi D.

مصطلحات موضوعية: ATTRv, Burden, Caregiving, Hereditary transthyretin amyloidosi, Professional support, Social network support, Adult, Amyloid Neuropathies, Familial, Human, Italy, Surveys and Questionnaire, Quality of Life, Social Support

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33827635; info:eu-repo/semantics/altIdentifier/wos/WOS:000638003000008; volume:16; issue:1; firstpage:163; lastpage:163; numberofpages:1; journal:ORPHANET JOURNAL OF RARE DISEASES; http://hdl.handle.net/2318/1805600Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85103998342

الإتاحة: https://doi.org/10.1186/s13023-021-01812-6Test
http://hdl.handle.net/2318/1805600Test

المؤلفون: Iorio A., De Angelis F., Di Girolamo M., Luigetti M., Pradotto L. G., Mazzeo A., Frusconi S., My F., Manfellotto D., Fuciarelli M., Polimanti R.

المساهمون: Iorio, A., De Angelis, F., Di Girolamo, M., Luigetti, M., Pradotto, L. G., Mazzeo, A., Frusconi, S., My, F., Manfellotto, D., Fuciarelli, M., Polimanti, R.

مصطلحات موضوعية: Amyloid, Gene expression, Genotype-phenotype correlation, Mutation, Transthyretin, Amyloidosi, Genotype, Human, Phenotype, Prealbumin, Gene Expression Regulation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28335735; info:eu-repo/semantics/altIdentifier/wos/WOS:000397086100008; volume:18; issue:1; firstpage:1; lastpage:8; numberofpages:8; journal:BMC GENOMICS; http://hdl.handle.net/11570/3169920Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85027024467

الإتاحة: https://doi.org/10.1186/s12864-017-3646-1Test
http://hdl.handle.net/11570/3169920Test

المؤلفون: Brugliera L., Filippi M., Del Carro U., Butera C., Bianchi F., Castellazzi P., Cimino P., Capodaglio P., Monti G., Mortini P., Pradotto L. G., Priano L., Spina A., Iannaccone S.

المساهمون: Brugliera, L., Filippi, M., Del Carro, U., Butera, C., Bianchi, F., Castellazzi, P., Cimino, P., Capodaglio, P., Monti, G., Mortini, P., Pradotto, L. G., Priano, L., Spina, A., Iannaccone, S.

مصطلحات موضوعية: Brachial plexus, Coronavirus, Prone position, Rehabilitation, Adult, Aged, COVID-19, Humans, Italy, Male, Middle Aged, Nerve Compression Syndromes, Patient Positioning, Respiration, Artificial, Retrospective Studies, SARS-CoV-2

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000632559000002; volume:102; issue:3; firstpage:359; lastpage:362; numberofpages:4; journal:ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION; http://hdl.handle.net/20.500.11768/114530Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85099905899

الإتاحة: https://doi.org/20.500.11768/114530Test
https://doi.org/10.1016/j.apmr.2020.10.131Test
https://hdl.handle.net/20.500.11768/114530Test

المؤلفون: Russo M, Merlini G, Obici L, Pacciolla P, Fabrizi G, Cavallaro T, Sabatelli M, Luigetti M, Bisogni G, Pareyson D, Fenu S, Calabrese D, Rapezzi C, Bartolomei I, Grandis M, Gemelli C, Mauro A, Pradotto L, Santoro L, Manganelli F, Antonini G, Leonardi L, Vanoli F, My F, Gentile L, Stancanelli C, Mazzeo A, Vita G

المساهمون: Russo, M, Merlini, G, Obici, L, Pacciolla, P, Fabrizi, G, Cavallaro, T, Sabatelli, M, Luigetti, M, Bisogni, G, Pareyson, D, Fenu, S, Calabrese, D, Rapezzi, C, Bartolomei, I, Grandis, M, Gemelli, C, Mauro, A, Pradotto, L, Santoro, L, Manganelli, F, Antonini, G, Leonardi, L, Vanoli, F, My, F, Gentile, L, Stancanelli, C, Mazzeo, A, Vita, G

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000464950800073; ispartofbook:Journal Peripheral Nervous System; Ninth Annual Meeting of the Italian Association for the Study of the Peripheral Nervous System (ASNP); volume:24; issue:Suppl 1; firstpage:S38; lastpage:S39; numberofpages:2; http://hdl.handle.net/11570/3151614Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85064771976

الإتاحة: https://doi.org/10.1111/jns.12312Test
http://hdl.handle.net/11570/3151614Test

المؤلفون: Russo M., Obici L., Bartolomei I., Cappelli F., Luigetti M., Fenu S., Cavallaro T., Chiappini M. G., Gemelli C., Pradotto L. G., Manganelli F., Leonardi L., My F., Sampaolo S., Briani C., Gentile L., Stancanelli C., Di Buduo E., Pacciolla P., Salvi F., Casagrande S., Bisogni G., Calabrese D., Vanoli F., Di Iorio G., Antonini G., Santoro L., Mauro A., Grandis M., Di Girolamo M., Fabrizi G. M., Pareyson D., Sabatelli M., Perfetto F., Rapezzi C., Merlini G., Mazzeo A., Vita G.

المساهمون: Russo, M., Obici, L., Bartolomei, I., Cappelli, F., Luigetti, M., Fenu, S., Cavallaro, T., Chiappini, M. G., Gemelli, C., Pradotto, L. G., Manganelli, F., Leonardi, L., My, F., Sampaolo, S., Briani, C., Gentile, L., Stancanelli, C., Di Buduo, E., Pacciolla, P., Salvi, F., Casagrande, S., Bisogni, G., Calabrese, D., Vanoli, F., Di Iorio, G., Antonini, G., Santoro, L., Mauro, A., Grandis, M., Di Girolamo, M., Fabrizi, G. M., Pareyson, D., Sabatelli, M., Perfetto, F., Rapezzi, C., Merlini, G., Mazzeo, A., Vita, G.

مصطلحات موضوعية: Amyloidosi, ATTRv, Italy, polyneuropathy, prevalence

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32696671; info:eu-repo/semantics/altIdentifier/wos/WOS:000550948300001; firstpage:1; lastpage:7; numberofpages:7; journal:AMYLOID; http://hdl.handle.net/11573/1441779Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85088483014

الإتاحة: https://doi.org/10.1080/13506129.2020.1794807Test
http://hdl.handle.net/11573/1441779Test

المؤلفون: Moglia C., Calvo A., Grassano M., Canosa A., Manera U., D'ovidio F., Bombaci A., Bersano E., Mazzini L., Mora G., Chio A., Cammarosano S., Vasta R., Torrieri M. C., Solero L., Clerico M., De Mercanti S., Mauro A., Pradotto L., De Marchi F., Sosso L., Leotta D., Appendino L., Imperiale D., Cavallo R., Geda C., Poglio F., Santimaria P., Massazza U., Villani A., Conti R., Ruiz L. C., Palermo M., Vergnano F., Rota E., Penza M. T., Aguggia M., Meineri P., Ghiglione P., Launaro N., Astegiano G., Corso G.

المساهمون: Moglia, C., Calvo, A., Grassano, M., Canosa, A., Manera, U., D'Ovidio, F., Bombaci, A., Bersano, E., Mazzini, L., Mora, G., Chio, A., Cammarosano, S., Vasta, R., Torrieri, M. C., Solero, L., Clerico, M., De Mercanti, S., Mauro, A., Pradotto, L., De Marchi, F., Sosso, L., Leotta, D., Appendino, L., Imperiale, D., Cavallo, R., Geda, C., Poglio, F., Santimaria, P., Massazza, U., Villani, A., Conti, R., Ruiz, L. C., Palermo, M., Vergnano, F., Rota, E., Penza, M. T., Aguggia, M., Meineri, P., Ghiglione, P., Launaro, N., Astegiano, G., Corso, G.

مصطلحات موضوعية: amyotrophic lateral sclerosis, body mass index, dysphagia, respiratory function, weight loss

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30630957; info:eu-repo/semantics/altIdentifier/wos/WOS:000471118100009; volume:90; issue:6; firstpage:666; lastpage:673; numberofpages:8; journal:JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY; https://hdl.handle.net/20.500.11768/159125Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85059804964; http://jnnp.bmj.comTest/

الإتاحة: https://doi.org/20.500.11768/159125Test
https://doi.org/10.1136/jnnp-2018-319611Test
https://hdl.handle.net/20.500.11768/159125Test
http://jnnp.bmj.comTest/

المؤلفون: Brussino, A, Vaula, G, Cagnoli, C, Mauro, A, Pradotto, L, Daniele, D, Di Gregorio, E, Barberis, M, Arduino, C, Squadrone, S, Abete, M C, Migone, N, Calabrese, O, Brusco, A

مصطلحات موضوعية: Short reports

وصف الملف: text/html

العلاقة: http://jnnp.bmj.com/cgi/content/short/80/2/237Test; http://dx.doi.org/10.1136/jnnp.2008.147330Test

الإتاحة: https://doi.org/10.1136/jnnp.2008.147330Test
http://jnnp.bmj.com/cgi/content/short/80/2/237Test

المؤلفون: Priano, L, Giaccone, G, Mangieri, M, Albani, G, Limido, L, Brioschi, A, Pradotto, L, Orsi, L, Mortara, P, Fociani, P, Mauro, A, Tagliavini, F

مصطلحات موضوعية: Short reports

وصف الملف: text/html

العلاقة: http://jnnp.bmj.com/cgi/content/short/80/8/924Test; http://dx.doi.org/10.1136/jnnp.2008.154815Test

الإتاحة: https://doi.org/10.1136/jnnp.2008.154815Test
http://jnnp.bmj.com/cgi/content/short/80/8/924Test

المؤلفون: Mancini C, Giorgio E, Rubegni A, Pradotto L, Bagnoli S, Rubino E, Prontera P, Cavalieri S, Di Gregorio E, Ferrero M, Pozzi E, Riberi E, Ferrero P, Nigro P, Mauro A, Zibetti M, Tessa A, Barghigiani M, Antenora A, Sirchia F, Piacentini S, Silvestri G, De Michele G, Filla A, Orsi L, Santorelli FM, Brusco A

المساهمون: Mancini, C, Giorgio, E, Rubegni, A, Pradotto, L, Bagnoli, S, Rubino, E, Prontera, P, Cavalieri, S, Di Gregorio, E, Ferrero, M, Pozzi, E, Riberi, E, Ferrero, P, Nigro, P, Mauro, A, Zibetti, M, Tessa, A, Barghigiani, M, Antenora, A, Sirchia, F, Piacentini, S, Silvestri, G, De Michele, G, Filla, A, Orsi, L, Santorelli, Fm, Brusco, A

مصطلحات موضوعية: Ala510Valhereditary ataxiaparapleginautosomal recessive spinocerebellar ataxiasspastic ataxiaSPG7

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000452969300011; volume:26; issue:1; firstpage:80; lastpage:86; numberofpages:7; journal:EUROPEAN JOURNAL OF NEUROLOGY; http://hdl.handle.net/11588/720976Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85052911703; Prevalence and phenotype of the c.1529C>T SPG7 variant in adult-onset cerebellar ataxia in Italy.

الإتاحة: https://doi.org/10.1111/ene.13768Test
http://hdl.handle.net/11588/720976Test