MANCARDI, GIOVANNI LUIGI
MANCARDI, GIOVANNI LUIGI
100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-Infantili
"Pure" meningeal carcinomatosis as the autopsy-proven sole manifestation of an undetected cancer
1992-01-01 Leonardi, A; Dagnino, N; Farinelli, M; Gambini, C; Ribizzi, G; Schenone, A; Mancardi, G L
'Apraxia' of eye opening in idiopathic Parkinson's disease.
1986-01-01 Brusa, A; Mancardi, GIOVANNI LUIGI; Meneghini, S; Piccardo, A; Brusa, G.
123I-FP-CIT SPECT validation of nigro-putaminal MRI tractography in dementia with Lewy bodies
2020-01-01 Pardini, Matteo; Nobili, Flavio; Arnaldi, Dario; Morbelli, Silvia; Bauckneht, Matteo; Rissotto, Roberto; Serrati, Carlo; Serafini, Gianluca; Lapucci, Caterina; Ghio, Lucio; Amore, Mario; Massucco, Davide; Sassos, Davide; Bonzano, Laura; Mancardi, Giovanni Luigi; Roccatagliata, Luca
17p11.2 duplication is a common finding in sporadic cases of charcot-marie-tooth type 1
1994-01-01 Mancardi, G. L.; Uccelli, A.; Bellone, E.; Sghirlanzoni, A.; Mandich, P.; Pareyson, D.; Schenone, A.; Abbruzzese, M.; Ajmar, F.
: Effect of total lymphoid irradiation (TLI) on circulating lymphocyte subsets in chronic progressive multiple sclerosis (CPMS) patients.
1993-01-01 Kunkle, A.; Valle, M. T.; Fenoglio, D.; Manca, F.; Vitale, V.; Corvo', RENZO GIACINTO; Giunti, D.; Capello, E.; Mancardi, GIOVANNI LUIGI; Rovida, S.
[Clinical aspects of cerebral arteriovenous malformations].
1986-01-01 Mancardi, GIOVANNI LUIGI
[Granular atrophy of the cerebellum. Apropos of an anatomo-clinical case].
1976-01-01 Mancardi, GIOVANNI LUIGI; Berio, Agostino; Mangiante, G.
[Hereditary sensory motor neuropathy: degenerative disease or a disease with an immune-mediated pathogenesis?].
1989-01-01 Cadoni, Angela; Zicca, Antonio; Mancardi, GIOVANNI LUIGI; DE MARTINI, Isabella; Schenone, Angelo; Zaccheo, D.
[Pathologic anatomy of cerebral arteriovenous malformations].
1986-01-01 Mancardi, GIOVANNI LUIGI
[Schwann cells in acute and chronic Guillain-Barré syndrome].
1987-01-01 Cadoni, Angela; Zicca, Antonio; Schenone, Angelo; DE MARTINI, Isabella; Mancardi, GIOVANNI LUIGI
[The culturing of human Schwann cells: a new contribution to the study of polyneuropathy].
1989-01-01 DE MARTINI, Isabella; Cadoni, Angela; Zicca, Antonio; Mancardi, GIOVANNI LUIGI; Bianchini, D; Zaccheo, D.
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
2011-01-01 Mandich, Paola; E., Majounie; A., Waite; J., Simón Sánchez; S., Rollinson; J. R., Gibbs; J. C., Schymick; H., Laaksovirta; J. C., Van; L., Myllykangas; H., Kalimo; A., Paetau; Y., Abramzon; A. M., Remes; A., Kaganovich; S. W., Scholz; J., Duckworth; J., Ding; D. W., Harmer; D. G., Hernandez; J. O., Johnson; K., Mok; M., Ryten; D., Trabzuni; R. J., Guerreiro; R. W., Orrell; J., Neal; A., Murray; J., Pearson; I. E., Jansen; D., Sondervan; H., Seelaar; D., Blake; K., Young; N., Halliwell; J. B., Callister; G., Toulson; A., Richardson; A., Gerhard; J., Snowden; D., Mann; D., Neary; M. A., Nalls; T., Peuralinna; L., Jansson; V., Isoviita; A., Kaivorinne; M., Hölttä Vuori; E., Ikonen; R., Sulkava; M., Benatar; J., Wuu; A., Chiò; G., Restagno; G., Borghero; M., Sabatelli; Mancardi, GIOVANNI LUIGI; D., Heckerman; E., Rogaeva; L., Zinman; J. D., Rothstein; M., Sendtner; C., Drepper; E. E., Eichler; C., Alkan; Z., Abdullaev; S. D., Pack; A., Dutra; E., Pak; J., Hardy; A., Singleton; N. M., Williams; P., Heutink; S., Pickering Brown; H. R., Morris; P. J., Tienari; B. J., Traynor
A major influence of the T cell receptor repertoire as compared to antigen processing-presentation in the selection of myelin basic protein epitopes in multiple sclerosis.
1999-01-01 G., Ristori; C., Montesperelli; Uccelli, Antonio; Giunti, Debora; C., Buttinelli; R., Bomprezzi; Mancardi, GIOVANNI LUIGI; M., Salvetti
A multicenter, randomized, double-blind, placebo-controlled trial of long-term ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL): the study protocol
2006-01-01 Pareyson, D; Schenone, A; Fabrizi, Gm; Santoro, L; Padua, L; Quattrone, A; Vita, G; Gemignani, F; Visioli, F; Solari, A; Salsano, E; Scaioli, V; Ciano, C; Rimoldi, M; Lauria, G; Rizzetto, E; Camozzi, F; Grandis, M; Narciso, E; Nobbio, L; Benedetti, L; Rizzuto, N; Cavallaro, T; Bertolasi, L; Casano, A; Manganelli, F; Nolano, M; Pazzaglia, C; Valentino, P; Nisticò, R; Pirritano, D; Lucisano, A; Canino, M; Mazzeo, A; Aguennouz, M; Di Leo, R; Girlanda, P; Majorana, G; Ciranni, A; Lanzano, N; Brindani, F; Lettieri, C; Bogani, P; Hughes, Rac; Mancardi, Gl; Cavaletti, G; Galimberti, S; Radice, D; Calabrese, D; Ferrari, G.
A New App for At-Home Cognitive Training: Description and Pilot Testing on Patients with Multiple Sclerosis
2015-01-01 Tacchino, Andrea; Pedulla', Ludovico; Bonzano, Laura; Vassallo, Claudio; Battaglia, Mario Alberto; Mancardi, GIOVANNI LUIGI; Bove, Marco; Brichetto, Giampaolo
A normative study of the Italian printed word version of the free and cued selective reminding test
2015-01-01 Girtler, NICOLA GIOVANNI; De Carli, F.; Amore, Mario; Arnaldi, Dario; Bosia, L. E.; Bruzzaniti, C.; Cappa, S. F.; Cocito, Leonardo; Colazzo, G.; Ghio, L.; Magi, E.; Mancardi, GIOVANNI LUIGI; Nobili, FLAVIO MARIANO; Pardini, Matteo; Picco, A.; Rissotto, R.; Serrati, C.; Brugnolo, Andrea
A novel hypothesis about mechanisms affecting conduction velocity of central myelinated fibers.
2011-01-01 Adriano, ENRICO GIOVANNI; Perasso, Luisa; Panfoli, Isabella; Ravera, Silvia; Gandolfo, Carlo; Mancardi, GIOVANNI LUIGI; Morelli, Alessandro; Balestrino, Maurizio
A novel prion protein gene-truncating mutation causing autonomic neuropathy and diarrhea
2018-01-01 Bommarito, G.; Cellerino, M.; Prada, V.; Venturi, C.; Capellari, S.; Cortelli, P.; Mancardi, G. L.; Parchi, P.; Schenone, A.
A numerical simulation for brain stroke microwave imaging by using the FVTD
2015-01-01 Cerruti, Matteo; Lavagetto, Fabio; Mancardi, GIOVANNI LUIGI; Pastorino, Matteo; Randazzo, Andrea
A patient with multiple sclerosis and Down's syndrome with a rare paroxysmal symptom at onset.
1999-01-01 C., Solaro; M. M., Uccelli; Mancardi, GIOVANNI LUIGI
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
"Pure" meningeal carcinomatosis as the autopsy-proven sole manifestation of an undetected cancer | 1-gen-1992 | Leonardi, A; Dagnino, N; Farinelli, M; Gambini, C; Ribizzi, G; Schenone, A; Mancardi, G L | |
'Apraxia' of eye opening in idiopathic Parkinson's disease. | 1-gen-1986 | Brusa, A; Mancardi, GIOVANNI LUIGI; Meneghini, S; Piccardo, A; Brusa, G. | |
123I-FP-CIT SPECT validation of nigro-putaminal MRI tractography in dementia with Lewy bodies | 1-gen-2020 | Pardini, Matteo; Nobili, Flavio; Arnaldi, Dario; Morbelli, Silvia; Bauckneht, Matteo; Rissotto, Roberto; Serrati, Carlo; Serafini, Gianluca; Lapucci, Caterina; Ghio, Lucio; Amore, Mario; Massucco, Davide; Sassos, Davide; Bonzano, Laura; Mancardi, Giovanni Luigi; Roccatagliata, Luca | |
17p11.2 duplication is a common finding in sporadic cases of charcot-marie-tooth type 1 | 1-gen-1994 | Mancardi, G. L.; Uccelli, A.; Bellone, E.; Sghirlanzoni, A.; Mandich, P.; Pareyson, D.; Schenone, A.; Abbruzzese, M.; Ajmar, F. | |
: Effect of total lymphoid irradiation (TLI) on circulating lymphocyte subsets in chronic progressive multiple sclerosis (CPMS) patients. | 1-gen-1993 | Kunkle, A.; Valle, M. T.; Fenoglio, D.; Manca, F.; Vitale, V.; Corvo', RENZO GIACINTO; Giunti, D.; Capello, E.; Mancardi, GIOVANNI LUIGI; Rovida, S. | |
[Clinical aspects of cerebral arteriovenous malformations]. | 1-gen-1986 | Mancardi, GIOVANNI LUIGI | |
[Granular atrophy of the cerebellum. Apropos of an anatomo-clinical case]. | 1-gen-1976 | Mancardi, GIOVANNI LUIGI; Berio, Agostino; Mangiante, G. | |
[Hereditary sensory motor neuropathy: degenerative disease or a disease with an immune-mediated pathogenesis?]. | 1-gen-1989 | Cadoni, Angela; Zicca, Antonio; Mancardi, GIOVANNI LUIGI; DE MARTINI, Isabella; Schenone, Angelo; Zaccheo, D. | |
[Pathologic anatomy of cerebral arteriovenous malformations]. | 1-gen-1986 | Mancardi, GIOVANNI LUIGI | |
[Schwann cells in acute and chronic Guillain-Barré syndrome]. | 1-gen-1987 | Cadoni, Angela; Zicca, Antonio; Schenone, Angelo; DE MARTINI, Isabella; Mancardi, GIOVANNI LUIGI | |
[The culturing of human Schwann cells: a new contribution to the study of polyneuropathy]. | 1-gen-1989 | DE MARTINI, Isabella; Cadoni, Angela; Zicca, Antonio; Mancardi, GIOVANNI LUIGI; Bianchini, D; Zaccheo, D. | |
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. | 1-gen-2011 | Mandich, Paola; E., Majounie; A., Waite; J., Simón Sánchez; S., Rollinson; J. R., Gibbs; J. C., Schymick; H., Laaksovirta; J. C., Van; L., Myllykangas; H., Kalimo; A., Paetau; Y., Abramzon; A. M., Remes; A., Kaganovich; S. W., Scholz; J., Duckworth; J., Ding; D. W., Harmer; D. G., Hernandez; J. O., Johnson; K., Mok; M., Ryten; D., Trabzuni; R. J., Guerreiro; R. W., Orrell; J., Neal; A., Murray; J., Pearson; I. E., Jansen; D., Sondervan; H., Seelaar; D., Blake; K., Young; N., Halliwell; J. B., Callister; G., Toulson; A., Richardson; A., Gerhard; J., Snowden; D., Mann; D., Neary; M. A., Nalls; T., Peuralinna; L., Jansson; V., Isoviita; A., Kaivorinne; M., Hölttä Vuori; E., Ikonen; R., Sulkava; M., Benatar; J., Wuu; A., Chiò; G., Restagno; G., Borghero; M., Sabatelli; Mancardi, GIOVANNI LUIGI; D., Heckerman; E., Rogaeva; L., Zinman; J. D., Rothstein; M., Sendtner; C., Drepper; E. E., Eichler; C., Alkan; Z., Abdullaev; S. D., Pack; A., Dutra; E., Pak; J., Hardy; A., Singleton; N. M., Williams; P., Heutink; S., Pickering Brown; H. R., Morris; P. J., Tienari; B. J., Traynor | |
A major influence of the T cell receptor repertoire as compared to antigen processing-presentation in the selection of myelin basic protein epitopes in multiple sclerosis. | 1-gen-1999 | G., Ristori; C., Montesperelli; Uccelli, Antonio; Giunti, Debora; C., Buttinelli; R., Bomprezzi; Mancardi, GIOVANNI LUIGI; M., Salvetti | |
A multicenter, randomized, double-blind, placebo-controlled trial of long-term ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL): the study protocol | 1-gen-2006 | Pareyson, D; Schenone, A; Fabrizi, Gm; Santoro, L; Padua, L; Quattrone, A; Vita, G; Gemignani, F; Visioli, F; Solari, A; Salsano, E; Scaioli, V; Ciano, C; Rimoldi, M; Lauria, G; Rizzetto, E; Camozzi, F; Grandis, M; Narciso, E; Nobbio, L; Benedetti, L; Rizzuto, N; Cavallaro, T; Bertolasi, L; Casano, A; Manganelli, F; Nolano, M; Pazzaglia, C; Valentino, P; Nisticò, R; Pirritano, D; Lucisano, A; Canino, M; Mazzeo, A; Aguennouz, M; Di Leo, R; Girlanda, P; Majorana, G; Ciranni, A; Lanzano, N; Brindani, F; Lettieri, C; Bogani, P; Hughes, Rac; Mancardi, Gl; Cavaletti, G; Galimberti, S; Radice, D; Calabrese, D; Ferrari, G. | |
A New App for At-Home Cognitive Training: Description and Pilot Testing on Patients with Multiple Sclerosis | 1-gen-2015 | Tacchino, Andrea; Pedulla', Ludovico; Bonzano, Laura; Vassallo, Claudio; Battaglia, Mario Alberto; Mancardi, GIOVANNI LUIGI; Bove, Marco; Brichetto, Giampaolo | |
A normative study of the Italian printed word version of the free and cued selective reminding test | 1-gen-2015 | Girtler, NICOLA GIOVANNI; De Carli, F.; Amore, Mario; Arnaldi, Dario; Bosia, L. E.; Bruzzaniti, C.; Cappa, S. F.; Cocito, Leonardo; Colazzo, G.; Ghio, L.; Magi, E.; Mancardi, GIOVANNI LUIGI; Nobili, FLAVIO MARIANO; Pardini, Matteo; Picco, A.; Rissotto, R.; Serrati, C.; Brugnolo, Andrea | |
A novel hypothesis about mechanisms affecting conduction velocity of central myelinated fibers. | 1-gen-2011 | Adriano, ENRICO GIOVANNI; Perasso, Luisa; Panfoli, Isabella; Ravera, Silvia; Gandolfo, Carlo; Mancardi, GIOVANNI LUIGI; Morelli, Alessandro; Balestrino, Maurizio | |
A novel prion protein gene-truncating mutation causing autonomic neuropathy and diarrhea | 1-gen-2018 | Bommarito, G.; Cellerino, M.; Prada, V.; Venturi, C.; Capellari, S.; Cortelli, P.; Mancardi, G. L.; Parchi, P.; Schenone, A. | |
A numerical simulation for brain stroke microwave imaging by using the FVTD | 1-gen-2015 | Cerruti, Matteo; Lavagetto, Fabio; Mancardi, GIOVANNI LUIGI; Pastorino, Matteo; Randazzo, Andrea | |
A patient with multiple sclerosis and Down's syndrome with a rare paroxysmal symptom at onset. | 1-gen-1999 | C., Solaro; M. M., Uccelli; Mancardi, GIOVANNI LUIGI |