Sfoglia per Autore
HYPEREKPLEXIA IN PATIENT WITH A BRAINSTEM VASCULAR ANOMALY
1999-01-01 Gambardella, A; Valentino, P; Annesi, G; Oliveri, Rl; Bono, F; Mazzei, Rl; Conforti, F; Bono, F; Aguglia, U; Zappia, M; Pardatscher, K; Quattrone, A
APOE AND RISK OF COGNITIVE IMPAIRMENT IN MULTIPLE SCLEROSIS
1999-01-01 Oliveri, Rl; Cittadella, R; Sibilia, G; Manna, I; Valentino, P; Gambardella, A; Aguglia, U; Zappia, M; Romeo, N; Andreoli, V; Bono, F; Et, Al
Hyperekplexia in a patient with a brainstem vascular anomaly
1999-01-01 Valentino, P; Annesi, G; Oliveri, Rl; Bono, F; Mazzei, R; Conforti, Fl; Aguglia, U; Zappia, M; Pardatscher, K; Quattrone, A.; Gambardella, A
Calf pseudohypertrophy in a patient with double neurogenic pathology
2000-01-01 Valentino, P; Santucci, M; Amorosi, A; Pittelli, M; Maltese, L; Volpentesta, G; Chirchiglia, D; Iannello, An; Ferraro, G; Signorelli, Cd; Lavano, A; Donato, G
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chomosome 1
2000-01-01 Gambardella, A; Annesi, G; DE FUSCO, M; Patrignani, A; Aguglia, U; Annesi, F; Spadafora, P; Oliveri, Rl; Valentino, P; Zappia, M; Ballabio, A; Et, Al
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1
2000-01-01 Gambardella, A; Annesi, G; DE FUSCO, M; Patrignani, A; Aguglia, U; Annesi, F; Pasqua, Aa; Spadafora, P; Oliveri, Rl; Valentino, P; Zappia, M; Ballabio, A; Casari, G; Quattrone, A.
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy
2001-01-01 Muglia, M; Zappia, M; Timmerman, V V; Valentino, P; Gabriele, Al; Conforti, Fl; DE JONGHE, P; Ragno, M; Mazzei, R; Sabatelli, M; Nicoletti, G; Patitucci, Am; Oliveri, Rl; Bono, F; Gambardella, A; Quattrone, A.
Juvenile Huntington's disease presenting as progressive myoclonic epilepsy
2001-01-01 Gambardella, A; Muglia, M.; Labate, A.; Magariello, A.; Gabriele, Al.; Mazzei, R.; Pirritano, D.; Conforti, Fl.; Patitucci, A.; Valentino, P.; Zappia, M.; Quattrone, A.
Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH
2001-01-01 Quattrone, A; Bono, F; Oliveri, Rl; Gambardella, A; Pirritano, D; Labate, A; Lucisano, A; Valentino, P; Zappia, M; Aguglia, U; Lavano, A; Fera, F; Pardatscher, K
Cerebral venous thrombosis and isolated intracrania hypertension without papilledema in CDH
2001-01-01 Quattrone, A; Bono, F; Oliveri, Rl; Gambardella, A; Pirritano, D; Labate, A; Lucisano, A; Valentino, P; Zappia, M; Aguglia, U; Lavano, A; Fera, F; Pardatscher, K
Clinical and genetic study of a large Charcot-Marie-Tooth type 2° family southern Italy
2001-01-01 Muglia, M; Zappia, M; Timmerman, V; Valentino, P; Gabriele, Al; Conforti, Fl; DE JONGHE, P; Ragno, M; Mazzei, R; Sabatelli, M; Nicoletti, G; Et, Al
Silent coeliac disease in patients with childhood localization-related epilepsies
2001-01-01 Labate, A; Gambardella, A.; Messina, D.; Tammaro, S.; LE PIANE, E.; Pirritano, D.; Cosco, C.; Doldo, P.; Mazzei, R.; Oliveti, R. L.; Bosco, D.; Zappia, M.; Valentino, P.; Aguglia, U.; Quattrone, A.
Silent celiac disease in patients with childhood localization-related epilepsies
2001-01-01 Labate, A; Messina, D; Tammaro, S; LE PIANE, E; Pirritano, D; Cosco, C; Mazzei, R; Oliveri, Rl; Bosco, D; Zappia, M; Aguglia, U; Quattrone, A.; Valentino, Paola; Doldo, P; Gambardella, Antonio
LACK OF ASSOCIATION BETWEEN ESTROGEN RECEPTOR 1 GENE POLYMORPHISMS AND MULTIPLE SCLEROSIS IN SOUTHERN ITALY IN HUMANS
2002-01-01 Savettieri, G; Cittadella, R; Valentino, P; Manna, I; Andreoli, V; Russa, A; Laporta, G; Ruscica, F; Ragonese, P; Pirritano, D; Bonavita, S; Et, Al
Temporal lobe epilepsy as a unique manifestation of multiple sclerosis
2003-01-01 Gambardella, A; Valentino, P; Labate, A; Sibilia, G; Ruscica, F; Colosimo, E; Nistico, R; Messina, D; Zappia, M; Quattrone, A.
CD45 AND MULTIPLE SCLEROSIS:THE EXON 4C77G POLYMORPHISM (ADDITIONAL STUDIES AND META-ANALYSIS) AND NEW MARKERS
2003-01-01 Gomezlira, M; Liguori, M; Magnani, C; Bonamini, D; Salviati, A; Leone, M; Andreoli, V; Trojano, M; Valentino, P; Savettieri, G; Quattrone, A; Pignatti, Pf; Momiglianorichiardi, P; Giordano, M.
APOLIPOPROTEIN E GENOTYPE DOES NOT INFLUENCE THE PROGRESSION OF MULTIPLE SCLEROSIS
2003-01-01 Savettieri, G; Andreoli, V; Bonavita, S; Cittadella, R; Caltagirone, C; Fazio, Mc; Girlanda, P; LE PIRA, F; Liguori, M; Locroscino, G; Lugaresi, A; Nocentini, U; Reggio, A; Salemi, G; Serra, P; Tedeschi, G; Toma, L; Trojano, M; Valentino, P; Quattrone, A.
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis?
2004-01-01 Mancuso, M; Conforti, Fl; Rocchi, A; Tessitore, A; Muglia, M; Tedeschi, G; Panza, D; Monsurro, M; Sola, P; Mandrioli, J; Choub, A; Delcorona, A; Manca, Ml; Mazzei, R; Sprovieri, T; Filosto, M; Salviati, A; Valentino, P; Bono, F; Caracciolo, M; Simone, Il; LA BELLA, V; Majorana, G; Siciliano, G; Murri, L; Quattrone, A.
Gene conversion events in adult-onset spinal muscular atrophy
2004-01-01 Mazzei, R; Gambardella, A; Conforti, Fl; Magariello, A; Patitucci, A; Gabriele, Al; Sprovieri, T; Labate, A; Valentino, P; Bono, F; Bonavita, S; Zappia, M; Muglia, M; Quattrone, A.
NARROWING OF THE CRITICAL REGION IN AUTOSOMAL RECESSIVE SPASTIC PARAPLEGIA LINKED TO THE SPG5 LOCUS
2004-01-01 Muglia, M; Criscuolo, C; Magariello, A; DE MICHELE, G; Scarano, V; D'Adamo, P; Ambrosio, G; Gabriele, Al; Patitucci, A; Mazzei, R; Confori, Fl; Sprovieri, T; Morgante, L; Epifano, A; LA SPINA, P; Valentino, P; Gasparini, P; Filla, A; Quattrone, A
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
HYPEREKPLEXIA IN PATIENT WITH A BRAINSTEM VASCULAR ANOMALY | 1-gen-1999 | Gambardella, A; Valentino, P; Annesi, G; Oliveri, Rl; Bono, F; Mazzei, Rl; Conforti, F; Bono, F; Aguglia, U; Zappia, M; Pardatscher, K; Quattrone, A | |
APOE AND RISK OF COGNITIVE IMPAIRMENT IN MULTIPLE SCLEROSIS | 1-gen-1999 | Oliveri, Rl; Cittadella, R; Sibilia, G; Manna, I; Valentino, P; Gambardella, A; Aguglia, U; Zappia, M; Romeo, N; Andreoli, V; Bono, F; Et, Al | |
Hyperekplexia in a patient with a brainstem vascular anomaly | 1-gen-1999 | Valentino, P; Annesi, G; Oliveri, Rl; Bono, F; Mazzei, R; Conforti, Fl; Aguglia, U; Zappia, M; Pardatscher, K; Quattrone, A.; Gambardella, A | |
Calf pseudohypertrophy in a patient with double neurogenic pathology | 1-gen-2000 | Valentino, P; Santucci, M; Amorosi, A; Pittelli, M; Maltese, L; Volpentesta, G; Chirchiglia, D; Iannello, An; Ferraro, G; Signorelli, Cd; Lavano, A; Donato, G | |
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chomosome 1 | 1-gen-2000 | Gambardella, A; Annesi, G; DE FUSCO, M; Patrignani, A; Aguglia, U; Annesi, F; Spadafora, P; Oliveri, Rl; Valentino, P; Zappia, M; Ballabio, A; Et, Al | |
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 | 1-gen-2000 | Gambardella, A; Annesi, G; DE FUSCO, M; Patrignani, A; Aguglia, U; Annesi, F; Pasqua, Aa; Spadafora, P; Oliveri, Rl; Valentino, P; Zappia, M; Ballabio, A; Casari, G; Quattrone, A. | |
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy | 1-gen-2001 | Muglia, M; Zappia, M; Timmerman, V V; Valentino, P; Gabriele, Al; Conforti, Fl; DE JONGHE, P; Ragno, M; Mazzei, R; Sabatelli, M; Nicoletti, G; Patitucci, Am; Oliveri, Rl; Bono, F; Gambardella, A; Quattrone, A. | |
Juvenile Huntington's disease presenting as progressive myoclonic epilepsy | 1-gen-2001 | Gambardella, A; Muglia, M.; Labate, A.; Magariello, A.; Gabriele, Al.; Mazzei, R.; Pirritano, D.; Conforti, Fl.; Patitucci, A.; Valentino, P.; Zappia, M.; Quattrone, A. | |
Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH | 1-gen-2001 | Quattrone, A; Bono, F; Oliveri, Rl; Gambardella, A; Pirritano, D; Labate, A; Lucisano, A; Valentino, P; Zappia, M; Aguglia, U; Lavano, A; Fera, F; Pardatscher, K | |
Cerebral venous thrombosis and isolated intracrania hypertension without papilledema in CDH | 1-gen-2001 | Quattrone, A; Bono, F; Oliveri, Rl; Gambardella, A; Pirritano, D; Labate, A; Lucisano, A; Valentino, P; Zappia, M; Aguglia, U; Lavano, A; Fera, F; Pardatscher, K | |
Clinical and genetic study of a large Charcot-Marie-Tooth type 2° family southern Italy | 1-gen-2001 | Muglia, M; Zappia, M; Timmerman, V; Valentino, P; Gabriele, Al; Conforti, Fl; DE JONGHE, P; Ragno, M; Mazzei, R; Sabatelli, M; Nicoletti, G; Et, Al | |
Silent coeliac disease in patients with childhood localization-related epilepsies | 1-gen-2001 | Labate, A; Gambardella, A.; Messina, D.; Tammaro, S.; LE PIANE, E.; Pirritano, D.; Cosco, C.; Doldo, P.; Mazzei, R.; Oliveti, R. L.; Bosco, D.; Zappia, M.; Valentino, P.; Aguglia, U.; Quattrone, A. | |
Silent celiac disease in patients with childhood localization-related epilepsies | 1-gen-2001 | Labate, A; Messina, D; Tammaro, S; LE PIANE, E; Pirritano, D; Cosco, C; Mazzei, R; Oliveri, Rl; Bosco, D; Zappia, M; Aguglia, U; Quattrone, A.; Valentino, Paola; Doldo, P; Gambardella, Antonio | |
LACK OF ASSOCIATION BETWEEN ESTROGEN RECEPTOR 1 GENE POLYMORPHISMS AND MULTIPLE SCLEROSIS IN SOUTHERN ITALY IN HUMANS | 1-gen-2002 | Savettieri, G; Cittadella, R; Valentino, P; Manna, I; Andreoli, V; Russa, A; Laporta, G; Ruscica, F; Ragonese, P; Pirritano, D; Bonavita, S; Et, Al | |
Temporal lobe epilepsy as a unique manifestation of multiple sclerosis | 1-gen-2003 | Gambardella, A; Valentino, P; Labate, A; Sibilia, G; Ruscica, F; Colosimo, E; Nistico, R; Messina, D; Zappia, M; Quattrone, A. | |
CD45 AND MULTIPLE SCLEROSIS:THE EXON 4C77G POLYMORPHISM (ADDITIONAL STUDIES AND META-ANALYSIS) AND NEW MARKERS | 1-gen-2003 | Gomezlira, M; Liguori, M; Magnani, C; Bonamini, D; Salviati, A; Leone, M; Andreoli, V; Trojano, M; Valentino, P; Savettieri, G; Quattrone, A; Pignatti, Pf; Momiglianorichiardi, P; Giordano, M. | |
APOLIPOPROTEIN E GENOTYPE DOES NOT INFLUENCE THE PROGRESSION OF MULTIPLE SCLEROSIS | 1-gen-2003 | Savettieri, G; Andreoli, V; Bonavita, S; Cittadella, R; Caltagirone, C; Fazio, Mc; Girlanda, P; LE PIRA, F; Liguori, M; Locroscino, G; Lugaresi, A; Nocentini, U; Reggio, A; Salemi, G; Serra, P; Tedeschi, G; Toma, L; Trojano, M; Valentino, P; Quattrone, A. | |
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? | 1-gen-2004 | Mancuso, M; Conforti, Fl; Rocchi, A; Tessitore, A; Muglia, M; Tedeschi, G; Panza, D; Monsurro, M; Sola, P; Mandrioli, J; Choub, A; Delcorona, A; Manca, Ml; Mazzei, R; Sprovieri, T; Filosto, M; Salviati, A; Valentino, P; Bono, F; Caracciolo, M; Simone, Il; LA BELLA, V; Majorana, G; Siciliano, G; Murri, L; Quattrone, A. | |
Gene conversion events in adult-onset spinal muscular atrophy | 1-gen-2004 | Mazzei, R; Gambardella, A; Conforti, Fl; Magariello, A; Patitucci, A; Gabriele, Al; Sprovieri, T; Labate, A; Valentino, P; Bono, F; Bonavita, S; Zappia, M; Muglia, M; Quattrone, A. | |
NARROWING OF THE CRITICAL REGION IN AUTOSOMAL RECESSIVE SPASTIC PARAPLEGIA LINKED TO THE SPG5 LOCUS | 1-gen-2004 | Muglia, M; Criscuolo, C; Magariello, A; DE MICHELE, G; Scarano, V; D'Adamo, P; Ambrosio, G; Gabriele, Al; Patitucci, A; Mazzei, R; Confori, Fl; Sprovieri, T; Morgante, L; Epifano, A; LA SPINA, P; Valentino, P; Gasparini, P; Filla, A; Quattrone, A |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile