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Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene.
2014-01-01 Manna, I; Mumoli, L; Citrigno, L; Ferlazzo, E; Quattrone, A; Labate, A; Aguglia, U; Gambardella, A
Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins.
2008-01-01 Diani, E; Di Bonaventura, C; Mecarelli, O; Elia, M; Bovo, G; Bisulli, F; Pinardi, F; Binelli, S; Egeo, G; Castellotti, B; Striano, P; Striano, S; Bianchi, A; Ferlazzo, E; Vianello, V; Coppola, G; Tinuper, P; Giallonardo, At; Michelucci, R; Nobile, C.; Aguglia, U; Gambardella, A
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.
1996-01-01 Quattrone, A; Gambardella, A; Bono, F; Aguglia, U; Bolino, A; Bruni, Ac; Montesi, Mp; Oliveri, Rl; Sabatelli, M; Tamburrini, O; Valentino, P; Van Broeckhoven, C; Zappia, M.
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths
1996-01-01 Quattrone, A.; Gambardella, A; Bono, F.; Aguglia, U.; Bolino, A.; Bruni, Ac.; Montesi, Mp.; Oliveri, Rl.; Sabatelli, M.; Tamburrini, O.; Valentino, P.; Van Broeckhoven, C.; Zappia, M.
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)
1999-01-01 Gambardella, A; Bono, F; Muglia, M; Quattrone, A; Valentino, P
Babylonian knowledge about temporal lobe epilepsy: distinguishing mesial from lateral forms
2022-01-01 Fortunato, Francesco; Labate, Angelo; Gambardella, Antonio
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity
2001-01-01 Malacarne, M; Gennaro, E; Madia, F; Pozzi, S; Vacca, D; Barone, B; Bernardina, Bd; Bianchi, A; Bonanni, P; DE MARCO, P; Gambardella, A; Giordano, L; Lispi, Ml; Romeo, A; Santorum, E; Vanadia, F; Vecchi, M; Veggiotti, P; Vigevano, F; Viri, F; Bricarelli, Fd; Zara, F.
Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy
2004-01-01 Berkovic, Sf; Heron, Se; Giordano, L; Marini, C; Guerrini, R; Kaplan, Re; Gambardella, A; Steinlein, Ok; Grinton, Be; Dean, Jt; Bordo, L; Hodgson, Bl; Yamamoto, T; Mulley, Jc; Zara, F; Scheffer, Ie.
Benign mesial temporal lobe epilepsy
2011-01-01 Labate, A; Gambardella, A; Andermann, E; Aguglia, U; Cendes, F; Berkovic, Sf; Andermann, F
Benign partial epilepsies of adolescence: a report of 37 new cases
2001-01-01 Capovilla, G; Gambardella, A; Romeo, A; Beccaria, F; Montagnini, A; Viri, M; Sgrò, V; Veggiotti, P; Labate, A
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene. | 1-gen-2014 | Manna, I; Mumoli, L; Citrigno, L; Ferlazzo, E; Quattrone, A; Labate, A; Aguglia, U; Gambardella, A | |
| Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins. | 1-gen-2008 | Diani, E; Di Bonaventura, C; Mecarelli, O; Elia, M; Bovo, G; Bisulli, F; Pinardi, F; Binelli, S; Egeo, G; Castellotti, B; Striano, P; Striano, S; Bianchi, A; Ferlazzo, E; Vianello, V; Coppola, G; Tinuper, P; Giallonardo, At; Michelucci, R; Nobile, C.; Aguglia, U; Gambardella, A | |
| Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family. | 1-gen-1996 | Quattrone, A; Gambardella, A; Bono, F; Aguglia, U; Bolino, A; Bruni, Ac; Montesi, Mp; Oliveri, Rl; Sabatelli, M; Tamburrini, O; Valentino, P; Van Broeckhoven, C; Zappia, M. | |
| Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths | 1-gen-1996 | Quattrone, A.; Gambardella, A; Bono, F.; Aguglia, U.; Bolino, A.; Bruni, Ac.; Montesi, Mp.; Oliveri, Rl.; Sabatelli, M.; Tamburrini, O.; Valentino, P.; Van Broeckhoven, C.; Zappia, M. | |
| Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B) | 1-gen-1999 | Gambardella, A; Bono, F; Muglia, M; Quattrone, A; Valentino, P | |
| Babylonian knowledge about temporal lobe epilepsy: distinguishing mesial from lateral forms | 1-gen-2022 | Fortunato, Francesco; Labate, Angelo; Gambardella, Antonio | |
| Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity | 1-gen-2001 | Malacarne, M; Gennaro, E; Madia, F; Pozzi, S; Vacca, D; Barone, B; Bernardina, Bd; Bianchi, A; Bonanni, P; DE MARCO, P; Gambardella, A; Giordano, L; Lispi, Ml; Romeo, A; Santorum, E; Vanadia, F; Vecchi, M; Veggiotti, P; Vigevano, F; Viri, F; Bricarelli, Fd; Zara, F. | |
| Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy | 1-gen-2004 | Berkovic, Sf; Heron, Se; Giordano, L; Marini, C; Guerrini, R; Kaplan, Re; Gambardella, A; Steinlein, Ok; Grinton, Be; Dean, Jt; Bordo, L; Hodgson, Bl; Yamamoto, T; Mulley, Jc; Zara, F; Scheffer, Ie. | |
| Benign mesial temporal lobe epilepsy | 1-gen-2011 | Labate, A; Gambardella, A; Andermann, E; Aguglia, U; Cendes, F; Berkovic, Sf; Andermann, F | |
| Benign partial epilepsies of adolescence: a report of 37 new cases | 1-gen-2001 | Capovilla, G; Gambardella, A; Romeo, A; Beccaria, F; Montagnini, A; Viri, M; Sgrò, V; Veggiotti, P; Labate, A |
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Opzioni
Scopri
Tipologia
- 1 Contributo su Rivista 473
- 1 Contributo su Rivista::1.1 Arti... 473
Data di pubblicazione
- In corso di stampa 1
- 2020 - 2024 99
- 2010 - 2019 203
- 2000 - 2009 104
- 1990 - 1999 65
- 1989 - 1989 1
Rivista
- EPILEPSIA 79
- NEUROLOGY 51
- EPILEPSY & BEHAVIOR 17
- EPILEPSY RESEARCH 17
- NEUROLOGICAL SCIENCES 17
- SEIZURE 15
- BRAIN 14
- ANNALS OF NEUROLOGY 11
- MOVEMENT DISORDERS 10
- EUROPEAN JOURNAL OF NEUROLOGY 9
Keyword
- Humans 14
- Epilepsy 13
- epilepsy 13
- temporal lobe epilepsy 11
- Temporal lobe epilepsy 10
- Adult 9
- Female 9
- MRI 9
- Male 8
- Middle Aged 6
Lingua
- eng 446
- ita 1
- scc 1
Accesso al fulltext
- no fulltext 473