AURILIA, CINZIA
AURILIA, CINZIA
A large Italian family with Gilles de la Tourette syndrome: clinical study and analysis of the SLITRK1 gene.
2007 Fabbrini, Giovanni; Pasquini, M; Aurilia, Cinzia; Berardelli, Isabella; Breedveld, G; Oostra, Ba; Bonifati, Vincenzo; Berardelli, Alfredo
Association between migraine and ACE gene (insertion/deletion) polymorphism: The BioBIM study
2014 Palmirotta, R.; Barbanti, P.; Ludovici, G.; De Marchis, M. L.; Ialongo, C.; Egeo, G.; Aurilia, C.; Fofi, L.; Abete, P.; Spila, A.; Ferroni, P.; Della-Morte, D.; Guadagni, F.
Dopamine-beta-hydroxylase 19-bp insertion/deletion polymorphism affects medication overuse in patients with chronic migraine
2019 Barbanti, P.; Guadagni, F.; De Marchis, M. L.; Ialongo, C.; Egeo, G.; Fofi, L.; Aurilia, C.; Lovero, D.; Della-Morte, D.; Ferroni, P.; Palmirotta, R.
EHMTI-0241. Association between migraine and sod1 and sod2 genes polymorphisms: the biobim study
2014 Barbanti, P; Palmirotta, R; De Marchis, M; Ludovici, G; Ialongo, C; Egeo, G; Aurilia, C; Fofi, L; Ferroni, P; Morte, Dd; Guadagni, F
Is SOD2 Ala16Val polymorphism associated with migraine with aura phenotype?
2015 Palmirotta, R.; Barbanti, P.; De Marchis, M. L.; Egeo, G.; Aurilia, C.; Fofi, L.; Ialongo, C.; Valente, M. G.; Ferroni, P.; Della-Morte, D.; Guadagni, F.
Look beyond Catechol-O-Methyltransferase genotype for cathecolamines derangement in migraine: the BioBIM rs4818 and rs4680 polymorphisms study
2015 DE MARCHIS, MARIA LAURA; Barbanti, P; Palmirotta, R; Egeo, G; Aurilia, C; Fofi, L; Piroso, S; Ialongo, C; Della-Morte, D; D'Andrea, G; Ferroni, P; Guadagni, F
O039. Case-control genetic association studies in migraine: a 7-year experience at the Interinstitutional Multidisciplinary Biobank (BioBIM) of IRCCS San Raffaele Pisana
2015 Barbanti, P.; Palmirotta, R.; De Marchis, M. L.; Ialongo, C.; Egeo, G.; Aurilia, C.; Fofi, L.; Piroso, S.; Fratangeli, F.; Valente, M. G.; Guadagni, F.
Pramipexole in Parkinson's disease. A short-term study using the combined levodopa-dopamine agonist test
2002 Fabbrini, Giovanni; P., Barbanti; Aurilia, Cinzia; Pauletti, Caterina; Meco, Giuseppe
Prion protein gene M129V polymorphism and variability in age at migraine onset
2013 Palmirotta, R.; Ludovici, G.; Egeo, G.; Ialongo, C.; Aurilia, C.; Fofi, L.; De Marchis, M. L.; Della-Morte, D.; Barbanti, P.; Guadagni, F.
Progesterone receptor gene (PROGINS) polymorphism correlates with late onset of migraine
2015 Palmirotta, R.; Barbanti, P.; Ialongo, C.; De Marchis, M. L.; Alessandroni, J.; Egeo, G.; Aurilia, C.; Fofi, L.; Valente, M. G.; Ferroni, P.; Della-Morte, D.; Guadagni, F.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A large Italian family with Gilles de la Tourette syndrome: clinical study and analysis of the SLITRK1 gene. | 2007 | Fabbrini, Giovanni; Pasquini, M; Aurilia, Cinzia; Berardelli, Isabella; Breedveld, G; Oostra, Ba; Bonifati, Vincenzo; Berardelli, Alfredo | |
| Association between migraine and ACE gene (insertion/deletion) polymorphism: The BioBIM study | 2014 | Palmirotta, R.; Barbanti, P.; Ludovici, G.; De Marchis, M. L.; Ialongo, C.; Egeo, G.; Aurilia, C.; Fofi, L.; Abete, P.; Spila, A.; Ferroni, P.; Della-Morte, D.; Guadagni, F. | |
| Dopamine-beta-hydroxylase 19-bp insertion/deletion polymorphism affects medication overuse in patients with chronic migraine | 2019 | Barbanti, P.; Guadagni, F.; De Marchis, M. L.; Ialongo, C.; Egeo, G.; Fofi, L.; Aurilia, C.; Lovero, D.; Della-Morte, D.; Ferroni, P.; Palmirotta, R. | |
| EHMTI-0241. Association between migraine and sod1 and sod2 genes polymorphisms: the biobim study | 2014 | Barbanti, P; Palmirotta, R; De Marchis, M; Ludovici, G; Ialongo, C; Egeo, G; Aurilia, C; Fofi, L; Ferroni, P; Morte, Dd; Guadagni, F | |
| Is SOD2 Ala16Val polymorphism associated with migraine with aura phenotype? | 2015 | Palmirotta, R.; Barbanti, P.; De Marchis, M. L.; Egeo, G.; Aurilia, C.; Fofi, L.; Ialongo, C.; Valente, M. G.; Ferroni, P.; Della-Morte, D.; Guadagni, F. | |
| Look beyond Catechol-O-Methyltransferase genotype for cathecolamines derangement in migraine: the BioBIM rs4818 and rs4680 polymorphisms study | 2015 | DE MARCHIS, MARIA LAURA; Barbanti, P; Palmirotta, R; Egeo, G; Aurilia, C; Fofi, L; Piroso, S; Ialongo, C; Della-Morte, D; D'Andrea, G; Ferroni, P; Guadagni, F | |
| O039. Case-control genetic association studies in migraine: a 7-year experience at the Interinstitutional Multidisciplinary Biobank (BioBIM) of IRCCS San Raffaele Pisana | 2015 | Barbanti, P.; Palmirotta, R.; De Marchis, M. L.; Ialongo, C.; Egeo, G.; Aurilia, C.; Fofi, L.; Piroso, S.; Fratangeli, F.; Valente, M. G.; Guadagni, F. | |
| Pramipexole in Parkinson's disease. A short-term study using the combined levodopa-dopamine agonist test | 2002 | Fabbrini, Giovanni; P., Barbanti; Aurilia, Cinzia; Pauletti, Caterina; Meco, Giuseppe | |
| Prion protein gene M129V polymorphism and variability in age at migraine onset | 2013 | Palmirotta, R.; Ludovici, G.; Egeo, G.; Ialongo, C.; Aurilia, C.; Fofi, L.; De Marchis, M. L.; Della-Morte, D.; Barbanti, P.; Guadagni, F. | |
| Progesterone receptor gene (PROGINS) polymorphism correlates with late onset of migraine | 2015 | Palmirotta, R.; Barbanti, P.; Ialongo, C.; De Marchis, M. L.; Alessandroni, J.; Egeo, G.; Aurilia, C.; Fofi, L.; Valente, M. G.; Ferroni, P.; Della-Morte, D.; Guadagni, F. |