GULLI, ROSSELLA
GULLI, ROSSELLA
8 - DIPARTIMENTO DI NEUROSCIENZE, OFTALMOLOGIA E GENETICA (attivo dal 01/06/2002 al 18/07/2012)
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise"
2018-01-01 Grandis, M; Geroldi, A; Gulli, R; Manganelli, F; Gotta, F; Lamp, M; Origone, P; Trevisan, L; Gemelli, C; Fabbri, S; Schenone, A; Tozza, S; Santoro, L; Bellone, E; Mandich, P.
Contribution of copy number variations in CMT1X: a retrospective study.
2015-01-01 Capponi, Simona; Geroldi, Alessandro; Pezzini, I; Gulli, Rossella; Ciotti, Paola; Ursino, Giulia; Lamp, Merit; Reni, L; Schenone, Angelo; Grandis, Marina; Mandich, Paola; Bellone, Emilia
Endothelial dysfunction in rheumatic autoimmune diseases.
2012-01-01 Murdaca, Giuseppe; Colombo, Bm; Cagnati, Paola; Gulli, R; Spanò, F; Puppo, Francesco
GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course
2016-01-01 Pezzini, I; Geroldi, Alessandro; Capponi, Simona; Gulli, Rossella; Schenone, Angelo; Grandis, Marina; Doria Lamba, L; La Piana, C; Cremonte, M; Pisciotta, C; Nolano, M; Manganelli, F; Santoro, L; Mandich, Paola; Bellone, Emilia
Gene symbol: GNE. Disease: Inclusion body myopathy.
2008-01-01 Bruno, C; Grandis, Marina; Cassandrini, D; Bellone, Emilia; Mandich, Paola; Gulli, Rossella
Genetic factors and systemic sclerosis
2016-01-01 Murdaca, Giuseppe; Contatore, Miriam; Gulli, Rossella; Mandich, Paola; Puppo, Francesco
Glutamate hypothesis of schizophrenia: No evidence that the N-Methyl-D-Aspartate receptor 2B gene (GRIN2B) is associated with susceptibility to schizophrenia
2001-01-01 Di Maria, E.; Gulli, R.; Pioli, R.; De Luca, A.; Novelli, G.; Gennarelli, M.; Mandich, P.
TNF-α gene polymorphisms: association with disease susceptibility and response to anti-TNF-α treatment in psoriatic arthritis
2014-01-01 Murdaca, Giuseppe; Gulli, Rossella; Spano', Francesca; Lantieri, Francesca; Burlando, Martina; Parodi, Aurora; Mandich, Paola; Puppo, Francesco
Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance.
2017-01-01 Geroldi, Alessandro; Lastella, P; Patruno, M; Gotta, Fabio; Resta, N; Devigili, G; Sabbà, C; Gulli, Rossella; Lamp, Merit; Origone, Paola; Mandich, Paola; Bellone, Emilia
Update upon efficacy and safety of etanercept for the treatment of spondyloarthritis and juvenile idiopathic arthritis
2018-01-01 Murdaca, Giuseppe; Negrini, Simone; Magnani, Ottavia; Penza, Elena; Pellecchio, Marco; Gulli, Rossella; Mandich, Paola; Puppo, Francesco
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise" | 1-gen-2018 | Grandis, M; Geroldi, A; Gulli, R; Manganelli, F; Gotta, F; Lamp, M; Origone, P; Trevisan, L; Gemelli, C; Fabbri, S; Schenone, A; Tozza, S; Santoro, L; Bellone, E; Mandich, P. | |
| Contribution of copy number variations in CMT1X: a retrospective study. | 1-gen-2015 | Capponi, Simona; Geroldi, Alessandro; Pezzini, I; Gulli, Rossella; Ciotti, Paola; Ursino, Giulia; Lamp, Merit; Reni, L; Schenone, Angelo; Grandis, Marina; Mandich, Paola; Bellone, Emilia | |
| Endothelial dysfunction in rheumatic autoimmune diseases. | 1-gen-2012 | Murdaca, Giuseppe; Colombo, Bm; Cagnati, Paola; Gulli, R; Spanò, F; Puppo, Francesco | |
| GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course | 1-gen-2016 | Pezzini, I; Geroldi, Alessandro; Capponi, Simona; Gulli, Rossella; Schenone, Angelo; Grandis, Marina; Doria Lamba, L; La Piana, C; Cremonte, M; Pisciotta, C; Nolano, M; Manganelli, F; Santoro, L; Mandich, Paola; Bellone, Emilia | |
| Gene symbol: GNE. Disease: Inclusion body myopathy. | 1-gen-2008 | Bruno, C; Grandis, Marina; Cassandrini, D; Bellone, Emilia; Mandich, Paola; Gulli, Rossella | |
| Genetic factors and systemic sclerosis | 1-gen-2016 | Murdaca, Giuseppe; Contatore, Miriam; Gulli, Rossella; Mandich, Paola; Puppo, Francesco | |
| Glutamate hypothesis of schizophrenia: No evidence that the N-Methyl-D-Aspartate receptor 2B gene (GRIN2B) is associated with susceptibility to schizophrenia | 1-gen-2001 | Di Maria, E.; Gulli, R.; Pioli, R.; De Luca, A.; Novelli, G.; Gennarelli, M.; Mandich, P. | |
| TNF-α gene polymorphisms: association with disease susceptibility and response to anti-TNF-α treatment in psoriatic arthritis | 1-gen-2014 | Murdaca, Giuseppe; Gulli, Rossella; Spano', Francesca; Lantieri, Francesca; Burlando, Martina; Parodi, Aurora; Mandich, Paola; Puppo, Francesco | |
| Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance. | 1-gen-2017 | Geroldi, Alessandro; Lastella, P; Patruno, M; Gotta, Fabio; Resta, N; Devigili, G; Sabbà, C; Gulli, Rossella; Lamp, Merit; Origone, Paola; Mandich, Paola; Bellone, Emilia | |
| Update upon efficacy and safety of etanercept for the treatment of spondyloarthritis and juvenile idiopathic arthritis | 1-gen-2018 | Murdaca, Giuseppe; Negrini, Simone; Magnani, Ottavia; Penza, Elena; Pellecchio, Marco; Gulli, Rossella; Mandich, Paola; Puppo, Francesco |