PATRONO, CLARICE
PATRONO, CLARICE
DIPARTIMENTO DI MEDICINA SPERIMENTALE E SCIENZE BIOCHIMICHE (attivo dal 07/07/1987 al 31/12/2013)
ALS phenotypes with mutations in SPG11
2009 Orlacchio, A; Babalini, C; Patrono, C; Montieri, P; Varlese, Ml; Borreca, A; Moschella, V; Mercuri, Nb; Bernardi, G; Kawarai, T
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: A novel mutation in the SPG11 gene and further evidence for genetic heterogeneity
2009 Pippucci, Tommaso; Panza, Emanuele; Pompilii, Eva; Donadio, Vincenzo; Borreca, Antonella; Babalini, Carla; Patrono, Clarice; Zuntini, Roberta; Kawarai, Toshitaka; Bernardi, Giorgio; Liguori, Rocco; Et, Al; Orlacchio, Antonio; Seri, Marco
Clinical and genetic findings of two Italian kindreds with Silver Syndrome
2006 Orlacchio, A; Patrono, C; Borreca, A; Babalini, C; Dionisi, L; Moschella, V; Orlacchio, A; Bernardi, G; Kawarai, T
Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4
2008 Orlacchio, Antonio; Patrono, Clarice; Gaudiello, Fabrizio; Rocchi, Camilla; Moschella, Vincenzo; Floris, Roberto; Bernardi, Giorgio; Kawarai, Toshitaka
Silver syndrome variant of hereditary spastic paraplegia: identification of a novel locus
2007 Orlacchio, A; Patrono, C; Gaudiello, F; Moschella, V; Borreca, A; Orlacchio, A; Floris, R; Bernardi, G; Kawarai, T
Spastic paraplegia in Romania: High prevalence of SPG4 mutations
2008 Orlacchio, Antonio; Patrono, Clarice; Borreca, Antonella; Babalini, Carla; Bernardi, Giorgio; Kawarai, Toshitaka
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis
2010 Orlacchio, Antonio; Babalini, Carla; Borreca, Antonella; Patrono, Clarice; Massa, Roberto; Basaran, Sarenur; Munhoz Renato, P.; Rogaeva Ekaterina, A; St George-Hyslop Peter, H; Bernardi, Giorgio; Kawarai, Toshitaka
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| ALS phenotypes with mutations in SPG11 | 2009 | Orlacchio, A; Babalini, C; Patrono, C; Montieri, P; Varlese, Ml; Borreca, A; Moschella, V; Mercuri, Nb; Bernardi, G; Kawarai, T | |
| Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: A novel mutation in the SPG11 gene and further evidence for genetic heterogeneity | 2009 | Pippucci, Tommaso; Panza, Emanuele; Pompilii, Eva; Donadio, Vincenzo; Borreca, Antonella; Babalini, Carla; Patrono, Clarice; Zuntini, Roberta; Kawarai, Toshitaka; Bernardi, Giorgio; Liguori, Rocco; Et, Al; Orlacchio, Antonio; Seri, Marco | |
| Clinical and genetic findings of two Italian kindreds with Silver Syndrome | 2006 | Orlacchio, A; Patrono, C; Borreca, A; Babalini, C; Dionisi, L; Moschella, V; Orlacchio, A; Bernardi, G; Kawarai, T | |
| Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4 | 2008 | Orlacchio, Antonio; Patrono, Clarice; Gaudiello, Fabrizio; Rocchi, Camilla; Moschella, Vincenzo; Floris, Roberto; Bernardi, Giorgio; Kawarai, Toshitaka | |
| Silver syndrome variant of hereditary spastic paraplegia: identification of a novel locus | 2007 | Orlacchio, A; Patrono, C; Gaudiello, F; Moschella, V; Borreca, A; Orlacchio, A; Floris, R; Bernardi, G; Kawarai, T | |
| Spastic paraplegia in Romania: High prevalence of SPG4 mutations | 2008 | Orlacchio, Antonio; Patrono, Clarice; Borreca, Antonella; Babalini, Carla; Bernardi, Giorgio; Kawarai, Toshitaka | |
| SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis | 2010 | Orlacchio, Antonio; Babalini, Carla; Borreca, Antonella; Patrono, Clarice; Massa, Roberto; Basaran, Sarenur; Munhoz Renato, P.; Rogaeva Ekaterina, A; St George-Hyslop Peter, H; Bernardi, Giorgio; Kawarai, Toshitaka |