| The spectrum of Notch3 mutations in 28 Italian CADASIL families MT Dotti, A Federico, R Mazzei, S Bianchi, O Scali, FL Conforti, ... Journal of Medical Genetics 42 (6), 478-478, 2005 | 113 | 2005 |
| Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? M Mancuso, FL Conforti, A Rocchi, A Tessitore, M Muglia, G Tedeschi, ... Neuroscience Letters 371 (2-3), 158-162, 2004 | 78 | 2004 |
| A prospective study of residual-disease monitoring of theALL1/AF4 transcript in patients with t(4;11) acute lymphoblastic leukemia G Cimino, L Elia, MC Rapanotti, T Sprovieri, M Mancini, A Cuneo, ... Blood, The Journal of the American Society of Hematology 95 (1), 96-101, 2000 | 77 | 2000 |
| ALL1 gene alterations in acute leukemia: biological and clinical aspects G Cimino, MC Rapanotti, T Sprovieri, L Elia Haematologica 83 (4), 350-357, 1998 | 77 | 1998 |
| A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy FL Conforti, T Sprovieri, R Mazzei, C Ungaro, V La Bella, A Tessitore, ... Neuromuscular Disorders 18 (1), 68-70, 2008 | 71 | 2008 |
| A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL R Mazzei, FL Conforti, PL Lanza, T Sprovieri, MR Lupo, O Gallo, ... Neurology 63 (3), 561-564, 2004 | 66 | 2004 |
| CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene C Ungaro, R Mazzei, FL Conforti, T Sprovieri, P Servillo, M Liguori, ... Journal of neuroscience research 87 (5), 1162-1167, 2009 | 41 | 2009 |
| Alternative splicing of ALS genes: misregulation and potential therapies B Perrone, V La Cognata, T Sprovieri, C Ungaro, FL Conforti, S Andò, ... Cellular and molecular neurobiology 40, 1-14, 2020 | 35 | 2020 |
| Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia A Magariello, M Muglia, A Patitucci, C Ungaro, R Mazzei, AL Gabriele, ... Journal of the neurological sciences 288 (1-2), 96-100, 2010 | 35 | 2010 |
| TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis FL Conforti, W Sproviero, IL Simone, R Mazzei, P Valentino, C Ungaro, ... Journal of Neurology, Neurosurgery & Psychiatry 82 (5), 587-588, 2011 | 31 | 2011 |
| A systems biology approach for personalized medicine in refractory epilepsy GD Naimo, M Guarnaccia, T Sprovieri, C Ungaro, FL Conforti, S Andò, ... International Journal of Molecular Sciences 20 (15), 3717, 2019 | 30 | 2019 |
| Sporadic ALS is not associated with VAPB gene mutations in Southern Italy FL Conforti, T Sprovieri, R Mazzei, C Ungaro, A Tessitore, G Tedeschi, ... Journal of negative results in biomedicine 5, 1-3, 2006 | 28 | 2006 |
| Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia A Magariello, M Muglia, A Patitucci, R Mazzei, FL Conforti, AL Gabriele, ... Neuromuscular Disorders 16 (6), 387-390, 2006 | 28 | 2006 |
| Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus M Muglia, C Criscuolo, A Magariello, G De Michele, V Scarano, ... Journal of the Peripheral Nervous System 9 (2), 124-124, 2004 | 27 | 2004 |
| A novel mutation in the X‐linked cyclin‐dependent kinase‐like 5 (CDKL5) gene associated with a severe Rett phenotype T Sprovieri, FL Conforti, A Fiumara, R Mazzei, C Ungaro, L Citrigno, ... American Journal of Medical Genetics Part A 149 (4), 722-725, 2009 | 26 | 2009 |
| Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P) P Valentino, FL Conforti, D Pirritano, R Nisticò, R Mazzei, A Patitucci, ... Neurology 64 (8), 1477-1478, 2005 | 26 | 2005 |
| Molecular evaluation of the NUP98/RAP1GDS1 gene frequency in adults with T-acute lymphoblastic leukemia G Cimino, T Sprovieri, MC Rapanotti, R Foà, C Mecucci, F Mandelli Haematologica 86 (4), 436-437, 2001 | 25 | 2001 |
| A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies M Muglia, A Patitucci, R Rizzi, C Ungaro, FL Conforti, AL Gabriele, ... Journal of the neurological sciences 263 (1-2), 194-197, 2007 | 23 | 2007 |
| Brain‐derived neurotrophic factor and risk for primary adult‐onset cranial‐cervical dystonia D Martino, M Muglia, G Abbruzzese, A Berardelli, P Girlanda, M Liguori, ... European journal of neurology 16 (8), 949-952, 2009 | 21 | 2009 |
| A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2) FL Conforti, M Muglia, R Mazzei, A Patitucci, P Valentino, A Magariello, ... Neurology 63 (7), 1327-1328, 2004 | 21 | 2004 |
Aldo QuattroneUniversità Magna Graecia CatanzaroVerified email at unicz.it
