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UNGARO, CARMINE

UNGARO, CARMINE  

Istituto sull'Inquinamento Atmosferico - IIA  

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Titolo Data di pubblicazione Autore(i) File
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy. 1-gen-2008 Conforti, Fl; Sprovieri, T; Mazzei, R; Ungaro, C; La Bella, V; Tessitore, A; Patitucci, A; Magariello, A; Gabriele, Al; Tedeschi, G; Simone, Il; Majorana, G; Valentino, P; Condino, F; Bono, F; Monsurrò, Mr; Muglia, M Quattrone A
A novel Angiogenin mutation a sporadic patient Amyotrophic Lateral Sclerosis from southern Italy 1-gen-2007 T. Sprovieri; M. Fusaro; C. Ungaro; R. Mazzei; A. Magariello; A. Patitucci; L. Citrigno; V. La Bella;A. Gabriele; M. Muglia; F.L. Conforti
A novel locus for dHMN with pyramidal features maps to chromosome 4q34.3-q35.2. 1-gen-2008 Muglia, M; Magariello, A; Citrigno, L; Passamonti, L; Sprovieri, T; Conforti, Fl; Mazzei, R; Patitucci, A; Gabriele, Al; Ungaro, C; Bellesi, M; Quattrone, A
A novel missense mutation (p.Arg309His) in the nuclear localization signal sequence of spastin protein causes a complicated form of Hereditary Spastic Paraplegia 1-gen-2012 A. Magariello; C. Tortorella; A. Patitucci; R. Tortelli; M. Liguori; R. Mazzei; F. L. Conforti; L. Citrigno; C. Ungaro; I. L. Simone; M. Muglia
A NOVEL MISSENSE MUTATION OF THE NF2 GENE IN A SEVERELY AFFECTED BOY AND HIS HEALTHY FATHER 1-gen-2007 A.L. Gabriele; M. Ruggieri; C. Nucifora; A. Patitucci; T. Sprovieri; A. Magariello; R. Mazzei; F.L. Conforti; C. Ungaro; M. Muglia; A. Quattrone
A novel missense mutation of the NF2 gene in a severely affected boy and his healthy father 1-gen-2007 A.L. Gabriele; M. Ruggieri; C. Nucifora; A. Patitucci; T. Sprovieri; A. Magariello; R. Mazzei; F.L. Conforti; C. Ungaro; M. Muglia; A. Quattrone
A NOVEL MUTATION IN CX32 IDENTIFIED IN A PATIENT WITH DEMYELINATING SENSORY-MOTOR NEUROPATHY AND SECONDARY AXONOPATHY 1-gen-2011 A. Patitucci; C. Tortorella; M. Liguori; A. Magariello; R. Mazzei; FL. Conforti; W. Sproviero; L. Citrigno; A. Morabito; C. Ungaro; A. Gambardella;M. Muglia
A novel mutation in the 3 UTR of SPG4 gene identified in an apparently sporadic patient affected by spastic paraplegia. 1-gen-2008 A Magariello; L Citrigno; A Patitucci; R. Mazzei; FL Conforti; AL Gabriele; T Sprovieri; C Ungaro; M Muglia.
A novel mutation in the exon 7 of the NOTCH3 gene in a patient affected by CADASIL 1-gen-2011 Mazzei, R; Ungaro, C; Conforti, Fl; Ruscica, F; Muglia, M; Sproviero, W; Patitucci, A; Citrigno, L; Magariello, A; Gambardella, A
A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotype. 1-gen-2009 Sprovieri T; Conforti FL; Fiumara A; Mazzei R; Ungaro C; Citrigno L; Muglia M; Arena A; Quattrone A.
A Novel Mutation In The X-Linked Cyclin-Dependent Kinase-Like 5 (CDKL5) Gene Associated With A Severe Rett Phenotype. 1-gen-2008 Sprovieri, T; Fiumara, A; Mazzei, R; Ungaro, C; Magariello, A; Patitucci, A; Citrigno, L; Arena, A; Gabriele, Al; Muglia, M; Conforti, Fl
A Novel Mutation in the X-Linked Cyclin-Dependent Kinaselike 5 (CDKL5) Gene Associated with a Severe Rett Phenotype 1-gen-2008 F. L. Conforti; T. Sprovieri; A. Fiumara; R. Mazzei; C. Ungaro; A. Magariello; A. Patitucci; L. Citrigno; A. Arena; A. Gabriele; M. Muglia; A. Quattrone.
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 1-gen-2010 Gabriele, Al; Ruggeri, M; Muglia, M; Patitucci, A; Magariello, A; Mazzei, R; Conforti, Fl; Ungaro, C; Di Palma, G; Citrigno, L; Sproviero, W; Gambardella, A; Quattrone, A
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 1-gen-2011 Gabriele AL; Ruggieri M; Patitucci A; Magariello A; Conforti FL; Mazzei R; Muglia M; Ungaro C; Di Palma G; Citrigno L; Sproviero W; Gambardella A; Quattrone A.
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 1-gen-2007 Mazzei, R; Ungaro, C; Conforti, Fl; Liguori, M; Sprovieri, T; DI PALMA, Gemma; Patitucci, A; Magariello, A; Gabriele, Al; Citrigno, L; Muglia, M; Quattrone, A
A Novel Notch3 Gene Mutation In A Patient With Cadasil From Southern Italy 1-gen-2007 Ungaro, C; Conforti, Fl; Muglia, M; Lanza, Pl; Patitucci, A; Magariello, A; Gabriele, Al; Citrigno, L; Mazzei, R
A novel Notch3 gene mutation in a patient with CADASIL from Southern Italy 1-gen-2006 Ungaro, C; Liguori, M; Conforti, Fl; Sprovieri, T; Di Palma, G; Patitucci, A; Magariello, A; Gabriele, Al; Muglia, M; Mazzei, R
A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy 1-gen-2007 Mazzei, R; Guidetti, D; Ungaro, C; Conforti, Fl; Muglia, M; G, Cenacchi; Lanza, P; Patitucci, A; Sprovieri, T; Riguzzi, P; Magariello, A; Gabriele, Al; Citrigno, L; Preda, P; Quattrone, A
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL 1-gen-2004 R. Mazzei; F. L. Conforti; T. Sprovieri; C. Ungaro; G. Di Palma; A. Patitucci; O. Gallo; A. Magariello; A. Gabriele; M. Muglia
A NOVEL POINT MUTATION IN PMP22 GENE IN AN ITALIAN FAMILY WITH HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES 1-gen-2007 Apatitucci, ; Muglia, M; Rizzi, R; Ungaro, C; L Conforti, F; L Gabriele, A; Magariello, A; Rmazzei, ; Motti, L; Saladini, R; Sprovieri, T; Nmarcello, ; Quattrone, A