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SPROVIERI, TERESA

SPROVIERI, TERESA  

Istituto sull'Inquinamento Atmosferico - IIA  

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Risultati 1 - 20 di 143 (tempo di esecuzione: 0.019 secondi).
Titolo Data di pubblicazione Autore(i) File
"A prospective study of residual- desease monitoring of ALL1/AF4 transcript in patients with t(4;11) acute lymphoblastic leukemia 1-gen-2000 Cimino, G; Elia, L; Rapanotti, Mc; Sprovieri, T; Mancini, M; Cuneo, A; Mecucci, C; Fioritoni, G; Carotenuto, M; Morra, E; Liso, V; Annino, L; Saglio, G; De Rossi, G; Foà, R; Mandelli, F
A CLINICAL AND MOLECULAR STUDY IN A CHILD UNDER 1 YEAR OF AGE AFFECTED BY NEUROFIBROMATOSIS TYPE 2 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 Clinical And Molecular Study In Children Under 1 Year Of Age Affected By Neurofibromatosis Type 2 1-gen-2006 L Gabriele, A; Ruggieri, M; Nucifora, C; Patitucci, A; Sprovieri, T; Magariello, A; Mazzei, R; L Conforti, F; Cungaro, ; Muglia, M; Quattrone, A
A label-free quantitative application of MALDI-TOF-MS to measure Thymosin beta 4 levels in human cerebrospinal fluid 1-gen-2010 E. Urso; M. Le Pera; S. Bossio; T. Sprovieri;A. Qualtieri
A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2). 1-gen-2004 Conforti, Fl; Muglia, M; Mazzei, R; Patitucci, A; Valentino, P; Magariello, A; Sprovieri, T; Bono, F; Bergmann, C; Gabriele, Al; Peluso, G; Nisticò, R; Senderek, J; Quattrone, A
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 Autosomal Dominant Distal Motor Neuronopathy maps to chromosome 4q-ter 1-gen-2007 Muglia, Maria; Magariello, Angela; Citrigno, Luigi; Passamonti, Luca; Patitucci, Alessandra; Conforti, FRANCESCA LUISA; Gabriele, ANNA LIA; Mazzei, Rosalucia; Sprovieri, Teresa; Ungaro, Carmine; Bellesi, Michele; Quattrone, Aldo
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 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 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 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 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-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 Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL. 1-gen-2004 Mazzei, R; Conforti, Fl; Lanza, Pl; Sprovieri, T; Lupo, Mr; Gallo, O; Patitucci, A; Magariello, A; Caracciolo, M; Gabriele, Al; Fera, F; Valentino, P; Bono, F; Cenacchi, G; Santoro, G; Muglia, M; Quattrone, A