DE ANGIOLETTI, MARIA
DE ANGIOLETTI, MARIA
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
(a)a5.3: A novel alpha+ thalassemia deletion with the breakpoints in the alpha2-globin gene and in close proximity to an Alu family repeat between the pseudoalpha2- and pseudoalpha1-globin genes.
1991 Lacerra, G; Fioretti, G; De Angioletti, M; Pagano, L; Guarino, E; de Bonis, C; Viola, A; Maglione, G; Scarallo, A; De Rosa, L; Carestia, ; C,
. Long-term expression of human glucose 6-phosphate dehydrogenase (G6PD) after lentiviral mediated transfer in primitive human hematopoietic cells engrafting NOD/SCID mice.
2001 Notaro R; De Angioletti M; FeinLevy C; Rovira A; Camacho Vanegas O; Sadelain M; Luzzatto; L
. Stable in vivo Expression of Human Glucose 6-Phosphate Deydrogenase (hG6PD) after Retroviral-Mediated Transfer into Murine and Human Hematopoietic Stem Cells (HSC)
2000 DE ANGIOLETTI, Maria; Rovira, Ana; Camacho Vanegas, Olga; Liu, Delong; Rosti, Vittorio; Gallardo, Humilidad; Feinlevy, Carolyn; Notaro, Rosario; Sadelain, Michel; Luzzatto, Lucio
aaaa anti-3.7 type II: a new alpha-globin gene rearrangement suggesting that the alpha-globin gene duplication could be caused by intrachromosomal recombination
1992 DE ANGIOLETTI, Maria; Lacerra, Giuseppina; Castaldo, C; Cutolo, Rita; de Bonis, Clemaria; Buonanno, Gennaro; Carestia, Clementina
ACUTE MYELOID LEUKEMIA (AML) ARISING FROM THE GPI-NEGATIVE HEMATOPOIETIC CELL POPULATION IN A PATIENT WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA (PNH)
2012 Sica, M.; Carpaneto, A.; Talini, G.; Caporale, R.; Berardi, M.; De Angioletti, M.; Montanaro, M.; Luzzatto, L.; Notaro, R.
alfa-talassemia: Un metodo rapido per la diagnosi molecolare di genotipo mediante PCR
1995 Lacerra G; De Angioletti M; Carestia C.
Alfa°-talassemia in Campania: Analisi di sei famiglie.
1987 Carestia C; Cutolo R; De Angioletti M; Lacerra G; Fioretti G; Mastrobuoni A; Pagano L; Proto AM; Ricciuti F.
alpha-thalassaemia deletions: Direct detection by agarose electrophoresis of PCR amplified DNA and correlation between genotypes and haematological phenotypes
1993 Lacerra G; De Angioletti M; Pagano L; Fioretti G; Viola A; Sciorio A; Fotino A; Libertino R; Di Girolamo R; Carestia C.
An unusually mild case of Hb H disease in a patient carrying an alpha3.7/-(alpha)20.5 genotype
1989 Lacerra, G; Sabato, V; De Angioletti, M; De Mattia, D; De Bonis, C; Schettini, F; Carestia, ; C,
Analisi molecolare della beta-talassemia in Campania
1992 Lacerra, G; de Bonis, C; De Angioletti, M; Maglione, G; Scarallo, A; Cutolo, R; Carestia, C; Fioretti, G; Pagano, L; De Rosa, L; Viola, A; Cimino, R
Aplotipo associato alla mutazione HB Lepore Boston
1987 Pagano, L; Fioretti, G; Mastrobuoni, ; Proto, Mg; Carestia, C; Cutolo, R; De Angioletti, M; Lacerra, G
Aspetti epidemiologici e diagnostici dei disordini dei geni globinici in Campania
1992 Pagano, L; Fioretti, G; De Rosa, L; Viola, A; Cimino, R; De Angioletti, M; Lacerra, G; de Bonis, C; Cutolo, R; Maglione, G; Scarallo, A; Carestia, C
Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24 MLH1 and MSH2 Gene Variants.
2017 Tricarico, Rossella; Kasela, Mariann; Mareni, Cristina; Thompson, Bryony A; Drouet, Aurelie; Staderini, Lucia; Gorelli, Greta; Crucianelli, Francesca; Ingrosso, Valentina; Kantelinen, Jukka; Papi, Laura; De Angioletti, Maria; Berardi, Margherita; Gaildrat, Pascaline; Soukarieh, Omar; Turchetti, Daniela; Martins, Alexandra; Spurdle, Amanda B; Nystrom, Minna; Genuardi, Maurizio
Association of -318 C/T and +49 A/G cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphisms with a clinical subset of Italian patients with systemic sclerosis
2007 Balbi, G; Ferrera, F; Rizzi, M; Piccioli, P; Morabito, A; Cardamone, L; Ghio, M; Palmisano, Gl; Carrara, P; Pedemonte, S; Sessarego, M; De Angioletti, M; Notaro, R; Indiveri, F; Pistillo, Mp
Base molecolare dell'alfa talassemia nella provincia di Caserta
1995 Lacerra, G; Sciorio, A; De Angioletti, M; Papa, G; Libertino, R; Pagnini, D; Di Girolamo, R; Carestia, C
Base molecolare della beta-talassemia in Campania
1995 Carestia, C; Pagano, L; Lacerra, G; Fioretti, G; De Angioletti, M
Beta - and alfa-globin genotypes in Albanian patients affected with beta-globin gene disorders
2002 DE ANGIOLETTI, Maria; Lacerra, Giuseppina; Boletini, Enis; Di Noce, Francesca; Musollino, Gennaro; Carestia, Clementina
Beta+45 G --> C: a novel silent beta-thalassaemia mutation, the first in the Kozak sequence
2004 De Angioletti M.; Lacerra G.; Sabato V.; Carestia C.
Beta-globin gene framework variant: an African type?
1991 Carestia C; Pagano L; Lacerra G; Fioretti G; De Angioletti M; de Bonis C; De Rosa L.
Beta-thalassaemia-87 C > G: relationship of the Hb F modulation and polymorphisms in compound heterozygous patients
2004 De Angioletti, M; Lacerra, G; Pagano, L; Alessi, M; D' Avino, R; Manca, L; Carestia, C
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| (a)a5.3: A novel alpha+ thalassemia deletion with the breakpoints in the alpha2-globin gene and in close proximity to an Alu family repeat between the pseudoalpha2- and pseudoalpha1-globin genes. | 1-gen-1991 | Lacerra, G; Fioretti, G; De Angioletti, M; Pagano, L; Guarino, E; de Bonis, C; Viola, A; Maglione, G; Scarallo, A; De Rosa, L; Carestia, ; C, | |
| . Long-term expression of human glucose 6-phosphate dehydrogenase (G6PD) after lentiviral mediated transfer in primitive human hematopoietic cells engrafting NOD/SCID mice. | 1-gen-2001 | Notaro R; De Angioletti M; FeinLevy C; Rovira A; Camacho Vanegas O; Sadelain M; Luzzatto; L | |
| . Stable in vivo Expression of Human Glucose 6-Phosphate Deydrogenase (hG6PD) after Retroviral-Mediated Transfer into Murine and Human Hematopoietic Stem Cells (HSC) | 1-gen-2000 | DE ANGIOLETTI, Maria; Rovira, Ana; Camacho Vanegas, Olga; Liu, Delong; Rosti, Vittorio; Gallardo, Humilidad; Feinlevy, Carolyn; Notaro, Rosario; Sadelain, Michel; Luzzatto, Lucio | |
| aaaa anti-3.7 type II: a new alpha-globin gene rearrangement suggesting that the alpha-globin gene duplication could be caused by intrachromosomal recombination | 1-gen-1992 | DE ANGIOLETTI, Maria; Lacerra, Giuseppina; Castaldo, C; Cutolo, Rita; de Bonis, Clemaria; Buonanno, Gennaro; Carestia, Clementina | |
| ACUTE MYELOID LEUKEMIA (AML) ARISING FROM THE GPI-NEGATIVE HEMATOPOIETIC CELL POPULATION IN A PATIENT WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA (PNH) | 1-gen-2012 | Sica, M.; Carpaneto, A.; Talini, G.; Caporale, R.; Berardi, M.; De Angioletti, M.; Montanaro, M.; Luzzatto, L.; Notaro, R. | |
| alfa-talassemia: Un metodo rapido per la diagnosi molecolare di genotipo mediante PCR | 1-gen-1995 | Lacerra G; De Angioletti M; Carestia C. | |
| Alfa°-talassemia in Campania: Analisi di sei famiglie. | 1-gen-1987 | Carestia C; Cutolo R; De Angioletti M; Lacerra G; Fioretti G; Mastrobuoni A; Pagano L; Proto AM; Ricciuti F. | |
| alpha-thalassaemia deletions: Direct detection by agarose electrophoresis of PCR amplified DNA and correlation between genotypes and haematological phenotypes | 1-gen-1993 | Lacerra G; De Angioletti M; Pagano L; Fioretti G; Viola A; Sciorio A; Fotino A; Libertino R; Di Girolamo R; Carestia C. | |
| An unusually mild case of Hb H disease in a patient carrying an alpha3.7/-(alpha)20.5 genotype | 1-gen-1989 | Lacerra, G; Sabato, V; De Angioletti, M; De Mattia, D; De Bonis, C; Schettini, F; Carestia, ; C, | |
| Analisi molecolare della beta-talassemia in Campania | 1-gen-1992 | Lacerra, G; de Bonis, C; De Angioletti, M; Maglione, G; Scarallo, A; Cutolo, R; Carestia, C; Fioretti, G; Pagano, L; De Rosa, L; Viola, A; Cimino, R | |
| Aplotipo associato alla mutazione HB Lepore Boston | 1-gen-1987 | Pagano, L; Fioretti, G; Mastrobuoni, ; Proto, Mg; Carestia, C; Cutolo, R; De Angioletti, M; Lacerra, G | |
| Aspetti epidemiologici e diagnostici dei disordini dei geni globinici in Campania | 1-gen-1992 | Pagano, L; Fioretti, G; De Rosa, L; Viola, A; Cimino, R; De Angioletti, M; Lacerra, G; de Bonis, C; Cutolo, R; Maglione, G; Scarallo, A; Carestia, C | |
| Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24 MLH1 and MSH2 Gene Variants. | 1-gen-2017 | Tricarico, Rossella; Kasela, Mariann; Mareni, Cristina; Thompson, Bryony A; Drouet, Aurelie; Staderini, Lucia; Gorelli, Greta; Crucianelli, Francesca; Ingrosso, Valentina; Kantelinen, Jukka; Papi, Laura; De Angioletti, Maria; Berardi, Margherita; Gaildrat, Pascaline; Soukarieh, Omar; Turchetti, Daniela; Martins, Alexandra; Spurdle, Amanda B; Nystrom, Minna; Genuardi, Maurizio | |
| Association of -318 C/T and +49 A/G cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphisms with a clinical subset of Italian patients with systemic sclerosis | 1-gen-2007 | Balbi, G; Ferrera, F; Rizzi, M; Piccioli, P; Morabito, A; Cardamone, L; Ghio, M; Palmisano, Gl; Carrara, P; Pedemonte, S; Sessarego, M; De Angioletti, M; Notaro, R; Indiveri, F; Pistillo, Mp | |
| Base molecolare dell'alfa talassemia nella provincia di Caserta | 1-gen-1995 | Lacerra, G; Sciorio, A; De Angioletti, M; Papa, G; Libertino, R; Pagnini, D; Di Girolamo, R; Carestia, C | |
| Base molecolare della beta-talassemia in Campania | 1-gen-1995 | Carestia, C; Pagano, L; Lacerra, G; Fioretti, G; De Angioletti, M | |
| Beta - and alfa-globin genotypes in Albanian patients affected with beta-globin gene disorders | 1-gen-2002 | DE ANGIOLETTI, Maria; Lacerra, Giuseppina; Boletini, Enis; Di Noce, Francesca; Musollino, Gennaro; Carestia, Clementina | |
| Beta+45 G --> C: a novel silent beta-thalassaemia mutation, the first in the Kozak sequence | 1-gen-2004 | De Angioletti M.; Lacerra G.; Sabato V.; Carestia C. | |
| Beta-globin gene framework variant: an African type? | 1-gen-1991 | Carestia C; Pagano L; Lacerra G; Fioretti G; De Angioletti M; de Bonis C; De Rosa L. | |
| Beta-thalassaemia-87 C > G: relationship of the Hb F modulation and polymorphisms in compound heterozygous patients | 1-gen-2004 | De Angioletti, M; Lacerra, G; Pagano, L; Alessi, M; D' Avino, R; Manca, L; Carestia, C |