Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsions
2002-01-01 Concolino, D; Iembo, Ma; Rossi, E; Giglio, Sabrina Rita; Coppola, G; Miraglia Del Giudice, E; Strisciuglio, P.
The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies
2007-01-01 Panza, E; Gimelli, G; Passalacqua, M; Cohen, A; Gimelli, S; Giglio, Sabrina Rita; Ghezzi, C; Sparatore, B; Heye, B; Zuffardi, O; Rugarli, E; Meitinger, T; Romeo, G; Ravazzolo, R; Seri, M.
STOP Pain Project—Opioid Response in Pediatric Cancer Patients and Gene Polymorphisms of Cytokine Pathways
2022-01-01 Crescioli, G.; Lombardi, N.; Vagnoli, L.; Bettiol, A.; Giunti, L.; Cetica, V.; Coniglio, M. L.; Provenzano, A.; Giglio, S.; Bonaiuti, R.; Mugelli, A.; Arico, M.; Messeri, A.; Vannacci, A.; Maggini, V.
A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family
2016-01-01 M., Callea; P., Nieminen; C. E., Willoughby; G., Clarich; I., Yavuz; A., Vinciguerra; M., Di Stazio; Giglio, Sabrina Rita; I., Sani; M., Maglione; S., Pensiero; G., Tadini; E., Bellacchio
Identification and characterization of a new human gene encoding a small protein with high homology to the proline-rich region of the SH3BGR gene
1998-01-01 A., Egeo; M., Mazzocco; P., Arrigo; J. M., Vidal Taboada; R., Oliva; B., Pirola; Giglio, Sabrina Rita; A., Rasore Quartino; P., Scartezzini
MYOCLONIC ASTATIC EPILEPSY IN A PATIENT WITH A DE NOVO 4q21.22q21.23 MICRODUPLICATION
2015-01-01 Ottaviani, V; Bartocci, A; Pantaleo, M; Giglio, Sabrina Rita; Cecconi, Massimiliano; Verrotti, A; Merla, G; Stangoni, G; Prontera, P.
Heterozygous Deletion of Long Noncoding RNA AK127244 Is a Susceptibility Factor for Neurodevelopmental Delay
2023-01-01 Coci, Emanuele G; Galesi, Ornella; Morgan, Thomas; Giglio, Sabrina; Ostergaard, Elsebet; Elia, Maurizio
Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q
2000-01-01 M. C., Bonaglia; R., Giorda; G., Poggi; M. E., Raggi; E., Rossi; A., Baroncini; Giglio, Sabrina Rita; R., Borgatti; O., Zuffardi
A SOX3 (Xq26.3-27.3) duplication in a boy with growth hormone deficiency, ocular dyspraxia, and intellectual disability: A long-term follow-up and literature review
2014-01-01 Stagi, Stefano; Elisabetta, Lapi; Marilena, Pantaleo; Giovanna, Traficante; Giglio, Sabrina Rita; Seminara, Salvatore; De Martino, Maurizio
Prevalence and prenatal ultrasound detection of clubfoot in a non-selected population: an analysis of 549 931 births in Tuscany
2015-01-01 Seravalli, Viola; Pierini, A; Bianchi, F; Giglio, Sabrina Rita; Vellucci, Fl; Cariati, E.
Focal dysplasia of the cerebral cortex and infantile spasms associated with somatic 1q21.1-q44 duplication including the AKT3gene
2015-01-01 Valerio, Conti; Marilena, Pantaleo; Carmen, Barba; Gianna, Baroni; Davide, Mei; Anna Maria, Buccoliero; Giglio, Sabrina Rita; Flavio, Giordano; Seung Tae, Baek; Joseph G., Gleeson; Guerrini, Renzo
Transient Neonatal Diabetes Mellitus in a Very Preterm Infant due to ABCC8 Mutation
2018-01-01 Piccini, Barbara; Coviello, Caterina; Drovandi, Livia; Rosangela, Artuso; Monzali, Francesca; Casalini, Emilio; Giglio, Sabrina; Toni, Sonia; Dani, Carlo
Phenotypic heterogeneity and mutational spectrum in a cohort of 45 Italian males subjects with X-linked ectodermal dysplasia
2015-01-01 L., Guazzarotti; G., Tadini; G. E., Mancini; Giglio, Sabrina Rita; C. E., Willoughby; M., Callea; I., Sani; P., Nannini; C., Mameli; A. A., Tenconi; S., Mauri; A., Bottero; A., Caimi; M., Morelli; G. V., Zuccotti
Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3
2015-01-01 Vetro, Annalisa; Reza Dehghani, Mohammad; Kraoua, Lilia; Giorda, Roberto; Beri, Silvana; Cardarelli, Laura; Merico, Maurizio; Manolakos, Emmanouil; Parada-Bustamante, Alexis; Castro, Andrea; Radi, Orietta; Camerino, Giovanna; Brusco, Alfredo; Sabaghian, Marjan; Sofocleous, Crystalena; Forzano, Francesca; Palumbo, Pietro; Palumbo, Orazio; Calvano, Savino; Zelante, Leopoldo; Grammatico, Paola; Giglio, Sabrina; Basly, Mohamed; Chaabouni, Myriam; Carella, Massimo; Russo, Gianni; Clara Bonaglia, Maria; Zuffardi, Orsetta
Non-Invasive Detection of a De Novo Frameshift Variant of STAG2 in a Female Fetus: Escape Genes Influence the Manifestation of X-Linked Diseases in Females
2022-01-01 Provenzano, Aldesia; La Barbera, Andrea; Lai, Francesco; Perra, Andrea; Farina, Antonio; Cariati, Ettore; Zuffardi, Orsetta; Giglio, Sabrina
Ovarian reserve of women with and without BRCA pathogenic variants: A systematic review and meta-analysis
2021-01-01 Gasparri, M. L.; Di Micco, R.; Zuber, V.; Taghavi, K.; Bianchini, G.; Bellaminutti, S.; Meani, F.; Graffeo, R.; Candiani, M.; Mueller, M. D.; Papadia, A.; Gentilini, O. D.
Cardiac resynchronization therapy acutely improves ventricular-arterial coupling by reducing the arterial load: Assessment by pressure-volume loops
2015-01-01 Pieragnoli, Paolo; Perego Giovanni, Battista; Ricciardi, Giuseppe; Sacchi, S; Padeletti, Margherita; Michelucci, Antonio; Valsecchi, Sergio; Padeletti, Luigi
A novel splicing variant of col2a1 in a fetus with achondrogenesis type ii: Interpretation of pathogenicity of in-frame deletions
2021-01-01 Bruni, V.; Spoleti, C. B.; La Barbera, A.; Dattilo, V.; Colao, E.; Votino, C.; Bellacchio, E.; Perrotti, N.; Giglio, S.; Iuliano, R.
Orientation-controlled conjugation of haloalkane dehalogenase fused homing peptides to multifunctional nanoparticles for the specific recognition of cancer cells
2013-01-01 Mazzucchelli, Serena; Colombo, Miriam; Verderio, Paolo; Rozek, E; Andreata, F; Galbiati, Elisabetta; Tortora, Paolo; Corsi, F; Prosperi, Davide
6q24 duplication and transient neonatal diabetes: a possible differential diagnosis with Beckwith-Wiedemann syndrome?
2007-01-01 Andreucci, E; Toni S. Ciccone R., De Gregori M; Giunti, L; Sani, I; Guarducci, ; S., Genuardi M; Zuffardi, O; Giglio, Sabrina Rita
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Familial pericentric inversion of chromosome 5 in a family with benign neonatal convulsions | 1-gen-2002 | Concolino, D; Iembo, Ma; Rossi, E; Giglio, Sabrina Rita; Coppola, G; Miraglia Del Giudice, E; Strisciuglio, P. | |
| The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies | 1-gen-2007 | Panza, E; Gimelli, G; Passalacqua, M; Cohen, A; Gimelli, S; Giglio, Sabrina Rita; Ghezzi, C; Sparatore, B; Heye, B; Zuffardi, O; Rugarli, E; Meitinger, T; Romeo, G; Ravazzolo, R; Seri, M. | |
| STOP Pain Project—Opioid Response in Pediatric Cancer Patients and Gene Polymorphisms of Cytokine Pathways | 1-gen-2022 | Crescioli, G.; Lombardi, N.; Vagnoli, L.; Bettiol, A.; Giunti, L.; Cetica, V.; Coniglio, M. L.; Provenzano, A.; Giglio, S.; Bonaiuti, R.; Mugelli, A.; Arico, M.; Messeri, A.; Vannacci, A.; Maggini, V. | |
| A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family | 1-gen-2016 | M., Callea; P., Nieminen; C. E., Willoughby; G., Clarich; I., Yavuz; A., Vinciguerra; M., Di Stazio; Giglio, Sabrina Rita; I., Sani; M., Maglione; S., Pensiero; G., Tadini; E., Bellacchio | |
| Identification and characterization of a new human gene encoding a small protein with high homology to the proline-rich region of the SH3BGR gene | 1-gen-1998 | A., Egeo; M., Mazzocco; P., Arrigo; J. M., Vidal Taboada; R., Oliva; B., Pirola; Giglio, Sabrina Rita; A., Rasore Quartino; P., Scartezzini | |
| MYOCLONIC ASTATIC EPILEPSY IN A PATIENT WITH A DE NOVO 4q21.22q21.23 MICRODUPLICATION | 1-gen-2015 | Ottaviani, V; Bartocci, A; Pantaleo, M; Giglio, Sabrina Rita; Cecconi, Massimiliano; Verrotti, A; Merla, G; Stangoni, G; Prontera, P. | |
| Heterozygous Deletion of Long Noncoding RNA AK127244 Is a Susceptibility Factor for Neurodevelopmental Delay | 1-gen-2023 | Coci, Emanuele G; Galesi, Ornella; Morgan, Thomas; Giglio, Sabrina; Ostergaard, Elsebet; Elia, Maurizio | |
| Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q | 1-gen-2000 | M. C., Bonaglia; R., Giorda; G., Poggi; M. E., Raggi; E., Rossi; A., Baroncini; Giglio, Sabrina Rita; R., Borgatti; O., Zuffardi | |
| A SOX3 (Xq26.3-27.3) duplication in a boy with growth hormone deficiency, ocular dyspraxia, and intellectual disability: A long-term follow-up and literature review | 1-gen-2014 | Stagi, Stefano; Elisabetta, Lapi; Marilena, Pantaleo; Giovanna, Traficante; Giglio, Sabrina Rita; Seminara, Salvatore; De Martino, Maurizio | |
| Prevalence and prenatal ultrasound detection of clubfoot in a non-selected population: an analysis of 549 931 births in Tuscany | 1-gen-2015 | Seravalli, Viola; Pierini, A; Bianchi, F; Giglio, Sabrina Rita; Vellucci, Fl; Cariati, E. | |
| Focal dysplasia of the cerebral cortex and infantile spasms associated with somatic 1q21.1-q44 duplication including the AKT3gene | 1-gen-2015 | Valerio, Conti; Marilena, Pantaleo; Carmen, Barba; Gianna, Baroni; Davide, Mei; Anna Maria, Buccoliero; Giglio, Sabrina Rita; Flavio, Giordano; Seung Tae, Baek; Joseph G., Gleeson; Guerrini, Renzo | |
| Transient Neonatal Diabetes Mellitus in a Very Preterm Infant due to ABCC8 Mutation | 1-gen-2018 | Piccini, Barbara; Coviello, Caterina; Drovandi, Livia; Rosangela, Artuso; Monzali, Francesca; Casalini, Emilio; Giglio, Sabrina; Toni, Sonia; Dani, Carlo | |
| Phenotypic heterogeneity and mutational spectrum in a cohort of 45 Italian males subjects with X-linked ectodermal dysplasia | 1-gen-2015 | L., Guazzarotti; G., Tadini; G. E., Mancini; Giglio, Sabrina Rita; C. E., Willoughby; M., Callea; I., Sani; P., Nannini; C., Mameli; A. A., Tenconi; S., Mauri; A., Bottero; A., Caimi; M., Morelli; G. V., Zuccotti | |
| Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3 | 1-gen-2015 | Vetro, Annalisa; Reza Dehghani, Mohammad; Kraoua, Lilia; Giorda, Roberto; Beri, Silvana; Cardarelli, Laura; Merico, Maurizio; Manolakos, Emmanouil; Parada-Bustamante, Alexis; Castro, Andrea; Radi, Orietta; Camerino, Giovanna; Brusco, Alfredo; Sabaghian, Marjan; Sofocleous, Crystalena; Forzano, Francesca; Palumbo, Pietro; Palumbo, Orazio; Calvano, Savino; Zelante, Leopoldo; Grammatico, Paola; Giglio, Sabrina; Basly, Mohamed; Chaabouni, Myriam; Carella, Massimo; Russo, Gianni; Clara Bonaglia, Maria; Zuffardi, Orsetta | |
| Non-Invasive Detection of a De Novo Frameshift Variant of STAG2 in a Female Fetus: Escape Genes Influence the Manifestation of X-Linked Diseases in Females | 1-gen-2022 | Provenzano, Aldesia; La Barbera, Andrea; Lai, Francesco; Perra, Andrea; Farina, Antonio; Cariati, Ettore; Zuffardi, Orsetta; Giglio, Sabrina | |
| Ovarian reserve of women with and without BRCA pathogenic variants: A systematic review and meta-analysis | 1-gen-2021 | Gasparri, M. L.; Di Micco, R.; Zuber, V.; Taghavi, K.; Bianchini, G.; Bellaminutti, S.; Meani, F.; Graffeo, R.; Candiani, M.; Mueller, M. D.; Papadia, A.; Gentilini, O. D. | |
| Cardiac resynchronization therapy acutely improves ventricular-arterial coupling by reducing the arterial load: Assessment by pressure-volume loops | 1-gen-2015 | Pieragnoli, Paolo; Perego Giovanni, Battista; Ricciardi, Giuseppe; Sacchi, S; Padeletti, Margherita; Michelucci, Antonio; Valsecchi, Sergio; Padeletti, Luigi | |
| A novel splicing variant of col2a1 in a fetus with achondrogenesis type ii: Interpretation of pathogenicity of in-frame deletions | 1-gen-2021 | Bruni, V.; Spoleti, C. B.; La Barbera, A.; Dattilo, V.; Colao, E.; Votino, C.; Bellacchio, E.; Perrotti, N.; Giglio, S.; Iuliano, R. | |
| Orientation-controlled conjugation of haloalkane dehalogenase fused homing peptides to multifunctional nanoparticles for the specific recognition of cancer cells | 1-gen-2013 | Mazzucchelli, Serena; Colombo, Miriam; Verderio, Paolo; Rozek, E; Andreata, F; Galbiati, Elisabetta; Tortora, Paolo; Corsi, F; Prosperi, Davide | |
| 6q24 duplication and transient neonatal diabetes: a possible differential diagnosis with Beckwith-Wiedemann syndrome? | 1-gen-2007 | Andreucci, E; Toni S. Ciccone R., De Gregori M; Giunti, L; Sani, I; Guarducci, ; S., Genuardi M; Zuffardi, O; Giglio, Sabrina Rita |
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