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1. AMICO galaxy clusters in KiDS-DR3: Constraints on cosmological parameters and on the normalisation of the mass-richness relation from clustering

Author

Lesci, G. F., Nanni, L., Marulli, F., Moscardini, L., Veropalumbo, A., Maturi, M., Sereno, M., Radovich, M., Bellagamba, F., Roncarelli, M., Bardelli, S., Castignani, G., Covone, G., Giocoli, C., Ingoglia, L., and Puddu, E.

Subjects
Astrophysics - Cosmology and Nongalactic Astrophysics
Abstract

We analysed the clustering of a photometric sample of galaxy clusters selected from the Third Data Release of the Kilo-Degree Survey, focusing on the redshift-space two-point correlation function (2PCF). We compared our measurements to theoretical predictions of the standard $\Lambda$ cold dark matter ($\Lambda$CDM) cosmological model. We measured the 2PCF of the sample in the cluster centric radial range $r\in[5,80]$ $h^{-1}$Mpc, considering 4934 galaxy clusters with richness $\lambda^*\geq15$ in the redshift range $z\in[0.1,0.6]$. A Markov chain Monte Carlo analysis has been performed to constrain the cosmological parameters $\Omega_{\rm m}$, $\sigma_8$, and $S_8 \equiv \sigma_8(\Omega_{\rm m}/0.3)^{0.5}$, assuming Gaussian priors on the mass-richness relation given by the posteriors obtained from a joint analysis of cluster counts and weak lensing. In addition, we constrained the normalisation of the mass-richness relation, $\alpha$, with fixed cosmological parameters. We obtained $\Omega_{\rm m}=0.28^{+0.05}_{-0.04}$, $\sigma_8=0.82^{+0.14}_{-0.12}$, and $S_8=0.80^{+0.08}_{-0.08}$. The constraint on $S_8$ is consistent within 1$\sigma$ with the results from WMAP and Planck. Furthermore, by fixing the cosmological parameters to those provided by Planck, we obtained $\alpha=0.12^{+0.06}_{-0.06}$, which is fully consistent with the result obtained from the joint analysis of cluster counts and weak lensing performed for this sample., Comment: 8 pages, 5 figures, 1 table. Submitted to A&A

Published
2022
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2. AMICO galaxy clusters in KiDS-DR3: cosmological constraints from counts and stacked weak-lensing

Author

Lesci, G. F., Marulli, F., Moscardini, L., Sereno, M., Veropalumbo, A., Maturi, M., Giocoli, C., Radovich, M., Bellagamba, F., Roncarelli, M., Bardelli, S., Contarini, S., Covone, G., Ingoglia, L., Nanni, L., and Puddu, E.

Subjects
Astrophysics - Cosmology and Nongalactic Astrophysics
Abstract

We present a cosmological analysis of abundances and stacked weak-lensing profiles of galaxy clusters, exploiting the AMICO KiDS-DR3 catalogue. The sample consists of 3652 galaxy clusters with intrinsic richness $\lambda^*\geq20$, over an effective area of 377 deg$^2$, in the redshift range $z\in[0.1,\,0.6]$. We quantified the purity and completeness of the sample through simulations. The statistical analysis has been performed by simultaneously modelling the comoving number density of galaxy clusters and the scaling relation between the intrinsic richnesses and the cluster masses, assessed through a stacked weak-lensing profile modelling. The fluctuations of the matter background density, caused by super-survey modes, have been taken into account in the likelihood. Assuming a flat $\Lambda$CDM model, we constrained $\Omega_{\rm m}$, $\sigma_8$, $S_8 \equiv \sigma_8(\Omega_{\rm m}/0.3)^{0.5}$, and the parameters of the mass-richness scaling relation. We obtained $\Omega_{\rm m}=0.24^{+0.03}_{-0.04}$, $\sigma_8=0.86^{+0.07}_{-0.07}$, $S_8=0.78^{+0.04}_{-0.04}$. The constraint on $S_8$ is consistent within 1$\sigma$ with the results from WMAP and Planck. Furthermore, we got constraints on the cluster mass scaling relation in agreement with those obtained from a previous weak-lensing only analysis., Comment: 12 pages, 7 figures, 2 tables. Accepted by A&A

Published
2020
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3. General Purpose (GenP) Bioimage Ensemble of Handcrafted and Learned Features with Data Augmentation

Author

Nanni, L., Brahnam, S., Ghidoni, S., and Maguolo, G.

Subjects
Computer Science - Computer Vision and Pattern Recognition, Computer Science - Machine Learning
Abstract

Bioimage classification plays a crucial role in many biological problems. In this work, we present a new General Purpose (GenP) ensemble that boosts performance by combining local features, dense sampling features, and deep learning approaches. First, we introduce three new methods for data augmentation based on PCA/DCT; second, we show that different data augmentation approaches can boost the performance of an ensemble of CNNs; and, finally, we propose a set of handcrafted/learned descriptors that are highly generalizable. Each handcrafted descriptor is used to train a different Support Vector Machine (SVM), and the different SVMs are combined with the ensemble of CNNs. Our method is evaluated on a diverse set of bioimage classification problems. Results demonstrate that the proposed GenP bioimage ensemble obtains state-of-the-art performance without any ad-hoc dataset tuning of parameters (thus avoiding the risk of overfitting/overtraining)., Comment: 27 pages, 1 figure, 5 tables, manuscript

Published
2019

4. PSMA-PET vs. conventional imaging for preoperative staging high-risk PCa patients underwent surgery for cN0M0 disease

Author

Bianchi, L., primary, Valerio, M., additional, Novello, Q., additional, Balestrazzi, E., additional, Bevilacqua, F., additional, Nanni, L., additional, Droghetti, M., additional, Piazza, P., additional, Gandaglia, G., additional, Ceci, F., additional, Farolfi, A., additional, Fanti, S., additional, Briganti, A., additional, Montorsi, F., additional, Schiavina, R., additional, and Brunocilla, E., additional

Published
2024
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8. Adaptive gene loss in the common bean pan-genome during range expansion and domestication

Author

Cortinovis, G., primary, Vincenzi, L., additional, Anderson, R., additional, Marturano, G., additional, Marsh, J. I., additional, Bayer, P. E., additional, Rocchetti, L., additional, Frascarelli, G., additional, Lanzavecchia, G., additional, Pieri, A., additional, Benazzo, A., additional, Bellucci, E., additional, Di Vittori, V., additional, Nanni, L., additional, Fernandez, J. J. Ferreira, additional, Rossato, M., additional, Aguilar, O. M., additional, Morrell, P. L., additional, Rodriguez, M., additional, Gioia, T., additional, Neumann, K., additional, Diaz, J. C. Alvarez, additional, Gratias-Weill, A., additional, Klopp, C., additional, Geffroy, V., additional, Bitocchi, E., additional, Delledonne, M., additional, Edwards, D., additional, and Papa, R., additional

Published
2023
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12. AMICO galaxy clusters in KiDS-DR3: Constraints on cosmological parameters and on the normalisation of the mass-richness relation from clustering

Author

Lesci, G. F., primary, Nanni, L., additional, Marulli, F., additional, Moscardini, L., additional, Veropalumbo, A., additional, Maturi, M., additional, Sereno, M., additional, Radovich, M., additional, Bellagamba, F., additional, Roncarelli, M., additional, Bardelli, S., additional, Castignani, G., additional, Covone, G., additional, Giocoli, C., additional, Ingoglia, L., additional, and Puddu, E., additional

Published
2022
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13. Children with special health care needs attending emergency department in Italy: analysis of 3479 cases

Author

Cianci, P, D'Apolito, V, Moretti, A, Barbagallo, M, Paci, S, Carbone, M, Lubrano, R, Urbino, A, Dionisi Vici, C, Memo, L, Zampino, G, La Marca, G, Villani, A, Corsello, G, Selicorni, A, Campania, A, Geremia, C, Castagno, E, Masi, S, Poggi, G, Vestri, M, Fossali, E, Rocchi, A, Dadalt, L, Arrighini, A, Chiappa, S, Renna, S, Piccotti, E, Borgna, C, Govoni, M, Biondi, A, Fossati, C, Iughetti, L, Bertolani, P, Salvatoni, A, Agosti, M, Fuca, F, Ilardi, A, Giuffrida, S, Diguardo, V, Boni, S, D'Antiga, L, Ruggeri, M, Chiaretti, A, Amarri, S, Peduto, A, Bernardi, F, Corsini, I, Deangelis, G, Ruberto, C, Zuccotti, G, Stringhi, C, Lombardi, G, Salladini, C, Dimichele, S, Parola, L, Porta, A, Biasucci, G, Bellini, M, Ortisi, M, Apuril, E, Midulla, F, Tarani, L, Parlapiano, G, Lietti, D, Sforzini, C, Marseglia, G, Savasta, S, Falsaperla, R, Vitaliti, M, Chiarelli, F, Rossi, N, Banderali, G, Giacchero, R, Bernardo, L, Pinto, F, Fabiani, E, Ficcadenti, A, Pellegrini, G, Giacoma, S, Biban, P, Spada, S, Tipo, V, Ghitti, C, Bolognini, S, Mariani, G, Russo, A, Colella, M, Verrico, A, Bruni, P, Poddighe, D, Cagnoli, G, Morandi, F, Gadaleta, A, Barbi, E, Bruno, I, Graziano, R, Sgaramella, P, Catalani, M, Baldoni, I, Colarusso, G, Galvagno, G, Barone, A, Longo, A, Nardella, G, Portale, G, Garigali, G, Bona, G, Erbela, M, Agostiniani, R, Nanni, L, Schieven, E, Dona, M, Varisco, T, Russo, F, Distefano, V, Dipietro, F, Tarallo, L, Imperato, L, Parisi, G, Salzano, R, Raiola, G, Talarico, V, Bellu, R, Cannone, A, Ferrante, P, Cianci P., D'Apolito V., Moretti A., Barbagallo M., Paci S., Carbone M. T., Lubrano R., Urbino A., Dionisi Vici C., Memo L., Zampino G., La Marca G., Villani A., Corsello G., Selicorni A., Campania A., Geremia C., Castagno E., Masi S., Poggi G., Vestri M., Fossali E., Rocchi A., DaDalt L., Arrighini A., Chiappa S., Renna S., Piccotti E., Borgna C., Govoni M. R., Biondi A., Fossati C., Iughetti L., Bertolani P., Salvatoni A., Agosti M., Fuca F., Ilardi A., Giuffrida S., DiGuardo V., Boni S., D'Antiga L., Ruggeri M., Chiaretti A., Amarri S., Peduto A., Bernardi F., Corsini I., DeAngelis G. L., Ruberto C., Zuccotti G. V., Stringhi C., Lombardi G., Salladini C., DiMichele S., Parola L., Porta A., Biasucci G., Bellini M., Ortisi M. T., Apuril E., Midulla F., Tarani L., Parlapiano G., Lietti D., Sforzini C., Marseglia G. L., Savasta S., Falsaperla R., Vitaliti M. C., Chiarelli F., Rossi N., Banderali G., Giacchero R., Bernardo L., Pinto F., Fabiani E., Ficcadenti A., Pellegrini G., Giacoma S., Biban P., Spada S., Tipo V., Ghitti C., Bolognini S., Mariani G., Russo A., Colella M. G., Verrico A., Bruni P., Poddighe D., Cagnoli G., Morandi F., Gadaleta A., Barbi E., Bruno I. I., Graziano R., Sgaramella P., Catalani M. P., Baldoni I., Colarusso G., Galvagno G., Barone A. P., Longo A., Nardella G., Portale G., Garigali G., Bona G., Erbela M., Agostiniani R., Nanni L., Schieven E., Dona M., Varisco T., Russo F., DiStefano V. A., DiPietro F., Tarallo L., Imperato L., Parisi G., Salzano R., Raiola G., Talarico V., Bellu R., Cannone A., Ferrante P., Cianci, P, D'Apolito, V, Moretti, A, Barbagallo, M, Paci, S, Carbone, M, Lubrano, R, Urbino, A, Dionisi Vici, C, Memo, L, Zampino, G, La Marca, G, Villani, A, Corsello, G, Selicorni, A, Campania, A, Geremia, C, Castagno, E, Masi, S, Poggi, G, Vestri, M, Fossali, E, Rocchi, A, Dadalt, L, Arrighini, A, Chiappa, S, Renna, S, Piccotti, E, Borgna, C, Govoni, M, Biondi, A, Fossati, C, Iughetti, L, Bertolani, P, Salvatoni, A, Agosti, M, Fuca, F, Ilardi, A, Giuffrida, S, Diguardo, V, Boni, S, D'Antiga, L, Ruggeri, M, Chiaretti, A, Amarri, S, Peduto, A, Bernardi, F, Corsini, I, Deangelis, G, Ruberto, C, Zuccotti, G, Stringhi, C, Lombardi, G, Salladini, C, Dimichele, S, Parola, L, Porta, A, Biasucci, G, Bellini, M, Ortisi, M, Apuril, E, Midulla, F, Tarani, L, Parlapiano, G, Lietti, D, Sforzini, C, Marseglia, G, Savasta, S, Falsaperla, R, Vitaliti, M, Chiarelli, F, Rossi, N, Banderali, G, Giacchero, R, Bernardo, L, Pinto, F, Fabiani, E, Ficcadenti, A, Pellegrini, G, Giacoma, S, Biban, P, Spada, S, Tipo, V, Ghitti, C, Bolognini, S, Mariani, G, Russo, A, Colella, M, Verrico, A, Bruni, P, Poddighe, D, Cagnoli, G, Morandi, F, Gadaleta, A, Barbi, E, Bruno, I, Graziano, R, Sgaramella, P, Catalani, M, Baldoni, I, Colarusso, G, Galvagno, G, Barone, A, Longo, A, Nardella, G, Portale, G, Garigali, G, Bona, G, Erbela, M, Agostiniani, R, Nanni, L, Schieven, E, Dona, M, Varisco, T, Russo, F, Distefano, V, Dipietro, F, Tarallo, L, Imperato, L, Parisi, G, Salzano, R, Raiola, G, Talarico, V, Bellu, R, Cannone, A, Ferrante, P, Cianci P., D'Apolito V., Moretti A., Barbagallo M., Paci S., Carbone M. T., Lubrano R., Urbino A., Dionisi Vici C., Memo L., Zampino G., La Marca G., Villani A., Corsello G., Selicorni A., Campania A., Geremia C., Castagno E., Masi S., Poggi G., Vestri M., Fossali E., Rocchi A., DaDalt L., Arrighini A., Chiappa S., Renna S., Piccotti E., Borgna C., Govoni M. R., Biondi A., Fossati C., Iughetti L., Bertolani P., Salvatoni A., Agosti M., Fuca F., Ilardi A., Giuffrida S., DiGuardo V., Boni S., D'Antiga L., Ruggeri M., Chiaretti A., Amarri S., Peduto A., Bernardi F., Corsini I., DeAngelis G. L., Ruberto C., Zuccotti G. V., Stringhi C., Lombardi G., Salladini C., DiMichele S., Parola L., Porta A., Biasucci G., Bellini M., Ortisi M. T., Apuril E., Midulla F., Tarani L., Parlapiano G., Lietti D., Sforzini C., Marseglia G. L., Savasta S., Falsaperla R., Vitaliti M. C., Chiarelli F., Rossi N., Banderali G., Giacchero R., Bernardo L., Pinto F., Fabiani E., Ficcadenti A., Pellegrini G., Giacoma S., Biban P., Spada S., Tipo V., Ghitti C., Bolognini S., Mariani G., Russo A., Colella M. G., Verrico A., Bruni P., Poddighe D., Cagnoli G., Morandi F., Gadaleta A., Barbi E., Bruno I. I., Graziano R., Sgaramella P., Catalani M. P., Baldoni I., Colarusso G., Galvagno G., Barone A. P., Longo A., Nardella G., Portale G., Garigali G., Bona G., Erbela M., Agostiniani R., Nanni L., Schieven E., Dona M., Varisco T., Russo F., DiStefano V. A., DiPietro F., Tarallo L., Imperato L., Parisi G., Salzano R., Raiola G., Talarico V., Bellu R., Cannone A., and Ferrante P.

Abstract

Background: Although children with special health care needs (CSHCN) represent a minority of the population, they go through more hospitalizations, more admissions to the Emergency Department (ED), and receive a major number of medical prescriptions, in comparison to general pediatric population. Objectives of the study were to determine the reasons for admission to the ED in Italian CSHCN, and to describe the association between patient’s demographic data, clinical history, and health services requirements. Methods: Ad hoc web site was created to collect retrospective data of 3479 visits of CSHCN to the ED in 58 Italian Hospitals. Results: Seventy-two percent of patients admitted to ED were affected by a previously defined medical condition. Most of the ED admissions were children with syndromic conditions (54%). 44.2% of the ED admissions were registered during the night-time and/or at the weekends. The hospitalization rate was of 45.6% among patients admitted to the ED. The most common reason for admission to the ED was the presence of respiratory symptoms (26.6%), followed by gastrointestinal problems (21.3%) and neurological disorders (18.2%). 51.4% of the access were classified as ‘urgent’, with a red/yellow triage code. Considering the type of ED, 61.9% of the visits were conducted at the Pediatric EDs (PedEDs), 33.5% at the Functional EDs (FunEDs) and 4.6% at the Dedicated EDs (DedEDs). Patients with more complex clinical presentation were more likely to be evaluated at the PedEDs. CSHCN underwent to a higher number of medical procedures at the PedEDs, more in comparison to other EDs. Children with medical devices were directed to a PedED quite exclusively when in need for medical attention. Subjects under multiple anti-epileptic drug therapy attended to PedEDs or FunEDs generally. Patients affected by metabolic diseases were more likely to look for medical attention at FunEDs. Syndromic patients mostly required medical attention at the DedEDs. Conclusions

Published
2020

15. Children with special health care needs attending emergency department in Italy: analysis of 3479 cases

Author

Cianci, P., D'Apolito, V., Moretti, A., Barbagallo, M., Paci, S., Carbone, M. T., Lubrano, R., Urbino, A., Dionisi Vici, C., Memo, L., Zampino, G., La Marca, G., Villani, A., Corsello, G., Selicorni, A., Campania, A., Geremia, C., Castagno, E., Masi, S., Poggi, G., Vestri, M., Fossali, E., Rocchi, A., Dadalt, L., Arrighini, A., Chiappa, S., Renna, S., Piccotti, E., Borgna, C., Govoni, M. R., Biondi, A., Fossati, C., Iughetti, L., Bertolani, P., Salvatoni, A., Agosti, M., Fuca, F., Ilardi, A., Giuffrida, S., Diguardo, V., Boni, S., D'Antiga, L., Ruggeri, M., Chiaretti, A., Amarri, S., Peduto, A., Bernardi, F., Corsini, I., Deangelis, G. L., Ruberto, C., Zuccotti, G. V., Stringhi, C., Lombardi, G., Salladini, C., Dimichele, S., Parola, L., Porta, A., Biasucci, G., Bellini, M., Ortisi, M. T., Apuril, E., Midulla, F., Tarani, L., Parlapiano, G., Lietti, D., Sforzini, C., Marseglia, G. L., Savasta, S., Falsaperla, R., Vitaliti, M. C., Chiarelli, F., Rossi, N., Banderali, G., Giacchero, R., Bernardo, L., Pinto, F., Fabiani, E., Ficcadenti, A., Pellegrini, G., Giacoma, S., Biban, P., Spada, S., Tipo, V., Ghitti, C., Bolognini, S., Mariani, G., Russo, A., Colella, M. G., Verrico, A., Bruni, P., Poddighe, D., Cagnoli, G., Morandi, F., Gadaleta, A., Barbi, E., Bruno, I. I., Graziano, R., Sgaramella, P., Catalani, M. P., Baldoni, I., Colarusso, G., Galvagno, G., Barone, A. P., Longo, A., Nardella, G., Portale, G., Garigali, G., Bona, G., Erbela, M., Agostiniani, R., Nanni, L., Schieven, E., Dona, M., Varisco, T., Russo, F., Distefano, V. A., Dipietro, F., Tarallo, L., Imperato, L., Parisi, G., Salzano, R., Raiola, G., Talarico, V., Bellu, R., Cannone, A., Ferrante, P., Cianci, P, D'Apolito, V, Moretti, A, Barbagallo, M, Paci, S, Carbone, M, Lubrano, R, Urbino, A, Dionisi Vici, C, Memo, L, Zampino, G, La Marca, G, Villani, A, Corsello, G, Selicorni, A, Campania, A, Geremia, C, Castagno, E, Masi, S, Poggi, G, Vestri, M, Fossali, E, Rocchi, A, Dadalt, L, Arrighini, A, Chiappa, S, Renna, S, Piccotti, E, Borgna, C, Govoni, M, Biondi, A, Fossati, C, Iughetti, L, Bertolani, P, Salvatoni, A, Agosti, M, Fuca, F, Ilardi, A, Giuffrida, S, Diguardo, V, Boni, S, D'Antiga, L, Ruggeri, M, Chiaretti, A, Amarri, S, Peduto, A, Bernardi, F, Corsini, I, Deangelis, G, Ruberto, C, Zuccotti, G, Stringhi, C, Lombardi, G, Salladini, C, Dimichele, S, Parola, L, Porta, A, Biasucci, G, Bellini, M, Ortisi, M, Apuril, E, Midulla, F, Tarani, L, Parlapiano, G, Lietti, D, Sforzini, C, Marseglia, G, Savasta, S, Falsaperla, R, Vitaliti, M, Chiarelli, F, Rossi, N, Banderali, G, Giacchero, R, Bernardo, L, Pinto, F, Fabiani, E, Ficcadenti, A, Pellegrini, G, Giacoma, S, Biban, P, Spada, S, Tipo, V, Ghitti, C, Bolognini, S, Mariani, G, Russo, A, Colella, M, Verrico, A, Bruni, P, Poddighe, D, Cagnoli, G, Morandi, F, Gadaleta, A, Barbi, E, Bruno, I, Graziano, R, Sgaramella, P, Catalani, M, Baldoni, I, Colarusso, G, Galvagno, G, Barone, A, Longo, A, Nardella, G, Portale, G, Garigali, G, Bona, G, Erbela, M, Agostiniani, R, Nanni, L, Schieven, E, Dona, M, Varisco, T, Russo, F, Distefano, V, Dipietro, F, Tarallo, L, Imperato, L, Parisi, G, Salzano, R, Raiola, G, Talarico, V, Bellu, R, Cannone, A, Ferrante, P, Paola Cianci, Valeria D'Apolito, Alex Moretti, Massimo Barbagallo, Sabrina Paci, Maria Teresa Carbone, Riccardo Lubrano, Antonio Urbino, Carlo Dionisi Vici, Luigi Memo, Giuseppe Zampino, Giancarlo La Marca, Alberto Villani, Giovanni Corsello, Angelo Selicorni, Cianci, P., D'Apolito, V., Moretti, A., Barbagallo, M., Paci, S., Carbone, M. T., Lubrano, R., Urbino, A., Dionisi Vici, C., Memo, L., Zampino, G., La Marca, G., Villani, A., Corsello, G., Selicorni, A., Campania, A., Geremia, C., Castagno, E., Masi, S., Poggi, G., Vestri, M., Fossali, E., Rocchi, A., Dadalt, L., Arrighini, A., Chiappa, S., Renna, S., Piccotti, E., Borgna, C., Govoni, M. R., Biondi, A., Fossati, C., Iughetti, L., Bertolani, P., Salvatoni, A., Agosti, M., Fuca, F., Ilardi, A., Giuffrida, S., Diguardo, V., Boni, S., D'Antiga, L., Ruggeri, M., Chiaretti, A., Amarri, S., Peduto, A., Bernardi, F., Corsini, I., Deangelis, G. L., Ruberto, C., Zuccotti, G. V., Stringhi, C., Lombardi, G., Salladini, C., Dimichele, S., Parola, L., Porta, A., Biasucci, G., Bellini, M., Ortisi, M. T., Apuril, E., Midulla, F., Tarani, L., Parlapiano, G., Lietti, D., Sforzini, C., Marseglia, G. L., Savasta, S., Falsaperla, R., Vitaliti, M. C., Chiarelli, F., Rossi, N., Banderali, G., Giacchero, R., Bernardo, L., Pinto, F., Fabiani, E., Ficcadenti, A., Pellegrini, G., Giacoma, S., Biban, P., Spada, S., Tipo, V., Ghitti, C., Bolognini, S., Mariani, G., Russo, A., Colella, M. G., Verrico, A., Bruni, P., Poddighe, D., Cagnoli, G., Morandi, F., Gadaleta, A., Barbi, E., Bruno, I. I., Graziano, R., Sgaramella, P., Catalani, M. P., Baldoni, I., Colarusso, G., Galvagno, G., Barone, A. P., Longo, A., Nardella, G., Portale, G., Garigali, G., Bona, G., Erbela, M., Agostiniani, R., Nanni, L., Schieven, E., Dona, M., Varisco, T., Russo, F., Distefano, V. A., Dipietro, F., Tarallo, L., Imperato, L., Parisi, G., Salzano, R., Raiola, G., Talarico, V., Bellu, R., Cannone, A., and Ferrante, P.

Subjects
Male, Metabolic disease, Hospitalization rate, Congenital skeletal condition, Children with special health care needs, Emergency department, Isolated CNS malformation, Metabolic diseases, Multiple AED therapy, Neuromuscular diseases, Syndromic disorders, True isolated microcephaly, 0302 clinical medicine, Clinical history, Medicine, Child, education.field_of_study, Neuromuscular disease, Settore MED/38, Disabled Children, Hospitalization, Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA, Italy, Child, Preschool, Female, Children with special health care need, Emergency Service, Hospital, medicine.medical_specialty, Adolescent, Population, Triage Code, 03 medical and health sciences, Pharmacotherapy, 030225 pediatrics, Humans, Medical prescription, education, Retrospective Studies, Health Services Needs and Demand, Syndromic disorder, business.industry, Research, Infant, Newborn, Infant, 030208 emergency & critical care medicine, Children with special health care needs, Congenital skeletal conditions,Emergency department, Hospitalization rate, Isolated CNS malformation, Metabolic diseases, Multiple AED therapy, Neuromuscular diseases, Syndromic disorders, True isolated microcephaly, Family medicine, Chronic Disease, business, Facilities and Services Utilization
Abstract

Background Although children with special health care needs (CSHCN) represent a minority of the population, they go through more hospitalizations, more admissions to the Emergency Department (ED), and receive a major number of medical prescriptions, in comparison to general pediatric population. Objectives of the study were to determine the reasons for admission to the ED in Italian CSHCN, and to describe the association between patient’s demographic data, clinical history, and health services requirements. Methods Ad hoc web site was created to collect retrospective data of 3479 visits of CSHCN to the ED in 58 Italian Hospitals. Results Seventy-two percent of patients admitted to ED were affected by a previously defined medical condition. Most of the ED admissions were children with syndromic conditions (54%). 44.2% of the ED admissions were registered during the night-time and/or at the weekends. The hospitalization rate was of 45.6% among patients admitted to the ED. The most common reason for admission to the ED was the presence of respiratory symptoms (26.6%), followed by gastrointestinal problems (21.3%) and neurological disorders (18.2%). 51.4% of the access were classified as ‘urgent’, with a red/yellow triage code. Considering the type of ED, 61.9% of the visits were conducted at the Pediatric EDs (PedEDs), 33.5% at the Functional EDs (FunEDs) and 4.6% at the Dedicated EDs (DedEDs). Patients with more complex clinical presentation were more likely to be evaluated at the PedEDs. CSHCN underwent to a higher number of medical procedures at the PedEDs, more in comparison to other EDs. Children with medical devices were directed to a PedED quite exclusively when in need for medical attention. Subjects under multiple anti-epileptic drug therapy attended to PedEDs or FunEDs generally. Patients affected by metabolic diseases were more likely to look for medical attention at FunEDs. Syndromic patients mostly required medical attention at the DedEDs. Conclusions Access of CSHCN to an ED is not infrequent. For this reason, it is fundamental for pediatricians working in any kind of ED to increase their general knowledge about CHSCN and to gain expertise in the management of such patients and their related medical complexity.

Published
2020

16. Prevalence of bladder cancer in Costello syndrome: New insights to drive clinical decision-making

Author

Leoni, Chiara, Paradiso, Filomena Valentina, Foschi, Nazario, Tedesco, Marta, Pierconti, Francesco, Silvaroli, S., Diego, M. D., Birritella, Lisa, Pantaleoni, F., Rendeli, Claudia, Onesimo, Roberta, Viscogliosi, Germana, Bassi, Pierfrancesco, Nanni, Lorenzo, Genuardi, Maurizio, Tartaglia, M., Zampino, Giuseppe, Leoni C., Paradiso F. V., Foschi N., Tedesco M., Pierconti F. (ORCID:0000-0003-0951-4131), Birritella L., Rendeli C. (ORCID:0000-0002-5948-1617), Onesimo R., Viscogliosi G., Bassi P. (ORCID:0000-0002-4313-8427), Nanni L. (ORCID:0000-0003-2569-8583), Genuardi M. (ORCID:0000-0002-7410-8351), Zampino G. (ORCID:0000-0003-3865-3253), Leoni, Chiara, Paradiso, Filomena Valentina, Foschi, Nazario, Tedesco, Marta, Pierconti, Francesco, Silvaroli, S., Diego, M. D., Birritella, Lisa, Pantaleoni, F., Rendeli, Claudia, Onesimo, Roberta, Viscogliosi, Germana, Bassi, Pierfrancesco, Nanni, Lorenzo, Genuardi, Maurizio, Tartaglia, M., Zampino, Giuseppe, Leoni C., Paradiso F. V., Foschi N., Tedesco M., Pierconti F. (ORCID:0000-0003-0951-4131), Birritella L., Rendeli C. (ORCID:0000-0002-5948-1617), Onesimo R., Viscogliosi G., Bassi P. (ORCID:0000-0002-4313-8427), Nanni L. (ORCID:0000-0003-2569-8583), Genuardi M. (ORCID:0000-0002-7410-8351), and Zampino G. (ORCID:0000-0003-3865-3253)

Abstract

Costello syndrome (CS) is a rare disorder affecting development and growth characterized by cancer predisposition and caused by mutations in HRAS proto-oncogene. Somatic HRAS mutations drive bladder carcinogenesis. The aim of this study was to analyze prevalence and histological characterization of bladder cancer (BC) in a cohort of patients with CS to help clinicians plan effective management strategies. This study included 13 patients above 10 years of age with molecular diagnosis of CS. Screening cystoscopies (31 total procedures) were performed to exclude BC. Any lesion was analyzed through cold-cup biopsy or trans-urethral resection of the bladder. According to histology, patients were followed-up with urinalysis and abdominal ultrasound yearly, and cystoscopies every 12–24 months. During study enrollment, bladder lesions (often multifocal) were detected in 11/13 patients. Histological analysis documented premalignant lesions in 90% of cystoscopies performed, epithelial dysplasia in 71%, and papillary urothelial neoplasm of low-malignant potential in 19%. BC G1/low grade (Ta) were removed in 10%. Overall, 76% of patients showed a bladder lesion at first cystoscopy. The present findings document that individuals with CS aged 10 years and older have high prevalence of bladder lesions (premalignant/malignant), highlighting the importance of personalized screening protocols.

Published
2022

17. A regional-based newborn hearing screening program: the Emilia-Romagna model after ten years of legislation.

Author

Bianchin, G., Palma, S., Polizzi, V., Kaleci, S., Stagi, P., Cappai, M., Baiocchi, M. P., Benincasa, P., Brandolini, C., Casadio, L., Di Sarro, S., Farneti, D., Galli, A., Ghiselli, S., Iadicicco, P., Landuzzi, E., Limarzi, M., Locatelli, C., Murri, A., and Nanni, L.

Subjects
NEWBORN infants, CONGENITAL disorders, HEALTH outcome assessment, EPIDEMIOLOGY, DEAFNESS
Abstract

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Published
2023
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19. AMICO galaxy clusters in KiDS-DR3: Cosmological constraints from counts and stacked weak lensing

Author

Lesci, G. F., primary, Marulli, F., additional, Moscardini, L., additional, Sereno, M., additional, Veropalumbo, A., additional, Maturi, M., additional, Giocoli, C., additional, Radovich, M., additional, Bellagamba, F., additional, Roncarelli, M., additional, Bardelli, S., additional, Contarini, S., additional, Covone, G., additional, Ingoglia, L., additional, Nanni, L., additional, and Puddu, E., additional

Published
2022
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24. Gut microbiome in DLBCL patients undergoing first‐line R‐CHOP regimen—The Oncopassport Study.

Author

Stefoni, V., Argnani, L., Casadei, B., Musuraca, G., Nanni, L., Pellegrini, C., Broccoli, A., Carella, M., Caldarulo, E., Mammoli, F., Conti, G., Turroni, S., Barone, M., Brigidi, P., and Zinzani, P. L.

Subjects
GUT microbiome, DIFFUSE large B-cell lymphomas, ANTINEOPLASTIC combined chemotherapy protocols
Abstract

Gut microbiome in DLBCL patients undergoing first-line R-CHOP regimen - The Oncopassport Study Reconstructing GM dynamics in DLBCL patients from diagnosis to the end of R-CHOP may provide important information for patient management. B Introduction: b The search of biomarkers that can predict and influence treatment outcomes of diffuse large B-cell lymphoma (DLBCL) is constantly evolving, especially in the front-line setting. [Extracted from the article]

Published
2023
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26. The INCREASE project: Intelligent Collections of food‐legume genetic resources for European agrofood systems

Author

Bellucci, E., Mario Aguilar, O., Alseekh, S., Bett, K., Brezeanu, C., Cook, D., De la Rosa, L., Delledonne, M., Dostatny, D.F., Ferreira, J.J., Geffroy, V., Ghitarrini, S., Kroc, M., Kumar Agrawal, S., Logozzo, G., Marino, M., Mary‐Huard, T., McClean, P., Meglič, V., Messer, T., Muel, F., Nanni, L., Neumann, K., Servalli, F., Străjeru, S., Varshney, R.K., Vasconcelos, M.W., Zaccardelli, M., Zavarzin, A., Bitocchi, E., Frontoni, E., Fernie, A.R., Gioia, T., Graner, A., Guasch, L., Prochnow, L., Oppermann, M., Susek, K., Tenaillon, M., Papa, R., Bellucci, E., Mario Aguilar, O., Alseekh, S., Bett, K., Brezeanu, C., Cook, D., De la Rosa, L., Delledonne, M., Dostatny, D.F., Ferreira, J.J., Geffroy, V., Ghitarrini, S., Kroc, M., Kumar Agrawal, S., Logozzo, G., Marino, M., Mary‐Huard, T., McClean, P., Meglič, V., Messer, T., Muel, F., Nanni, L., Neumann, K., Servalli, F., Străjeru, S., Varshney, R.K., Vasconcelos, M.W., Zaccardelli, M., Zavarzin, A., Bitocchi, E., Frontoni, E., Fernie, A.R., Gioia, T., Graner, A., Guasch, L., Prochnow, L., Oppermann, M., Susek, K., Tenaillon, M., and Papa, R.

Abstract

Food legumes are crucial for all agriculture-related societal challenges, including climate change mitigation, agrobiodiversity conservation, sustainable agriculture, food security and human health. The transition to plant-based diets, largely based on food legumes, could present major opportunities for adaptation and mitigation, generating significant co-benefits for human health. The characterization, maintenance and exploitation of food-legume genetic resources, to date largely unexploited, form the core development of both sustainable agriculture and a healthy food system. INCREASE will implement, on chickpea (Cicer arietinum), common bean (Phaseolus vulgaris), lentil (Lens culinaris) and lupin (Lupinus albus and L. mutabilis), a new approach to conserve, manage and characterize genetic resources. Intelligent Collections, consisting of nested core collections composed of single-seed descent-purified accessions (i.e., inbred lines), will be developed, exploiting germplasm available both from genebanks and on-farm and subjected to different levels of genotypic and phenotypic characterization. Phenotyping and gene discovery activities will meet, via a participatory approach, the needs of various actors, including breeders, scientists, farmers and agri-food and non-food industries, exploiting also the power of massive metabolomics and transcriptomics and of artificial intelligence and smart tools. Moreover, INCREASE will test, with a citizen science experiment, an innovative system of conservation and use of genetic resources based on a decentralized approach for data management and dynamic conservation. By promoting the use of food legumes, improving their quality, adaptation and yield and boosting the competitiveness of the agriculture and food sector, the INCREASE strategy will have a major impact on economy and society and represents a case study of integrative and participatory approaches towards conservation and exploitation of crop genetic resources.

Published
2021

27. Contactless: a new personalised telehealth model in chronic pediatric diseases and disability during the COVID-19 era

Author

Mercuri, Eugenio Maria, Zampino, Giuseppe, Morsella, Alisha, Pane, Marika, Onesimo, Roberta, Angioletti, C., Valentini, Piero, Rendeli, Claudia, Ruggiero, Antonio, Nanni, Lorenzo, Chiaretti, Antonio, Vento, Giovanni, Korn, D., Meneschincheri, Emilio, Sergi, P., Scambia, Giovanni, Ricciardi, Walter, Cambieri, Andrea, De Belvis, Antonio, Mercuri E. (ORCID:0000-0002-9851-5365), Zampino G. (ORCID:0000-0003-3865-3253), Morsella A., Pane M. (ORCID:0000-0002-4851-6124), Onesimo R., Valentini P. (ORCID:0000-0001-6095-9510), Rendeli C. (ORCID:0000-0002-5948-1617), Ruggiero A. (ORCID:0000-0002-6052-3511), Nanni L. (ORCID:0000-0003-2569-8583), Chiaretti A. (ORCID:0000-0002-9971-1640), Vento G. (ORCID:0000-0002-8132-5127), Meneschincheri E., Scambia G. (ORCID:0000-0003-2758-1063), Ricciardi W. (ORCID:0000-0002-5655-688X), Cambieri A., De Belvis A. (ORCID:0000-0003-4456-1937), Mercuri, Eugenio Maria, Zampino, Giuseppe, Morsella, Alisha, Pane, Marika, Onesimo, Roberta, Angioletti, C., Valentini, Piero, Rendeli, Claudia, Ruggiero, Antonio, Nanni, Lorenzo, Chiaretti, Antonio, Vento, Giovanni, Korn, D., Meneschincheri, Emilio, Sergi, P., Scambia, Giovanni, Ricciardi, Walter, Cambieri, Andrea, De Belvis, Antonio, Mercuri E. (ORCID:0000-0002-9851-5365), Zampino G. (ORCID:0000-0003-3865-3253), Morsella A., Pane M. (ORCID:0000-0002-4851-6124), Onesimo R., Valentini P. (ORCID:0000-0001-6095-9510), Rendeli C. (ORCID:0000-0002-5948-1617), Ruggiero A. (ORCID:0000-0002-6052-3511), Nanni L. (ORCID:0000-0003-2569-8583), Chiaretti A. (ORCID:0000-0002-9971-1640), Vento G. (ORCID:0000-0002-8132-5127), Meneschincheri E., Scambia G. (ORCID:0000-0003-2758-1063), Ricciardi W. (ORCID:0000-0002-5655-688X), Cambieri A., and De Belvis A. (ORCID:0000-0003-4456-1937)

Abstract

Background: Suspending ordinary care activities during the COVID-19 pandemic made it necessary to find alternative routes to comply with care recommendations not only for acute health needs but also for patients requiring follow-up and multidisciplinary visits. We present the ‘Contactless’ model, a comprehensive operational tool including a plurality of services delivered remotely, structured according to a complexity gradient, aimed to cover diagnostic procedures and monitor disease progression in chronic pediatric patients. Methods: A multidisciplinary and multiprofessional project team was recruited, in collaboration with patients’ associations, to map a panel of available Evidence-Based solutions and address individual needs in full respect of the concept of personalized medicine. The solutions include a number of services from videoconsultations to more structure videotraining sessions. Results: A modular framework made up of four three Macro-levels of complexity - Contactless Basic, Intermediate and Advanced - was displayed as an incremental set of services and operational planning establishing each phase, from factors influencing eligibility to the delivery of the most accurate and complex levels of care. Conclusion: The multimodal, multidisciplinary ‘Contactless’ model allowed the inclusion of all Units of our Pediatric Department and families with children with disability or complex chronic conditions. The strengths of this project rely on its replicability outside of pediatrics and in the limited resources needed to practically impact patients, caregivers and professionals involved in the process of care. Its implementation in the future may contribute to reduce the duration of hospital admissions, money and parental absence from work.

Published
2021

35. ZBTB12 DNA methylation is associated with coagulation- and inflammation-related blood cell parameters: findings from the Moli-family cohort

Author

Noro, F., Gianfagna, F., Gialluisi, A., De Curtis, A., Di Castelnuovo, A., Napoleone, E., Cerletti, C., Donati, M. B., de Gaetano, G., Hoylaerts, M. F., Iacoviello, L., Izzi, B., Vohnout, B., Arca, M., Lorenzet, R., di Castelnuovo, A., Costanzo, S., di Giuseppe, R., Cutrone, A., Magnacca, S., Crescente, M., Pampuch, A., Tamburrelli, C., Zurlo, F., and Nanni, L.

Subjects
Male, 0301 basic medicine, Myocardial Infarction, Cohort Studies, Pathogenesis, Blood cell, Leukocyte Count, 0302 clinical medicine, PLATELET, Genetics (clinical), Genetics & Heredity, DNA methylation, Granulocyte counts, White blood cell counts, Whole blood coagulation time, Zinc fingers, Cardiovascular risk, Principal Component Analysis, DNA methylation, TRANSCRIPTIONAL REGULATION, Methylation, Middle Aged, Blood Coagulation Factors, DNA-Binding Proteins, MEDITERRANEAN DIET, Haematopoiesis, Granulocyte counts, Zinc fingers, medicine.anatomical_structure, Oncology, CpG site, MONOCYTES, 030220 oncology & carcinogenesis, Female, Life Sciences & Biomedicine, Adult, Biology, Granulocyte, REGION, Young Adult, 03 medical and health sciences, ADHERENCE, White blood cell, Cardiovascular risk, White blood cell counts, Whole blood coagulation time, Genetics, medicine, Humans, Blood Coagulation, Molecular Biology, Science & Technology, Tumor Necrosis Factor-alpha, Research, 030104 developmental biology, TISSUE FACTOR, Immunology, CpG Islands, Granulocytes, Transcription Factors, Developmental Biology
Abstract

Background Zinc finger and BTB domain-containing protein 12 (ZBTB12) is a predicted transcription factor with potential role in hematopoietic development. Recent evidence linked low methylation level of ZBTB12 exon1 to myocardial infarction (MI) risk. However, the role of ZBTB12 in the pathogenesis of MI and cardiovascular disease in general is not yet clarified. We investigated the relation between ZBTB12 methylation and several blood parameters related to cardio-cerebrovascular risk in an Italian family-based cohort. Results ZBTB12 methylation was analyzed on white blood cells from the Moli-family cohort using the Sequenom EpiTYPER MassARRAY (Agena). A total of 13 CpG Sequenom units were analyzed in the small CpG island located in the only translated ZBTB12 exon. Principal component analysis (PCA) was performed to identify groups of CpG units with similar methylation estimates. Linear mixed effect regressions showed a positive association between methylation of ZBTB12 Factor 2 (including CpG units 8, 9–10, 16, 21) and TNF-ɑ stimulated procoagulant activity, a measure of procoagulant and inflammatory potential of blood cells. In addition, we also found a negative association between methylation of ZBTB12 Factor 1 (mainly characterized by CpG units 1, 3–4, 5, 11, and 26) and white blood cell and granulocyte counts. An in silico prediction analysis identified granulopoiesis- and hematopoiesis-specific transcription factors to potentially bind DNA sequences encompassing CpG1, CpG3–4, and CpG11. Conclusions ZBTB12 hypomethylation is linked to shorter TNF-ɑ stimulated whole blood coagulation time and increased WBC and granulocyte counts, further elucidating the possible link between ZBTB12 methylation and cardiovascular disease risk. Electronic supplementary material The online version of this article (10.1186/s13148-019-0665-6) contains supplementary material, which is available to authorized users.

Published
2019

36. Variation of PEAR1 DNA methylation influences platelet and leukocyte function

Author

Izzi, B., Gianfagna, F., Yang, W. -Y., Cludts, K., De Curtis, A., Verhamme, P., Di Castelnuovo, A., Cerletti, C., Donati, M. B., De Gaetano, G., Staessen, J. A., Hoylaerts, M. F., Iacoviello, L., Vohnout, B., Arca, M., Lorenzet, R., Costanzo, S., Di Giuseppe, R., Cutrone, A., Magnacca, S., Crescente, M., Pampuch, A., Tamburrelli, C., Napoleone, E., Zurlo, F., and Nanni, L.

Subjects
Adult, Blood Platelets, Male, 0301 basic medicine, medicine.medical_specialty, Population, Receptors, Cell Surface, DNA methylation, leukocyte function, platelet, PEAR1, 030204 cardiovascular system & hematology, Biology, Epigenesis, Genetic, Cohort Studies, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Leukocytes, Genetics, medicine, Humans, Platelet, Platelet activation, Epigenetics, education, Molecular Biology, Genetics (clinical), epidemiology, public health, epigenetics, platelet aggregation, inflammation, education.field_of_study, Research, Platelet Distribution Width, Methylation, DNA Methylation, Middle Aged, Blood Cell Count, Pedigree, 030104 developmental biology, Endocrinology, Italy, CpG site, Moli-family Investigators, DNA methylation, Female, Developmental Biology
Abstract

BackgroundPlatelet-endothelial aggregation receptor 1 (PEAR-1) is a transmembrane receptor involved in platelet activation and megakaryopoiesis whose expression is driven by DNA methylation.PEAR1variants were associated with differential platelet response to activation and cardiovascular outcomes. We aimed at investigating the link betweenPEAR1methylation and platelet and leukocyte function markers in a family-based population.ResultsWe measuredPEAR1methylation in 605 Moli-family participants with available blood counts, plasma P-selectin and C-reactive protein, whole blood platelet P-selectin, and platelet-leukocyte mixed conjugate measurements. We performed principal component analysis (PCA) to identify groups of highly correlated CpG sites. We used linear mixed regression models (using age, gender, BMI, smoking, alcohol drinking, being a proband for family recruitment, being a member of myocardial infarction (MI) family as fixed effects, and family as a random effect) to evaluate associations betweenPEAR1methylation and phenotypes.PEAR1methylation Factor2, characterized by the previously identified megakaryocyte-specific CpG sites, was inversely associated with platelet-monocyte conjugates, P-selectin, and WBC counts, while positively associated with the platelet distribution width (PDW) and with leukocyte CD11b and L-selectin. Moreover,PEAR1Factor2 methylation was negatively associated with INFLAscore, a low-grade inflammation score. The latter was partially mediated by thePEAR1methylation effect on platelet variables.PEAR1methylation association with WBC measurements and INFLAscore was confirmed in the independent cohort FLEMENGHO.ConclusionsWe report a significant link between epigenetic signatures in a platelet functional gene and inflammation-dependent platelet function variability measured in two independent cohorts.

Published
2019

40. Extensive epigenomic integration of the glucocorticoid response in primary human monocytes and in vitro derived macrophages

Author

Wang, C, Nanni, L, Novakovic, B, Megchelenbrink, W, Kuznetsova, T, Stunnenberg, HG, Ceri, S, Logie, C, Wang, C, Nanni, L, Novakovic, B, Megchelenbrink, W, Kuznetsova, T, Stunnenberg, HG, Ceri, S, and Logie, C

Abstract

Glucocorticoid receptor is a transcription factor that is ubiquitously expressed. Glucocorticoids are circadian steroids that regulate a wide range of bodily functions, including immunity. Here we report that synthetic glucocorticoids affect 1035 mRNAs in isolated healthy human blood monocytes but only 165 in the respective six day-old monocyte-derived macrophages. The majority of the glucocorticoid response in monocytes concerns genes that are dynamic upon monocyte to macrophage differentiation, whereby macrophage-like mRNA levels are often reached in monocytes within four hours of treatment. Concomitantly, over 5000 chromosomal H3K27ac regions undergo remodelling, of which 60% involve increased H3K27ac signal. We find that chromosomal glucocorticoid receptor binding sites correlate with positive but not with negative local epigenomic effects. To investigate further we assigned our data to topologically associating domains (TADs). This shows that about 10% of macrophage TADs harbour at least one GR binding site and that half of all the glucocorticoid-induced H3K27ac regions are confined to these TADs. Our analyses are therefore consistent with the notion that TADs naturally accommodate information from sets of distal glucocorticoid response elements.

Published
2019

48. Correction to: Multimodal treatment of pediatric patients with Askin's tumors: Our experience (World Journal of Surgical Oncology (2018) 16 (140) DOI: 10.1186/s12957-018-1434-2)

Author

Triarico, S., Attina, G., Maurizi, Palma, Mastrangelo, Stefano, Nanni, Lorenzo, Briganti, V., Meacci, Elisa, Margaritora, Stefano, Balducci, Mario, Ruggiero, Antonio, Maurizi P. (ORCID:0000-0002-5930-0193), Mastrangelo S. (ORCID:0000-0002-3305-6014), Nanni L. (ORCID:0000-0003-2569-8583), Meacci E. (ORCID:0000-0001-8424-3816), Margaritora S. (ORCID:0000-0002-9796-760X), Balducci M. (ORCID:0000-0003-0398-9726), Ruggiero A. (ORCID:0000-0002-6052-3511), Triarico, S., Attina, G., Maurizi, Palma, Mastrangelo, Stefano, Nanni, Lorenzo, Briganti, V., Meacci, Elisa, Margaritora, Stefano, Balducci, Mario, Ruggiero, Antonio, Maurizi P. (ORCID:0000-0002-5930-0193), Mastrangelo S. (ORCID:0000-0002-3305-6014), Nanni L. (ORCID:0000-0003-2569-8583), Meacci E. (ORCID:0000-0001-8424-3816), Margaritora S. (ORCID:0000-0002-9796-760X), Balducci M. (ORCID:0000-0003-0398-9726), and Ruggiero A. (ORCID:0000-0002-6052-3511)

Abstract

In the original article mentioned above, the name of the sixth author was wrongly mentioned as "Vincenzo Briganti" instead of "Vito Briganti". The original article has been corrected.

Published
2018

49. Pancreatic head mass and jaundice as revealing signs of autoimmune pancreatitis type 2 in a 15-year-old girl

Author

Rigante, Donato, Pagliari, Danilo, Masiello, Enrico, Filoni, Simona, Giorgio, Valentina, Gatto, Antonio, Nanni, Lorenzo, Paradiso, Filomena Valentina, Lazzareschi, Ilaria, Valentini, Piero, Rigante D (ORCID:0000-0001-7032-7779), Pagliari D, Filoni S, Giorgio V, Gatto A, Nanni L (ORCID:0000-0003-2569-8583), Paradiso FV, Lazzareschi I (ORCID:0000-0001-7221-2983), Valentini P (ORCID:0000-0001-6095-9510), Rigante, Donato, Pagliari, Danilo, Masiello, Enrico, Filoni, Simona, Giorgio, Valentina, Gatto, Antonio, Nanni, Lorenzo, Paradiso, Filomena Valentina, Lazzareschi, Ilaria, Valentini, Piero, Rigante D (ORCID:0000-0001-7032-7779), Pagliari D, Filoni S, Giorgio V, Gatto A, Nanni L (ORCID:0000-0003-2569-8583), Paradiso FV, Lazzareschi I (ORCID:0000-0001-7221-2983), and Valentini P (ORCID:0000-0001-6095-9510)

Abstract

The description of this patient highlights that autoimmune pancreatitis should be taken into consideration when a pancreatic mass is combined with jaundice also in young patients.

Published
2018

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