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2. Prevalence of neurological diseases associated with cervical pain and/or signs of cervical myelopathy in French bulldogs: a retrospective analysis of 105 cases.

Author

Capasso, Michele, Canal, Sara, and Balducci, Federica

Subjects
NEUROLOGICAL disorders, SYRINGOMYELIA, NECK pain, BULLDOG, DISEASE prevalence, SPINAL cord diseases, INTERVERTEBRAL disk
Abstract

Introduction: French bulldogs can be affected by several neurological diseases, with myelopathies representing the most frequent cause of neurological signs. Studies focusing on the epidemiology of cervical diseases in this breed are lacking. This study aims to describe the prevalence of neurological pathologies responsible for cervical pain and/or signs of cervical myelopathy, assuming that intervertebral disc herniation represents the most common disease; a second aim was to evaluate how often different pathologies coexist in this spinal region in French bulldogs. Materials and methods: A retrospective analysis of medical records from the database of a single referral center (AniCura I Portoni Rossi Veterinary Hospital--Zola Predosa, Bologna, Italy) was performed, including French bulldogs presented for neck pain and/or neurological deficits consistent with cervical myelopathy. Clinical and imaging data were reviewed and used as inclusion criteria. Based on the number of MRI-diagnosed diseases, the eligible dogs were divided into three groups. Results: One hundred five French bulldogs met the inclusion criteria. The most commonly diagnosed condition was an intervertebral disc herniation (66.9%), followed by C2 idiopathic hypertrophic ganglioneuritis (15.1%), cervical syringomyelia (11.5%), congenital osseous malformations (1.4%), spinal arachnoid diverticula (1.4%), neoplasms (1.4%), steroid-responsive meningitis-arteritis (0.7%), traumatic vertebral fractures (0.7%), and other (0.7%). For the vast majority of dogs (75/105) a single pathology was diagnosed, with intervertebral disc herniations accounting for 86.7% of cases, involving C3-C4 IVD most commonly. In the remaining 30 dogs, two or three different and concurrent diseases were detected. Among these 30 dogs, intervertebral disc herniations still remained the most diagnosed condition, in combination with C2 idiopathic hypertrophic ganglioneuritis and syringomyelia in 19 and seven cases, respectively. Conclusion: The results of this study highlight that different pathologies can affect the cervical spinal cord in French bulldogs, with intervertebral disc herniations representing the most frequent condition, as previously described in the veterinary literature. In almost a third of cases, different pathologies can coexist at the cervical level. However, for cases in which different pathologies are present at the same time, it is not always possible to clearly establish their clinical significance. [ABSTRACT FROM AUTHOR]

Published
2024
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5. Positive predictive values and outcomes for uninformative cell‐free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study)

Author

Grati, Francesca Romana, primary, Bestetti, Ilaria, additional, De Siero, Daria, additional, Malvestiti, Francesca, additional, Villa, Nicoletta, additional, Sala, Elena, additional, Crosti, Francesca, additional, Parisi, Valentina, additional, Nardone, Anna Maria, additional, Di Giacomo, Gianluca, additional, Pettinari, Antonella, additional, Tortora, Giada, additional, Montaldi, Annamaria, additional, Calò, Annapaola, additional, Saccilotto, Donatella, additional, Zanchetti, Sara, additional, Celli, Paola, additional, Guerneri, Silvana, additional, Silipigni, Rosamaria, additional, Cardarelli, Laura, additional, Lippi, Elisabetta, additional, Cavani, Simona, additional, Malacarne, Michela, additional, Genesio, Rita, additional, Beltrami, Nicola, additional, Pittalis, Maria Carla, additional, Desiderio, Laura, additional, Gentile, Mattia, additional, Ficarella, Romina, additional, Recalcati, Maria Paola, additional, Catusi, Ilaria, additional, Garzo, Maria, additional, Miele, Lorena, additional, Corti, Cecilia, additional, Ghezzo, Sara, additional, Bertini, Veronica, additional, Cambi, Francesca, additional, Valetto, Angelo, additional, Facchinetti, Barbara, additional, Bernardini, Laura, additional, Capalbo, Anna, additional, Balducci, Federica, additional, Pelo, Elisabetta, additional, Minuti, Barbara, additional, Pescucci, Chiara, additional, Giuliani, Costanza, additional, Renieri, Alessandra, additional, Longo, Ilaria, additional, Tita, Rossella, additional, Castello, Giuseppe, additional, Casalone, Rosario, additional, Righi, Rossana, additional, Raso, Barbara, additional, Civolani, Alessandro, additional, Muzi, Maria Cristina, additional, di Natale, Manuela, additional, Varriale, Luigia, additional, Gasperini, Daniela, additional, Nuzzi, Maria Cristina, additional, Cellamare, Angelo, additional, Casieri, Paola, additional, Busuito, Rosa, additional, Ceccarini, Caterina, additional, Cesarano, Carla, additional, Privitera, Orsola, additional, Melani, Daniela, additional, Menozzi, Cristina, additional, Falcinelli, Cristina, additional, Calabrese, Olga, additional, Battaglia, Paola, additional, Tanzariello, Antonella, additional, Stampalija, Tamara, additional, Ardisia, Carmela, additional, Gasparini, Paolo, additional, Benn, Peter, additional, and Novelli, Antonio, additional

Published
2022
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10. 818 Impaired clinical outcome and increased postoperative complications in COVID-19 patients undergoing cardiopulmonary bypass

Author

Chiariello, Giovanni A., primary, Bruno, Piergiorgio, additional, Pavone, Natalia, additional, D’avino, Serena, additional, Ferraro, Francesco, additional, Nesta, Marialisa, additional, Pasquini, Annalisa, additional, Cammertoni, Federico, additional, Farina, Piero, additional, Mazza, Andrea, additional, Balducci, Federica, additional, Calabrese, Maria, additional, Montone, Rocco A., additional, Montini, Luca, additional, and Massetti, Massimo, additional

Published
2021
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12. Missed linkage to care for patients who screened positive for Hepatitis C in a tertiary care centre: Results of the Telepass project

Author

Ponziani, Francesca Romana, Santopaolo, Francesco, Siciliano, Massimo, De Belvis, A. G., Tortora, Annalisa, Mora, Vincenzina, Fanali, Chiara, Morsella, Alisha, Balducci, Federica, Vetrugno, Giuseppe, D'Alfonso, Maria Elena, Cambieri, Andrea, Cauda, Roberto, Bellantone, Rocco Domenico Alfonso, Sanguinetti, Maurizio, Pompili, Maurizio, Gasbarrini, Antonio, Ponziani F. R. (ORCID:0000-0002-5924-6238), Santopaolo F., Siciliano M., Tortora A., Mora V., Fanali C., Morsella A., Balducci F., Vetrugno G. (ORCID:0000-0003-0181-2855), D'Alfonso M. E., Cambieri A., Cauda R. (ORCID:0000-0002-1498-4229), Bellantone R. (ORCID:0000-0002-0844-3469), Sanguinetti M. (ORCID:0000-0002-9780-7059), Pompili M. (ORCID:0000-0001-6699-7980), Gasbarrini A. (ORCID:0000-0002-7278-4823), Ponziani, Francesca Romana, Santopaolo, Francesco, Siciliano, Massimo, De Belvis, A. G., Tortora, Annalisa, Mora, Vincenzina, Fanali, Chiara, Morsella, Alisha, Balducci, Federica, Vetrugno, Giuseppe, D'Alfonso, Maria Elena, Cambieri, Andrea, Cauda, Roberto, Bellantone, Rocco Domenico Alfonso, Sanguinetti, Maurizio, Pompili, Maurizio, Gasbarrini, Antonio, Ponziani F. R. (ORCID:0000-0002-5924-6238), Santopaolo F., Siciliano M., Tortora A., Mora V., Fanali C., Morsella A., Balducci F., Vetrugno G. (ORCID:0000-0003-0181-2855), D'Alfonso M. E., Cambieri A., Cauda R. (ORCID:0000-0002-1498-4229), Bellantone R. (ORCID:0000-0002-0844-3469), Sanguinetti M. (ORCID:0000-0002-9780-7059), Pompili M. (ORCID:0000-0001-6699-7980), and Gasbarrini A. (ORCID:0000-0002-7278-4823)

Abstract

Italy is one of the countries on track with the WHO’s agenda to eliminate hepatitis C virus (HCV) by 2030. Healthcare facilities play a crucial role in seeking patients who are infected but have not yet been treated. We assessed the effectiveness of a recall strategy, named ‘Telepass’ project, for patients exposed to HCV infection who have not yet been linked to care in a large tertiary care centre. The ‘Telepass’ project was structured in two phases: (a) a retrospective analysis first identified all anti–HCV-positive subjects among patients who underwent pre-operative assessment in the facility in the course of one year; (b) a following prospective phase, aimed to recall patients in need either of further diagnostic tests (ie HCV-RNA) or treatment. A total of 12246 records of patients tested for HCV antibodies were reviewed. The overall prevalence of anti–HCV-positive subjects was 1.83% (224/12246) with a male/female ratio of 2.07. Out of the 224 anti–HCV-positive patients, 123 (54.91%) did not have documented HCV-RNA tests and were therefore selected for recall. Of these, 123 were reachable and 26 (21.13%) were successfully linked to care. Ten patients (38.46%) tested HCV-RNA positive and initiated treatment with direct-acting antivirals (DAAs). The Telepass study highlights that a recall strategy starting from internal hospital databases can help identify patients with chronic HCV infection who have not yet been linked to care, and provides an epidemiological insight into the prevalence of HCV infection in Italy in the late DAAs era.

Published
2021

14. Positive Predictive Values and Outcomes for Uninformative Cell-Free DNA Tests: An Italian Multicentric Cytogenetic and Cytogenomic Audit of DiagnOstic Testing (ICARO Study)

Author

Grati, Francesca Romana, Bestetti, Ilaria, de Siero, Daria, Malvestiti, Francesca, Villa, Nicoletta, Sala, Elena, Crosti, Francesca, Parisi, Valentina, Nardone, Anna Maria, Di Giacomo, Gianluca, Pettinari, Antonella, Tortora, Giada, Montaldi, Annamaria, Calò, Annapaola, Saccilotto, Donatella, Zanchetti, Sara, Celli, Paola, Guerneri, Silvana, Silipigni, Rosamaria, Cardarelli, Laura, Lippi, Elisabetta, Cavani, Simona, Malacarne, Michela, Genesio, Rita, Beltrami, Nicola, Pittalis, Maria Carla, Desiderio, Laura, Gentile, Mattia, Ficarella, Romina, Recalcati, Maria Paola, Catusi, Ilaria, Garzo, Maria, Miele, Lorena, Corti, Cecilia, Ghezzo, Sara, Bertini, Veronica, Cambi, Francesca, Valetto, Angelo, Facchinetti, Barbara, Bernardini, Laura, Capalbo, Anna, Balducci, Federica, Pelo, Elisabetta, Minuti, Barbara, Pescucci, Chiara, Giuliani, Costanza, Renieri, Alessandra, Longo, Ilaria, Tita, Rossella, Castello, Giuseppe, Casalone, Rosario, Righi, Rossana, Raso, Barbara, Civolani, Alessandro, Muzi, Maria Cristina, di Natale, Manuela, Varriale, Luigia, Gasperini, Daniela, Nuzzi, Maria Cristina, Cellamare, Angelo, Casieri, Paola, Busuito, Rosa, Ceccarini, Caterina, Cesarano, Carla, Privitera, Orsola, Melani, Daniela, Menozzi, Cristina, Falcinelli, Cristina, Calabrese, Olga, Battaglia, Paola, Tanzariello, Antonella, Stampalija, Tamara, Ardisia, Carmela, Gasparini, Paolo, Benn, Peter, and Novelli, Antonio

Abstract

(Abstracted from Prenat Diagn2022;42:1575–1586Methods for diagnosis of genetic abnormalities have recently undergone substantial improvement. Noninvasive prenatal testing (NIPT) is performed early in pregnancy, typically at the end of the first trimester using cell-free DNA (cfDNA) to identify 3 commonly occurring trisomies (13, 18, and 21).

Published
2023
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17. The ReSTE course: 6-Hours course on resuscitation and resternotomy after cardiac surgery

Author

Arlotta, Gabriella, primary, Verdicchio, Loredana, additional, Gaetani, Cristina, additional, Di Cola, Rita, additional, Buralli, Daniela, additional, D’Antonio, Diego, additional, Balducci, Federica, additional, Mazza, Andrea, additional, Nesta, Marialisa, additional, Cavaliere, Franco, additional, Martinelli, Lorenzo, additional, Calabrese, Maria, additional, Antoniucci, Maria Enrica, additional, Guarneri, Sergio, additional, Corrado, Michele, additional, De Paulis, Stefano, additional, Zamparelli, Roberto, additional, Conti, Francesco, additional, Corsi, Filippo, additional, Bevilacqua, Francesca, additional, and Scapigliati, Andrea, additional

Published
2018
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21. Neurogenic urinary retention in cats following severe cluster seizures.

Author

Balducci, Federica, De Risio, Luisa, Shea, Anita, Canal, Sara, Stabile, Fabio, and Bernardini, Marco

Abstract

Case series summary Four cats that presented with severe cluster seizures developed neurogenic urinary retention in the postictal phase. None of the cats had previous seizures. Micturition was reported as normal in all cats for 3 or more years before seizure onset. All cats required a continuous rate infusion of propofol to control the seizure activity. In all cats manual bladder expression was performed every 8 h until recovery of normal micturition. One cat was started on phenoxybenzamine to reduce internal urethral sphincter tone. All cats recovered normal micturition within 4 weeks of the last cluster of seizures. Relevance and novel information Transient neurogenic urinary retention has not previously been reported in cats or dogs following severe cluster seizures. Urinary retention should be considered a potential postictal deficit, requiring prompt recognition and treatment to avoid urinary tract infection and detrusor muscle atony. [ABSTRACT FROM AUTHOR]

Published
2017
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22. A Different Shade of Pink: Literary Thresholds and Cultural Intersections in Italian Chick Lit

Author

Bernardi, Claudia, Balducci, Federica, Bernardi, Claudia, and Balducci, Federica

Abstract

This thesis investigates the Italian production of chick lit, a particular segment of contemporary women’s popular fiction developed in the mid 1990s in Anglophone countries. A worldwide phenomenon born out of Helen Fielding’s Bridget Jones’s Diary (1996) and the HBO TV show Sex and the City (1998), chick lit novels portray the professional, emotional and sentimental anxieties of white, middle-class, heterosexual and financially independent women in a witty and humorous tone. The arrival of chick lit and its successful translation into Italian in the late 1990s has prompted many local writers to engage with the genre, but the growing body of chick lit written in Italian and its place in the cultural and literary landscape have yet to be assessed. This thesis explores recurring themes, narrative strategies and stylistic features deployed in Italian chick lit novels not only against their Anglo-American models, but also in relation to Western popular media culture and the Italian tradition of romanzo rosa, its cultures and practices as well as its legacy. It shows the presence of distinct intertextual patterns in dealing with key generic features, such as the identification with the female protagonist and her journey toward self-empowerment, the relationship with consumerism and popular media culture, and the humorous style. This thesis also assesses the nature of chick lit as both a literary genre and a sociocultural phenomenon across countries and languages through theoretical perspectives of cultural studies and feminist theories on women’s popular culture and Western popular postfeminism.

Published
2011

24. Positive predictive values and outcomes for uninformative cell-free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO Study)

Author

Francesca Romana Grati, Ilaria Bestetti, Daria De Siero, Francesca Malvestiti, Nicoletta Villa, Elena Sala, Francesca Crosti, Valentina Parisi, Anna Maria Nardone, Gianluca Di Giacomo, Antonella Pettinari, Giada Tortora, Annamaria Montaldi, Annapaola Calò, Donatella Saccilotto, Sara Zanchetti, Paola Celli, Silvana Guerneri, Rosamaria Silipigni, Laura Cardarelli, Elisabetta Lippi, Simona Cavani, Michela Malacarne, Rita Genesio, Nicola Beltrami, Maria Carla Pittalis, Laura Desiderio, Mattia Gentile, Romina Ficarella, Maria Paola Recalcati, Ilaria Catusi, Maria Garzo, Lorena Miele, Cecilia Corti, Sara Ghezzo, Veronica Bertini, Francesca Cambi, Angelo Valetto, Barbara Facchinetti, Laura Bernardini, Anna Capalbo, Federica Balducci, Elisabetta Pelo, Barbara Minuti, Chiara Pescucci, Costanza Giuliani, Alessandra Renieri, Ilaria Longo, Rossella Tita, Giuseppe Castello, Rosario Casalone, Rossana Righi, Barbara Raso, Alessandro Civolani, Maria Cristina Muzi, Manuela di Natale, Luigia Varriale, Daniela Gasperini, Maria Cristina Nuzzi, Angelo Cellamare, Paola Casieri, Rosa Busuito, Caterina Ceccarini, Carla Cesarano, Orsola Privitera, Daniela Melani, Cristina Menozzi, Cristina Falcinelli, Olga Calabrese, Paola Battaglia, Antonella Tanzariello, Tamara Stampalija, Carmela Ardisia, Paolo Gasparini, Peter Benn, Antonio Novelli, Grati, Francesca Romana, Bestetti, Ilaria, De Siero, Daria, Malvestiti, Francesca, Villa, Nicoletta, Sala, Elena, Crosti, Francesca, Parisi, Valentina, Nardone, Anna Maria, Di Giacomo, Gianluca, Pettinari, Antonella, Tortora, Giada, Montaldi, Annamaria, Calò, Annapaola, Saccilotto, Donatella, Zanchetti, Sara, Celli, Paola, Guerneri, Silvana, Silipigni, Rosamaria, Cardarelli, Laura, Lippi, Elisabetta, Cavani, Simona, Malacarne, Michela, Genesio, Rita, Beltrami, Nicola, Pittalis, Maria Carla, Desiderio, Laura, Gentile, Mattia, Ficarella, Romina, Recalcati, Maria Paola, Catusi, Ilaria, Garzo, Maria, Miele, Lorena, Corti, Cecilia, Ghezzo, Sara, Bertini, Veronica, Cambi, Francesca, Valetto, Angelo, Facchinetti, Barbara, Bernardini, Laura, Capalbo, Anna, Balducci, Federica, Pelo, Elisabetta, Minuti, Barbara, Pescucci, Chiara, Giuliani, Costanza, Renieri, Alessandra, Longo, Ilaria, Tita, Rossella, Castello, Giuseppe, Casalone, Rosario, Righi, Rossana, Raso, Barbara, Civolani, Alessandro, Muzi, Maria Cristina, di Natale, Manuela, Varriale, Luigia, Gasperini, Daniela, Nuzzi, Maria Cristina, Cellamare, Angelo, Casieri, Paola, Busuito, Rosa, Ceccarini, Caterina, Cesarano, Carla, Privitera, Orsola, Melani, Daniela, Menozzi, Cristina, Falcinelli, Cristina, Calabrese, Olga, Battaglia, Paola, Tanzariello, Antonella, Stampalija, Tamara, Ardisia, Carmela, Gasparini, Paolo, Benn, Peter, and Novelli, Antonio

Subjects
cfDNAtesting, Obstetrics and Gynecology, Genetics (clinical)
Abstract

Objectives: To establish the positive predictive values (PPV) of cfDNA testing based on data from a nationwide survey of independent clinical cytogenetics laboratories. Methods: Prenatal diagnostic test results obtained by Italian laboratories between 2013 and March 2020 were compiled for women with positive non-invasive prenatal tests (NIPT), without an NIPT result, and cases where there was sex discordancy between the NIPT and ultrasound. PPV and other summary data were reviewed. Results: Diagnostic test results were collected for 1327 women with a positive NIPT. The highest PPVs were for Trisomy (T) 21 (624/671, 93%) and XYY (26/27, 96.3%), while rare autosomal trisomies (9/47, 19.1%) and recurrent microdeletions (8/55, 14.5%) had the lowest PPVs. PPVs for T21, T18, and T13 were significantly higher when diagnostic confirmation was carried out on chorionic villi (97.5%) compared to amniotic fluid (89.5%) (p < 0.001). In 19/139 (13.9%), of no result cases, a cytogenetic abnormality was detected. Follow-up genetic testing provided explanations for 3/6 cases with a fetal sex discordancy between NIPT and ultrasound. Conclusions: NIPT PPVs differ across the conditions screened and the tissues studied in diagnostic testing. This variability, issues associated with fetal sex discordancy, and no results, illustrate the importance of pre- and post-test counselling.

Published
2022

25. Mild mental retardation in a child with a de novo interstitial deletion of 15q21.2q22.1: A comparison with previously described cases

Author

Valeria Politi, Danila Sollima, Barbara Sinigaglia, Sergio Tempesta, Loredana Santarini, Luciano Bovicelli, Marina Stefani, Sara Ghezzo, Roberta Cernetti, Orsetta Zuffardi, Antonino Restuccia, Bommina Celso, Roberto Ciccone, Federica Balducci, Cinzia Marzocchi, Tempesta, Sergio, Sollima, Danila, Ghezzo, Sara, Politi, Valeria, Sinigaglia, Barbara, Balducci, Federica, Celso, Bommina, Restuccia, Antonino, Stefani, Marina, Cernetti, Roberta, Marzocchi, Cinzia, Ciccone, Roberto, Zuffardi, Orsetta, Bovicelli, Luciano, and Santarini, Loredana

Subjects
Array-CGH, 15q21 Deletion, Biology, Corpus callosum, Chromosome 15, FISH, Genetic, Intellectual Disability, Hypotelorism, Genetics, medicine, Humans, Abnormalities, Multiple, In Situ Hybridization, Fluorescence, Genetics (clinical), Chromosomes, Human, Pair 15, medicine.diagnostic_test, Nucleic Acid Hybridization, Mental retardation, General Medicine, medicine.disease, Blepharophimosis, Hypoplasia, Developmental disorder, Child, Preschool, %22">Fish , Female, Chromosome Deletion, Human, Fluorescence in situ hybridization
Abstract

We report on a child with mild mental retardation, hypotelorism, blepharophimosis, face slight asymmetry and partial hypoplasia of corpus callosum, with an interstitial deletion of a chromosome 15. The deletion was molecularly characterized by array-CGH and FISH techniques. This rearrangement has a 7.18 Mb extension and maps to 15q21.2q22.1. To date, there have been only six individuals reported with a deletion of 15q21; in three cases, the rearrangement was characterized by molecular cytogenetic techniques. After a comparison with these three cases, it appeared that the deletion we found is one of the smallest and it overlaps the distal portion of the ones taken into account. Finally, we tried to delineate the genotype-phenotype correlation in patients with a deletion of 15q21. © 2008 Elsevier Masson SAS. All rights reserved.

Published
2008
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26. Hereditary breast and ovarian cancer genetic testing in unselected patients: example of private supplementation of public healthcare service.

Author

Fiorentino F, Innella G, Balducci F, Marullo L, Lanzoni G, Miccoli S, Cardarelli L, Turchetti D, and Tempesta S

Subjects
Humans, Female, Middle Aged, Adult, Aged, Breast Neoplasms genetics, BRCA1 Protein genetics, Italy, Genetic Predisposition to Disease, Ataxia Telangiectasia Mutated Proteins genetics, Hereditary Breast and Ovarian Cancer Syndrome genetics, DNA-Binding Proteins, Genetic Testing methods, Genetic Testing statistics & numerical data, Checkpoint Kinase 2 genetics, BRCA2 Protein genetics, Ovarian Neoplasms genetics
Abstract

In the Emilia-Romagna region (Northern Italy), the identification and management of women at familial/hereditary risk of breast and ovarian cancer is guided by a well-established regional protocol. Here we report the results of the experience of private supplementation of public healthcare service in offering the possibility to undergo BRCA1/2 testing and/or multigene panel testing (MGPT) within a well-defined pathway to women unfulfilling regional criteria. Out of 177 patients referred to our center who underwent BRCA1/2 testing, 175 tested negative while two (1.1%) resulted carriers of pathogenic variants in BRCA2; 69 patients also underwent MGPT, and in four cases (5.8%) a pathogenic variant were found (two in ATM and one in CHEK2 and RAD51C, respectively). Overall, this private supplementation of territorial public healthcare system has made it possible to confirm the validity of regional criteria for genetic testing access (concordance: 98.9%), but also to identify carriers of pathogenic variants of BRCA1/2 that would have escaped regional protocol, to support the effectiveness of MGPT for the identification of rare cases (not BRCA) at mild/high risk, and to provide reassurance to women who were found to be non-carriers of pathogenic variants, who may benefit from a more accurate assessment of their risk., Competing Interests: Declarations. Conflict of interest: The authors declare no competing interests., (© 2024. The Author(s), under exclusive licence to Springer Nature B.V.)

Published
2024
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