Mutation of Angiopoietin-1 Gene Associates with a New Type of Hereditary Angioedema
Bafunno, Valeria, MSc, PhD, Firinu, Davide, MD, D’Apolito, Maria, MSc, PhD, Cordisco, Giorgia, BSc, Loffredo, Stefania, MD, Leccese, Angelica, BSc, Bova, Maria, MD, Barca, Maria Pina, MD, Santacroce, Rosa, MSc, PhD, Cicardi, Marco, MD, Del Giacco, Stefano, MD, Margaglione., Maurizio, MD
Published in Journal of allergy and clinical immunology (01.03.2018)
Published in Journal of allergy and clinical immunology (01.03.2018)
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Neurologic and Psychiatric Manifestations of Bradykinin-Mediated Angioedema: Old and New Challenges
Mormile, Ilaria, Palestra, Francesco, Petraroli, Angelica, Loffredo, Stefania, Rossi, Francesca Wanda, Spadaro, Giuseppe, de Paulis, Amato, Bova, Maria
Published in International journal of molecular sciences (29.07.2023)
Published in International journal of molecular sciences (29.07.2023)
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A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy
Zanichelli, Andrea, Arcoleo, Francesco, Barca, Maria Pina, Borrelli, Paolo, Bova, Maria, Cancian, Mauro, Cicardi, Marco, Cillari, Enrico, De Carolis, Caterina, De Pasquale, Tiziana, Del Corso, Isabella, Di Rocco, Paola Cesinaro, Guarino, Maria Domenica, Massaro, Ilaria, Minale, Paola, Montinaro, Vincenzo, Neri, Sergio, Perricone, Roberto, Pucci, Stefano, Quattrocchi, Paolina, Rossi, Oliviero, Triggiani, Massimo, Zanierato, Giuseppina, Zoli, Alessandra
Published in Orphanet journal of rare diseases (06.02.2015)
Published in Orphanet journal of rare diseases (06.02.2015)
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Psychological processes in the experience of hereditary angioedema in adult patients: an observational study
Savarese, Livia, Bova, Maria, Maiello, Assunta, Petraroli, Angelica, Mormile, Ilaria, Cancian, Mauro, Senter, Riccardo, Zanichelli, Andrea, Spadaro, Giuseppe, Freda, Maria Francesca
Published in Orphanet journal of rare diseases (09.01.2021)
Published in Orphanet journal of rare diseases (09.01.2021)
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Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency
Loffredo, Stefania, Ferrara, Anne Lise, Bova, Maria, Borriello, Francesco, Suffritti, Chiara, Veszeli, Nóra, Petraroli, Angelica, Galdiero, Maria Rosaria, Varricchi, Gilda, Granata, Francescopaolo, Zanichelli, Andrea, Farkas, Henriette, Cicardi, Marco, Lambeau, Gérard, Marone, Gianni
Published in Frontiers in immunology (23.07.2018)
Published in Frontiers in immunology (23.07.2018)
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Emotional processes and stress in children affected by hereditary angioedema with C1-inhibitor deficiency: a multicenter, prospective study
Savarese, Livia, Bova, Maria, De Falco, Raffaella, Guarino, Maria Domenica, De Luca Picione, Raffaele, Petraroli, Angelica, Senter, Riccardo, Traverso, Claudia, Zabotto, Matteo, Zanichelli, Andrea, Zito, Eugenio, Alessio, Maria, Cancian, Mauro, Cicardi, Marco, Franzese, Adriana, Perricone, Roberto, Marone, Gianni, Valerio, Paolo, Freda, Maria Francesca
Published in Orphanet journal of rare diseases (13.07.2018)
Published in Orphanet journal of rare diseases (13.07.2018)
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Lanadelumab Injection Treatment For The Prevention Of Hereditary Angioedema (HAE): Design, Development And Place In Therapy
Bova, Maria, Valerieva, Anna, Wu, Maddalena Alessandra, Senter, Riccardo, Perego, Francesca
Published in Drug design, development and therapy (01.10.2019)
Published in Drug design, development and therapy (01.10.2019)
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Episodic Angioedema with Hypereosinophilia (Gleich's Syndrome): A Case Report and Extensive Review of the Literature
Mormile, Ilaria, Petraroli, Angelica, Loffredo, Stefania, Rossi, Francesca Wanda, Mormile, Mauro, Del Mastro, Andrea, Spadaro, Giuseppe, de Paulis, Amato, Bova, Maria
Published in Journal of clinical medicine (01.04.2021)
Published in Journal of clinical medicine (01.04.2021)
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Deciphering the Genetics of Primary Angioedema with Normal Levels of C1 Inhibitor
Loules, Gedeon, Parsopoulou, Faidra, Zamanakou, Maria, Csuka, Dorottya, Bova, Maria, González-Quevedo, Teresa, Psarros, Fotis, Porebski, Gregor, Speletas, Matthaios, Firinu, Davide, del Giacco, Stefano, Suffritti, Chiara, Makris, Michael, Vatsiou, Sofia, Zanichelli, Andrea, Farkas, Henriette, Germenis, Anastasios E.
Published in Journal of clinical medicine (23.10.2020)
Published in Journal of clinical medicine (23.10.2020)
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Molecular Genetics of GLUT1DS Italian Pediatric Cohort: 10 Novel Disease-Related Variants and Structural Analysis
Mauri, Alessia, Duse, Alessandra, Palm, Giacomo, Previtali, Roberto, Bova, Stefania Maria, Olivotto, Sara, Benedetti, Sara, Coscia, Francesca, Veggiotti, Pierangelo, Cereda, Cristina
Published in International journal of molecular sciences (01.11.2022)
Published in International journal of molecular sciences (01.11.2022)
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Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases
Olivotto, Sara, Duse, Alessandra, Bova, Stefania Maria, Leonardi, Valeria, Biganzoli, Elia, Milanese, Alberto, Cereda, Cristina, Bertoli, Simona, Previtali, Roberto, Veggiotti, Pierangelo
Published in Orphanet journal of rare diseases (24.09.2022)
Published in Orphanet journal of rare diseases (24.09.2022)
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Case report: Early-onset parkinsonism among the neurological features in children with PHACTR1 variants
Previtali, Roberto, Leidi, Alessia, Basso, Martina, Izzo, Giana, Stignani, Cecilia, Spaccini, Luigina, Iascone, Maria, Veggiotti, Pierangelo, Bova, Stefania Maria
Published in Frontiers in neurology (06.07.2023)
Published in Frontiers in neurology (06.07.2023)
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Expert Perspectives on Hereditary Angioedema: Key Areas for Advancements in Care across the Patient Journey
Banerji, Aleena, Baş, Murat, Bernstein, Jonathan A., Boccon-Gibod, Isabelle, Bova, Maria, Dempster, John, Grumach, Anete Sevciovic, Magerl, Markus, Poarch, Kimberly, Ferreira, Manuel Branco
Published in Allergy & rhinology (Providence, R.I.) (01.01.2016)
Published in Allergy & rhinology (Providence, R.I.) (01.01.2016)
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The experience of living with a chronic disease in pediatrics from the mothers’ narratives: The Clinical Interview on Parental Sense of Grip on the Disease
Savarese, Livia, Freda, Maria Francesca, De Luca Picione, Raffaele, Dolce, Pasquale, De Falco, Raffaella, Alessio, Maria, Cancian, Mauro, Franzese, Adriana, Guarino, Maria Domenica, Perricone, Roberto, Petraroli, Angelica, Senter, Riccardo, Traverso, Claudia, Zanichelli, Andrea, Zito, Eugenio, Bova, Maria
Published in Health psychology open (01.07.2020)
Published in Health psychology open (01.07.2020)
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Visual–perceptual impairment in children with periventricular leukomalacia
Fazzi, Elisa, Bova, Stefania Maria, Uggetti, Carla, Signorini, Sabrina Giovanna, Bianchi, Paolo Emilio, Maraucci, Ilaria, Zoppello, Marina, Lanzi, Giovanni
Published in Brain & development (Tokyo. 1979) (01.12.2004)
Published in Brain & development (Tokyo. 1979) (01.12.2004)
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Six-month multidisciplinary follow-up in multisystem inflammatory syndrome in children: An Italian single-center experience
Zuccotti, Gianvincenzo, Calcaterra, Valeria, Mannarino, Savina, D'Auria, Enza, Bova, Stefania Maria, Fiori, Laura, Verduci, Elvira, Milanese, Alberto, Marano, Giuseppe, Garbin, Massimo, Zirpoli, Salvatore, Fabiano, Valentina, Carlucci, Patrizia, Olivotto, Sara, Gianolio, Laura, De Santis, Raffaella, Pelizzo, Gloria, Zoia, Elena, Dilillo, Dario, Biganzoli, Elia Mario
Published in Frontiers in pediatrics (26.01.2023)
Published in Frontiers in pediatrics (26.01.2023)
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Successful use of perampanel in GABRA1-related myoclonic epilepsy with photosensitivity
Olivotto, Sara, Freddi, Anna, Lavatelli, Rossella, Basso, Eleonora, Leidi, Alessia, Castellotti, Barbara, Spaccini, Luigina, Bova, Stefania Maria, Veggiotti, Pierangelo
Published in Epilepsy & behavior reports (01.01.2022)
Published in Epilepsy & behavior reports (01.01.2022)
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Spectrum of visual disorders in children with cerebral visual impairment
Fazzi, Elisa, Signorini, Sabrina Giovanna, Bova, Stefania Maria, La Piana, Roberta, Ondei, Paola, Bertone, Chiara, Misefari, Walter, Bianchi, Paolo Emilio
Published in Journal of child neurology (01.03.2007)
Published in Journal of child neurology (01.03.2007)
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A myoferlin gain‐of‐function variant associates with a new type of hereditary angioedema
Ariano, Anastasia, D'Apolito, Maria, Bova, Maria, Bellanti, Francesco, Loffredo, Stefania, D'Andrea, Giovanna, Intrieri, Mariano, Petraroli, Angelica, Maffione, Angela Bruna, Spadaro, Giuseppe, Santacroce, Rosa, Margaglione, Maurizio
Published in Allergy (Copenhagen) (01.11.2020)
Published in Allergy (Copenhagen) (01.11.2020)
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