Anwar Baban (A Baban)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 26

Top Topics

Left Ventricular

Congenital Heart Disease

Transcranial Magnetic Stimulation

Top Venues

American journal of medical genetics. Part A

Clinical genetics

European heart journal

Journal of cardiovascular development and disease

This page only lists publications with an associated author ORCID identifier.

Publications

Juan Pablo Pablo Kaski, Gabrielle Norrish, Juan Ramon Gimeno-Blanes, Philippe Charron, Perry Mark Elliott, Luigi Tavazzi, Michal Tendera, Cécile Laroche, Aldo Pietro Maggioni, Anwar Baban, Diala Khraiche, Lidia Ziółkowska, Giuseppe Limongelli, Tiina H Ojala, Matthias Gorenflo, Aris Anastasakis, Shaimaa A Mostafa, Alida Linda Patrizia Caforio, null null
Cardiomyopathies in children and adolescents: aetiology, management, and outcomes in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Registry. European heart journal (2024)
Anwar Baban, Giovanni Parlapiano, Marianna Cicenia, Michela Armando, Alessio Franceschini, Concettina Pacifico, Arianna Panfili, Gaetano Zinzanella, Antonino Romanzo, Adelaide Fusco, Martina Caiazza, Gianluigi Perri, Lorenzo Galletti, Maria Christina Digilio, Paola Sabrina Buonuomo, Andrea Bartuli, Antonio Novelli, Massimiliano Raponi, Giuseppe Limongelli
Unique Features of Cardiovascular Involvement and Progression in Children with Marfan Syndrome Justify Dedicated Multidisciplinary Care. Journal of cardiovascular development and disease 11 (4) (2024)
Anwar Baban, Giovanni Parlapiano, Marianna Cicenia, Michela Armando, Alessio Franceschini, Concettina Pacifico, Arianna Panfili, Gaetano Zinzanella, Antonino Romanzo, Adelaide Fusco, Martina Caiazza, Gianluigi Perri, Lorenzo Galletti, Maria Christina Digilio, Paola Sabrina Buonuomo, Andrea Bartuli, Antonio Novelli, Massimiliano Raponi, Giuseppe Limongelli
Unique Features of Cardiovascular Involvement and Progression in Children with Marfan Syndrome Justify Dedicated Multidisciplinary Care. Journal of cardiovascular development and disease 11 (4) (2024)
Arianna Esposito, Marcello Niceta, Antonio Novelli, Monia Magliozzi, Giovanni Parlapiano, Anwar Baban, Marco Alfonso Perrone
Massive pericardial effusion in an infant with Aymé-Gripp syndrome: A case report and review of the literature. American journal of medical genetics. Part A 194 (9) (2024)
Arianna Esposito, Marcello Niceta, Antonio Novelli, Monia Magliozzi, Giovanni Parlapiano, Anwar Baban, Marco Alfonso Perrone
Massive pericardial effusion in an infant with Aymé-Gripp syndrome: A case report and review of the literature. American journal of medical genetics. Part A (2024)
Arianna Esposito, Marcello Niceta, Antonio Novelli, Monia Magliozzi, Giovanni Parlapiano, Anwar Baban, Marco Alfonso Perrone
Massive pericardial effusion in an infant with Aymé-Gripp syndrome: A case report and review of the literature. American journal of medical genetics. Part A 194 (9) (2024)
Arianna Esposito, Marcello Niceta, Antonio Novelli, Monia Magliozzi, Giovanni Parlapiano, Anwar Baban, Marco Alfonso Perrone
Massive pericardial effusion in an infant with Aymé-Gripp syndrome: A case report and review of the literature. American journal of medical genetics. Part A 194 (9) (2024)
Maria Gnazzo, Giulia Pascolini, Giovanni Parlapiano, Francesco Petrizzelli, Daniele Perrino, Luigina Porco, Andrea Bartuli, Antonio Novelli, Anwar Baban
Usmani-Riazuddin syndrome can have a recognizable phenotype: Report of a novel AP1G1 variant. Clinical genetics 106 (1) (2024)
Anwar Baban, Giovanni Parlapiano, Marianna Cicenia, Michela Armando, Alessio Franceschini, Concettina Pacifico, Arianna Panfili, Gaetano Zinzanella, Antonino Romanzo, Adelaide Fusco, Martina Caiazza, Gianluigi Perri, Lorenzo Galletti, Maria Christina Digilio, Paola Sabrina Buonuomo, Andrea Bartuli, Antonio Novelli, Massimiliano Raponi, Giuseppe Limongelli
Unique Features of Cardiovascular Involvement and Progression in Children with Marfan Syndrome Justify Dedicated Multidisciplinary Care. Journal of cardiovascular development and disease 11 (4) (2024)
Juan Pablo Pablo Kaski, Gabrielle Norrish, Juan Ramon Gimeno-Blanes, Philippe Charron, Perry Mark Elliott, Luigi Tavazzi, Michal Tendera, Cécile Laroche, Aldo Pietro Maggioni, Anwar Baban, Diala Khraiche, Lidia Ziółkowska, Giuseppe Limongelli, Tiina H Ojala, Matthias Gorenflo, Aris Anastasakis, Shaimaa A Mostafa, Alida Linda Patrizia Caforio, null null
Cardiomyopathies in children and adolescents: aetiology, management, and outcomes in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Registry. European heart journal 45 (16) (2024)
Maria Gnazzo, Giulia Pascolini, Giovanni Parlapiano, Francesco Petrizzelli, Daniele Perrino, Luigina Porco, Andrea Bartuli, Antonio Novelli, Anwar Baban
Usmani-Riazuddin syndrome can have a recognizable phenotype: Report of a novel AP1G1 variant. Clinical genetics (2024)
Lia Crotti, Carla Spazzolini, Mette Nygaard, Michael Toft Overgaard, Maria-Christina Kotta, Federica Dagradi, Luca Sala, Takeshi Aiba, Mark D Ayers, Anwar Baban, Julien Barc, Cheyenne M Beach, Elijah R Behr, J Martijn Bos, Marina Cerrone, Peter Covi, Bettina F Cuneo, Isabelle Denjoy, Birgit Donner, Adrienne Elbert, Håkan Eliasson, Susan P Etheridge, Megumi Fukuyama, Francesca Girolami, Robert M Hamilton, Minoru Horie, Maria Iascone, Juan Jiménez Jaimez, Henrik Kjaerulf Jensen, Prince J Kannankeril, Juan Pablo Pablo Kaski, Naomasa Makita, Carmen Muñoz-Esparza, Hans Henrik Odland, Seiko Ohno, John Papagiannis, Alessandra Pia Porretta, Christopher Prandstetter, Vincent Probst, Tomas Robyns, Eric Rosenthal, Ferran Roses Y Noguer, Nicole Sekarski, Anoop Singh, Georgia Spentzou, Fridrike Stute, Jacob Tfelt Hansen, Jan Till, Kathryn E Tobert, Jeffrey M Vinocur, Gregory Webster, Arthur A M Wilde, Cordula M Wolf, Michael J Ackerman, Peter J Schwartz
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry. European heart journal (2023)
Gabrielle Norrish, Tao Ding, Ella Field, Elena Cervi, Lidia Ziółkowska, Iacopo Olivotto, Diala Khraiche, Giuseppe Limongelli, Aris Anastasakis, Robert G Weintraub, Elena Biagini, Luca Ragni, Terence W Prendiville, Sophie Duignan, Karen McLeod, Maria Ilina, Adrián Fernández, Chiara Marrone, Regina Bökenkamp, Anwar Baban, Peter Kubus, Piers E F Daubeney, Georgia Sarquella Brugada, Sergi César, Sabine Klaassen, Tiina H Ojala, Vinay Bhole, Constancio Medrano, Orhan Uzun, Elspeth Brown, Ferran Gran, Gianfranco Sinagra, Francisco J Castro, A Graham Stuart, Gabriele Vignati, Hirokuni Yamazawa, Roberto Barriales Villa, Luis García-Guereta, Satish Adwani, Katie Linter, Tara Bharucha, Pablo Garcia-Pavia, Ana Siles, Torsten B Rasmussen, Margherita Calcagnino, Caroline B Jones, Hans De Wilde, Toru Kubo, Tiziana Felice, Anca Popoiu, Jens Mogensen, Sujeev Mathur, Fernando Centeno, Zdenka Reinhardt, Sylvie Schouvey, Costas O'Mahony, Rumana Z Omar, Perry Mark Elliott, Juan Pablo Pablo Kaski
Relationship Between Maximal Left Ventricular Wall Thickness and Sudden Cardiac Death in Childhood Onset Hypertrophic Cardiomyopathy. Circulation. Arrhythmia and electrophysiology 15 (5) (2022)
Maria Christina Digilio, Giulio Calcagni, Maria Gnazzo, Paolo Versacci, Maria Lisa Dentici, Rossella Capolino, Lorenzo Sinibaldi, Anwar Baban, Carolina Putotto, Paolo Alfieri, Marta Unolt, Francesca Romana Lepri, Viola Alesi, Silvia Genovesea, Antonio Novelli, Bruno Marino, Bruno Dallapiccola
Congenital heart defects in molecularly confirmed KBG syndrome patients. American journal of medical genetics. Part A 188 (4) (2021)
Marianna Cicenia, Viola Alesi, Valeria Orlando, Monia Magliozzi, Silvia Di Tommaso, Francesca G Iodice, Emanuela Pompei, Alessandra Toscano, Maria C Digilio, Fabrizio Drago, Antonio Novelli, Anwar Baban
8p23.1 deletion: Look out for left ventricular hypertrabeculation and not only congenital heart diseases. Single-center experience and literature revision. American journal of medical genetics. Part A 188 (3) (2021)
Anwar Baban, Francesca G Iodice, Arianna Di Molfetta, Marianna Cicenia, Caterina Rizzo, Emanuele Agolini, Fabrizio Drago, Antonio Novelli, Luca Di Chiara, Giuseppina Testa, Antonio Amodeo
Deciphering Genetic Variants of Warfarin Metabolism in Children With Ventricular Assist Devices. Pediatric cardiology 42 (5) (2021)
Nicoletta Cantarutti, Rachele Adorisio, Anwar Baban, Arianna Di Molfetta, Antonio Amodeo, Fabrizio Drago
Persistent myocardial atrophy despite LV reverse remodeling in Duchenne cardiomyopathy treated by LVAD. Pediatric transplantation 25 (2) (2020)
Maria Gnazzo, Francesca Romana Lepri, Maria Lisa Dentici, Rossella Capolino, Elisa Pisaneschi, Emanuele Agolini, Martina Rinelli, Viola Alesi, Paolo Versacci, Silvia Genovesea, Claudia Cesario, Lorenzo Sinibaldi, Anwar Baban, Andrea Bartuli, Bruno Marino, Marco Cappa, Bruno Dallapiccola, Antonio Novelli, Maria Christina Digilio
KBG syndrome: Common and uncommon clinical features based on 31 new patients. American journal of medical genetics. Part A 182 (5) (2020)
Anwar Baban, Nicole Olivini, Nicoletta Cantarutti, Federica Calì, Carmen Vitello, Diletta Valentini, Rachele Adorisio, Giulio Calcagni, Viola Alesi, Corrado Di Mambro, Alberto Villani, Bruno Dallapiccola, Maria Cristina Digilio, Bruno Marino, Adriano Carotti, Fabrizio Drago
Differences in morbidity and mortality in Down syndrome are related to the type of congenital heart defect. American journal of medical genetics. Part A 182 (6) (2020)
Viola Alesi, Sara Loddo, Federica Calì, Valeria Orlando, Silvia Genovesea, Daniele Ferretti, Chiara Calacci, Giusy Calvieri, Roberto Falasca, Lucia Ulgheri, Fabrizio Drago, Bruno Dallapiccola, Anwar Baban, Antonio Novelli
A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome. American journal of medical genetics. Part A 179 (8) (2019)
Anwar Baban, Rachele Adorisio, Bernadette Corica, Cristiano Rizzo, Federica Calì, Michela Semeraro, Roberta Taurisano, Monia Magliozzi, Rosalba Carrozzo, Francesco Parisi, Bruno Dallapiccola, Frédéric M Vaz, Fabrizio Drago, Carlo Dionisi-Vici
Delayed appearance of 3-methylglutaconic aciduria in neonates with early onset metabolic cardiomyopathies: A potential pitfall for the diagnosis. American journal of medical genetics. Part A 182 (1) (2019)
Anwar Baban, Nicole Olivini, Francesca Romana Lepri, Federica Calì, Mafalda Mucciolo, Maria C Digilio, Giulio Calcagni, Corrado di Mambro, Bruno Dallapiccola, Rachele Adorisio, Antonio Novelli, Fabrizio Drago
SOS1 mutations in Noonan syndrome: Cardiomyopathies and not only congenital heart defects! Report of six patients including two novel variants and literature review. American journal of medical genetics. Part A 179 (10) (2019)
Jirko Kühnisch, Christopher Herbst, Nadya Al-Wakeel-Marquard, Josephine Dartsch, Manuel Holtgrewe, Anwar Baban, Giulia Mearini, Juliane Hardt, Konstantinos Kolokotronis, Brenda Gerull, Lucie Carrier, Dieter Beule, Stephan Schubert, Daniel R Messroghli, Franziska Degener, Felix Berger, Sabine Klaassen
Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3. Clinical genetics 96 (6) (2019)
Anwar Baban, Monia Magliozzi, Bart Loeys, Rachele Adorisio, Viola Alesi, Aurelio Secinaro, Bernadette Corica, Luca Vricella, Harry C Dietz, Fabrizio Drago, Antonio Novelli, Antonio Amodeo
First evidence of maternally inherited mosaicism in TGFBR1 and subtle primary myocardial changes in Loeys-Dietz syndrome: a case report. BMC medical genetics 19 (1) (2018)
Maria Christina Digilio, F Pugnaloni, A De Luca, G Calcagni, Anwar Baban, Maria Lisa Dentici, P Versacci, B Dallapiccola, M Tartaglia, B Marino
Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog. Clinical genetics 95 (2) (2018)
Silvia Morlino, Viola Alesi, Federica Calì, Francesca Romana Lepri, Aurelio Secinaro, Paola Grammatico, Antonio Novelli, Fabrizio Drago, Marco Castori, Anwar Baban
LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant. American journal of medical genetics. Part A 179 (1) (2018)