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Author/Creator Baban, Anwar

1. A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome. Issue 8 (30th May 2019)

Authors:
Alesi, Viola; Loddo, Sara; Calì, Federica; Orlando, Valeria; Genovese, Silvia; Ferretti, Daniele; Calacci, Chiara; Calvieri, Giusy; Falasca, Roberto; Ulgheri, Lucia; Drago, Fabrizio; Dallapiccola, Bruno; Baban, Anwar; Novelli, Antonio
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 8(2019)
Page Start:
1615
Record Type:
Journal Article
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2. Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3. Issue 6 (22nd October 2019)

Authors:
Kühnisch, Jirko; Herbst, Christopher; Al‐Wakeel‐Marquard, Nadya; Dartsch, Josephine; Holtgrewe, Manuel; Baban, Anwar; Mearini, Giulia; Hardt, Juliane; Kolokotronis, Konstantinos; Gerull, Brenda; Carrier, Lucie; Beule, Dieter; Schubert, Stephan; Messroghli, Daniel; Degener, Franziska; Berger, Feli...
Journal:
Clinical genetics
Issue:
Volume 96:Issue 6(2019)
Page Start:
549
Record Type:
Journal Article
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3. Atypical cardiac defects in patients with RASopathies: Updated data on CARNET study. Issue 10 (18th June 2020)

Authors:
Calcagni, Giulio; Gagliostro, Giulia; Limongelli, Giuseppe; Unolt, Marta; De Luca, Enrica; Digilio, Maria C.; Baban, Anwar; Albanese, Sonia B.; Ferrero, Giovanni B.; Baldassarre, Giuseppina; Agnoletti, Gabriella; Banaudi, Elena; Marek, Jan; Kaski, Juan P.; Tuo, Giulia; Marasini, Maurizio; Cairell...
Other Names:
Watanabe Michiko guestEditor.
Journal:
Birth defects research
Issue:
Volume 112:Issue 10(2020)
Page Start:
725
Record Type:
Journal Article
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4. Differences in morbidity and mortality in Down syndrome are related to the type of congenital heart defect. Issue 6 (22nd April 2020)

Authors:
Baban, Anwar; Olivini, Nicole; Cantarutti, Nicoletta; Calì, Federica; Vitello, Carmen; Valentini, Diletta; Adorisio, Rachele; Calcagni, Giulio; Alesi, Viola; Di Mambro, Corrado; Villani, Alberto; Dallapiccola, Bruno; Digilio, Maria Cristina; Marino, Bruno; Carotti, Adriano; Drago, Fabrizio
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 6(2020)
Page Start:
1342
Record Type:
Journal Article
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5. KBG syndrome: Common and uncommon clinical features based on 31 new patients. Issue 5 (3rd March 2020)

Authors:
Gnazzo, Maria; Lepri, Francesca R; Dentici, Maria Lisa; Capolino, Rossella; Pisaneschi, Elisa; Agolini, Emanuele; Rinelli, Martina; Alesi, Viola; Versacci, Paolo; Genovese, Silvia; Cesario, Claudia; Sinibaldi, Lorenzo; Baban, Anwar; Bartuli, Andrea; Marino, Bruno; Cappa, Marco; Dallapiccola, Brun...
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 5(2020)
Page Start:
1073
Record Type:
Journal Article
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6. 245 Arrhythmogenic cardiomyopathy in children according to 'padua criteria': single paediatric centre experience. (8th December 2021)

Authors:
Cicenia, Marianna; Cantarutti, Nicoletta; Adorisio, Rachele; Silvetti, Massimo Stefano; Secinaro, Aurelio; Ciancarella, Paolo; Di Mambro, Corrado; Magliozzi, Monia; Novelli, Antonio; Amodeo, Antonio; Baban, Anwar; Drago, Fabrizio
Journal:
European heart journal supplements
Issue:
Volume 23(2021)Supplement G
Page Start:
Record Type:
Journal Article
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7. Congenital heart defects in molecularly confirmed KBG syndrome patients. Issue 4 (31st December 2021)

Authors:
Digilio, Maria Cristina; Calcagni, Giulio; Gnazzo, Maria; Versacci, Paolo; Dentici, Maria Lisa; Capolino, Rossella; Sinibaldi, Lorenzo; Baban, Anwar; Putotto, Carolina; Alfieri, Paolo; Unolt, Marta; Lepri, Francesca R.; Alesi, Viola; Genovese, Silvia; Novelli, Antonio; Marino, Bruno; Dallapiccola...
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 4(2022)
Page Start:
1149
Record Type:
Journal Article
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8. Arrhythmogenic cardiomyopathy in children according to "Padua criteria": Single pediatric center experience. (1st March 2022)

Authors:
Cicenia, Marianna; Cantarutti, Nicoletta; Adorisio, Rachele; Silvetti, Massimo Stefano; Secinaro, Aurelio; Ciancarella, Paolo; Di Mambro, Corrado; Magliozzi, Monia; Novelli, Antonio; Amodeo, Antonio; Baban, Anwar; Drago, Fabrizio
Journal:
International journal of cardiology
Issue:
Volume 350(2022)
Page Start:
83
Record Type:
Journal Article
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9. Delayed appearance of 3‐methylglutaconic aciduria in neonates with early onset metabolic cardiomyopathies: A potential pitfall for the diagnosis. Issue 1 (15th November 2019)

Authors:
Baban, Anwar; Adorisio, Rachele; Corica, Bernadette; Rizzo, Cristiano; Calì, Federica; Semeraro, Michela; Taurisano, Roberta; Magliozzi, Monia; Carrozzo, Rosalba; Parisi, Francesco; Dallapiccola, Bruno; Vaz, Frédéric M.; Drago, Fabrizio; Dionisi‐Vici, Carlo
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 1(2020)
Page Start:
64
Record Type:
Journal Article
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10. The MAP3K7 gene: Further delineation of clinical characteristics and genotype/phenotype correlations. Issue 10 (29th July 2022)

Authors:
van Woerden, Geeske M.; Senden, Richelle; de Konink, Charlotte; Trezza, Rossella A.; Baban, Anwar; Bassetti, Jennifer A.; van Bever, Yolande; Bird, Lynne M.; van Bon, Bregje W.; Brooks, Alice S.; Guan, Qiaoning; Klee, Eric W.; Marcelis, Carlo; Rosado, Joel M.; Schimmenti, Lisa A.; Shikany, Amy R....
Journal:
Human mutation
Issue:
Volume 43:Issue 10(2022)
Page Start:
1377
Record Type:
Journal Article
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