All papers authored by Anwar Baban
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2023
Lia Crotti 
,
Carla Spazzolini ,
Mette Nyegaard ,
Michael T. 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
and 40 other authors
,
Carla Spazzolini ,
Mette Nyegaard ,
Michael T. 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
and 40 other authors
Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry
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2022
Gabrielle Norrish,
Tao Ding,
Ella Field ,
Elena Cervi ,
Lidia Ziółkowska ,
Iacopo Olivotto ,
Diala Khraiche,
Giuseppe Limongelli ,
Aris Anastasakis,
Robert Weintraub ,
Elena Biagini ,
Luca Ragni,
Terrence Prendiville ,
Sophie Duignan ,
Karen McLeod
and 44 other authors
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,
Elena Cervi ,
Lidia Ziółkowska ,
Iacopo Olivotto ,
Diala Khraiche,
Giuseppe Limongelli ,
Aris Anastasakis,
Robert Weintraub ,
Elena Biagini ,
Luca Ragni,
Terrence Prendiville ,
Sophie Duignan ,
Karen McLeod
and 44 other authors
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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
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,
Monia Magliozzi,
Silvia Di Tommaso,
Francesca G. Iodice,
Emanuela Pompei,
Alessandra Toscano,
Maria C. Digilio,
Fabrizio Drago,
Antonio Novelli,
Anwar Baban
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2020
Maria Gnazzo,
Francesca R. Lepri ,
Maria Lisa Dentici ,
Rossella Capolino,
Elisa Pisaneschi,
Emanuele Agolini ,
Martina Rinelli ,
Viola Alesi,
Paolo Versacci,
Silvia Genovese ,
Claudia Cesario,
Lorenzo Sinibaldi,
Anwar Baban ,
Andrea Bartuli,
Bruno Marino
and 4 other authors
,
Maria Lisa Dentici ,
Rossella Capolino,
Elisa Pisaneschi,
Emanuele Agolini ,
Martina Rinelli ,
Viola Alesi,
Paolo Versacci,
Silvia Genovese ,
Claudia Cesario,
Lorenzo Sinibaldi,
Anwar Baban ,
Andrea Bartuli,
Bruno Marino
and 4 other authors
KBG syndrome: Common and uncommon clinical features based on 31 new patients
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2019
Viola Alesi ,
Sara Loddo ,
Federica Calì,
Valeria Orlando ,
Silvia Genovese ,
Daniele Ferretti,
Chiara Calacci,
Giusy Calvieri,
Roberto Falasca,
Lucia Ulgheri,
Fabrizio Drago,
Bruno Dallapiccola,
Anwar Baban ,
Antonio Novelli
,
Sara Loddo ,
Federica Calì,
Valeria Orlando ,
Silvia Genovese ,
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
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