MARINO TAUSSIG DE BODONIA, Bruno
MARINO TAUSSIG DE BODONIA, Bruno
DIPARTIMENTO MATERNO INFANTILE E SCIENZE UROLOGICHE
16p subtelomeric duplication: a clinically recognizable syndrome
2009 Maria Cristina, Digilio; Laura, Bernardini; Anna, Capalbo; Rossella, Capolino; Maria Giulia, Gagliardi; MARINO TAUSSIG DE BODONIA, Bruno; Antonio, Novelli; Bruno, Dallapiccola
22q11 Deletion syndrome: a review of some developmental biology aspects of the cardiovascular system
2006 Angelo, Restivo; Anna, Sarkozy; Maria Cristina, Digilio; DALLA PICCOLA, Bruno; MARINO TAUSSIG DE BODONIA, Bruno
22q11.2 deletion syndrome
2015 McDonald-McGinn, Donna M.; Sullivan, Kathleen E.; Marino, Bruno; Philip, Nicole; Swillen, Ann; Vorstman, Jacob A. S.; Zackai, Elaine H.; Emanuel, Beverly S.; Vermeesch, Joris R.; Morrow, Bernice E.; Scambler, Peter J.; Bassett, Anne S.
22q11.2 Deletion Syndrome. Impact of Genetics in the Treatment of Conotruncal Heart Defects
2022 Putotto, C.; Pugnaloni, F.; Unolt, M.; Maiolo, S.; Trezzi, M.; Digilio, M. C.; Cirillo, A.; Limongelli, G.; Marino, B.; Calcagni, G.; Versacci, P.
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago
1997 Francalanci, P; Gallo, Pietro; DALLA PICCOLA, Bruno; Calabrese, G; MARINO TAUSSIG DE BODONIA, Bruno
A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries in mice
2006 Daria, Cipollone; Francesca, Amati; Rita, Carsetti; Silvia, Placidi; Michela, Biancolella; D'Amati, Giulia; Giuseppe, Novelli; Gregorio, Siracusa; MARINO TAUSSIG DE BODONIA, Bruno
A rare case of cystic variety of angiomatoid fibrous histiocytoma
2010 Filingeri, V.; Bellini, I.; Marino, B.; Fratoni, S.; Schiaroli, S.
A rare case of cystic variety of angiomatoid fibrous histiocytoma
2010 Filingeri, V.; Bellini, I.; Marino, B.; Fratoni, S.; Schiaroli, S.
A rare case of cystic variety of angiomatoid fibrous histiocytoma (European Review for Medical and Pharmacological Sciences (2010) 14, 10 (887-890))
2010 Filingeri, V.; Bellini, I.; Marino, B.; Frantoni, S.; Schiaroli, S.
A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot
2013 Guida, V; Ferese, R; Rocchetti, M; Bonetti, M; Sarkozy, A; Cecchetti, S; Gelmetti, V; Lepri, F; Copetti, M; Lamorte, G; Digilio, Mc; MARINO TAUSSIG DE BODONIA, Bruno; Zaza, A; den Hertog, J; DALLA PICCOLA, Bruno; De Luca, A.
Absent pulmonary valve with intact ventricular septum and patent ductus arteriosus: a specific cardiac phenotype associated with deletion 18q syndrome
2005 Versacci, P; DIGILIO M., C; Sauer, U; DALLA PICCOLA, B; MARINO TAUSSIG DE BODONIA, B.
Additional evidence that PTPN11 mutations play only a minor role in the pathogenesis of non-syndromic atrioventricular canal defect
2006 Sarkozy, A; Lepri, F; MARINO TAUSSIG DE BODONIA, Bruno; Pizzuti, Antonio; Digilio, Mc; DALLA PICCOLA, Bruno
Age at operation for children with atrioventricular canal.
2001 MARINO TAUSSIG DE BODONIA, Bruno; Anaclerio, S.; DI DONATO, R.
Anatomical substrate for biventricular repair in patients with left isomerism
2021 Madrigali, A.; Putotto, C.; Marino, B.; Versacci, P.
Anatomically corrected malposition of the great arteries (S,L,D) with mutation of Nodal gene
2022 Putotto, Carolina; Caruso, Elio; MARINO TAUSSIG DE BODONIA, Bruno; Cristina Digilio, Maria; Novelli, Antonio; Agati, Salvatore
Association of deletion 22 and trisomy 21: A likely random association in patients with conotruncal heart defects
2005 Maria Cristina, Digilio; Bruno, Dallapiccola; MARINO TAUSSIG DE BODONIA, Bruno
Association of Di George anomaly and caudal dysplasia sequence in neonate born to a diabetic mother.
2013 Dentici, Ml; Placidi, S; Francalanci, P; Capolino, R; Rinelli, G; MARINO TAUSSIG DE BODONIA, Bruno; Digilio, Mc; DALLA PICCOLA, Bruno
Atrioventricular canal defect and associated genetic disorders: new insights into polydactyly syndromes
2011 Digilio, Mc; Versacci, P; Lepri, F; Baban, A; DALLA PICCOLA, Bruno; MARINO TAUSSIG DE BODONIA, Bruno
Atrioventricular canal defect and genetic syndromes: the unifying role of sonic hedgehog
2019 Digilio, M C; Pugnaloni, F; De Luca, A; Calcagni, G; Baban, A; Dentici, M L; Versacci, P; Dallapiccola, B; Tartaglia, M; Marino, B
Atrioventricular canal defect and hypoplastic left heart syndrome as discirdant congenital heart defects in twins.
1999 Digilio, Mc; MARINO TAUSSIG DE BODONIA, Bruno; Giannico, S; Giannotti, A; Dallapiccola, B.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 16p subtelomeric duplication: a clinically recognizable syndrome | 2009 | Maria Cristina, Digilio; Laura, Bernardini; Anna, Capalbo; Rossella, Capolino; Maria Giulia, Gagliardi; MARINO TAUSSIG DE BODONIA, Bruno; Antonio, Novelli; Bruno, Dallapiccola | |
| 22q11 Deletion syndrome: a review of some developmental biology aspects of the cardiovascular system | 2006 | Angelo, Restivo; Anna, Sarkozy; Maria Cristina, Digilio; DALLA PICCOLA, Bruno; MARINO TAUSSIG DE BODONIA, Bruno | |
| 22q11.2 deletion syndrome | 2015 | McDonald-McGinn, Donna M.; Sullivan, Kathleen E.; Marino, Bruno; Philip, Nicole; Swillen, Ann; Vorstman, Jacob A. S.; Zackai, Elaine H.; Emanuel, Beverly S.; Vermeesch, Joris R.; Morrow, Bernice E.; Scambler, Peter J.; Bassett, Anne S. | |
| 22q11.2 Deletion Syndrome. Impact of Genetics in the Treatment of Conotruncal Heart Defects | 2022 | Putotto, C.; Pugnaloni, F.; Unolt, M.; Maiolo, S.; Trezzi, M.; Digilio, M. C.; Cirillo, A.; Limongelli, G.; Marino, B.; Calcagni, G.; Versacci, P. | |
| A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago | 1997 | Francalanci, P; Gallo, Pietro; DALLA PICCOLA, Bruno; Calabrese, G; MARINO TAUSSIG DE BODONIA, Bruno | |
| A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries in mice | 2006 | Daria, Cipollone; Francesca, Amati; Rita, Carsetti; Silvia, Placidi; Michela, Biancolella; D'Amati, Giulia; Giuseppe, Novelli; Gregorio, Siracusa; MARINO TAUSSIG DE BODONIA, Bruno | |
| A rare case of cystic variety of angiomatoid fibrous histiocytoma | 2010 | Filingeri, V.; Bellini, I.; Marino, B.; Fratoni, S.; Schiaroli, S. | |
| A rare case of cystic variety of angiomatoid fibrous histiocytoma | 2010 | Filingeri, V.; Bellini, I.; Marino, B.; Fratoni, S.; Schiaroli, S. | |
| A rare case of cystic variety of angiomatoid fibrous histiocytoma (European Review for Medical and Pharmacological Sciences (2010) 14, 10 (887-890)) | 2010 | Filingeri, V.; Bellini, I.; Marino, B.; Frantoni, S.; Schiaroli, S. | |
| A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot | 2013 | Guida, V; Ferese, R; Rocchetti, M; Bonetti, M; Sarkozy, A; Cecchetti, S; Gelmetti, V; Lepri, F; Copetti, M; Lamorte, G; Digilio, Mc; MARINO TAUSSIG DE BODONIA, Bruno; Zaza, A; den Hertog, J; DALLA PICCOLA, Bruno; De Luca, A. | |
| Absent pulmonary valve with intact ventricular septum and patent ductus arteriosus: a specific cardiac phenotype associated with deletion 18q syndrome | 2005 | Versacci, P; DIGILIO M., C; Sauer, U; DALLA PICCOLA, B; MARINO TAUSSIG DE BODONIA, B. | |
| Additional evidence that PTPN11 mutations play only a minor role in the pathogenesis of non-syndromic atrioventricular canal defect | 2006 | Sarkozy, A; Lepri, F; MARINO TAUSSIG DE BODONIA, Bruno; Pizzuti, Antonio; Digilio, Mc; DALLA PICCOLA, Bruno | |
| Age at operation for children with atrioventricular canal. | 2001 | MARINO TAUSSIG DE BODONIA, Bruno; Anaclerio, S.; DI DONATO, R. | |
| Anatomical substrate for biventricular repair in patients with left isomerism | 2021 | Madrigali, A.; Putotto, C.; Marino, B.; Versacci, P. | |
| Anatomically corrected malposition of the great arteries (S,L,D) with mutation of Nodal gene | 2022 | Putotto, Carolina; Caruso, Elio; MARINO TAUSSIG DE BODONIA, Bruno; Cristina Digilio, Maria; Novelli, Antonio; Agati, Salvatore | |
| Association of deletion 22 and trisomy 21: A likely random association in patients with conotruncal heart defects | 2005 | Maria Cristina, Digilio; Bruno, Dallapiccola; MARINO TAUSSIG DE BODONIA, Bruno | |
| Association of Di George anomaly and caudal dysplasia sequence in neonate born to a diabetic mother. | 2013 | Dentici, Ml; Placidi, S; Francalanci, P; Capolino, R; Rinelli, G; MARINO TAUSSIG DE BODONIA, Bruno; Digilio, Mc; DALLA PICCOLA, Bruno | |
| Atrioventricular canal defect and associated genetic disorders: new insights into polydactyly syndromes | 2011 | Digilio, Mc; Versacci, P; Lepri, F; Baban, A; DALLA PICCOLA, Bruno; MARINO TAUSSIG DE BODONIA, Bruno | |
| Atrioventricular canal defect and genetic syndromes: the unifying role of sonic hedgehog | 2019 | Digilio, M C; Pugnaloni, F; De Luca, A; Calcagni, G; Baban, A; Dentici, M L; Versacci, P; Dallapiccola, B; Tartaglia, M; Marino, B | |
| Atrioventricular canal defect and hypoplastic left heart syndrome as discirdant congenital heart defects in twins. | 1999 | Digilio, Mc; MARINO TAUSSIG DE BODONIA, Bruno; Giannico, S; Giannotti, A; Dallapiccola, B. |