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Refinado por: assunto: Cardiology. Vascular System remover assunto: Child, Preschool remover
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1
Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion
Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion
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Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion

Digilio, M C ; Marino, B ; Giannotti, A ; Toscano, A ; Dallapiccola, B

Journal of medical genetics, 1997-03, Vol.34 (3), p.188-190 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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2
Atrioventricular canal defect and hypoplastic left heart syndrome as discordant congenital heart defects in twins
Atrioventricular canal defect and hypoplastic left heart syndrome as discordant congenital heart defects in twins
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Atrioventricular canal defect and hypoplastic left heart syndrome as discordant congenital heart defects in twins

Digilio, Maria Cristina ; Marino, Bruno ; Giannico, Salvatore ; Giannotti, Aldo ; Dallapiccola, Bruno

Teratology (Philadelphia), 1999-10, Vol.60 (4), p.206-208

New York: John Wiley & Sons, Inc

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3
Complete transposition of the great arteries: Patterns of congenital heart disease in familial precurrence
Complete transposition of the great arteries: Patterns of congenital heart disease in familial precurrence
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Complete transposition of the great arteries: Patterns of congenital heart disease in familial precurrence

DIGILIO, Maria Cristina ; CASEY, Brett ; TOSCANO, Alessandra ; CALABRO, Raffaele ; PACILEO, Giuseppe ; MARASINI, Maurizio ; BANAUDI, Elena ; GIANNOTTI, Aldo ; DALLAPICCOLA, Bruno ; MARINO, Bruno

Circulation (New York, N.Y.), 2001-12, Vol.104 (23), p.2809-2814 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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4
Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects
Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects
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Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects

GIGLIO, S ; GRAW, S. L ; DIGILIO, M. C ; GIANNOTTI, A ; MARINO, B ; CARROZZO, R ; KORENBERG, J. R ; DANESINO, C ; SUJANSKY, E ; DALLAPICCOLA, B ; ZUFFARDI, O ; GIMELLI, G ; PIROLA, B ; VARONE, P ; VOULLAIRE, L ; LERZO, F ; ROSSI, E ; DELLAVECCHIA, C ; BONAGLIA, M. C

Circulation (New York, N.Y.), 2000-07, Vol.102 (4), p.432-437 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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5
Associated cardiac anomalies in isolated and syndromic patients with tetralogy of fallot
Associated cardiac anomalies in isolated and syndromic patients with tetralogy of fallot
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Associated cardiac anomalies in isolated and syndromic patients with tetralogy of fallot

Marino, Bruno ; Digilio, Maria Cristina ; Grazioli, Sabina ; Formigari, Roberto ; Mingarelli, Rita ; Giannotti, Aldo ; Dallapiccola, Bruno

The American journal of cardiology, 1996-03, Vol.77 (7), p.505-508 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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6
22q11 deletions in isolated and syndromic patients with tetralogy of fallot
22q11 deletions in isolated and syndromic patients with tetralogy of fallot
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22q11 deletions in isolated and syndromic patients with tetralogy of fallot

AMATI, F ; MARI, A ; DIGILIO, M. C ; MINGARELLI, R ; MERINO, B ; GIANNOTTI, A ; NOVELLI, G ; DALLAPICCOLA, B

Human genetics, 1995-05, Vol.95 (5), p.479-482 [Periódico revisado por pares]

Heidelberg: Springer

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7
Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia
Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia
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Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia

Digilio, Maria Cristina ; Marino, Bruno ; Grazioli, Sabina ; Agostino, Domenico ; Giannotti, Aldo ; Dallapiccola, Bruno

The American journal of cardiology, 1996-06, Vol.77 (15), p.1375-1376 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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8
Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomalies
Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomalies
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Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomalies

TOSCANO, Alessandra ; ANACLERIO, Silvia ; DIGILIO, Maria Cristina ; GIANNOTTI, Aldo ; FARIELLO, Giuseppe ; DALLAPICCOLA, Bruno ; MARINO, Bruno

European journal of pediatrics, 2002-02, Vol.161 (2), p.116-117 [Periódico revisado por pares]

Heidelberg: Springer

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9
Noonan syndrome : structural abnormalities of the mitral valve causing subaortic obstruction
Noonan syndrome : structural abnormalities of the mitral valve causing subaortic obstruction
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Noonan syndrome : structural abnormalities of the mitral valve causing subaortic obstruction

MARINO, B ; GAGLIARDI, M. G ; DIGILIO, M. C ; POLLETTA, B ; GRAZIOLI, S ; AGOSTINO, D ; GIANNOTTI, A ; DALLAPICCOLA, B

European journal of pediatrics, 1995-12, Vol.154 (12), p.949-952 [Periódico revisado por pares]

Heidelberg: Springer

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10
Are ECG abnormalities in Noonan syndrome characteristic for the syndrome?
Are ECG abnormalities in Noonan syndrome characteristic for the syndrome?
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Are ECG abnormalities in Noonan syndrome characteristic for the syndrome?

Raaijmakers, R. ; Noordam, C. ; Noonan, J. A. ; Croonen, E. A. ; van der Burgt, C. J. A. M. ; Draaisma, J. M. T.

European journal of pediatrics, 2008-12, Vol.167 (12), p.1363-1367 [Periódico revisado por pares]

Berlin/Heidelberg: Springer-Verlag

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