Baban A - Search Results

1

Cardiovascular Involvement in Pediatric FLNC Variants: A Case Series of Fourteen Patients.

Baban A, Alesi V, Magliozzi M, Parlapiano G, Genovese S, Cicenia M, Loddo S, Lodato V, Di Chiara L, Fattori F, D'Amico A, Francalanci P, Amodeo A, Novelli A, Drago F. Baban A, et al. J Cardiovasc Dev Dis. 2022 Sep 30;9(10):332. doi: 10.3390/jcdd9100332. J Cardiovasc Dev Dis. 2022. PMID: 36286284 Free PMC article.

2

Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1.

Digilio MC, Bernardini L, Lepri F, Giuffrida MG, Guida V, Baban A, Versacci P, Capolino R, Torres B, De Luca A, Novelli A, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: baban a. Am J Med Genet A. 2011 Sep;155A(9):2196-202. doi: 10.1002/ajmg.a.34131. Epub 2011 Aug 3. Am J Med Genet A. 2011. PMID: 21815254

3

Syndromic non-compaction of the left ventricle: associated chromosomal anomalies.

Digilio MC, Bernardini L, Gagliardi MG, Versacci P, Baban A, Capolino R, Dentici ML, Roberti MC, Angioni A, Novelli A, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: baban a. Clin Genet. 2013 Oct;84(4):362-7. doi: 10.1111/cge.12069. Epub 2012 Dec 28. Clin Genet. 2013. PMID: 23210894

4

Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: rare association with pulmonary valve stenosis.

Digilio MC, Bernardini L, Consoli F, Lepri FR, Giuffrida MG, Baban A, Surace C, Ferese R, Angioni A, Novelli A, Marino B, De Luca A, Dallapiccola B. Digilio MC, et al. Among authors: baban a. Eur J Med Genet. 2013 Mar;56(3):144-9. doi: 10.1016/j.ejmg.2012.12.004. Epub 2012 Dec 25. Eur J Med Genet. 2013. PMID: 23270675

5

Congenital heart defects in molecularly proven Kabuki syndrome patients.

Digilio MC, Gnazzo M, Lepri F, Dentici ML, Pisaneschi E, Baban A, Passarelli C, Capolino R, Angioni A, Novelli A, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: baban a. Am J Med Genet A. 2017 Nov;173(11):2912-2922. doi: 10.1002/ajmg.a.38417. Epub 2017 Sep 8. Am J Med Genet A. 2017. PMID: 28884922

6

Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies.

Calcagni G, Adorisio R, Martinelli S, Grutter G, Baban A, Versacci P, Digilio MC, Drago F, Gelb BD, Tartaglia M, Marino B. Calcagni G, et al. Among authors: baban a. Heart Fail Clin. 2018 Apr;14(2):225-235. doi: 10.1016/j.hfc.2017.12.005. Heart Fail Clin. 2018. PMID: 29525650 Review.

7

Bradyarrhythmias in Repaired Atrioventricular Septal Defects: Single-Center Experience Based on 34 Years of Follow-Up of 522 Patients.

Di Mambro C, Calvieri C, Silvetti MS, Tamburri I, Giannico S, Baban A, Albanese S, Brancaccio G, Carotti A, Iorio FS, Drago F. Di Mambro C, et al. Among authors: baban a. Pediatr Cardiol. 2018 Dec;39(8):1590-1597. doi: 10.1007/s00246-018-1934-4. Epub 2018 Jun 13. Pediatr Cardiol. 2018. PMID: 29948031

8

Long-term survival and phenotypic spectrum in heterotaxy syndrome: A 25-year follow-up experience.

Baban A, Cantarutti N, Adorisio R, Lombardi R, Calcagni G, Piano Mortari E, Dallapiccola B, Marino B, Iorio FS, Carsetti R, Digilio MC, Giannico S, Drago F, Carotti A. Baban A, et al. Int J Cardiol. 2018 Oct 1;268:100-105. doi: 10.1016/j.ijcard.2018.02.050. Int J Cardiol. 2018. PMID: 30041775

9

First evidence of maternally inherited mosaicism in TGFBR1 and subtle primary myocardial changes in Loeys-Dietz syndrome: a case report.

Baban A, Magliozzi M, Loeys B, Adorisio R, Alesi V, Secinaro A, Corica B, Vricella L, Dietz HC, Drago F, Novelli A, Amodeo A. Baban A, et al. BMC Med Genet. 2018 Sep 15;19(1):170. doi: 10.1186/s12881-018-0661-2. BMC Med Genet. 2018. PMID: 30219046 Free PMC article.

10

LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant.

Morlino S, Alesi V, Calì F, Lepri FR, Secinaro A, Grammatico P, Novelli A, Drago F, Castori M, Baban A. Morlino S, et al. Among authors: baban a. Am J Med Genet A. 2019 Jan;179(1):104-112. doi: 10.1002/ajmg.a.10. Epub 2018 Dec 18. Am J Med Genet A. 2019. PMID: 30565850

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