Selicorni A - Search Results

1

Increased nocturnal heart rate and wave reflection are early markers of cardiovascular disease in Williams-Beuren syndrome children.

Maloberti A, Cesana F, Hametner B, Dozio D, Villa P, Hulpke-Wette M, Schwarz A, Selicorni A, Wassertheurer S, Mancia G, Giannattasio C. Maloberti A, et al. Among authors: selicorni a. J Hypertens. 2015 Apr;33(4):804-9; discussion 809. doi: 10.1097/HJH.0000000000000454. J Hypertens. 2015. PMID: 25915885

2

Balance function in patients with Williams syndrome.

Barozzi S, Soi D, Gagliardi C, Selicorni A, Bedeschi MF, Forti S, Di Berardino F, Cesarani A, Brambilla D. Barozzi S, et al. Among authors: selicorni a. Gait Posture. 2013 Jun;38(2):221-5. doi: 10.1016/j.gaitpost.2012.11.012. Epub 2012 Dec 7. Gait Posture. 2013. PMID: 23219788

3

Genotype-phenotype correlation in two sets of monozygotic twins with Williams syndrome.

Castorina P, Selicorni A, Bedeschi F, Dalprà L, Larizza L. Castorina P, et al. Among authors: selicorni a. Am J Med Genet. 1997 Mar 3;69(1):107-11. doi: 10.1002/(sici)1096-8628(19970303)69:1<107::aid-ajmg21>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9066894

4

Renal tract ultrasonography and calcium homeostasis in Williams-Beuren syndrome.

Sforzini C, Milani D, Fossali E, Barbato A, Grumieri G, Bianchetti MG, Selicorni A. Sforzini C, et al. Among authors: selicorni a. Pediatr Nephrol. 2002 Nov;17(11):899-902. doi: 10.1007/s00467-002-0889-z. Epub 2002 Oct 9. Pediatr Nephrol. 2002. PMID: 12432430 Clinical Trial.

5

Thyroid anomalies in Williams syndrome: investigation of 95 patients.

Selicorni A, Fratoni A, Pavesi MA, Bottigelli M, Arnaboldi E, Milani D. Selicorni A, et al. Am J Med Genet A. 2006 May 15;140(10):1098-101. doi: 10.1002/ajmg.a.31210. Am J Med Genet A. 2006. PMID: 16596673

6

Clinical follow-up of young adults affected by Williams syndrome: experience of 45 Italian patients.

Bedeschi MF, Bianchi V, Colli AM, Natacci F, Cereda A, Milani D, Maitz S, Lalatta F, Selicorni A. Bedeschi MF, et al. Among authors: selicorni a. Am J Med Genet A. 2011 Feb;155A(2):353-9. doi: 10.1002/ajmg.a.33819. Epub 2011 Jan 13. Am J Med Genet A. 2011. PMID: 21271653

7

Immunogenicity, safety and tolerability of monovalent 2009 pandemic influenza A/H1N1 MF59-adjuvanted vaccine in children and adolescents with Williams or Cornelia De Lange syndrome.

Esposito S, Selicorni A, Daleno C, Valzano A, Cerutti M, Galeone C, Consolo S, Menni F, Principi N. Esposito S, et al. Among authors: selicorni a. Hum Vaccin. 2011 Jun;7(6):613-7. doi: 10.4161/hv.7.6.15133. Epub 2011 Jun 1. Hum Vaccin. 2011. PMID: 21508673

8

Audiological findings in Williams syndrome: a study of 69 patients.

Barozzi S, Soi D, Comiotto E, Borghi A, Gavioli C, Spreafico E, Gagliardi C, Selicorni A, Forti S, Ambrosetti U, Cesarani A, Brambilla D. Barozzi S, et al. Among authors: selicorni a. Am J Med Genet A. 2012 Apr;158A(4):759-71. doi: 10.1002/ajmg.a.35241. Epub 2012 Mar 12. Am J Med Genet A. 2012. PMID: 22411878

9

Prevalence of diabetes and pre-diabetes in a cohort of Italian young adults with Williams syndrome.

Masserini B, Bedeschi MF, Bianchi V, Scuvera G, Beck-Peccoz P, Lalatta F, Selicorni A, Orsi E. Masserini B, et al. Among authors: selicorni a. Am J Med Genet A. 2013 Apr;161A(4):817-21. doi: 10.1002/ajmg.a.35655. Epub 2013 Mar 12. Am J Med Genet A. 2013. PMID: 23495209

10

Audiological follow-up of 24 patients affected by Williams syndrome.

Barozzi S, Soi D, Spreafico E, Borghi A, Comiotto E, Gagliardi C, Selicorni A, Forti S, Cesarani A, Brambilla D. Barozzi S, et al. Among authors: selicorni a. Eur J Med Genet. 2013 Sep;56(9):490-6. doi: 10.1016/j.ejmg.2013.07.001. Epub 2013 Jul 22. Eur J Med Genet. 2013. PMID: 23886711

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