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Year Number of Results
2002 1
2010 1
2011 1
2012 2
2013 3
2014 2
2017 1
2020 1
2021 1
2024 0

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Page 1
Cilia and Ear.
Piatti G, De Santi MM, Torretta S, Pignataro L, Soi D, Ambrosetti U. Piatti G, et al. Among authors: soi d. Ann Otol Rhinol Laryngol. 2017 Apr;126(4):322-327. doi: 10.1177/0003489417691299. Epub 2017 Feb 12. Ann Otol Rhinol Laryngol. 2017. PMID: 28290230
Vestibular and audiological findings in the Alport syndrome.
Barozzi S, Soi D, Intieri E, Giani M, Aldè M, Tonon E, Signorini L, Renieri A, Fallerini C, Perin P, Montini G, Ambrosetti U. Barozzi S, et al. Among authors: soi d. Am J Med Genet A. 2020 Oct;182(10):2345-2358. doi: 10.1002/ajmg.a.61796. Epub 2020 Aug 20. Am J Med Genet A. 2020. PMID: 32820599
Reliability of postural control measures in children and young adolescents.
Barozzi S, Socci M, Soi D, Di Berardino F, Fabio G, Forti S, Gasbarre AM, Brambilla D, Cesarani A. Barozzi S, et al. Among authors: soi d. Eur Arch Otorhinolaryngol. 2014 Jul;271(7):2069-77. doi: 10.1007/s00405-014-2930-9. Epub 2014 Feb 21. Eur Arch Otorhinolaryngol. 2014. PMID: 24557440 Free article.
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: soi d. 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
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: soi d. 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
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: soi d. 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
11 results