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Looking for CALR mutations in familial myeloproliferative neoplasms.
Leukemia. 2014 Jun;28(6):1357-60. doi: 10.1038/leu.2014.33. Epub 2014 Jan 20.
Leukemia. 2014.
PMID: 24441291
No abstract available.
The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss.
Bussini A, Righi R, Pessina C, Genoni A, Cristofari E, Meli A, Granata P, Meroni E, Broccolo F, Casalone R.
Bussini A, et al.
Int J Pediatr Otorhinolaryngol. 2019 Dec;127:109653. doi: 10.1016/j.ijporl.2019.109653. Epub 2019 Aug 22.
Int J Pediatr Otorhinolaryngol. 2019.
PMID: 31472357
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Molecular detection of SARS-CoV-2 eta VOI in Northern Italy: a case report.
Broccolo F, Giovanetti M, Colombo A, Perrelli N, Bussini A, Cavalli S, Ciccozzi M, Zollo M.
Broccolo F, et al. Among authors: bussini a.
Clin Chem Lab Med. 2021 Dec 2;60(3):61-63. doi: 10.1515/cclm-2021-1230. Print 2022 Feb 23.
Clin Chem Lab Med. 2021.
PMID: 34854655
Free article.
No abstract available.
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Durable molecular response despite F317L and E255K mutations: Successful treatment of chronic myeloid leukemia with sequential imatinib, nilotinib and dasatinib.
Intermesoli T, Castagnetti F, Soverini S, Bussini A, Spinelli O, Gnani A, Bassan R, Rosti G.
Intermesoli T, et al. Among authors: bussini a.
Leuk Res. 2012 Jan;36(1):e10-1. doi: 10.1016/j.leukres.2011.09.002. Epub 2011 Oct 1.
Leuk Res. 2012.
PMID: 21962337
No abstract available.
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