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540 results

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Page 1
Acute respiratory failure in a child after talc inhalation.
Patarino F, Norbedo S, Barbi E, Poli F, Furlan S, Savron F. Patarino F, et al. Among authors: poli f. Respiration. 2010;79(4):340. doi: 10.1159/000181013. Epub 2008 Dec 2. Respiration. 2010. PMID: 19052443 Free article. No abstract available.
Treatment of low bone density in young people with cystic fibrosis: a multicentre, prospective, open-label observational study of calcium and calcifediol followed by a randomised placebo-controlled trial of alendronate.
Bianchi ML, Colombo C, Assael BM, Dubini A, Lombardo M, Quattrucci S, Bella S, Collura M, Messore B, Raia V, Poli F, Bini R, Albanese CV, De Rose V, Costantini D, Romano G, Pustorino E, Magazzù G, Bertasi S, Lucidi V, Traverso G, Coruzzo A, Grzejdziak AD. Bianchi ML, et al. Among authors: poli f. Lancet Respir Med. 2013 Jul;1(5):377-85. doi: 10.1016/S2213-2600(13)70064-X. Epub 2013 Jun 2. Lancet Respir Med. 2013. PMID: 24429202 Clinical Trial.
Diagnosis of diabetes. What about cystic fibrosis?
Marchetti F, Tornese G, Faleschini E, Poli F. Marchetti F, et al. Among authors: poli f. BMJ. 2009 Dec 31;339:b5644. doi: 10.1136/bmj.b5644. BMJ. 2009. PMID: 20044398 No abstract available.
MBL2 polymorphisms screening in a regional Italian CF Center.
Trevisiol C, Boniotto M, Giglio L, Poli F, Morgutti M, Crovella S. Trevisiol C, et al. Among authors: poli f. J Cyst Fibros. 2005 Sep;4(3):189-91. doi: 10.1016/j.jcf.2005.04.001. J Cyst Fibros. 2005. PMID: 16046196 Free article.
Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome.
Nacci L, Danesino C, Sainati L, Longoni D, Poli F, Cipolli M, Perobelli S, Nicolis E, Cannioto Z, Morini J, Valli R, Pasquali F, Minelli A. Nacci L, et al. Among authors: poli f. Br J Haematol. 2014 May;165(4):573-5. doi: 10.1111/bjh.12767. Epub 2014 Feb 1. Br J Haematol. 2014. PMID: 24484588 Free article. No abstract available.
The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome.
Minelli A, Maserati E, Nicolis E, Zecca M, Sainati L, Longoni D, Lo Curto F, Menna G, Poli F, De Paoli E, Cipolli M, Locatelli F, Pasquali F, Danesino C. Minelli A, et al. Among authors: poli f. Leukemia. 2009 Apr;23(4):708-11. doi: 10.1038/leu.2008.369. Epub 2009 Jan 15. Leukemia. 2009. PMID: 19148133
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.
Maserati E, Pressato B, Valli R, Minelli A, Sainati L, Patitucci F, Marletta C, Mastronuzzi A, Poli F, Lo Curto F, Locatelli F, Danesino C, Pasquali F. Maserati E, et al. Among authors: poli f. Br J Haematol. 2009 Apr;145(2):190-7. doi: 10.1111/j.1365-2141.2009.07611.x. Epub 2009 Feb 17. Br J Haematol. 2009. PMID: 19222471 Free article.
540 results