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Items: 22

1.

Skeletal involvement in type 1 Gaucher disease: Not just bone mineral density.

Baldini M, Casirati G, Ulivieri FM, Cassinerio E, Khouri Chalouhi K, Poggiali E, Borin L, Burghignoli V, Cesana BM, Cappellini MD.

Blood Cells Mol Dis. 2018 Feb;68:148-152. doi: 10.1016/j.bcmd.2017.06.003. Epub 2017 Jun 16.

PMID:
28693786
2.

The role of cardiac magnetic resonance in assessing the cardiac involvement in Gaucher type 1 patients: morphological and functional evaluations.

Roghi A, Poggiali E, Cassinerio E, Pedrotti P, Giuditta M, Milazzo A, Quattrocchi G, Cappellini MD.

J Cardiovasc Med (Hagerstown). 2017 Apr;18(4):244-248. doi: 10.2459/JCM.0000000000000326.

PMID:
27136700
3.

Dual therapy with peg-interferon and ribavirin in thalassemia major patients with chronic HCV infection: Is there still an indication?

Di Marco V, D'Ambrosio R, Bronte F, Saracco G, Lanza AG, Forni G, Poggiali E, Calvaruso V; on behalf ITHACA (Italy for THAalassemia, hepatitis C Advances) Group.

Dig Liver Dis. 2016 Jun;48(6):650-5. doi: 10.1016/j.dld.2016.02.004. Epub 2016 Feb 21.

PMID:
27012446
4.

Response to Zanella et al.

Elli L, Poggiali E.

Am J Gastroenterol. 2015 Aug;110(8):1241. doi: 10.1038/ajg.2015.201. No abstract available.

PMID:
26263363
5.

Role of Non-Transferrin-Bound Iron in the pathogenesis of cardiotoxicity in patients with ST-elevation myocardial infarction assessed by Cardiac Magnetic Resonance Imaging.

Roghi A, Poggiali E, Duca L, Mafrici A, Pedrotti P, Paccagnini S, Brenna S, Galli A, Consonni D, Cappellini MD.

Int J Cardiol. 2015 Nov 15;199:326-32. doi: 10.1016/j.ijcard.2015.07.056. Epub 2015 Jul 23.

PMID:
26241638
6.

A multicentre observational study for early diagnosis of Gaucher disease in patients with Splenomegaly and/or Thrombocytopenia.

Motta I, Filocamo M, Poggiali E, Stroppiano M, Dragani A, Consonni D, Barcellini W, Gaidano G, Facchini L, Specchia G, Cappellini MD; Splenomegaly Gaucher Disease study group.

Eur J Haematol. 2016 Apr;96(4):352-9. doi: 10.1111/ejh.12596. Epub 2015 Jun 11.

PMID:
26033455
7.

Anemia and splenomegaly: what lies behind?

Migone De Amicis M, Fattizzo B, Poggiali E, Minonzio F, Gianelli U, Cappellini MD.

Intern Emerg Med. 2015 Sep;10(6):711-4. doi: 10.1007/s11739-015-1254-0. Epub 2015 May 19. No abstract available.

PMID:
25986481
8.

Anemia in elderly hospitalized patients: prevalence and clinical impact.

Migone De Amicis M, Poggiali E, Motta I, Minonzio F, Fabio G, Hu C, Cappellini MD.

Intern Emerg Med. 2015 Aug;10(5):581-6. doi: 10.1007/s11739-015-1197-5. Epub 2015 Jan 30.

PMID:
25633233
9.

Does TMPRSS6 RS855791 polymorphism contribute to iron deficiency in treated celiac disease?

Elli L, Poggiali E, Tomba C, Andreozzi F, Nava I, Bardella MT, Campostrini N, Girelli D, Conte D, Cappellini MD.

Am J Gastroenterol. 2015 Jan;110(1):200-2. doi: 10.1038/ajg.2014.354. No abstract available.

PMID:
25567183
10.

A 5-year follow-up in deferasirox treatment: improvement of cardiac and hepatic iron overload and amelioration in cardiac function in thalassemia major patients.

Cassinerio E, Roghi A, Orofino N, Pedrotti P, Zanaboni L, Poggiali E, Giuditta M, Consonni D, Cappellini MD.

Ann Hematol. 2015 Jun;94(6):939-45. doi: 10.1007/s00277-014-2291-x. Epub 2015 Jan 8.

PMID:
25563596
11.

The role of TMPRSS6 polymorphisms in iron deficiency anemia partially responsive to oral iron treatment.

Poggiali E, Andreozzi F, Nava I, Consonni D, Graziadei G, Cappellini MD.

Am J Hematol. 2015 Apr;90(4):306-9. doi: 10.1002/ajh.23929. Epub 2015 Mar 2.

12.

Myocardial and hepatic iron overload assessment by region-based and pixel-wise T2* mapping analysis: technical pitfalls and clinical warnings.

Roghi A, Poggiali E, Pedrotti P, Milazzo A, Quattrocchi G, Cassinerio E, Cappellini MD.

J Comput Assist Tomogr. 2015 Jan-Feb;39(1):128-33. doi: 10.1097/RCT.0000000000000159.

PMID:
25279849
13.

Combination of deferasirox and deferoxamine in clinical practice: an alternative scheme of chelation in thalassemia major patients.

Cassinerio E, Orofino N, Roghi A, Duca L, Poggiali E, Fraquelli M, Zanaboni L, Cappellini MD.

Blood Cells Mol Dis. 2014 Sep;53(3):164-7. doi: 10.1016/j.bcmd.2014.04.006. Epub 2014 May 17.

PMID:
24846580
14.

Gaucher disease: a diagnostic challenge for internists.

Cassinerio E, Graziadei G, Poggiali E.

Eur J Intern Med. 2014 Feb;25(2):117-24. doi: 10.1016/j.ejim.2013.09.006. Epub 2013 Oct 1. Review.

PMID:
24090739
15.

Anemia of chronic disease: a unique defect of iron recycling for many different chronic diseases.

Poggiali E, Migone De Amicis M, Motta I.

Eur J Intern Med. 2014 Jan;25(1):12-7. doi: 10.1016/j.ejim.2013.07.011. Epub 2013 Aug 26. Review.

PMID:
23988263
16.

Hypercoagulability in β-thalassemia: a status quo.

Cappellini MD, Poggiali E, Taher AT, Musallam KM.

Expert Rev Hematol. 2012 Oct;5(5):505-11; quiz 512. doi: 10.1586/ehm.12.42. Review.

PMID:
23146054
17.

An update on iron chelation therapy.

Poggiali E, Cassinerio E, Zanaboni L, Cappellini MD.

Blood Transfus. 2012 Oct;10(4):411-22. doi: 10.2450/2012.0008-12. Epub 2012 Jun 27. Review. No abstract available.

18.

Hypercoagulability in non-transfusion-dependent thalassemia.

Cappellini MD, Musallam KM, Poggiali E, Taher AT.

Blood Rev. 2012 Apr;26 Suppl 1:S20-3. doi: 10.1016/S0268-960X(12)70007-3. Review.

PMID:
22631037
19.

Inherited disorders of iron metabolism.

Camaschella C, Poggiali E.

Curr Opin Pediatr. 2011 Feb;23(1):14-20. doi: 10.1097/MOP.0b013e3283425591. Review.

PMID:
21150441
20.

Rare types of genetic hemochromatosis.

Camaschella C, Poggiali E.

Acta Haematol. 2009;122(2-3):140-5. doi: 10.1159/000243798. Epub 2009 Nov 10.

PMID:
19907151
21.

Towards explaining "unexplained hyperferritinemia".

Camaschella C, Poggiali E.

Haematologica. 2009 Mar;94(3):307-9. doi: 10.3324/haematol.2008.005405. No abstract available.

22.

Blunted hepcidin response to oral iron challenge in HFE-related hemochromatosis.

Piperno A, Girelli D, Nemeth E, Trombini P, Bozzini C, Poggiali E, Phung Y, Ganz T, Camaschella C.

Blood. 2007 Dec 1;110(12):4096-100. Epub 2007 Aug 27.

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