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Items: 13

1.

Eltrombopag for the treatment of inherited thrombocytopenias: a phase 2 clinical trial.

Zaninetti C, Gresele P, Bertomoro A, Klersy C, De Candia E, Veneri D, Barozzi S, Fierro T, Alberelli MA, Musella V, Noris P, Fabris F, Balduini CL, Pecci A.

Haematologica. 2019 Jul 4. pii: haematol.2019.223966. doi: 10.3324/haematol.2019.223966. [Epub ahead of print]

2.

Eltrombopag in preparation for surgery in patients with severe MYH9-related thrombocytopenia.

Zaninetti C, Barozzi S, Bozzi V, Gresele P, Balduini CL, Pecci A.

Am J Hematol. 2019 Aug;94(8):E199-E201. doi: 10.1002/ajh.25500. Epub 2019 May 8. No abstract available.

PMID:
31034630
3.

MYH9-related disease mutations cause abnormal red blood cell morphology through increased myosin-actin binding at the membrane.

Smith AS, Pal K, Nowak RB, Demenko A, Zaninetti C, Da Costa L, Favier R, Pecci A, Fowler VM.

Am J Hematol. 2019 Jun;94(6):667-677. doi: 10.1002/ajh.25472. Epub 2019 Apr 17.

PMID:
30916803
4.

MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder.

Zaninetti C, De Rocco D, Giangregorio T, Bozzi V, Demeter J, Leoni P, Noris P, Ryhänen S, Barozzi S, Pecci A, Savoia A.

Hamostaseologie. 2019 Feb;39(1):87-94. doi: 10.1055/s-0038-1645840. Epub 2018 Jul 11.

PMID:
29996171
5.

Prevalence of anemia in hospitalized internal medicine patients: Correlations with comorbidities and length of hospital stay.

Zaninetti C, Klersy C, Scavariello C, Bastia R, Balduini CL, Invernizzi R.

Eur J Intern Med. 2018 May;51:11-17. doi: 10.1016/j.ejim.2017.11.001. Epub 2017 Nov 16.

PMID:
29153343
6.

Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases.

Zaninetti C, Santini V, Tiniakou M, Barozzi S, Savoia A, Pecci A.

J Thromb Haemost. 2017 Dec;15(12):2388-2392. doi: 10.1111/jth.13855. Epub 2017 Oct 28.

PMID:
28976612
7.

Extramedullary hematopoiesis: a new feature of inherited thrombocytopenias?

Zaninetti C, Melazzini F, Croci GA, Boveri E, Balduini CL.

J Thromb Haemost. 2017 Nov;15(11):2226-2229. doi: 10.1111/jth.13850. Epub 2017 Oct 13.

PMID:
28921865
8.

Bleeding is not the main clinical issue in many patients with inherited thrombocytopaenias.

Melazzini F, Zaninetti C, Balduini CL.

Haemophilia. 2017 Sep;23(5):673-681. doi: 10.1111/hae.13255. Epub 2017 Jun 8. Review.

PMID:
28594466
9.

Massive mediastinal enlargement due to extramedullary haematopoiesis in a patient with MYH9-related thrombocytopenia.

Zaninetti C, Boveri E, Melazzini F.

Br J Haematol. 2017 Jul;178(1):10. doi: 10.1111/bjh.14676. Epub 2017 May 17. No abstract available.

PMID:
28516481
10.

Severe to profound deafness may be associated with MYH9-related disease: report of 4 patients.

Canzi P, Pecci A, Manfrin M, Rebecchi E, Zaninetti C, Bozzi V, Benazzo M.

Acta Otorhinolaryngol Ital. 2016 Oct;36(5):415-420. doi: 10.14639/0392-100X-702.

11.

SLFN14-related thrombocytopenia: identification within a large series of patients with inherited thrombocytopenia.

Marconi C, Di Buduo CA, Barozzi S, Palombo F, Pardini S, Zaninetti C, Pippucci T, Noris P, Balduini A, Seri M, Pecci A.

Thromb Haemost. 2016 May 2;115(5):1076-9. doi: 10.1160/TH15-11-0884. Epub 2016 Jan 14. No abstract available.

PMID:
26769223
12.

Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia.

Zaninetti C, Biino G, Noris P, Melazzini F, Civaschi E, Balduini CL.

Haematologica. 2015 Sep;100(9):e338-40. doi: 10.3324/haematol.2015.127597. Epub 2015 May 8. No abstract available.

13.

MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.

Pecci A, Klersy C, Gresele P, Lee KJ, De Rocco D, Bozzi V, Russo G, Heller PG, Loffredo G, Ballmaier M, Fabris F, Beggiato E, Kahr WH, Pujol-Moix N, Platokouki H, Van Geet C, Noris P, Yerram P, Hermans C, Gerber B, Economou M, De Groot M, Zieger B, De Candia E, Fraticelli V, Kersseboom R, Piccoli GB, Zimmermann S, Fierro T, Glembotsky AC, Vianello F, Zaninetti C, Nicchia E, Güthner C, Baronci C, Seri M, Knight PJ, Balduini CL, Savoia A.

Hum Mutat. 2014 Feb;35(2):236-47. doi: 10.1002/humu.22476. Epub 2013 Dec 12.

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