Balduini CL - Search Results

1

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

Zaninetti C, Barozzi S, Bozzi V, Gresele P, Balduini CL, Pecci A. Zaninetti C, et al. Among authors: balduini cl. Am J Hematol. 2019 Aug;94(8):E199-E201. doi: 10.1002/ajh.25500. Epub 2019 May 8. Am J Hematol. 2019. PMID: 31034630 Free article. No abstract available.

2

Megakaryocytes of patients with MYH9-related thrombocytopenia present an altered proplatelet formation.

Pecci A, Malara A, Badalucco S, Bozzi V, Torti M, Balduini CL, Balduini A. Pecci A, et al. Among authors: balduini cl, balduini a. Thromb Haemost. 2009 Jul;102(1):90-6. doi: 10.1160/TH09-01-0068. Thromb Haemost. 2009. PMID: 19572073

3

Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations.

Pecci A, Gresele P, Klersy C, Savoia A, Noris P, Fierro T, Bozzi V, Mezzasoma AM, Melazzini F, Balduini CL. Pecci A, et al. Among authors: balduini cl. Blood. 2010 Dec 23;116(26):5832-7. doi: 10.1182/blood-2010-08-304725. Epub 2010 Sep 15. Blood. 2010. PMID: 20844233 Free article. Clinical Trial.

4

Eltrombopag for the treatment of inherited thrombocytopenias: a phase II 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. Zaninetti C, et al. Among authors: balduini cl. Haematologica. 2020 Mar;105(3):820-828. doi: 10.3324/haematol.2019.223966. Epub 2019 Jul 4. Haematologica. 2020. PMID: 31273088 Free PMC article. Clinical Trial.

5

Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease.

Pecci A, Panza E, Pujol-Moix N, Klersy C, Di Bari F, Bozzi V, Gresele P, Lethagen S, Fabris F, Dufour C, Granata A, Doubek M, Pecoraro C, Koivisto PA, Heller PG, Iolascon A, Alvisi P, Schwabe D, De Candia E, Rocca B, Russo U, Ramenghi U, Noris P, Seri M, Balduini CL, Savoia A. Pecci A, et al. Among authors: balduini cl. Hum Mutat. 2008 Mar;29(3):409-17. doi: 10.1002/humu.20661. Hum Mutat. 2008. PMID: 18059020

6

Renin-angiotensin system blockade is effective in reducing proteinuria of patients with progressive nephropathy caused by MYH9 mutations (Fechtner-Epstein syndrome).

Pecci A, Granata A, Fiore CE, Balduini CL. Pecci A, et al. Among authors: balduini cl. Nephrol Dial Transplant. 2008 Aug;23(8):2690-2. doi: 10.1093/ndt/gfn277. Epub 2008 May 23. Nephrol Dial Transplant. 2008. PMID: 18503011 No abstract available.

7

Pecci A, Panza E, De Rocco D, Pujol-Moix N, Girotto G, Podda L, Paparo C, Bozzi V, Pastore A, Balduini CL, Seri M, Savoia A. Pecci A, et al. Among authors: balduini cl. Eur J Haematol. 2010 Apr;84(4):291-7. doi: 10.1111/j.1600-0609.2009.01398.x. Epub 2009 Dec 11. Eur J Haematol. 2010. PMID: 20002731 Clinical Trial.

8

Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias.

Balduini CL, Pecci A, Savoia A. Balduini CL, et al. Br J Haematol. 2011 Jul;154(2):161-74. doi: 10.1111/j.1365-2141.2011.08716.x. Epub 2011 May 4. Br J Haematol. 2011. PMID: 21542825 Free article. Review.

9

Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cells.

Pecci A, Bozzi V, Panza E, Barozzi S, Gruppi C, Seri M, Balduini CL. Pecci A, et al. Among authors: balduini cl. Thromb Haemost. 2011 Oct;106(4):693-704. doi: 10.1160/TH11-02-0126. Epub 2011 Aug 11. Thromb Haemost. 2011. PMID: 21833445

10

Short-term eltrombopag for surgical preparation of a patient with inherited thrombocytopenia deriving from MYH9 mutation.

Pecci A, Barozzi S, d'Amico S, Balduini CL. Pecci A, et al. Among authors: balduini cl. Thromb Haemost. 2012 Jun;107(6):1188-9. doi: 10.1160/TH12-01-0005. Epub 2012 Mar 8. Thromb Haemost. 2012. PMID: 22398565 No abstract available.

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