Pecci A - Search Results

1

A A386G biallelic GPIbα gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesis.

Vettore S, Tezza F, Malara A, Vianello F, Pecci A, Scandellari R, Floris M, Balduini A, Fabris F. Vettore S, et al. Among authors: pecci a. Haematologica. 2011 Dec;96(12):1878-82. doi: 10.3324/haematol.2010.039008. Epub 2011 Oct 11. Haematologica. 2011. PMID: 21993687 Free PMC article. Clinical Trial.

2

Defective expression of GPIb/IX/V complex in platelets from patients with May-Hegglin anomaly and Sebastian syndrome.

Di Pumpo M, Noris P, Pecci A, Savoia A, Seri M, Ceresa IF, Balduini CL. Di Pumpo M, et al. Among authors: pecci a. Haematologica. 2002 Sep;87(9):943-7. Haematologica. 2002. PMID: 12217806

3

Expression, activation, and subcellular localization of the Rap1 GTPase in cord blood-derived human megakaryocytes.

Balduini A, Pecci A, Lova P, Arezzi N, Marseglia C, Bellora F, Perotti C, Balduini C, Balduini CL, Torti M. Balduini A, et al. Among authors: pecci a. Exp Cell Res. 2004 Oct 15;300(1):84-93. doi: 10.1016/j.yexcr.2004.07.011. Exp Cell Res. 2004. PMID: 15383317

4

Application of a diagnostic algorithm for inherited thrombocytopenias to 46 consecutive patients.

Noris P, Pecci A, Di Bari F, Di Stazio MT, Di Pumpo M, Ceresa IF, Arezzi N, Ambaglio C, Savoia A, Balduini CL. Noris P, et al. Among authors: pecci a. Haematologica. 2004 Oct;89(10):1219-25. Haematologica. 2004. PMID: 15477207

5

Altered cytoskeleton organization in platelets from patients with MYH9-related disease.

Canobbio I, Noris P, Pecci A, Balduini A, Balduini CL, Torti M. Canobbio I, et al. Among authors: pecci a. J Thromb Haemost. 2005 May;3(5):1026-35. doi: 10.1111/j.1538-7836.2005.01244.x. J Thromb Haemost. 2005. PMID: 15869600 Free article.

6

Pathogenetic mechanisms of hematological abnormalities of patients with MYH9 mutations.

Pecci A, Canobbio I, Balduini A, Stefanini L, Cisterna B, Marseglia C, Noris P, Savoia A, Balduini CL, Torti M. Pecci A, et al. Hum Mol Genet. 2005 Nov 1;14(21):3169-78. doi: 10.1093/hmg/ddi344. Epub 2005 Sep 14. Hum Mol Genet. 2005. PMID: 16162639

7

Adhesive receptors, extracellular proteins and myosin IIA orchestrate proplatelet formation by human megakaryocytes.

Balduini A, Pallotta I, Malara A, Lova P, Pecci A, Viarengo G, Balduini CL, Torti M. Balduini A, et al. Among authors: pecci a. J Thromb Haemost. 2008 Nov;6(11):1900-7. doi: 10.1111/j.1538-7836.2008.03132.x. Epub 2008 Aug 22. J Thromb Haemost. 2008. PMID: 18752571 Free article.

8

Proplatelet formation in heterozygous Bernard-Soulier syndrome type Bolzano.

Balduini A, Malara A, Pecci A, Badalucco S, Bozzi V, Pallotta I, Noris P, Torti M, Balduini CL. Balduini A, et al. Among authors: pecci a. J Thromb Haemost. 2009 Mar;7(3):478-84. doi: 10.1111/j.1538-7836.2008.03255.x. Epub 2008 Dec 4. J Thromb Haemost. 2009. PMID: 19067792 Free article.

9

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. Thromb Haemost. 2009 Jul;102(1):90-6. doi: 10.1160/TH09-01-0068. Thromb Haemost. 2009. PMID: 19572073

10

Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder.

Savoia A, De Rocco D, Panza E, Bozzi V, Scandellari R, Loffredo G, Mumford A, Heller PG, Noris P, De Groot MR, Giani M, Freddi P, Scognamiglio F, Riondino S, Pujol-Moix N, Fabris F, Seri M, Balduini CL, Pecci A. Savoia A, et al. Among authors: pecci a. Thromb Haemost. 2010 Apr;103(4):826-32. doi: 10.1160/TH09-08-0593. Epub 2010 Feb 19. Thromb Haemost. 2010. PMID: 20174760

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