Pecci A - Search Results

1

Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2.

Pippucci T, Savoia A, Perrotta S, Pujol-Moix N, Noris P, Castegnaro G, Pecci A, Gnan C, Punzo F, Marconi C, Gherardi S, Loffredo G, De Rocco D, Scianguetta S, Barozzi S, Magini P, Bozzi V, Dezzani L, Di Stazio M, Ferraro M, Perini G, Seri M, Balduini CL. Pippucci T, et al. Among authors: pecci a. Am J Hum Genet. 2011 Jan 7;88(1):115-20. doi: 10.1016/j.ajhg.2010.12.006. Am J Hum Genet. 2011. PMID: 21211618 Free PMC article.

2

Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders.

Pecci A, Noris P, Invernizzi R, Savoia A, Seri M, Ghiggeri GM, Sartore S, Gangarossa S, Bizzaro N, Balduini CL. Pecci A, et al. Br J Haematol. 2002 Apr;117(1):164-7. doi: 10.1046/j.1365-2141.2002.03385.x. Br J Haematol. 2002. PMID: 11918549 Free article.

3

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

4

Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome).

Ghiggeri GM, Caridi G, Magrini U, Sessa A, Savoia A, Seri M, Pecci A, Romagnoli R, Gangarossa S, Noris P, Sartore S, Necchi V, Ravazzolo R, Balduini CL. Ghiggeri GM, et al. Among authors: pecci a. Am J Kidney Dis. 2003 Jan;41(1):95-104. doi: 10.1053/ajkd.2003.50028. Am J Kidney Dis. 2003. PMID: 12500226

5

Seri M, Pecci A, Di Bari F, Cusano R, Savino M, Panza E, Nigro A, Noris P, Gangarossa S, Rocca B, Gresele P, Bizzaro N, Malatesta P, Koivisto PA, Longo I, Musso R, Pecoraro C, Iolascon A, Magrini U, Rodriguez Soriano J, Renieri A, Ghiggeri GM, Ravazzolo R, Balduini CL, Savoia A. Seri M, et al. Among authors: pecci a. Medicine (Baltimore). 2003 May;82(3):203-15. doi: 10.1097/01.md.0000076006.64510.5c. Medicine (Baltimore). 2003. PMID: 12792306 Free article.

6

Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis.

Balduini CL, Pecci A, Loffredo G, Izzo P, Noris P, Grosso M, Bergamaschi G, Rosti V, Magrini U, Ceresa IF, Conti V, Poggi V, Savoia A. Balduini CL, et al. Among authors: pecci a. Thromb Haemost. 2004 Jan;91(1):129-40. doi: 10.1160/TH03-05-0290. Thromb Haemost. 2004. PMID: 14691578

7

Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains.

Marigo V, Nigro A, Pecci A, Montanaro D, Di Stazio M, Balduini CL, Savoia A. Marigo V, et al. Among authors: pecci a. Genomics. 2004 Jun;83(6):1125-33. doi: 10.1016/j.ygeno.2003.12.012. Genomics. 2004. PMID: 15177565

8

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

9

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.

10

Dissecting clinical findings: platelet defects segregate independently of deafness and cataract in a family affected by an apparent syndromic form of macrothrombocytopenia.

Gangarossa S, Seri M, Pecci A, Di Bari F, Cusano R, Balduini C, Gasparini P, Savoia A. Gangarossa S, et al. Among authors: pecci a. Int J Mol Med. 2005 Sep;16(3):437-41. Int J Mol Med. 2005. PMID: 16077952

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