Balduini CL - Search Results

1

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: balduini cl. Medicine (Baltimore). 2003 May;82(3):203-15. doi: 10.1097/01.md.0000076006.64510.5c. Medicine (Baltimore). 2003. PMID: 12792306 Free 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. Among authors: balduini cl. 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

Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene.

Seri M, Savino M, Bordo D, Cusano R, Rocca B, Meloni I, Di Bari F, Koivisto PA, Bolognesi M, Ghiggeri GM, Landolfi R, Balduini CL, Zelante L, Ravazzolo R, Renieri A, Savoia A. Seri M, et al. Among authors: balduini cl. Hum Genet. 2002 Feb;110(2):182-6. doi: 10.1007/s00439-001-0659-1. Epub 2001 Dec 14. Hum Genet. 2002. PMID: 11935325

4

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: balduini cl. Haematologica. 2002 Sep;87(9):943-7. Haematologica. 2002. PMID: 12217806

5

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: balduini cl. Am J Kidney Dis. 2003 Jan;41(1):95-104. doi: 10.1053/ajkd.2003.50028. Am J Kidney Dis. 2003. PMID: 12500226

6

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

7

Inherited thrombocytopenias: from genes to therapy.

Balduini CL, Iolascon A, Savoia A. Balduini CL, et al. Haematologica. 2002 Aug;87(8):860-80. Haematologica. 2002. PMID: 12161364 Review.

8

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: balduini cl. Genomics. 2004 Jun;83(6):1125-33. doi: 10.1016/j.ygeno.2003.12.012. Genomics. 2004. PMID: 15177565

9

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. Among authors: balduini cl, balduini a. 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

10

Identification of the first duplication in MYH9-related disease: a hot spot for unequal crossing-over within exon 24 of the MYH9 gene.

De Rocco D, Pujol-Moix N, Pecci A, Faletra F, Bozzi V, Balduini CL, Savoia A. De Rocco D, et al. Among authors: balduini cl. Eur J Med Genet. 2009 Jul-Aug;52(4):191-4. doi: 10.1016/j.ejmg.2009.01.006. Epub 2009 Feb 9. Eur J Med Genet. 2009. PMID: 19450438

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