Savoia A - Search Results

1

International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country.

Glembotsky AC, Marta RF, Pecci A, De Rocco D, Gnan C, Espasandin YR, Goette NP, Negro F, Noris P, Savoia A, Balduini CL, Molinas FC, Heller PG. Glembotsky AC, et al. Among authors: savoia a. J Thromb Haemost. 2012 Aug;10(8):1653-61. doi: 10.1111/j.1538-7836.2012.04805.x. J Thromb Haemost. 2012. PMID: 22672365 Free article.

2

The gene for May-Hegglin anomaly localizes to a <1-Mb region on chromosome 22q12.3-13.1.

Martignetti JA, Heath KE, Harris J, Bizzaro N, Savoia A, Balduini CL, Desnick RJ. Martignetti JA, et al. Among authors: savoia a. Am J Hum Genet. 2000 Apr;66(4):1449-54. doi: 10.1086/302873. Epub 2000 Mar 17. Am J Hum Genet. 2000. PMID: 10739770 Free PMC article.

3

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.

Seri M, Cusano R, Gangarossa S, Caridi G, Bordo D, Lo Nigro C, Ghiggeri GM, Ravazzolo R, Savino M, Del Vecchio M, d'Apolito M, Iolascon A, Zelante LL, Savoia A, Balduini CL, Noris P, Magrini U, Belletti S, Heath KE, Babcock M, Glucksman MJ, Aliprandis E, Bizzaro N, Desnick RJ, Martignetti JA. Seri M, et al. Among authors: savoia a. Nat Genet. 2000 Sep;26(1):103-5. doi: 10.1038/79063. Nat Genet. 2000. PMID: 10973259

4

Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome.

Savoia A, Balduini CL, Savino M, Noris P, Del Vecchio M, Perrotta S, Belletti S, Poggi, Iolascon A. Savoia A, et al. Blood. 2001 Mar 1;97(5):1330-5. doi: 10.1182/blood.v97.5.1330. Blood. 2001. PMID: 11222377 Free article.

5

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: savoia a. 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.

6

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: savoia a. Hum Genet. 2002 Feb;110(2):182-6. doi: 10.1007/s00439-001-0659-1. Epub 2001 Dec 14. Hum Genet. 2002. PMID: 11935325

7

Inherited thrombocytopenias: from genes to therapy.

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

8

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: savoia a. Haematologica. 2002 Sep;87(9):943-7. Haematologica. 2002. PMID: 12217806

9

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

10

Inherited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle Piastrine.

Balduini CL, Cattaneo M, Fabris F, Gresele P, Iolascon A, Pulcinelli FM, Savoia A; Italian Gruppo di Studio delle Piastrine. Balduini CL, et al. Among authors: savoia a. Haematologica. 2003 May;88(5):582-92. Haematologica. 2003. PMID: 12745278

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