Sacchi E - Search Results

1

A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype.

Bernardi F, Faioni EM, Castoldi E, Lunghi B, Castaman G, Sacchi E, Mannucci PM. Bernardi F, et al. Among authors: sacchi e. Blood. 1997 Aug 15;90(4):1552-7. Blood. 1997. PMID: 9269773 Free article.

2

Protein S mRNA in patients with protein S deficiency.

Sacchi E, Pinotti M, Marchetti G, Merati G, Tagliabue L, Mannucci PM, Bernardi F. Sacchi E, et al. Thromb Haemost. 1995 May;73(5):746-9. Thromb Haemost. 1995. PMID: 7482397

3

Plasma factor VII levels are influenced by a polymorphism in the promoter region of the FVII gene.

Sacchi E, Tagliabue L, Scoglio R, Baroncini C, Coppola R, Bernardi F, Mannucci PM. Sacchi E, et al. Blood Coagul Fibrinolysis. 1996 Mar;7(2):114-7. doi: 10.1097/00001721-199603000-00002. Blood Coagul Fibrinolysis. 1996. PMID: 8735799

4

Resistance to activated protein C in nine thrombophilic families: interference in a protein S functional assay.

Faioni EM, Franchi F, Asti D, Sacchi E, Bernardi F, Mannucci PM. Faioni EM, et al. Among authors: sacchi e. Thromb Haemost. 1993 Dec 20;70(6):1067-71. Thromb Haemost. 1993. PMID: 8165605

5

The genetic defect of type I von Willebrand disease "Vicenza" is linked to the von Willebrand factor gene.

Randi AM, Sacchi E, Castaman GC, Rodeghiero F, Mannucci PM. Randi AM, et al. Among authors: sacchi e. Thromb Haemost. 1993 Feb 1;69(2):173-6. Thromb Haemost. 1993. PMID: 8456430

6

Two additional TaqI RFLPs in von Willebrand factor gene (VWF) and pseudogene.

Marchetti G, Sacchi E, Patracchini P, Randi AM, Sampietro M, Bernardi F. Marchetti G, et al. Among authors: sacchi e. Nucleic Acids Res. 1989 Apr 25;17(8):3329. doi: 10.1093/nar/17.8.3329. Nucleic Acids Res. 1989. PMID: 2566970 Free PMC article.

7

Prenatal diagnosis and carrier detection of hemophilia A.

Sampietro M, Sacchi E, Randi AM, Tagliavacca L, Stefanile C, Krachmalnicoff A, Travi M, Brambati B, Fiorelli G, Mannucci PM. Sampietro M, et al. Among authors: sacchi e. Curr Stud Hematol Blood Transfus. 1991;(58):84-7. doi: 10.1159/000419343. Curr Stud Hematol Blood Transfus. 1991. PMID: 1683275 No abstract available.

8

Carrier detection and feasibility of prenatal diagnosis of hemophilia B by multiplex polymerase chain reaction.

Tagliavacca L, Sacchi E, Mannucci PM. Tagliavacca L, et al. Among authors: sacchi e. Int J Clin Lab Res. 1993;23(3):169-71. doi: 10.1007/BF02592304. Int J Clin Lab Res. 1993. PMID: 8104543

9

High risk of cerebral-vein thrombosis in carriers of a prothrombin-gene mutation and in users of oral contraceptives.

Martinelli I, Sacchi E, Landi G, Taioli E, Duca F, Mannucci PM. Martinelli I, et al. Among authors: sacchi e. N Engl J Med. 1998 Jun 18;338(25):1793-7. doi: 10.1056/NEJM199806183382502. N Engl J Med. 1998. PMID: 9632445 Free article.

10

Diagnosis of hemophilia A in a female subject by using restriction fragment length polymorphisms linked to the factor VIII gene.

Randi AM, Sacchi E, Sampietro M, Papaleo G, Muleo G, Mannucci PM. Randi AM, et al. Among authors: sacchi e. Ric Clin Lab. 1989 Jan-Mar;19(1):75-9. doi: 10.1007/BF02871795. Ric Clin Lab. 1989. PMID: 2569759

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