Baronciani L - Search Results

1

Abnormal VWF modifies megakaryocytopoiesis: studies of platelets and megakaryocyte cultures from patients with von Willebrand disease type 2B.

Nurden P, Gobbi G, Nurden A, Enouf J, Youlyouz-Marfak I, Carubbi C, La Marca S, Punzo M, Baronciani L, De Marco L, Vitale M, Federici AB. Nurden P, et al. Among authors: baronciani l. Blood. 2010 Apr 1;115(13):2649-56. doi: 10.1182/blood-2009-07-231886. Epub 2010 Jan 29. Blood. 2010. PMID: 20118404 Free article.

2

Erratum to 'A comparative study in type 2 von Willebrand disease patients using four different platelet-dependent von Willebrand factor assays.' [Research and Practice in Thrombosis and Haemostasis Volume 7, Issue 3, March 2023, 100139].

Colpani P, Baronciani L, Stufano F, Cozzi G, Boscarino M, Pagliari MT, Biguzzi E, Peyvandi F. Colpani P, et al. Among authors: baronciani l. Res Pract Thromb Haemost. 2023 Jul 8;7(5):102141. doi: 10.1016/j.rpth.2023.102141. eCollection 2023 Jul. Res Pract Thromb Haemost. 2023. PMID: 37601023 Free PMC article.

3

Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease.

Baronciani L, Cozzi G, Canciani MT, Peyvandi F, Srivastava A, Federici AB, Mannucci PM. Baronciani L, et al. Thromb Haemost. 2000 Oct;84(4):536-40. Thromb Haemost. 2000. PMID: 11057846

4

Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients.

Baronciani L, Cozzi G, Canciani MT, Peyvandi F, Srivastava A, Federici AB, Mannucci PM. Baronciani L, et al. Blood Cells Mol Dis. 2003 May-Jun;30(3):264-70. doi: 10.1016/s1079-9796(03)00033-0. Blood Cells Mol Dis. 2003. PMID: 12737944

5

An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees.

Kunicki TJ, Federici AB, Salomon DR, Koziol JA, Head SR, Mondala TS, Chismar JD, Baronciani L, Canciani MT, Peake IR. Kunicki TJ, et al. Among authors: baronciani l. Blood. 2004 Oct 15;104(8):2359-67. doi: 10.1182/blood-2004-01-0349. Epub 2004 Jun 29. Blood. 2004. PMID: 15226188 Free article.

6

A new candidate mutation, G1629R, in a patient with type 2A von Willebrand's disease: basic mechanisms and clinical implications.

Hilbert L, Federici AB, Baronciani L, Dallagiovanna S, Mazurier C. Hilbert L, et al. Among authors: baronciani l. Haematologica. 2004 Sep;89(9):1128-33. Haematologica. 2004. PMID: 15377475 Free article.

7

Expression studies on a novel type 2B variant of the von Willebrand factor gene (R1308L) characterized by defective collagen binding.

Baronciani L, Federici AB, Beretta M, Cozzi G, Canciani MT, Mannucci PM. Baronciani L, et al. J Thromb Haemost. 2005 Dec;3(12):2689-94. doi: 10.1111/j.1538-7836.2005.01638.x. Epub 2005 Oct 25. J Thromb Haemost. 2005. PMID: 16246252 Free article.

8

An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigrees.

Kunicki TJ, Baronciani L, Canciani MT, Gianniello F, Head SR, Mondala TS, Salomon DR, Federici AB. Kunicki TJ, et al. Among authors: baronciani l. J Thromb Haemost. 2006 Jan;4(1):137-47. doi: 10.1111/j.1538-7836.2005.01675.x. J Thromb Haemost. 2006. PMID: 16409463 Free article.

9

von Willebrand disease type 2B must be always considered in the differential diagnosis of genetic thrombocytopenias with giant platelets.

Loffredo G, Baronciani L, Noris P, Menna F, Federici AB, Balduini CL. Loffredo G, et al. Among authors: baronciani l. Platelets. 2006 May;17(3):149-52. doi: 10.1080/09537100500441150. Platelets. 2006. PMID: 16702040 Free article.

10

Molecular mapping of the chloride-binding site in von Willebrand factor (VWF): energetics and conformational effects on the VWF/ADAMTS-13 interaction.

De Cristofaro R, Peyvandi F, Baronciani L, Palla R, Lavoretano S, Lombardi R, Di Stasio E, Federici AB, Mannucci PM. De Cristofaro R, et al. Among authors: baronciani l. J Biol Chem. 2006 Oct 13;281(41):30400-11. doi: 10.1074/jbc.M603321200. Epub 2006 Aug 9. J Biol Chem. 2006. PMID: 16899464 Free article.

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