Margaglione M - Search Results

1

A myoferlin gain-of-function variant associates with a new type of hereditary angioedema.

Ariano A, D'Apolito M, Bova M, Bellanti F, Loffredo S, D'Andrea G, Intrieri M, Petraroli A, Maffione AB, Spadaro G, Santacroce R, Margaglione M. Ariano A, et al. Among authors: margaglione m. Allergy. 2020 Nov;75(11):2989-2992. doi: 10.1111/all.14454. Epub 2020 Jul 1. Allergy. 2020. PMID: 32542751 No abstract available.

2

A comprehensive on-line digestion-liquid chromatography/mass spectrometry/collision-induced dissociation mass spectrometry approach for the characterization of human fibrinogen.

Vecchione G, Casetta B, Santacroce R, Margaglione M. Vecchione G, et al. Among authors: margaglione m. Rapid Commun Mass Spectrom. 2001;15(16):1383-90. doi: 10.1002/rcm.355. Rapid Commun Mass Spectrom. 2001. PMID: 11507749

3

The factor V (FV) gene ASP79HIS polymorphism modulates FV plasma levels and affects the activated protein C resistance phenotype in presence of the FV Leiden mutation.

Bossone A, Cappucci F, D'Andrea G, Brancaccio V, Cibelli G, Iannaccone L, Grandone E, Margaglione M. Bossone A, et al. Among authors: margaglione m. Haematologica. 2003 Mar;88(3):286-9. Haematologica. 2003. PMID: 12651267

4

Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism.

D'Andrea G, Margaglione M; Glansmann's Thrombasthemia Italian Team (GLATIT). D'Andrea G, et al. Among authors: margaglione m. Haematologica. 2003 Dec;88(12):1378-82. Haematologica. 2003. PMID: 14687991

5

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin.

D'Andrea G, D'Ambrosio RL, Di Perna P, Chetta M, Santacroce R, Brancaccio V, Grandone E, Margaglione M. D'Andrea G, et al. Among authors: margaglione m. Blood. 2005 Jan 15;105(2):645-9. doi: 10.1182/blood-2004-06-2111. Epub 2004 Sep 9. Blood. 2005. PMID: 15358623 Free article. Clinical Trial.

6

Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.

Santacroce R, Cappucci F, Pisanelli D, Perricone F, Papa ML, Santoro R, Grandone E, Margaglione M. Santacroce R, et al. Among authors: margaglione m. Blood Coagul Fibrinolysis. 2006 Jun;17(4):235-40. doi: 10.1097/01.mbc.0000224841.48463.be. Blood Coagul Fibrinolysis. 2006. PMID: 16651864

7

Low protein Z levels and risk of occurrence of deep vein thrombosis.

Santacroce R, Sarno M, Cappucci F, Sessa F, Colaizzo D, Brancaccio V, Grandone E, Margaglione M. Santacroce R, et al. Among authors: margaglione m. J Thromb Haemost. 2006 Nov;4(11):2417-22. doi: 10.1111/j.1538-7836.2006.02186.x. Epub 2006 Aug 25. J Thromb Haemost. 2006. PMID: 16938126 Free article. Clinical Trial.

8

A new case of combined factor V and factor VIII deficiency further suggests that the LMAN1 M1T mutation is a frequent cause in Italian patients.

D'Ambrosio R, Santacroce R, Di Perna P, Sarno M, Romondia A, Margaglione M. D'Ambrosio R, et al. Among authors: margaglione m. Blood Coagul Fibrinolysis. 2007 Mar;18(2):203-4. doi: 10.1097/MBC.0b013e328012b615. Blood Coagul Fibrinolysis. 2007. PMID: 17287640

9

Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes.

Zefferino R, Piccaluga S, Lasalvia M, D' Andrea G, Margaglione M, Ambrosi L. Zefferino R, et al. Among authors: margaglione m. Int J Immunopathol Pharmacol. 2006 Oct-Dec;19(4 Suppl):15-20. Int J Immunopathol Pharmacol. 2006. PMID: 17291401

10

Oral anticoagulants: Pharmacogenetics Relationship between genetic and non-genetic factors.

D'Andrea G, D'Ambrosio R, Margaglione M. D'Andrea G, et al. Among authors: margaglione m. Blood Rev. 2008 May;22(3):127-40. doi: 10.1016/j.blre.2007.11.004. Epub 2008 Jan 30. Blood Rev. 2008. PMID: 18234403 Review.

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