Margaglione M - Search Results

1

Genome-Wide Association Study Identifies First Locus Associated with Susceptibility to Cerebral Venous Thrombosis.

Ken-Dror G, Cotlarciuc I, Martinelli I, Grandone E, Hiltunen S, Lindgren E, Margaglione M, Duchez VLC, Triquenot AB, Zedde M, Mancuso M, Ruigrok YM, Marjot T, Worrall B, Majersik JJ, Metso TM, Putaala J, Haapaniemi E, Zuurbier SM, Brouwer MC, Passamonti SM, Abbattista M, Bucciarelli P, Mitchell BD, Kittner SJ, Lemmens R, Jern C, Pappalardo E, Costa P, Colombi M, de Sousa DA, Rodrigues S, Canhão P, Tkach A, Santacroce R, Favuzzi G, Arauz A, Colaizzo D, Spengos K, Hodge A, Ditta R, Pezzini A, Debette S, Coutinho JM, Thijs V, Jood K, Pare G, Tatlisumak T, Ferro JM, Sharma P. Ken-Dror G, et al. Among authors: margaglione m. Ann Neurol. 2021 Nov;90(5):777-788. doi: 10.1002/ana.26205. Epub 2021 Sep 29. Ann Neurol. 2021. PMID: 34459509 Free PMC article.

2

Plasma predictors of ischemic complications of atherosclerosis: open issues.

Margaglione M, Grandone E, Di Minno G. Margaglione M, et al. Biomed Pharmacother. 1993;47(10):445-9. doi: 10.1016/0753-3322(93)90341-h. Biomed Pharmacother. 1993. PMID: 8061244 Review.

3

Drugs affecting plasma fibrinogen levels. Implications for new antithrombotic strategies.

Margaglione M, Grandone E, Mancini FP, Di Minno G. Margaglione M, et al. Prog Drug Res. 1996;46:169-81. doi: 10.1007/978-3-0348-8996-4_4. Prog Drug Res. 1996. PMID: 8754205 Review.

4

Factor V Leiden is associated with repeated and recurrent unexplained fetal losses.

Grandone E, Margaglione M, Colaizzo D, d'Addedda M, Cappucci G, Vecchione G, Sciannamé N, Pavone G, Di Minno G. Grandone E, et al. Among authors: margaglione m. Thromb Haemost. 1997 May;77(5):822-4. Thromb Haemost. 1997. PMID: 9184385

5

Clinical relevance of polymorphic markers of arterial thrombosis.

Di Minno G, Grandone E, Margaglione M. Di Minno G, et al. Among authors: margaglione m. Thromb Haemost. 1997 Jul;78(1):462-6. Thromb Haemost. 1997. PMID: 9198197 Review.

6

Factor V Leiden, C > T MTHFR polymorphism and genetic susceptibility to preeclampsia.

Grandone E, Margaglione M, Colaizzo D, Cappucci G, Paladini D, Martinelli P, Montanaro S, Pavone G, Di Minno G. Grandone E, et al. Among authors: margaglione m. Thromb Haemost. 1997 Jun;77(6):1052-4. Thromb Haemost. 1997. PMID: 9241730

7

The PAI-1 gene locus 4G/5G polymorphism is associated with a family history of coronary artery disease.

Margaglione M, Cappucci G, Colaizzo D, Giuliani N, Vecchione G, Grandone E, Pennelli O, Di Minno G. Margaglione M, et al. Arterioscler Thromb Vasc Biol. 1998 Feb;18(2):152-6. doi: 10.1161/01.atv.18.2.152. Arterioscler Thromb Vasc Biol. 1998. PMID: 9484978

8

Relation between PAI-1 gene locus polymorphism and family history of coronary artery disease.

Margaglione M, Grandone E, Di Minno G. Margaglione M, et al. Ann Intern Med. 1998 Mar 15;128(6):508-9. doi: 10.7326/0003-4819-128-6-199803150-00028. Ann Intern Med. 1998. PMID: 9499345 No abstract available.

9

The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation.

Margaglione M, D'Andrea G, d'Addedda M, Giuliani N, Cappucci G, Iannaccone L, Vecchione G, Grandone E, Brancaccio V, Di Minno G. Margaglione M, et al. Thromb Haemost. 1998 May;79(5):907-11. Thromb Haemost. 1998. PMID: 9609218

10

Reduction of mononuclear cytokine production in hemodialysis patients treated with steam-sterilized low-flux polysulphone membranes.

Aucella F, Vigilante M, Grandone E, Colaizzo D, Margaglione M, Modoni S, Orlandini G, Stallone C. Aucella F, et al. Among authors: margaglione m. Int J Artif Organs. 1998 Apr;21(4):210-5. Int J Artif Organs. 1998. PMID: 9649062 Clinical Trial.

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