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Items: 1 to 20 of 90


Factor VII deficiency: a novel missense variant and genotype-phenotype correlation in patients from Southern Italy.

Tiscia G, Favuzzi G, Chinni E, Colaizzo D, Fischetti L, Intrieri M, Margaglione M, Grandone E.

Hum Genome Var. 2017 Nov 2;4:17048. doi: 10.1038/hgv.2017.48. eCollection 2017.


Ultrasound-guided fine-needle aspiration biopsy of thyroid nodules in patients on oral anticoagulants.

Grandone E, Barcellona D, Colaizzo D, Marongiu F.

J Endocrinol Invest. 2017 Jul;40(7):785-786. doi: 10.1007/s40618-017-0610-5. Epub 2017 Feb 17. No abstract available.


Towards the genetic basis of cerebral venous thrombosis-the BEAST Consortium: a study protocol.

Cotlarciuc I, Marjot T, Khan MS, Hiltunen S, Haapaniemi E, Metso TM, Putaala J, Zuurbier SM, Brouwer MC, Passamonti SM, Bucciarelli P, Pappalardo E, Patel T, Costa P, Colombi M, Canhão P, Tkach A, Santacroce R, Margaglione M, Favuzzi G, Grandone E, Colaizzo D, Spengos K, Arauz A, Hodge A, Ditta R, Debette S, Zedde M, Pare G, Ferro JM, Thijs V, Pezzini A, Majersik JJ, Martinelli I, Coutinho JM, Tatlisumak T, Sharma P; ISGC (International Stroke Genetics Consortium) and BEAST investigators.

BMJ Open. 2016 Nov 22;6(11):e012351. doi: 10.1136/bmjopen-2016-012351.


Postpartum haemorrhage in a woman with essential thrombocythemia carrying calreticulin mutation: a case report.

Villani M, Colaizzo D, Tiscia GL, Chinni E, Bodenizza C, Cascavilla N, Grandone E.

Blood Coagul Fibrinolysis. 2016 Sep;27(6):727-8. doi: 10.1097/MBC.0000000000000473.


Pregnancy-related venous thrombosis: comparison between spontaneous and ART conception in an Italian cohort.

Villani M, Dentali F, Colaizzo D, Tiscia GL, Vergura P, Petruccelli T, Petruzzelli F, Ageno W, Margaglione M, Grandone E.

BMJ Open. 2015 Oct 6;5(10):e008213. doi: 10.1136/bmjopen-2015-008213.


Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis.

Colaizzo D, Amitrano L, Guardascione MA, Favuzzi G, Tiscia GL, D'Andrea G, Santacroce R, Grandone E, Margaglione M.

Thromb Haemost. 2015 Jun;113(6):1381-2. doi: 10.1160/TH14-12-1055. Epub 2015 Mar 12. No abstract available.


Influence of hCG on inducible nitric oxide synthase gene expression in ram testicular arteries.

Matteo M, Rizzo A, Cicinelli E, Grandone E, Cardo G, Colaizzo D, Minoia G, Castellana L, Indraccolo U, Marrocchella S, Greco P, Sciorsci RL.

Arch Ital Urol Androl. 2014 Sep 30;86(3):183-7. doi: 10.4081/aiua.2014.3.183.


Low-molecular -weight heparin in pregnancies after ART -a retrospective study-.

Grandone E, Villani M, Dentali F, Tiscia GL, Colaizzo D, Cappucci F, Fischetti L, Ageno W, Margaglione M.

Thromb Res. 2014 Aug;134(2):336-9. doi: 10.1016/j.thromres.2014.06.004. Epub 2014 Jun 11.


Clinical utility of antithrombotic prophylaxis in ART procedures: an Italian experience.

Grandone E, Villani M, Tiscia GL, Dentali F, Colaizzo D, Cappucci F, Fischetti L, Ageno W, Margaglione M.

PLoS One. 2014 May 28;9(5):e97604. doi: 10.1371/journal.pone.0097604. eCollection 2014.


Clinical Pregnancies and Live Births in women approaching ART: a follow-up analysis of 157 women after thrombophilia screening.

Grandone E, Villani M, Tiscia GL, Dentali F, Colaizzo D, Cappucci F, Chinni E, Ageno W, Margaglione M.

Thromb Res. 2014 Feb;133(2):168-72. doi: 10.1016/j.thromres.2013.11.016. Epub 2013 Nov 22.


Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation.

Colaizzo D, Amitrano L, Guardascione MA, Tiscia GL, D'Andrea G, Longo VA, Grandone E, Margaglione M.

Thromb Res. 2013 Aug;132(2):e99-e104. doi: 10.1016/j.thromres.2013.07.014. Epub 2013 Aug 1.


TET2 mutations in Ph-negative myeloproliferative neoplasms: identification of three novel mutations and relationship with clinical and laboratory findings.

Patriarca A, Colaizzo D, Tiscia G, Spadano R, Di Zacomo S, Spadano A, Villanova I, Margaglione M, Grandone E, Dragani A.

Biomed Res Int. 2013;2013:929840. doi: 10.1155/2013/929840. Epub 2013 May 25.


The M2 haplotype in the ANXA5 gene is an independent risk factor for idiopathic small-for-gestational age newborns.

Tiscia G, Colaizzo D, Favuzzi G, Vergura P, Martinelli P, Margaglione M, Grandone E.

Mol Hum Reprod. 2012 Oct;18(10):510-3. Epub 2012 Jun 7.


Aspirin for preventing the recurrence of venous thromboembolism.

Becattini C, Agnelli G, Schenone A, Eichinger S, Bucherini E, Silingardi M, Bianchi M, Moia M, Ageno W, Vandelli MR, Grandone E, Prandoni P; WARFASA Investigators.

N Engl J Med. 2012 May 24;366(21):1959-67. doi: 10.1056/NEJMoa1114238. Erratum in: N Engl J Med. 2012 Oct 18;367(16):1573.


Risk of obstetric and thromboembolic complications in family members of women with previous adverse obstetric outcomes carrying common inherited thombophilias.

Villani M, Tiscia GL, Margaglione M, Colaizzo D, Fischetti L, Vergura P, Grandone E.

J Thromb Haemost. 2012 Feb;10(2):223-8. doi: 10.1111/j.1538-7836.2011.04583.x.


Sex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis.

Colaizzo D, Tiscia GL, Bafunno V, Amitrano L, Vergura P, Lupone MR, Grandone E, Guardascione MA, Margaglione M.

Thromb Res. 2011 Sep;128(3):233-6. doi: 10.1016/j.thromres.2011.03.024. Epub 2011 Apr 16.


Increased warfarin consumption and residual fibrin turnover in thrombotic patients with primary antiphospholipid syndrome.

Ames PR, Margaglione M, Ciampa A, Colaizzo D, Ferrara F, Iannaccone L, Vincenzobrancaccio.

Thromb Res. 2011 Jun;127(6):595-9. doi: 10.1016/j.thromres.2011.01.014. Epub 2011 Mar 2.


Subclinical atherosclerosis and genetic risk markers in healthy offspring of patients with premature myocardial infarction.

Barra S, Scala S, Cuomo V, Guarini P, Colaizzo D, Margaglione M, Materazzi C, Vitagliano G, Gaeta G, Faiella A.

Minerva Cardioangiol. 2011 Apr;59(2):127-34.


Impact of common thrombophilias and JAK2 V617F on pregnancy outcomes in unselected Italian women.

Grandone E, Colaizzo D, Tiscia G, Vergura P, Cappucci F, Greco L, Margaglione M, Martinelli P; PRENACEL Study Group.

J Thromb Haemost. 2011 Mar;9(3):496-501. doi: 10.1111/j.1538-7836.2011.04183.x.


Role of the M2 haplotype within the annexin A5 gene in the occurrence of pregnancy-related venous thromboembolism.

Grandone E, Tiscia G, Colaizzo D, Chinni E, Pisanelli D, Bafunno V, Margaglione M.

Am J Obstet Gynecol. 2010 Nov;203(5):461.e1-5. doi: 10.1016/j.ajog.2010.06.007.


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