1 - 25 of 69 results for author:"Margaglione M." in Literature citations
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| 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. 18:510-513(2012) · Mapped (3) |
| F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis. Gouw S.C., van den Berg H.M., Oldenburg J., Astermark J., de Groot P.G., Margaglione M., Thompson A.R., van Heerde W., Boekhorst J., Miller C.H. et al. Blood 119:2922-2934(2012) · Mapped (12) |
| Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family. Cafolla A., D'Andrea G., Baldacci E., Margaglione M., Mazzucconi M.G., Foa R. Eur. J. Haematol. 88:336-339(2012) · Mapped (33) |
| Sex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosis. Colaizzo D., Tiscia G.L., Bafunno V., Amitrano L., Vergura P., Lupone M.R., Grandone E., Guardascione M.A., Margaglione M. Thromb. Res. 128:233-236(2011) · Mapped (6) |
| The spectrum of subclinical Best vitelliform macular dystrophy in subjects with mutations in BEST1 gene. Querques G., Zerbib J., Santacroce R., Margaglione M., Delphin N., Querques L., Rozet J.M., Kaplan J., Souied E.H. Invest. Ophthalmol. Vis. Sci. 52:4678-4684(2011) · Mapped (9) |
| Gene polymorphisms and sport attitude in Italian athletes. Sessa F., Chetta M., Petito A., Franzetti M., Bafunno V., Pisanelli D., Sarno M., Iuso S., Margaglione M. Genet Test Mol Biomarkers 15:285-290(2011) · Mapped (8) |
| 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. J. Thromb. Haemost. 9:496-501(2011) · Mapped (6) |
| 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. 203:461.e1-5(2010) · Mapped (3) |
| The haplotype M2 within the ANXA5 gene is independently associated with the occurrence of deep venous thrombosis. Grandone E., Tiscia G., Colaizzo D., Vergura P., Pisanelli D., Margaglione M. Thromb. Haemost. 103:1102-1103(2010) · Mapped (24) |
| New TET2 gene mutations in patients with myeloproliferative neoplasms and splanchnic vein thrombosis. Colaizzo D., Tiscia G.L., Pisanelli D., Bafunno V., Amitrano L., Grandone E., Guardascione M.A., Margaglione M. J. Thromb. Haemost. 8:1142-1144(2010) · Mapped (2) |
| Functional and clinical data of Best vitelliform macular dystrophy patients with mutations in the BEST1 gene. Querques G., Zerbib J., Santacroce R., Margaglione M., Delphin N., Rozet J.M., Kaplan J., Martinelli D., Delle Noci N., Soubrane G. et al. Mol. Vis. 15:2960-2972(2009) · Mapped (9) |
| Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. Bafunno V., Santacroce R., Chetta M., D'Andrea G., Pisanelli D., Sessa F., Trotta T., Tagariello G., Peyvandi F., Margaglione M. Haemophilia 16:469-473(2010) · Mapped (42) |
| The JAK2 rs12343867 CC genotype frequently occurs in patients with splanchnic venous thrombosis without the JAK2V617F mutation: a retrospective study. Colaizzo D., Tiscia G.L., Bafunno V., Amitrano L., Vergura P., Grandone E., Guardascione M.A., Margaglione M. J. Thromb. Haemost. 8:413-416(2010) · Mapped (27) |
| Factor VIII gene (F8) mutations as predictors of outcome in immune tolerance induction of hemophilia A patients with high-responding inhibitors. Coppola A., Margaglione M., Santagostino E., Rocino A., Grandone E., Mannucci P.M., Di Minno G. J. Thromb. Haemost. 7:1809-1815(2009) · Mapped (12) |
| Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification. Santacroce R., Longo V., Bafunno V., Sessa F., Chetta M., Sarno M., Bukvic N., D'Andrea G., Tomaiuolo M., Margaglione M. Genet Test Mol Biomarkers 13:573-576(2009) · Mapped (12) |
| Haplotype M2 in the annexin A5 (ANXA5) gene and the occurrence of obstetric complications. Tiscia G., Colaizzo D., Chinni E., Pisanelli D., Scianname N., Favuzzi G., Margaglione M., Grandone E. Thromb. Haemost. 102:309-313(2009) · Mapped (3) |
| Protein Z g-42a variant and the risk of pregnancy-related venous thromboembolism in a cohort of Italian patients. Grandone E., Favuzzi G., De Stefano V., Chinni E., Rossi E., Cappucci F., Margaglione M. Thromb. Res. 123:848-850(2009) · Mapped (1) |
| A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. D'Andrea G., Bafunno V., Del Vecchio L., Amoriello A., Morabito P., Vecchione G., Grandone E., Margaglione M. Blood Coagul. Fibrinolysis 19:657-662(2008) · Mapped (5) |
| Occurrence of the JAK2 V617F mutation in the Budd-Chiari syndrome. Colaizzo D., Amitrano L., Tiscia G.L., Iannaccone L., Gallone A., Grandone E., Guardascione M.A., Margaglione M. Blood Coagul. Fibrinolysis 19:459-462(2008) · Mapped (6) |
| Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism. Piccoli C., Ripoli M., Quarato G., Scrima R., D'Aprile A., Boffoli D., Margaglione M., Criscuolo C., De Michele G., Sardanelli A. et al. J. Med. Genet. 45:596-602(2008) · Mapped (1) |
| Identification of GLA gene deletions in Fabry patients by Multiplex Ligation-dependent Probe Amplification (MLPA). Schirinzi A., Centra M., Prattichizzo C., Gigante M., De Fabritiis M., Giancaspro V., Petrarulo F., Santacroce R., Margaglione M., Gesualdo L. et al. Mol. Genet. Metab. 94:382-385(2008) · Mapped (5) |
| Annexin V expression in human placenta is influenced by the carriership of the common haplotype M2. Chinni E., Tiscia G.L., Colaizzo D., Vergura P., Margaglione M., Grandone E. Fertil. Steril. 91:940-942(2009) · Mapped (3) |
| An unreported mutation within protein Z gene is associated with very low protein levels in women with fetal loss. Grandone E., Colaizzo D., Cappucci F., D'Ambrosio R.L., Vecchione G., Margaglione M. Fertil. Steril. 90:864-865(2008) · Mapped (6) |
| Screening of mutations of hemophilia A in 40 Italian patients: a novel G-to-A mutation in intron 10 of the F8 gene as a putative cause of mild hemophilia A in southern Italy. Santacroce R., Santoro R., Sessa F., Iannaccaro P., Sarno M., Longo V., Gallone A., Vecchione G., Muleo G., Margaglione M. Blood Coagul. Fibrinolysis 19:197-202(2008) · Mapped (12) |
| The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype. Margaglione M., Castaman G., Morfini M., Rocino A., Santagostino E., Tagariello G., Tagliaferri A.R., Zanon E., Bicocchi M.P., Castaldo G. et al. Haematologica 93:722-728(2008) · Mapped (12) |