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Results:
1-12
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Results: 12
Authors:
Martinelli, P
Grandone, E
Colaizzo, D
Paladini, D
Scianname, N
Margaglione, M
Di Minno, G
Citation: P. Martinelli et al., Familial thrombophilia and the occurrence of fetal growth restriction, HAEMATOLOG, 86(4), 2001, pp. 428-431
Authors:
Margaglione, M
Bossone, A
Cappucci, G
Colaizzo, D
Grandone, E
Di Minno, G
Citation: M. Margaglione et al., The effect of interleukin-6 C/G-174 polymorphism and circulating interleukin-6 on fibrinogen plasma levels, HAEMATOLOG, 86(2), 2001, pp. 199-204
Authors:
Grandone, E
Colaizzo, D
Lo Bue, A
Checola, MG
Cittadini, E
Margaglione, M
Citation: E. Grandone et al., Inherited thrombophilia and in vitro fertilization implantation failure, FERT STERIL, 76(1), 2001, pp. 201-202
Authors:
Paolisso, G
Tagliamonte, MR
De Lucia, D
Palmieri, F
Manzella, D
Rinaldi, C
Bossone, A
Colaizzo, D
Margaglione, M
Varricchio, M
Citation: G. Paolisso et al., ACE gene polymorphism and insulin action in older subjects and healthy centenarians, J AM GER SO, 49(5), 2001, pp. 610-614
Authors:
Margaglione, M
Cappucci, G
Colaizzo, D
Vecchione, G
Grandone, E
Di Minno, G
Citation: M. Margaglione et al., C-reactive protein in offspring is associated with the occurrence of myocardial infarction in first-degree relatives, ART THROM V, 20(1), 2000, pp. 198-203
Authors:
Margaglione, M
Colaizzo, D
D'Andrea, G
Brancaccio, V
Clampa, A
Grandone, E
Di Minno, G
Citation: M. Margaglione et al., Genetic modulation of oral anticoagulation with warfarin, THROMB HAEM, 84(5), 2000, pp. 775-778
Authors:
Margaglione, M
Santacroce, R
Colaizzo, D
Seripa, D
Vecchione, G
Lupone, MR
De Lucia, D
Fortina, P
Grandone, E
Perricone, C
Di Minno, G
Citation: M. Margaglione et al., A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing, BLOOD, 96(7), 2000, pp. 2501-2505
Authors:
De Cosmo, S
Margaglione, M
Tassi, V
Garrubba, M
Thomas, S
Olivetti, C
Piras, GP
Trevisan, R
Vedovato, M
Perin, PC
Bacci, S
Colaizzo, D
Cisternino, C
Zucaro, L
Di Minno, G
Trischitta, V
Viberti, GC
Citation: S. De Cosmo et al., ACE, PAI-1, decorin and Warner helicase genes are not associated with the development of renal disease in European patients with Type 1 diabetes, DIABET M R, 15(4), 1999, pp. 247-253
Authors:
Margaglione, M
D'Andrea, G
Colaizzo, D
Cappucci, G
del Popolo, A
Brancaccio, V
Ciampa, A
Grandone, E
Di Minno, G
Citation: M. Margaglione et al., Coexistence of Factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism, THROMB HAEM, 82(6), 1999, pp. 1583-1587
Genetic polymorphism of 5,10-MTHFR reductase gene in offspring of patientswith myocardial infarction
Authors:
Margaglione, M
Colaizzo, D
Cappucci, G
del Popolo, A
Vecchione, G
Grandone, E
Di Minno, G
Citation: M. Margaglione et al., Genetic polymorphism of 5,10-MTHFR reductase gene in offspring of patientswith myocardial infarction, THROMB HAEM, 82(1), 1999, pp. 19-23
Authors:
Grandone, E
Margaglione, M
Colaizzo, D
Cappucci, G
Scianname, N
Montanaro, S
Paladini, D
Martinelli, P
Di Minno, G
Citation: E. Grandone et al., Prothrombotic genetic risk factors and the occurrence of gestational hypertension with or without proteinuria, THROMB HAEM, 81(3), 1999, pp. 349-352
Authors:
Vecchione, G
Margaglione, M
Grandone, E
Colaizzo, D
Cappucci, G
Fermo, I
D'Angelo, A
Di Minno, G
Citation: G. Vecchione et al., Determining sulfur-containing amino acids by capillary electrophoresis: A fast novel method for total homocyst(e)ine human plasma, ELECTROPHOR, 20(3), 1999, pp. 569-574
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