-
1
-
-
0036040213
-
Factor VII Deficiency
-
Perry D.J. Factor VII Deficiency. Br J Haematol 2002, 118:689-700.
-
(2002)
Br J Haematol
, vol.118
, pp. 689-700
-
-
Perry, D.J.1
-
2
-
-
0018192517
-
Burul A. Factor VII Padua: a congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern
-
Girolami A., Fabris F., Dal Bo Zanon R., Ghiotto G. Burul A. Factor VII Padua: a congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern. J Lab Clin Med 1978, 91:387-395.
-
(1978)
J Lab Clin Med
, vol.91
, pp. 387-395
-
-
Girolami, A.1
Fabris, F.2
Dal Bo Zanon, R.3
Ghiotto, G.4
-
3
-
-
0018646780
-
Another family with the Factor VII Padua clotting defect
-
Girolami A., Patrassi G., Cappellato G., Casonato A. Another family with the Factor VII Padua clotting defect. Acta Haematol 1979, 62:4-11.
-
(1979)
Acta Haematol
, vol.62
, pp. 4-11
-
-
Girolami, A.1
Patrassi, G.2
Cappellato, G.3
Casonato, A.4
-
4
-
-
0019995501
-
Further studies on FVII Padua defect: the report of the fourth homozygous patient
-
Girolami A., Gaio A., Procidano M., Saltarin P. Further studies on FVII Padua defect: the report of the fourth homozygous patient. Blut 1982, 44:363-369.
-
(1982)
Blut
, vol.44
, pp. 363-369
-
-
Girolami, A.1
Gaio, A.2
Procidano, M.3
Saltarin, P.4
-
5
-
-
0020689250
-
Report of the fifth homozygous patient with FVII Padua defect
-
Girolami A., Dal Bo Zanon R., Caenazzo A., Scattolo N. Report of the fifth homozygous patient with FVII Padua defect. Folia Haematol 1983, 110:447-454.
-
(1983)
Folia Haematol
, vol.110
, pp. 447-454
-
-
Girolami, A.1
Dal Bo Zanon, R.2
Caenazzo, A.3
Scattolo, N.4
-
6
-
-
78650175151
-
Variant coagulation factor X and VII point mutations in a highly conserved model in the substrate binding pocket. Comparative molecular modeling
-
(Abstract Book).
-
James H.L., Kumar A., Girolami A., Hubbard J.G., Fair D.S. Variant coagulation factor X and VII point mutations in a highly conserved model in the substrate binding pocket. Comparative molecular modeling. Thromb Haemost 1991, 65:137. (Abstract Book).
-
(1991)
Thromb Haemost
, vol.65
, pp. 137
-
-
James, H.L.1
Kumar, A.2
Girolami, A.3
Hubbard, J.G.4
Fair, D.S.5
-
7
-
-
0027528846
-
The dysfunction of coagulation factor VII Padua results from substitution of arginine 304 with glutamine
-
James H., Girolami A., Hubbard J.G., Kumar A., Fair D.S. The dysfunction of coagulation factor VII Padua results from substitution of arginine 304 with glutamine. Chem Biophys Acta 1993, 1172:301-305.
-
(1993)
Chem Biophys Acta
, vol.1172
, pp. 301-305
-
-
James, H.1
Girolami, A.2
Hubbard, J.G.3
Kumar, A.4
Fair, D.S.5
-
8
-
-
0025871447
-
Purification and characterization of factor VII 304-Gln: a variant molecule with reduced activity isolated from a clinically unaffected male
-
O'Brien D.P., Gale K.M., Anderson J.S., et al. Purification and characterization of factor VII 304-Gln: a variant molecule with reduced activity isolated from a clinically unaffected male. Blood 1991, 78:132-140.
-
(1991)
Blood
, vol.78
, pp. 132-140
-
-
O'Brien, D.P.1
Gale, K.M.2
Anderson, J.S.3
-
9
-
-
22444446252
-
Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation
-
Fromovich-Amit Y., Zivelin A., Rosenberg N., Landau M., Rosa J.P., Seligsohn U. Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation. Blood Coagul Fibrinolysis 2005, 16:369-374.
-
(2005)
Blood Coagul Fibrinolysis
, vol.16
, pp. 369-374
-
-
Fromovich-Amit, Y.1
Zivelin, A.2
Rosenberg, N.3
Landau, M.4
Rosa, J.P.5
Seligsohn, U.6
-
10
-
-
0035131432
-
Study Group of Factor Seven Deficiency. Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency
-
Giansily-Blaizot M., Aguilar-Martinez P., Biron-Andreani C., Jeanjean P., Igual H. Study Group of Factor Seven Deficiency. Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency. Eur J Hum Genet 2001, 9:105-112.
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 105-112
-
-
Giansily-Blaizot, M.1
Aguilar-Martinez, P.2
Biron-Andreani, C.3
Jeanjean, P.4
Igual, H.5
-
11
-
-
77957754703
-
Dysfunctional human FVII variants and single-strand conformational polymorphism (SSC5)
-
Takamiya O., McVey I., Kemhell-Cook G., Tuddenham E. Dysfunctional human FVII variants and single-strand conformational polymorphism (SSC5). Thromb Hemost 1993, 69:1291. (Suppl).
-
(1993)
Thromb Hemost
, vol.69
, Issue.SUPPL
, pp. 1291
-
-
Takamiya, O.1
McVey, I.2
Kemhell-Cook, G.3
Tuddenham, E.4
-
12
-
-
77957753648
-
Factor VII genotype and clinical profile in 6 Iranian patients with congenital factor VII deficiency
-
Rastager-Iari
-
Tahatahary A., Ravanbod S., Baghaipour M., Enayar M., Ala F., Rastager-Iari Factor VII genotype and clinical profile in 6 Iranian patients with congenital factor VII deficiency. J Thromb Hemost 2007, 5:208. Suppl.
-
(2007)
J Thromb Hemost
, vol.5
, Issue.SUPPL
, pp. 208
-
-
Tahatahary, A.1
Ravanbod, S.2
Baghaipour, M.3
Enayar, M.4
Ala, F.5
-
13
-
-
0006541684
-
Factor VII deficiency (FVII Richmond) associated with thrombosis
-
Sabharwal A., KuppusWarmy M., Foster D. Factor VII deficiency (FVII Richmond) associated with thrombosis. Circul 1992, 88:679. (Suppl).
-
(1992)
Circul
, vol.88
, Issue.SUPPL
, pp. 679
-
-
Sabharwal, A.1
KuppusWarmy, M.2
Foster, D.3
-
14
-
-
0028340150
-
Impaired human tissue factor mediated activity in blood clotting Factor VII Nagoya (Arg304Trp)
-
Matsushita T., Kojima T., Emi N., Takahashi I., Saito H. Impaired human tissue factor mediated activity in blood clotting Factor VII Nagoya (Arg304Trp). J Biol Chem 1994, 269:7355-7363.
-
(1994)
J Biol Chem
, vol.269
, pp. 7355-7363
-
-
Matsushita, T.1
Kojima, T.2
Emi, N.3
Takahashi, I.4
Saito, H.5
|