-
1
-
-
33747432663
-
Myocardial infarction and other arterial occlusions in hemophilia A Patients: A cardiological evaluation of all 42 cases reported in the literature
-
DOI 10.1159/000093642
-
Girolami A, Ruzzon E, Fabris F, Varvarikis C, Sartori R, Girolami B (2006) Myocardial infarction and other arterial occlusions in Hemophilia A patients. Acta Haematol 116:120-125 (Pubitemid 44252768)
-
(2006)
Acta Haematologica
, vol.116
, Issue.2
, pp. 120-125
-
-
Girolami, A.1
Ruzzon, E.2
Fabris, F.3
Varvarikis, C.4
Sartori, R.5
Girolami, B.6
-
2
-
-
12344313430
-
Thrombotic complications in patients with hereditary bleeding disorders
-
Franchini M (2004) Thrombotic complications in patients with hereditary bleeding disorders. Throm Haemost 92:298-304 (Pubitemid 39172310)
-
(2004)
Thrombosis and Haemostasis
, vol.92
, Issue.2
, pp. 298-304
-
-
Franchini, M.1
-
3
-
-
34248387034
-
Arterial and venous thrombosis in rare congenital bleeding disorders
-
16834733 10.1111/j.1365-2516.2006.01299.x 1:STN:280: DC%2BD28vht1Orug%3D%3D
-
Girolami A, Ruzzon E, Tezza F, Scandellari R, Vettore S, Girolami B (2006) arterial and venous thrombosis in rare congenital bleeding disorders. Haemophilia 12:345-351
-
(2006)
Haemophilia
, vol.12
, pp. 345-351
-
-
Girolami, A.1
Ruzzon, E.2
Tezza, F.3
Scandellari, R.4
Vettore, S.5
Girolami, B.6
-
4
-
-
77957938334
-
The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiency
-
19412729 10.1007/s11239-009-0342-2
-
Girolami A, Candeo N, Vettore S, Lombardi AM, Girolami B (2010) The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiency. J Thromb Thrombolysis 29:299-302
-
(2010)
J Thromb Thrombolysis
, vol.29
, pp. 299-302
-
-
Girolami, A.1
Candeo, N.2
Vettore, S.3
Lombardi, A.M.4
Girolami, B.5
-
5
-
-
35548977521
-
Venous thrombosis in Glanzmann's thrombasthenia [1]
-
DOI 10.1111/j.1365-2516.2007.01555.x
-
Phillips R, Richards M (2007) Venous thrombosis in Glanzmann's thrombasthenia. Haemophilia 13:758-759 (Pubitemid 350018268)
-
(2007)
Haemophilia
, vol.13
, Issue.6
, pp. 758-759
-
-
Phillips, R.1
Richards, M.2
-
6
-
-
0030854922
-
Severe proximal deep vein thrombosis in a Glanzmann thrombasthenia variant successfully treated with a low molecular weight heparin [2]
-
Gruel Y, Pacouret G, Bellucci S, Caen J (1997) Severe proximal deep vein thrombosis in a Glanzmann thrombasthenia variant successfully treated with a low molecular weight heparin. Blood 90:888-890 (Pubitemid 27299131)
-
(1997)
Blood
, vol.90
, Issue.2
, pp. 888-890
-
-
Gruel, Y.1
Pacouret, G.2
Bellucci, S.3
Caen, J.4
-
7
-
-
51249098043
-
Pulmonary embolus in Glanzmann's thrombasthenia trated with warfarin
-
18624697 10.1111/j.1365-2516.2008.01804.x 1:STN:280: DC%2BD1cnntlGmtA%3D%3D
-
Seretny M, Senadheera N, Miller E, Keeling D (2008) Pulmonary embolus in Glanzmann's thrombasthenia trated with warfarin. Haemophilia 14:1138-1139
-
(2008)
Haemophilia
, vol.14
, pp. 1138-1139
-
-
Seretny, M.1
Senadheera, N.2
Miller, E.3
Keeling, D.4
-
8
-
-
83555166022
-
Secondary prophilaxis with warfarin for recurrent thrombosis in a patient with Glanzmann thrombastenia and F5 G1691A
-
10.1111/j.1365-2141.2011.08821 21848888 10.1111/j.1365-2141.2011.08821.x
-
Rezende S (2012) Secondary prophilaxis with warfarin for recurrent thrombosis in a patient with Glanzmann thrombastenia and F5 G1691A. Br J Haematol 156(1):144. doi: 10.1111/j.1365-2141.2011.08821
-
(2012)
Br J Haematol
, vol.156
, Issue.1
, pp. 144
-
-
Rezende, S.1
-
9
-
-
82955248033
-
Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May-Hegglin, Sebastian, Fechtner and Epstein syndromes)
-
21842307 10.1007/s11239-011-0603-8
-
Girolami A, Vettore S, Bonamigo E, Fabris F (2011) Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May-Hegglin, Sebastian, Fechtner and Epstein syndromes). J Thromb Thrombolysis 32:474-477
-
(2011)
J Thromb Thrombolysis
, vol.32
, pp. 474-477
-
-
Girolami, A.1
Vettore, S.2
Bonamigo, E.3
Fabris, F.4
-
10
-
-
77952703684
-
Modem management of severe platelet function disorders
-
10.1111/j.1365-2141.2010.08191.x
-
Alamelu J, Liesner RJ (2010) Modem management of severe platelet function disorders. Brit J Haematol 149:813-823
-
(2010)
Brit J Haematol
, vol.149
, pp. 813-823
-
-
Alamelu, J.1
Liesner, R.J.2
-
11
-
-
0141609789
-
Inherited platelet based bleeding disorders
-
12871299 10.1046/j.1538-7836.2003.00266.x 1:CAS:528:DC%2BD2cXktFOjtLw%3D
-
Cattaneo M (2003) Inherited platelet based bleeding disorders. J Thromb Haemost 1:1628-1636
-
(2003)
J Thromb Haemost
, vol.1
, pp. 1628-1636
-
-
Cattaneo, M.1
-
12
-
-
41149168746
-
Inherited traits affecting platelet function
-
18180086 10.1016/j.blre.2007.11.002 1:CAS:528:DC%2BD1cXmsl2qtLs%3D
-
Salles I, Feys H, Iserlyt B, De Meyer S, Varrhoorelleke K, Deckmyn H (2008) Inherited traits affecting platelet function. Blood Rev 22:155-172
-
(2008)
Blood Rev
, vol.22
, pp. 155-172
-
-
Salles, I.1
Feys, H.2
Iserlyt, B.3
De Meyer, S.4
Varrhoorelleke, K.5
Deckmyn, H.6
-
13
-
-
0026651068
-
Atherosclerosis and unstable angina in Bernard-Soulier syndrome
-
1575209 1:STN:280:DyaK383ks1Wmsw%3D%3D
-
Humphries JE, Yirinec BA, Hess CE (1992) Atherosclerosis and unstable angina in Bernard-Soulier syndrome. Am J Clin Pathol 97:652-655
-
(1992)
Am J Clin Pathol
, vol.97
, pp. 652-655
-
-
Humphries, J.E.1
Yirinec, B.A.2
Hess, C.E.3
-
14
-
-
0035034321
-
Are patients with Glanzmann thrombasthenia and the Bernard-Soulier syndrome protected against atherosclerosis?
-
Nurden A, Nurden P, George JN (2001) Are patients with Glanzmann thrombasthenia and the Bernard-Soulier syndrome protected against atherosclerosis? Adv Exp Med Biol 489:13-29 (Pubitemid 32374630)
-
(2001)
Advances in Experimental Medicine and Biology
, vol.489
, pp. 13-29
-
-
Nurden, A.T.1
Nurden, P.2
George, J.N.3
-
15
-
-
33847618245
-
Decreased thrombotic tendency in mouse models of the Bernard-Soulier syndrome
-
DOI 10.1161/01.ATV.0000251992.47053.75, PII 0004360520070100000036
-
Strassel C, Nonne A, Eckly A, David T, Leon C, Freund M, Cazenave J-P, Gachet C, Lanza F (2007) Decreased thrombotic tendency in mouse models of the Bernard-Soulier syndrome. Arterioscler Thromb Vasc Biol 27:241-247 (Pubitemid 46360405)
-
(2007)
Arteriosclerosis, Thrombosis, and Vascular Biology
, vol.27
, Issue.1
, pp. 241-247
-
-
Strassel, C.1
Nonne, C.2
Eckly, A.3
David, T.4
Leon, C.5
Freund, M.6
Cazenave, J.-P.7
Gachet, C.8
Lanza, F.9
-
16
-
-
0022646192
-
Platelet adhesion and thrombus formation on subendothelium in platelets deficient in glycoproteins IIb-IIIa, Ib, and storage granules
-
Weiss HJ, Turitto VT, Baumgartner HR (1986) Platelet adhesion and thrombus formation on subendothelium in platelets deficient in glycoproteins IIb-IIIa, Ib, and storage granules. Blood 67(2):322-330 (Pubitemid 16164643)
-
(1986)
Blood
, vol.67
, Issue.2
, pp. 322-330
-
-
Weiss, H.J.1
Turitto, V.T.2
Baumgartner, H.R.3
-
17
-
-
0022495893
-
The role of platelet membrane glycoproteins Ib and IIb-IIIa in platelet adherence to human artery subendothelium
-
Sakariassen KS, Nievelstein PF, Coller BS, Sixma JJ (1986) The role of platelet membrane glycoproteins Ib and IIb-IIIa in platelet adherence to human artery subendothelium. Br J Haematol 63(4):681-691 (Pubitemid 16033606)
-
(1986)
British Journal of Haematology
, vol.63
, Issue.4
, pp. 681-691
-
-
Sakariassen, K.S.1
Nievelstein, P.F.E.M.2
Coller, B.S.3
Sixma, J.J.4
-
18
-
-
2342425765
-
The role of the platelet glycoprotein IIb/IIIa in thrombosis and haemostasis
-
DOI 10.2174/1381612043384682
-
Fullard JF (2004) The role of the platelet glycoprotein IIb/IIIa in thrombosis and haemostasis. Curr Pharm Des 10(14):1567-1576 (Pubitemid 38559768)
-
(2004)
Current Pharmaceutical Design
, vol.10
, Issue.14
, pp. 1567-1576
-
-
Fullard, J.F.1
-
19
-
-
55549095626
-
Novel point mutation in a leucine rich repeat of the GPIbα chain of the platelet von Willebrand factor receptor, GPIb/V/IX, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: The N41H variant
-
18815197 10.3324/haematol.12830 1:CAS:528:DC%2BD1cXhsFansbvF
-
Vettore S, Scandellari R, Moro S, Lombardi AM, Scapin M, Randi ML, Fabris F (2008) Novel point mutation in a leucine rich repeat of the GPIbα chain of the platelet von Willebrand factor receptor, GPIb/V/IX, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant. Haematologica 93:1743-1747
-
(2008)
Haematologica
, vol.93
, pp. 1743-1747
-
-
Vettore, S.1
Scandellari, R.2
Moro, S.3
Lombardi, A.M.4
Scapin, M.5
Randi, M.L.6
Fabris, F.7
-
20
-
-
84875606477
-
Sur une nouvelle varietè de distrophie thrombocitaire hemorragipare congenital
-
Bernard J, Soulier JP (1948) Sur une nouvelle varietè de distrophie thrombocitaire hemorragipare congenital. Sem Hop Paris 24:2317-2322
-
(1948)
Sem Hop Paris
, vol.24
, pp. 2317-2322
-
-
Bernard, J.1
Soulier, J.P.2
-
21
-
-
0035282727
-
Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome
-
DOI 10.1182/blood.V97.5.1330
-
Savoia A, Balduini CL, Savino M, Noris P, Del Vecchio M, Perrotta S, Belletti S, Poggi V, Iolascon A (2001) Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome. Blood 97:1330-1335 (Pubitemid 32183756)
-
(2001)
Blood
, vol.97
, Issue.5
, pp. 1330-1335
-
-
Savoia, A.1
Balduini, C.L.2
Savino, M.3
Noris, P.4
Del Vecchio, M.5
Perrotta, S.6
Belletti, S.7
Poggi, V.8
Iolascon, A.9
-
22
-
-
0025283519
-
Variant Bernard-Soulier syndrome type Bolzano. A congenital bleeding disorder due to a structural and functional abnormality of the platelet glycoprotein Ib-IX complex
-
De Marco L, Mazzucato M, Fabris F, De Roia D, Coser P, Girolami A (1990) Variant Bernard-Soulier syndrome, type Bolzano. A congenital bleeding disorder due to a structural and functional abnormality of the platelet glycoprotein Ib-IX complex. J Clin Invest 86:25-31 (Pubitemid 20226970)
-
(1990)
Journal of Clinical Investigation
, vol.86
, Issue.1
, pp. 25-31
-
-
De Marco, L.1
Mazzucato, M.2
Fabris, F.3
De Roia, D.4
Coser, P.5
Girolami, A.6
Vicente, V.7
Ruggeri, Z.M.8
-
23
-
-
0001210482
-
Hereditare haemorrhagesche thrombasthenie. Ein Beitrag zur pathologie der blut plachetten
-
Glanzmann E (1918) Hereditare haemorrhagesche thrombasthenie. Ein Beitrag zur pathologie der blut plachetten. J Kinderkranken 88:113-120
-
(1918)
J Kinderkranken
, vol.88
, pp. 113-120
-
-
Glanzmann, E.1
-
24
-
-
0037022915
-
3 receptors are not protected from atherosclerosis
-
DOI 10.1161/hc0902.104676
-
Shpilberg O, Rabi I, Schiller K, Walden R, Herats D, Tyrrel KS, Coller B, Sebigsohn U (2002) Patients with Glanzmann thrombastenia lacking platelet glycoprotein α2β3 (GPIIb/IIIa) and α2β3 receptor are not protected from aterosclerosis. Circulation 105:1044-1048 (Pubitemid 34212611)
-
(2002)
Circulation
, vol.105
, Issue.9
, pp. 1044-1048
-
-
Shpilberg, O.1
Rabi, I.2
Schiller, K.3
Walden, R.4
Harats, D.5
Tyrrell, K.S.6
Coller, B.7
Seligsohn, U.8
-
25
-
-
33845201642
-
Glanzmann thrombasthenia with endomyocardial fibrosis: A thrombotic paradox
-
DOI 10.1016/j.ijcard.2005.11.094, PII S0167527306001148
-
Tullu MS, Vaideeswar P, Pandit SP, Lahiri KR (2007) Glanzmann thrombastenia with endomyocardial fibrosis: a thrombotic paradox. Int J Cardiol 114:401-402 (Pubitemid 44855897)
-
(2007)
International Journal of Cardiology
, vol.114
, Issue.3
, pp. 401-402
-
-
Tullu, M.S.1
Vaideeswar, P.2
Pandit, S.P.3
Lahiri, K.R.4
-
26
-
-
51849126451
-
A case of Bernard-Soulier syndrome due to a homozygous four bases deletion (TGAG) of GPIbα gene: Lack of GPIbα but absence of bleeding
-
18791947 10.1080/09537100801949976 1:CAS:528:DC%2BD1cXhtFaisrrP
-
Vettore S, Scandellari R, Scapin M, Lombardi AM, Duner E, Randi ML, Fabris F (2008) A case of Bernard-Soulier syndrome due to a homozygous four bases deletion (TGAG) of GPIbα gene: lack of GPIbα but absence of bleeding. Platelets 19:388-391
-
(2008)
Platelets
, vol.19
, pp. 388-391
-
-
Vettore, S.1
Scandellari, R.2
Scapin, M.3
Lombardi, A.M.4
Duner, E.5
Randi, M.L.6
Fabris, F.7
-
27
-
-
82855163998
-
A A386G biallelic GPIbα gene mutation with anomalous behavior: A new mechanism suggested for Bernard-Soulier syndrome pathogenesis
-
21993687 10.3324/haematol.2010.039008
-
Vettore S, Tezza F, Malara A, Vianello F, Pecci A, Scandellari R, Floris M, Balduini A, Fabris F (2011) A A386G biallelic GPIbα gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesis. Haematologica 96:1878-1882
-
(2011)
Haematologica
, vol.96
, pp. 1878-1882
-
-
Vettore, S.1
Tezza, F.2
Malara, A.3
Vianello, F.4
Pecci, A.5
Scandellari, R.6
Floris, M.7
Balduini, A.8
Fabris, F.9
-
28
-
-
0023913919
-
Deep vein thrombosis induced by tranexamic acid in idiopathic thrombocytopenic purpura
-
3373703 10.1001/jama.1988.03720240023026 1:STN:280:DyaL1c3jtVyjug%3D%3D
-
Endo Y, Nishimura S, Miura A (1988) Deep vein thrombosis induced by tranexamic acid in idiopathic thrombocytopenic purpura. JAMA 259:3561-3562
-
(1988)
JAMA
, vol.259
, pp. 3561-3562
-
-
Endo, Y.1
Nishimura, S.2
Miura, A.3
-
29
-
-
76749158403
-
Primary PCI for acute myocardial infarction in a patient with idiopathic thrombocytopenic purpura
-
10.1007/s00059-010-3262-1
-
Neskevic A, Stankovic I, Miliecevic P, Aleksic A, Vlahovic-Stipec A, Calija B, Putnikovic B (2000) Primary PCI for acute myocardial infarction in a patient with idiopathic thrombocytopenic purpura. Herz 35:43-49
-
(2000)
Herz
, vol.35
, pp. 43-49
-
-
Neskevic, A.1
Stankovic, I.2
Miliecevic, P.3
Aleksic, A.4
Vlahovic-Stipec, A.5
Calija, B.6
Putnikovic, B.7
|