-
1
-
-
0001345297
-
Sur une nouvelle variété de dystrophie thrombocytaire hémorragipare congénitale
-
Bernard J, Soulier JP. Sur une nouvelle variété de dystrophie thrombocytaire hémorragipare congénitale. Sem Hop Paris 1948; 97: 3217-23.
-
(1948)
Sem Hop Paris
, vol.97
, pp. 3217-3223
-
-
Bernard, J.1
Soulier, J.P.2
-
2
-
-
0016862422
-
Specific roles for surface glycoproteins in platelet function
-
Nurden AT, Caen JP. Specific roles for surface glycoproteins in platelet function. Nature 1975; 255: 720-2.
-
(1975)
Nature
, vol.255
, pp. 720-722
-
-
Nurden, A.T.1
Caen, J.P.2
-
3
-
-
0018717263
-
Platelet membrane glycoproteins in thrombasthenia, Bernard-Soulier syndrome and storage pool disease
-
Jamieson GA, Okumura T, Fishback B, Johnson MM, Egan JJ, Weiss HJ. Platelet membrane glycoproteins in thrombasthenia, Bernard-Soulier syndrome and storage pool disease. J Lab Clin Med 1979; 93: 652-60.
-
(1979)
J Lab Clin Med
, vol.93
, pp. 652-660
-
-
Jamieson, G.A.1
Okumura, T.2
Fishback, B.3
Johnson, M.M.4
Egan, J.J.5
Weiss, H.J.6
-
4
-
-
0019973882
-
Characterization of the platelet membrane glycoprotein abnormality in Bernard-Soulier syndrome and comparison with normal by surface-labeling techniques and high resolution two-dimensional gel electrophpresis
-
Clemetson KJ, Mc Gregor JL, James E, Dechavanne M, Luscher EF. Characterization of the platelet membrane glycoprotein abnormality in Bernard-Soulier syndrome and comparison with normal by surface-labeling techniques and high resolution two-dimensional gel electrophpresis. J Clin Invest 1982; 70: 304-11.
-
(1982)
J Clin Invest
, vol.70
, pp. 304-311
-
-
Clemetson, K.J.1
Mc Gregor, J.L.2
James, E.3
Dechavanne, M.4
Luscher, E.F.5
-
5
-
-
0020986895
-
The defective prothrombin consumption in Bernard-Soulier syndrome. Hypotheses from 1948 to 1982
-
Caen J, Bellucci S. The defective prothrombin consumption in Bernard-Soulier syndrome. Hypotheses from 1948 to 1982. Blood Cells 1983; 9: 389-99.
-
(1983)
Blood Cells
, vol.9
, pp. 389-399
-
-
Caen, J.1
Bellucci, S.2
-
6
-
-
0016488991
-
Hereditary giant platelet syndrome: Absence of collagen-induced coagulant activity and deficiency of factor XI binding to platelets
-
Walsh PN, Mills DCB, Pareti FI, Stewart GJ, Macfarlane DE, Johnson MM, Egan JJ. Hereditary giant platelet syndrome: absence of collagen-induced coagulant activity and deficiency of factor XI binding to platelets. Brit J Haematol 1975; 29: 639-55.
-
(1975)
Brit J Haematol
, vol.29
, pp. 639-655
-
-
Walsh, P.N.1
Mills, D.C.B.2
Pareti, F.I.3
Stewart, G.J.4
De Macfarlane5
Johnson, M.M.6
Egan, J.J.7
-
7
-
-
0015645726
-
La dystrophie thrombocytaire hemorragipare (Interaction des plaquettes et du facteur Willebrand)
-
Caen J, Lévy-Toledano S, Sultan Y, Bernard J. La dystrophie thrombocytaire hemorragipare (Interaction des plaquettes et du facteur Willebrand). Nouv Rev Fr Hematol 1973; 13: 595-602.
-
(1973)
Nouv Rev Fr Hematol
, vol.13
, pp. 595-602
-
-
Caen, J.1
Lévy-Toledano, S.2
Sultan, Y.3
Bernard, J.4
-
8
-
-
0022545920
-
Platelet prothrombin converting activity in hereditary disorders of platelet function
-
Bevers EM, Comfurius P, Nieuwenhuis K, Lévy-Toledano S, Einouf J, Bellucci S, Caen JP, Zwaal RFA. Platelet prothrombin converting activity in hereditary disorders of platelet function. Brit J Hematol 1986; 63: 335-45.
-
(1986)
Brit J Hematol
, vol.63
, pp. 335-345
-
-
Bevers, E.M.1
Comfurius, P.2
Nieuwenhuis, K.3
Lévy-Toledano, S.4
Einouf, J.5
Bellucci, S.6
Caen, J.P.7
Zwaal, R.F.A.8
-
9
-
-
0005697367
-
La dystrophie thrombocytaire hémorragipare congénitale
-
Bernard J, Caen JP, Maroteaux P. La dystrophie thrombocytaire hémorragipare congénitale. Revue d'Hématologie 1957; 12: 222-49.
-
(1957)
Revue d'Hématologie
, vol.12
, pp. 222-249
-
-
Bernard, J.1
Caen, J.P.2
Maroteaux, P.3
-
10
-
-
0017276144
-
Bernard-Soulier syndrome, a new platelet glycoprotein abnormality: Its relationship with platelet adhesion to subendothelium and with the factor VIII von Willebrand protein
-
Caen JP, Nurden AT, Jeanneau C, Michel H, Tobelem G, Lévy-Toledano S, Sultan Y, Valensi F, Bernard J. Bernard-Soulier syndrome, a new platelet glycoprotein abnormality: its relationship with platelet adhesion to subendothelium and with the factor VIII von Willebrand protein. J Lab Clin Med 1976; 87: 586-96.
-
(1976)
J Lab Clin Med
, vol.87
, pp. 586-596
-
-
Caen, J.P.1
Nurden, A.T.2
Jeanneau, C.3
Michel, H.4
Tobelem, G.5
Lévy-Toledano, S.6
Sultan, Y.7
Valensi, F.8
Bernard, J.9
-
11
-
-
0025646605
-
Studies on the megakaryocytes of a patient with the Bernard-Soulier syndrome
-
Hourdille P, Pico M, Jandrot-Perrus M, Lacaze D, Lozano M, Nurden AT. Studies on the megakaryocytes of a patient with the Bernard-Soulier syndrome. Brit J Haematol 1990; 76: 521-30.
-
(1990)
Brit J Haematol
, vol.76
, pp. 521-530
-
-
Hourdille, P.1
Pico, M.2
Jandrot-Perrus, M.3
Lacaze, D.4
Lozano, M.5
Nurden, A.T.6
-
12
-
-
0028171639
-
Cys209 Ser mutation in the platelet membrane glycoprotein Iba gene is associated with Bernard-Soulier Syndrome
-
Simsek S, Noris P, Lozano M, Pico M, von dem Borne AEGKr, Ribera A, Gallardo D. Cys209 Ser mutation in the platelet membrane glycoprotein Iba gene is associated with Bernard-Soulier Syndrome. Brit J Haematol 1994; 88: 839-44.
-
(1994)
Brit J Haematol
, vol.88
, pp. 839-844
-
-
Simsek, S.1
Noris, P.2
Lozano, M.3
Pico, M.4
Von Dem Borne, A.E.G.Kr.5
Ribera, A.6
Gallardo, D.7
-
13
-
-
0000913739
-
The prothrombin consumption test
-
Quick AJ, Favre-Gilly JE. The prothrombin consumption test. Blood 1949; 4: 1281-6.
-
(1949)
Blood
, vol.4
, pp. 1281-1286
-
-
Quick, A.J.1
Favre-Gilly, J.E.2
-
14
-
-
0025119629
-
Ristocetin and botrocetin involve two distinct domains of von Willebrand Factor for binding to platelet membrane glycoprotein Ib
-
Girma JP, Takahashi Y, Yoshioka A, Diaz J, Meyer D. Ristocetin and botrocetin involve two distinct domains of von Willebrand Factor for binding to platelet membrane glycoprotein Ib. Thromb Haemost 1990; 64: 326-32.
-
(1990)
Thromb Haemost
, vol.64
, pp. 326-332
-
-
Girma, J.P.1
Takahashi, Y.2
Yoshioka, A.3
Diaz, J.4
Meyer, D.5
-
15
-
-
0024425034
-
New variant of von Willebrand disease with defective binding to Factor VIII
-
Nishino M, Girma JP, Rothschild C, Fressinaud E, Meyer D. New variant of von Willebrand disease with defective binding to Factor VIII. Blood 1989; 74: 1591-99.
-
(1989)
Blood
, vol.74
, pp. 1591-1599
-
-
Nishino, M.1
Girma, J.P.2
Rothschild, C.3
Fressinaud, E.4
Meyer, D.5
-
16
-
-
0021184617
-
Hybridoma antibodies to human von Willebrand Factor I. Characterization of seven clones
-
Meyer D, Zimmerman TS, Obert B, Edgington TS. Hybridoma antibodies to human von Willebrand Factor I. Characterization of seven clones. Brit J Haematol 1984; 57: 597-608.
-
(1984)
Brit J Haematol
, vol.57
, pp. 597-608
-
-
Meyer, D.1
Zimmerman, T.S.2
Obert, B.3
Edgington, T.S.4
-
17
-
-
0018907213
-
The role of phospholipids and factor Va in the prothrombinase complex
-
Rosing J, Tans G, Govers-Riemslag JWP, Zwaal RFA, Hemker HC. The role of phospholipids and factor Va in the prothrombinase complex. J Biol Chem 1980; 255: 274-83.
-
(1980)
J Biol Chem
, vol.255
, pp. 274-283
-
-
Rosing, J.1
Tans, G.2
Govers-Riemslag, J.W.P.3
Zwaal, R.F.A.4
Hemker, H.C.5
-
18
-
-
0019831499
-
The role of phospholipid and factor VIIIa in the activation of bovine factor X
-
Van Dieijen G, Tans G, Rosing J, Hemker HC. The role of phospholipid and factor VIIIa in the activation of bovine factor X. J Biol Chem 1981; 256: 3433-3442.
-
(1981)
J Biol Chem
, vol.256
, pp. 3433-3442
-
-
Van Dieijen, G.1
Tans, G.2
Rosing, J.3
Hemker, H.C.4
-
19
-
-
0021077199
-
Abnormal phospholipid organization in Bernard-Soulier platelets
-
Perret B, Lévy-Toledano S, Plantavid M, Bredoux R, Chap H, Tobelem G, Douste-Blazy L, Caen JP. Abnormal phospholipid organization in Bernard-Soulier platelets. Thromb Res 1983; 31: 529-37.
-
(1983)
Thromb Res
, vol.31
, pp. 529-537
-
-
Perret, B.1
Lévy-Toledano, S.2
Plantavid, M.3
Bredoux, R.4
Chap, H.5
Tobelem, G.6
Douste-Blazy, L.7
Caen, J.P.8
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