AAAAAA
Results:
1-9
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Results: 9
Authors:
Freson, K
Hoylaerts, MF
Jaeken, J
Eyssen, M
Arnout, J
Vermylen, J
Van Geet, C
Citation: K. Freson et al., Genetic variation of the extra-large stimulatory G protein alpha-subunit leads to Gs hyperfunction in platelets and is a risk factor for bleeding, THROMB HAEM, 86(3), 2001, pp. 733-738
Authors:
Van Geet, C
Jaeken, J
Freson, K
Lenaerts, T
Arnout, J
Vermylen, J
Hoylaerts, MF
Citation: C. Van Geet et al., Congenital disorders of glycosylation type Ia and IIa are associated with different primary haemostatic complications, J INH MET D, 24(4), 2001, pp. 477-492
Authors:
Casteels-Van Daele, M
Van Geet, C
Wouters, C
Eggermont, E
Citation: M. Casteels-van Daele et al., Reye's syndrome, LANCET, 358(9278), 2001, pp. 334-334
Authors:
Poon, MC
d'Oiron, R
Hann, I
Negrier, C
de Lumley, L
Thomas, A
Karafoulidou, A
Demers, C
Street, A
Huth-Kuhne, A
Petrini, P
Fressinaud, E
Morfini, M
Tengborn, L
Marques-Verdier, A
Musso, R
Devecioglu, O
Houston, DS
Lethagen, S
Van Geet, C
von Depka, M
Berger, C
Beurrier, P
Britton, HA
Gerrits, W
Guthner, C
Kuhle, S
Lorenzo, JJ
Makris, PE
Nohe, N
Paugy, P
Pautard, B
Torchet, MF
Trillot, N
Vicariot, M
Wilde, J
Winter, M
Chambost, H
Ingerslev, J
Peters, M
Strauss, G
Citation: Mc. Poon et al., Use of recombinant factor VIIa (NovoSeven (R)) in patients with Glanzmann thrombasthenia, SEM HEMATOL, 38(4), 2001, pp. 21-25
Authors:
Freson, K
Devriendt, K
Matthijs, G
Van Hoof, A
De Vos, R
Thys, C
Minner, K
Hoylaerts, MF
Vermylen, J
Van Geet, C
Citation: K. Freson et al., Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation, BLOOD, 98(1), 2001, pp. 85-92
Authors:
Ferster, A
Tahriri, P
Vermylen, C
Sturbois, G
Corazza, F
Fondu, P
Devalck, C
Dresse, MF
Feremans, W
Hunninck, K
Toppet, M
Philippet, P
Van Geet, C
Sariban, E
Citation: A. Ferster et al., Five years of experience with hydroxyurea in children and young adults with sickle cell disease, BLOOD, 97(11), 2001, pp. 3628-3632
Authors:
Ljung, R
Aronis-Vournas, S
Kurnik-Auberger, K
Van den Berg, M
Chambost, H
Claeyssens, S
Van Geet, C
Glomstein, A
Hann, I
Hill, F
Kobelt, R
Kreuz, W
Mancuso, G
Muntean, W
Petrini, P
Rosado, L
Scheibel, E
Siimes, M
Smith, O
Tusell, J
Citation: R. Ljung et al., Treatment of children with haemophilia in Europe: a survey of 20 centres in 16 countries, HAEMOPHILIA, 6(6), 2000, pp. 619-624
Authors:
Casteels-Van Daele, M
Van Geet, C
Wouters, C
Eggermont, E
Citation: M. Casteels-van Daele et al., Reye syndrome revisited: a descriptive term covering a group of heterogeneous disorders, EUR J PED, 159(9), 2000, pp. 641-648
Authors:
Oury, C
Toth-Zsamboki, E
Van Geet, C
Thys, C
Wei, L
Nilius, B
Vermylen, J
Hoylaerts, MF
Citation: C. Oury et al., A natural dominant negative P2X1 receptor due to deletion of a single amino acid residue, J BIOL CHEM, 275(30), 2000, pp. 22611-22614
Risultati:
1-9
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