Inhibitor development against exogenous factor VIII is a severe impairment of replacement therapy affecting 18% of Argentine patients with severe haemophilia A (HA). To study the molecular predisposition for inhibitor development, we genotyped 260 HA patients with and without inhibitors, countrywide. The inhibitor-positive population (19 transients, 15 low responders, LR and 70 high responders, HR) of 104 severe-HA patients showed 59 Inv22 (intron 22 inversions), 18 small ins/del-frameshifts, 12 gross deletions, 12 nonsense, one splicing defect and two missense, p.Arg531Pro and p.Leu575Pro, both LR and thought to impair FVIII A2 domain secondary structure. In addition, a patient with mild HA and HR showed the missense p.Glu1704Lys associate...
This systematic review was designed to provide more precise effect estimates of inhibitor developmen...
Neutralizing antibodies (inhibitors) toward factor VIII form a severe complication in nonsevere hemo...
Neutralizing antibodies (inhibitors) toward factor VIII form a severe complication in nonsevere hemo...
Hemophilia A is an X-linked bleeding disorder caused by mutations in the FVIII gene. Genetic factors...
In haemophilia B (HB) (factor IX [FIX] deficiency), F9 genotype largely determines clinical phenotyp...
Hemophilia A (HA) is caused by heterogeneous mutations in the factor VIII gene (F8). This paper repo...
Introduction: Inhibitor development is a severe complication of mild/ moderate hemophilia A (MHA) an...
The development of neutralizing antibodies (inhibitors) against coagulation factor VIII (FVIII) is t...
Background: The development of neutralizing antibodies (inhibitors) towards factor VIII is a major c...
El desarrollo de inhibidores de FVIII en hemofilia A (HA) es considerado un rasgo complejo, ya que i...
Haemophilia A (HA) (OMIM#306700) and haemophilia B (HB) (OMIM#306900) are X-linked disorders charact...
Background: A severe and challenging complication in the treatment of hemophilia A is the developmen...
Contains fulltext : 70262.pdf (publisher's version ) (Closed access)The appearance...
This systematic review was designed to provide more precise effect estimates of inhibitor developmen...
Neutralizing antibodies (inhibitors) toward factor VIII form a severe complication in nonsevere hemo...
This systematic review was designed to provide more precise effect estimates of inhibitor developmen...
Neutralizing antibodies (inhibitors) toward factor VIII form a severe complication in nonsevere hemo...
Neutralizing antibodies (inhibitors) toward factor VIII form a severe complication in nonsevere hemo...
Hemophilia A is an X-linked bleeding disorder caused by mutations in the FVIII gene. Genetic factors...
In haemophilia B (HB) (factor IX [FIX] deficiency), F9 genotype largely determines clinical phenotyp...
Hemophilia A (HA) is caused by heterogeneous mutations in the factor VIII gene (F8). This paper repo...
Introduction: Inhibitor development is a severe complication of mild/ moderate hemophilia A (MHA) an...
The development of neutralizing antibodies (inhibitors) against coagulation factor VIII (FVIII) is t...
Background: The development of neutralizing antibodies (inhibitors) towards factor VIII is a major c...
El desarrollo de inhibidores de FVIII en hemofilia A (HA) es considerado un rasgo complejo, ya que i...
Haemophilia A (HA) (OMIM#306700) and haemophilia B (HB) (OMIM#306900) are X-linked disorders charact...
Background: A severe and challenging complication in the treatment of hemophilia A is the developmen...
Contains fulltext : 70262.pdf (publisher's version ) (Closed access)The appearance...
This systematic review was designed to provide more precise effect estimates of inhibitor developmen...
Neutralizing antibodies (inhibitors) toward factor VIII form a severe complication in nonsevere hemo...
This systematic review was designed to provide more precise effect estimates of inhibitor developmen...
Neutralizing antibodies (inhibitors) toward factor VIII form a severe complication in nonsevere hemo...
Neutralizing antibodies (inhibitors) toward factor VIII form a severe complication in nonsevere hemo...