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Predictive factors of immune tolerance treatment response in severe haemophilia A patients with inhibitors: A real‐world report from a single centre, mixed retrospective‐prospective long‐term study.
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- Haemophilia, 2019, v. 25, n. 2, p. e97, doi. 10.1111/hae.13660
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- Article
Identification of a new candidate mutation, G1629R, in a family with type 2A von Willebrand disease.
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- American Journal of Hematology, 1999, v. 60, n. 4, p. 309, doi. 10.1002/(SICI)1096-8652(199904)60:4<309::AID-AJH10>3.0.CO;2-P
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- Article
Search for mutations in a segment of the exon 28 of the human von Willebrand factor gene: New mutations, R1315C and R1341W, associated with type 2M and 2B variants.
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- American Journal of Hematology, 1998, v. 59, n. 1, p. 57, doi. 10.1002/(SICI)1096-8652(199809)59:1<57::AID-AJH11>3.0.CO;2-Z
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- Article
Large deletion in the Factor VIII gene ( F8) involving segmental duplications in int22h shows no haematological phenotype in female carriers, but may be embryonic lethal in males.
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- British Journal of Haematology, 2012, v. 158, n. 1, p. 138, doi. 10.1111/j.1365-2141.2012.09092.x
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- Article
First application of MLPA method in severe von Willebrand disease. Confirmation of a new large VWF gene deletion and identification of heterozygous carriers.
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- British Journal of Haematology, 2011, v. 152, n. 2, p. 240, doi. 10.1111/j.1365-2141.2010.08400.x
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- Article
Significant linkage and non-linkage of type 1 von Willebrand disease to the von Willebrand factor gene.
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- British Journal of Haematology, 2001, v. 115, n. 3, p. 692, doi. 10.1046/j.1365-2141.2001.03132.x
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- Article
Q1311X: a novel nonsense mutation of putative ancient origin in the von Willebrand factor gene.
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- British Journal of Haematology, 2000, v. 111, n. 2, p. 552, doi. 10.1046/j.1365-2141.2000.02410.x
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- Article
Immunotolerance Induction Treatments in Hemophilia.
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- Journal of Coagulation Disorders, 2010, v. 2, n. 2, p. 1
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- Article
Immunotolerance Induction Treatments in Hemophilia.
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- Journal of Coagulation Disorders, 2009, v. 1, n. 1, p. 1
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- Article
Novel missense mutation c.2685G>C (p.Q895H) in VWF gene associated with very low levels of VWF mRNA.
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- Annals of Hematology, 2009, v. 88, n. 3, p. 245, doi. 10.1007/s00277-008-0576-7
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- Article