Found: 17
Select item for more details and to access through your institution.
Updates on Novel Non-Replacement Drugs for Hemophilia.
- Published in:
- Pharmaceuticals (14248247), 2022, v. 15, n. 10, p. 1183, doi. 10.3390/ph15101183
- By:
- Publication type:
- Article
Reproductive care in human immunodeficiency virus serodiscordant couples with haemophilia.
- Published in:
- Blood Transfusion (17232007), 2013, v. 11, n. 3, p. 469, doi. 10.2450/2012.0079-12
- By:
- Publication type:
- Article
Development of a Specific Monoclonal Antibody to Detect Male Cells Expressing the RPS4Y1 Protein.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 4, p. 2001, doi. 10.3390/ijms22042001
- By:
- Publication type:
- Article
Immune Responses to Plasma-Derived Versus Recombinant FVIII Products.
- Published in:
- Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2020.591878
- By:
- Publication type:
- Article
A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients: evidence for a founder effect.
- Published in:
- Molecular Genetics & Genomic Medicine, 2016, v. 4, n. 2, p. 152, doi. 10.1002/mgg3.189
- By:
- Publication type:
- Article
Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII.
- Published in:
- American Journal of Hematology, 2005, v. 79, n. 4, p. 262, doi. 10.1002/ajh.20397
- By:
- Publication type:
- Article
A rare inherited coagulation disorder: Combined homozygous factor VII and factor X deficiency.
- Published in:
- American Journal of Hematology, 2004, v. 77, n. 1, p. 90, doi. 10.1002/ajh.20132
- By:
- Publication type:
- Article
The P303T mutation in the human factor VII (FVII) gene alters the conformational state of the enzyme and causes a severe functional deficiency.
- Published in:
- British Journal of Haematology, 2004, v. 127, n. 5, p. 576, doi. 10.1111/j.1365-2141.2004.05241.x
- By:
- Publication type:
- Article
Pitfalls in molecular diagnosis in a family with severe factor VII (FVII) deficiencymisdiagnosis by direct sequence analysis using a PCR product.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 9, p. 731, doi. 10.1002/pd.679
- By:
- Publication type:
- Article
ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura.
- Published in:
- 2010
- By:
- Publication type:
- Other
Gender equity in hemophilia: need for healthcare, familial, and societal advocacy.
- Published in:
- Frontiers in Medicine, 2024, p. 1, doi. 10.3389/fmed.2024.1345496
- By:
- Publication type:
- Article
Psychological and cognitive factors involved in decision‐making process of haemophilia carriers in reproductive choices.
- Published in:
- Haemophilia, 2023, v. 29, n. 5, p. 1313, doi. 10.1111/hae.14836
- By:
- Publication type:
- Article
Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A.
- Published in:
- Haemophilia, 2022, v. 28, n. 2, p. 270, doi. 10.1111/hae.14503
- By:
- Publication type:
- Article
Performance of a clinical risk prediction model for inhibitor formation in severe haemophilia A.
- Published in:
- Haemophilia, 2021, v. 27, n. 4, p. e441, doi. 10.1111/hae.14325
- By:
- Publication type:
- Article
Real‐life experience in switching to new extended half‐life products at European haemophilia centres.
- Published in:
- Haemophilia, 2019, v. 25, n. 6, p. 946, doi. 10.1111/hae.13834
- By:
- Publication type:
- Article
Clinical advances in gene therapy updates on clinical trials of gene therapy in haemophilia.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. 738, doi. 10.1111/hae.13816
- By:
- Publication type:
- Article
Genetic Variants Identified by Whole Exome Sequencing in a Large Italian Family with High Plasma Levels of Factor VIII and Von Willebrand Factor.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 18, p. 14167, doi. 10.3390/ijms241814167
- By:
- Publication type:
- Article