138 results on '"Wulff, Karin"'
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2. An Ordinary Day – OAAT Team, Malmö
3. Team and Progress
4. Inheritance Pattern of Hereditary Angioedema Indicates Mutation-Dependent Selective Effects During Early Embryonic Development
5. Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation
6. Making the Leap with Couples in Sweden: One-at-a-Time Mindset in Action
7. Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence
8. Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene
9. Mutant plasminogen in hereditary angioedema is bypassing FXII/kallikrein to generate bradykinin
10. Inheritance pattern of hereditary angioedema indicates mutation-dependent selective effects during early embryonic development
11. Common polymorphisms and cardiovascular factors in patients with myocardial infarction of Costa Rica
12. Molecular diagnosis of hemophilia A and B. Report of five families from Costa Rica
13. Faktor-XII-Mangel, APC-Resistenz, Hyperhomocysteinämie und von-Willebrand-Erkrankung Typ 1 in einer Familie
14. Hereditäres Angioödem in einer Familie mit spezifischen Mutationen sowohl im Plasminogen‐ als auch im SERPING1‐Gen
15. Hereditary angioedema in a single family with specific mutations in both plasminogen and SERPING1 genes
16. Treatment of Hereditary Angioedema with the Mutation c.988A>G (p.K330E) in the Plasminogen Gene
17. Hereditary angioedema caused by missense mutations in the factor XII gene: Clinical features, trigger factors, and therapy
18. Antihistamine-resistant Angioedema in Women with Negative Family History: Estrogens and F12 Gene Mutations
19. The FXIIIVal34Leu, common and risk factors of venous thrombosis in early middle-age Costa Rican patients
20. HOMOZYGOUS FACTOR X GENE MUTATIONS GLY380ARG AND TYR163DELAT ARE ASSOCIATED WITH PERINATAL INTRACRANIAL HEMORRHAGE
21. Lithuanian haemophilia A and B registry comprising phenotypic and genotypic data
22. Molecular Biology and Clinical Manifestation of Hereditary Factor VII Deficiency
23. Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N‐terminal cleavage site of bradykinin
24. Ett Samtal i Taget: Parterapi på en gång
25. World distribution of factor V Leiden mutation
26. Severe Tongue Swellings In Hereditary Angioedema With A Specific Mutation In The Plasminogen Gene
27. Prevalence of eight molecular markers associated with thrombotic diseases in six Amerindian tribes and two African groups of Costa Rica
28. Tamoxifen, a Trigger Factor of Hereditary Angioedema with Normal C1-INH with a Specific Mutation in the F12 Gene (HAE-FXII)
29. Hereditary Angioedema with Normal C1-INH with Versus without a Specific Mutation in the F12 Gene
30. Molecular diagnosis of hemophilia A and B. Report of five families from Costa Rica
31. Common polymorphisms and cardiovascular factors in patients with myocardial infarction of Costa Rica
32. 83 Hereditary Angioedema and Normal C1-Inhibitor (HAE TYPE III)
33. A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor
34. Characterization of a Novel Aberrant Splice Site, 79bp Downstream of Exon 5 in the Human Factor 7 Gene Detected in Patients with Severe Congenital Factor VII Deficiency.
35. Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic Republic
36. Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyadh anomaly
37. The FXIIIVal34Leu, common and risk factors of venous thrombosis in early middle‐age Costa Rican patients
38. Analysis of Structural Changes of the Factor VIII Gene: Intron 1 and 22, in Costarrican Families with Severe Haemophilia A.
39. Influence of Factor V HR2 on Thrombin Generation and Clinical Manifestation in Rare Bleeding Disorders
40. Prevalence of eight molecular markers associated with thrombotic diseases in six Amerindian tribes and two African groups of Costa Rica
41. Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency)
42. Twenty two novel mutations of the factor VII gene in factor VII deficiency
43. Severe clinical expression in X-linked Emery–Dreifuss muscular dystrophy
44. Molekulare Genanalyse und Gendiagnostik bei Hämophilie B und Faktor-VII-Mangel
45. Six novel mutations in the emerin gene causing X‐linked Emery‐Dreifuss muscular dystrophy
46. Haemophilia B in Female Twins Caused by a Point Mutation in one Factor IX Gene and Nonrandom Inactivation Patterns of the X-Chromosomes
47. World distribution of factor V Leiden mutation
48. Twenty-five novel mutations of the factor IX gene in haemophilia B
49. Mutations of the iduronate-2-sulfatase (IDS) gene in patients with hunter syndrome (mucopolysaccharidosis II)
50. Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic Republic.
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