613 results on '"Wulff K."'
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2. Sleep-related memory consolidation in the psychosis spectrum phenotype
3. Achieving accurate estimates of fetal gestational age and personalised predictions of fetal growth based on data from an international prospective cohort study: a population-based machine learning study
4. Modellbasierte Folgeregelung fur nichtlineare Regelstrecken am Beispiel der Ladedruckregelung – Ein applikationsnaher Entwurf
5. Hereditary angioedema with a mutation in the plasminogen gene
6. Therapeutical Options for Congenital FVII Deficiency — The HK 7 Project of the International Greifswald Registry of the Congenital FVII Deficiency (GR-HK-7)
7. Characterization of a Mutation in Exon 1 of the FVII Gene — a Case of RNA Editing?
8. Factor VII Deficiency: Clinical Manifestation and Molecular Genetics of 718 Subjects with FVII Gene Mutations
9. Influence of Factor VHR2 on Endogenous Thrombin Potential and Clinical Phenotype in Factor VII Deficiency
10. Characterization of Three Novel Mutations in the Sodium Binding Site of Coagulation Factor X
11. Characterization of a Mutation in the 5′ Flanking Region and a Novel IVS7 Splice site Mutation in a Patient with Severe FVII Deficiency
12. U.S. Congregational Life Survey, 2001, Seventh-Day Adventist Leaders
13. U.S. Congregational Life Survey, 2001, United Methodist Leaders
14. U.S. Congregational Life Survey, 2001, Fast-Growing Presbyterian Profile
15. U.S. Congregational Life Survey, 2001, Random Attenders
16. U.S. Congregational Life Survey, 2001, Southern Baptist Attenders
17. U.S. Congregational Life Survey, 2001, Seventh-Day Adventist Profile
18. U.S. Congregational Life Survey, 2001, Racial Ethnic Presbyterian Leaders
19. U.S. Congregational Life Survey, 2001, Presbyterian Attenders
20. U.S. Congregational Life Survey, 2001, Presbyterian Leaders
21. U.S. Congregational Life Survey, 2001, Church of the Nazarene Leaders
22. U.S. Congregational Life Survey, 2001, Southern Baptist Profile
23. U.S. Congregational Life Survey, 2001, Seventh-Day Adventist Attenders
24. U.S. Congregational Life Survey, 2001, Lutheran Attenders
25. U.S. Congregational Life Survey, 2001, Church of the Nazarene Attenders
26. U.S. Congregational Life Survey, 2001, United Church of Christ Leaders
27. U.S. Congregational Life Survey, 2001, Fast-Growing Presbyterian Leaders
28. U.S. Congregational Life Survey, 2001, Lutheran Profile
29. U.S. Congregational Life Survey, 2001, United Methodist Profile
30. U.S. Congregational Life Survey, 2001, Presbyterian Profile
31. U.S. Congregational Life Survey, 2001, United Methodist Attenders
32. U.S. Congregational Life Survey, 2001, Racial Ethnic Presbyterian Attenders
33. U.S. Congregational Life Survey, 2001, United Church of Christ Profile
34. U.S. Congregational Life Survey, 2001, Church of the Nazarene Profile
35. U.S. Congregational Life Survey, 2001, Random Profile
36. U.S. Congregational Life Survey, 2001, Random Attenders Backfile
37. U.S. Congregational Life Survey, 2001, United Church of Christ Attenders
38. Individual differences in slow wave sleep architecture relate to variation in white matter microstructure across adulthood
39. Three Novel Microdeletions and the First Insertion / Deletion in Patients with Factor X Deficiency
40. Homozygous Factor X Gene Mutation Gly380Arg is Associated to Perinatal Intracranial Hemorrhage
41. Factor V Leiden and other thrombotic risk factors in CHD and myocardial Infarction
42. Molecular Analysis of Hemophilia B: »Greifswald Registry FIX Deficiency (Hemophilia B)«
43. Gly222Asp and Ser379Lys — Novel Factor X Gene Mutations in severe FX Deficiency — Greifswald Registry of Factor X congenital Deficiency
44. Hereditary Antithrombin Deficiency — Results of a Family Study
45. Lithuanian Hemophilia A and B Register Comprising Phenotypic and Genotypic Data
46. Greifswald Hemophilia B Study
47. Twenty-Two Novel Mutations of Factor VII Gene in Factor VII Deficiency
48. Prevalence of Common Mutations and Polymorphisms of the Genes of FII, FV, FVII, FXII, FXIII, MTHFR and ACE — Identified As Risk Factors for Venous and Arterial Thrombosis — in Germany and Different Ethnic Groups (Indians, Blacks) of Costa Rica
49. Treatment for hereditary angioedema with normal C1‐INH and specific mutations in the F12 gene (HAE‐FXII)
50. Analyse von Genmutationen bei hereditärem Faktor-VII-Mangel
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