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1. Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG

2. New insights into the genetic etiology of Alzheimer's disease and related dementias

3. Military supply, everyday demand, and reindeer:zooarchaeology of Nazi German Second World War military presence in Finnish Lapland, Northernmost Europe

4. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

7. Genetic architecture of human plasma lipidome and its link to cardiovascular disease

8. Genetic architecture of human plasma lipidome and its link to cardiovascular disease

9. The effects of interleukin-8, VEGF and CFH polymorphisms on the long-term response to bevacizumab therapy in exudative age-related macular degeneration

14. Single nucleotide polymorphisms of the tenomodulin gene (TNMD) in age-related macular degeneration

19. Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG.

20. A founder mutation in CERKL is a major cause of retinal dystrophy in Finland.

21. Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degeneration†.

22. The genetic variant rs4073 A→T of the Interleukin-8 promoter region is associated with the earlier onset of exudative age-related macular degeneration.

23. The IL-8, VEGF, and CFH polymorphisms and bevacizumab in age-related macular degeneration.

24. Interleukin 8 promoter polymorphism predicts the initial response to bevacizumab treatment for exudative age-related macular degeneration.

25. Leucocyte telomere length in age-related macular degeneration.

26. Adiponectin receptor 1 gene (ADIPOR1) variant is associated with advanced age-related macular degeneration in Finnish population.

27. Lack of complement inhibitors in the outer intracranial artery aneurysm wall associates with complement terminal pathway activation.

28. Screening of DNA-variants in the properdin gene (CFP) in age-related macular degeneration (AMD).

29. Vascular endothelial growth factor gene variation and the response to photodynamic therapy in age-related macular degeneration.

30. [Properdin mutations a risk factor for meningitis].

31. [Pathogenesis of age-related macular degeneration].

32. [Identification of susceptibility genes for age-related macular degeneration--a success story of molecular genetics].

33. Single nucleotide polymorphisms of the tenomodulin gene (TNMD) in age-related macular degeneration.

34. Complement factor H Y402H polymorphism and characteristics of exudative age-related macular degeneration lesions.

35. Y402H polymorphism of complement factor H affects binding affinity to C-reactive protein.

36. Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish population.

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