26 results on '"Yaouanq, Jacqueline"'
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2. REEP1 mutations in SPG31: Frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction
3. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
4. Evidence for a two-stage disability progression in multiple sclerosis
5. A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations
6. Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE)
7. Human leukocyte antigen (HLA) association and typing in hemochromatosis
8. Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis
9. Founder Effect in Patients with Unverricht-Lundborg Disease on Reunion Island
10. HLA class I gene polymorphism in genetic hemochromatosis
11. Evidence for Linkage Disequilibrium between HLA-DRB1 Gene and Multiple Sclerosis
12. Genetic analysis of multiple sclerosis in Europeans: French data
13. Small-area distribution of multiple sclerosis incidence in western France: in search of environmental triggers
14. DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family
15. Ferritin H gene polymorphism in idiopathic hemochromatosis
16. NOD2/CARD15 gene polymorphisms in Crohn's disease
17. Genetic interaction ofCTLA-4 with HLA-DR15 in multiple sclerosis patients
18. Haemochromatosis and HLA–H
19. The role of HLA-DR-DR and HLA-DR-DP interactions in genetic susceptibility to rheumatoid arthritis
20. Primary liver cancer in genetic hemochromatosis: A clinical, pathological, and pathogenetic study of 54 cases
21. Renal scintigraphy in insulin-dependent diabetes mellitus: Early glomerular and urologic dysfunction
22. Genetics of Hemochromatosis: HLA Association and Mode of Inheritancea.
23. Genetic interaction of CTLA‐4with HLA‐DR15 in multiple sclerosis patients
24. Genetic interaction of <TOGGLE>CTLA-4</TOGGLE> with HLA-DR15 in multiple sclerosis patients<FNR HREF="fn1"></FNR><FN ID="fn1"> Additional members of the Italian Group for MS Genetics and the Portuguese Group for MS Genetics are listed in the Appendix on page 122.</FN>
25. Genetics of Hemochromatosis: HLA Association and Mode of Inheritance
26. Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients.
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