153 results on '"Momigliano-Richiardi P"'
Search Results
2. A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy
3. Concordance, disease progression, and heritability of coeliac disease in Italian twins
4. Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5′ regulatory region
5. Genetics of Multiple Sclerosis: Linkage and Association Studies
6. Detection of AGXT gene mutations by denaturing high-performance liquid chromatography for diagnosis of hyperoxyluria type 1
7. HLA class I in acute promyelocytic leukemia (APL): possible correlation with clinical outcome
8. HLA-class I markers and multiple sclerosis susceptibility in the Italian population
9. A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population
10. Two Single-Nucleotide Polymorphisms in the 5′ and 3′ Ends of the Osteopontin Gene Contribute to Susceptibility to Systemic Lupus Erythematosus
11. Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency
12. Additional factor in some HLA DR3/DQ2 haplotypes confers a fourfold increased genetic risk of celiac disease
13. New polymorphisms in the IL-10 promoter region
14. The IL12B gene does not confer susceptibility to coeliac disease
15. MICA and MICB microsatellite alleles in HLA extended haplotypes
16. HLA CLASS I AND SUSCEPTIBILITY TO ACUTE PROMYELOCYTIC LEUKEMIA
17. MAPPING OF A PUTATIVE RECOMBINATION HOT SPOT IN THE HLA CENTRAL REGION
18. Association between polymorphisms in the TNF region and systemic lupus erythematosus in the Italian population
19. Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families
20. Role of SOCS2 in regulating Gh signaling: screening of variations associated with idiopathic short stature, preliminary data
21. Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans
22. HLA-multiple sclerosis association in continental Italy and correlation with disease prevalence in Europe
23. Prolactin and prolactin receptor gene polymorphisms in multiple sclerosis and systemic lupus erythematosus
24. CD45 and Multiple Sclerosis: the exon 4 C77G polymorphism and new markers
25. Identification of single nucleotide variations in the coding and regulatory regions of the myelin-associated glycoprotein gene and study of their association with multiple sclerosis
26. Molecular Analysis of Growth Hormone Releasing Hormone Receptor Gene (GHRH-R) in isolated growth hormone deficiency: identification of a likely etiological mutation in the signal peptide
27. Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families
28. An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population
29. Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects
30. HLA-class I markers and multiple sclerosis susceptibility in the Italian population
31. A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy
32. SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS)
33. Two single‐nucleotide polymorphisms in the 5′ and 3′ ends of the osteopontin gene contribute to susceptibility to systemic lupus erythematosus
34. Genetic defects in GH synthesis and secretion
35. TheIL12Bgene does not confer susceptibility to coeliac disease
36. Molecular Analysis of the Growth Hormone Releasing Hormone Receptor (GHRH-R) Gene in Isolated Growth Hormone Deficiency: Identification of a Likely Etiological Mutation in the Signal Peptide
37. Molecular Analysis of the Growth Hormone Gene (GH1) in Isolated Growth Hormone Deficiency
38. Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families
39. Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease
40. Similar ectopic expression of ICAM-1 and HLA Class II molecules in hypertrophic scars following thermal injury
41. Neuropeptide S Receptor 1 Gene Polymorphism Is Associated With Susceptibility to Inflammatory Bowel Disease.
42. Reassessment of the Specificity of Lens Opacities in Myotonic Dystrophy.
43. A novel recessive splicing mutation in the POU1F1gene causing combined pituitary hormone deficiency
44. Genetic interaction of CTLA‐4with HLA‐DR15 in multiple sclerosis patients
45. 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>
46. Determination of SNP allele frequencies in pooled DNAs by primer extension genotyping and denaturing high-performance liquid chromatography
47. Systemic lupus erythematosus candidate genes in the Italian population: Evidence for a significant association with interleukin-10
48. Historical recombinant sites in extended HLA haplotypes
49. Molecular analysis of the growth hormone releasing hormone receptor gene (GHRH-R) in isolated growth hormone deficiency: Identification of a likely etiological mutation in the signal peptide
50. Maternal effect in multiple sclerosis.
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