154 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. SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS)
8. HLA class I in acute promyelocytic leukemia (APL): possible correlation with clinical outcome
9. HLA-class I markers and multiple sclerosis susceptibility in the Italian population
10. A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population
11. Two Single-Nucleotide Polymorphisms in the 5′ and 3′ Ends of the Osteopontin Gene Contribute to Susceptibility to Systemic Lupus Erythematosus
12. Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency
13. Additional factor in some HLA DR3/DQ2 haplotypes confers a fourfold increased genetic risk of celiac disease
14. New polymorphisms in the IL-10 promoter region
15. The IL12B gene does not confer susceptibility to coeliac disease
16. MICA and MICB microsatellite alleles in HLA extended haplotypes
17. HLA CLASS I AND SUSCEPTIBILITY TO ACUTE PROMYELOCYTIC LEUKEMIA
18. MAPPING OF A PUTATIVE RECOMBINATION HOT SPOT IN THE HLA CENTRAL REGION
19. Association between polymorphisms in the TNF region and systemic lupus erythematosus in the Italian population
20. Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families
21. Role of SOCS2 in regulating Gh signaling: screening of variations associated with idiopathic short stature, preliminary data
22. Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans
23. HLA-multiple sclerosis association in continental Italy and correlation with disease prevalence in Europe
24. Prolactin and prolactin receptor gene polymorphisms in multiple sclerosis and systemic lupus erythematosus
25. CD45 and Multiple Sclerosis: the exon 4 C77G polymorphism and new markers
26. 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
27. 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
28. Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families
29. An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population
30. Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects
31. HLA-class I markers and multiple sclerosis susceptibility in the Italian population
32. A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy
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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