Pages that link to "Q67981677"

The following pages link to Diagnostic criteria for multiple sclerosis research involving multiply affected families (Q67981677):

Displaying 25 items.

• IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patients (Q24599179) (← links)
• Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis (Q28218229) (← links)
• Familial multiple sclerosis: MRI findings in clinically affected and unaffected siblings (Q33591696) (← links)
• HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course (Q33904555) (← links)
• A second-generation genomic screen for multiple sclerosis (Q33910544) (← links)
• Genetic burden in multiple sclerosis families (Q33916650) (← links)
• A high-density screen for linkage in multiple sclerosis (Q34021149) (← links)
• Alzheimer diseases: a model of gene mutations and susceptibility polymorphisms for complex psychiatric diseases (Q34461295) (← links)
• Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis (Q34993579) (← links)
• Genetics and pathogenesis of multiple sclerosis (Q35004746) (← links)
• Clonal expansions of activated gamma/delta T cells in recent-onset multiple sclerosis (Q36081667) (← links)
• Aggregation of multiple sclerosis genetic risk variants in multiple and single case families (Q36438926) (← links)
• The T‐cell response to myelin basic protein in familial multiple sclerosis: Diversity of fine specificity, restricting elements, and T‐cell receptor usage (Q41532565) (← links)
• Cytokines in genetic susceptibility to multiple sclerosis: a candidate gene approach. French Multiple Sclerosis Genetics Group. (Q42616750) (← links)
• Pharmacogenomic analysis of interferon receptor polymorphisms in multiple sclerosis. (Q42695938) (← links)
• PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients (Q44118357) (← links)
• Intercellular adhesion molecule-1: a protective haplotype against multiple sclerosis. (Q45022950) (← links)
• Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis (Q45416078) (← links)
• Sequence variation in the transforming growth factor-beta1 (TGFB1) gene and multiple sclerosis susceptibility (Q46450678) (← links)
• Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study (Q47408285) (← links)
• CTLA4 is associated with susceptibility to multiple sclerosis (Q56904087) (← links)
• The HLA locus and multiple sclerosis in Spain. Role in disease susceptibility, clinical course and response to interferon-β (Q57602052) (← links)
• The R131 low-affinity allele of the Fc gamma RIIA receptor is associated with systemic lupus erythematosus but not with other autoimmune diseases in French Caucasians (Q57812260) (← links)
• A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group (Q71230101) (← links)
• A vulnerability locus to multiple sclerosis maps to 7p15 in a region syntenic to an EAE locus in the rat (Q75305446) (← links)