Variation in major histocompatibility complex genes on chromosome 6p21. 3, specifically the
human leukocyte antigen HLA-DR2 or DRB1* 1501-DQB1* 0602 extended haplotype …

Detection of gene variants affecting the risk for multiple sclerosis provides insights into
mechanisms central for autoaggressive neuroinflammation. Major histocompatibility …

Eae5 in rats was originally identified in two F 2 intercrosses,(DA× BN) and (E3× DA),
displaying linkage to CNS inflammation and disease severity in experimental autoimmune …

The DR15 allele at the HLA DRB1 locus is a marker for immune-mediated bone marrow
failure syndromes. We hypothesized that HLA DR15 plays a role in T-cell interactions with …

We examined the influence of alleles at the HLA loci, previously found to be associated with
multiple sclerosis (MS) in Sardinia, on the clinical course of the disease in 835 relapsing (R) …

purpose. To investigate whether polymorphisms in the gene encoding the chemokine
receptor CX 3 CR1, which has been linked to changes in functional ligand-binding activity …

It has long been recognized that, despite living at geographical latitudes where multiple
sclerosis (MS) is common, genetically isolated ethnic groups—including Gypsies in Hungary …

Η πολλαπλή σκλήρυνση είναι αυτοάνοση φλεγμονώδης νόσος που χαρακτηρίζεται από
απομυελίνωση και εκφύλιση του κεντρικού νευρικού συστήματος. Η αυτοάνοση παθογένεσή …

Abstract In approximately 10-15% of cases Multiple Sclerosis follows a progressive rather
than a relapsing course and this is known as Primary Progressive Multiple Sclerosis …