HLA genotype-clinical phenotype correlations are not established for multiple sclerosis (MS)
and neuromyelitis optica spectrum disorders (NMOSD). We studied HLA-DRB1/DPB1 …

Objective Multiple sclerosis (MS) is a partially heritable autoimmune disease. HLA-DR2 is
the largest identified genetic risk factor for MS. The largest identified genetic risk factor is …

Background: The genetic predisposition to multiple sclerosis (MS) is associated with HLA
alleles, especially HLA-DRB1* 15: 01. Objective: To identify associations between findings …

Multiple sclerosis (MS) is an autoimmune disease of the central nervous system (CNS) that
is characterized by injury to the myelin sheath and subsequent neurodegeneration. The …

Increasing our knowledge of the HLA system, including both the complete sequence
description and the assessment of its diversity at the worldwide human population-level, is of …

Background: Previous studies have shown that people with a family history are more likely to
develop multiple sclerosis (MS). The purpose of this study was to investigate the relationship …

Increasing our knowledge of the HLA system, including both the complete sequence
description and the assessment of its diversity at the worldwide human population-level, is of …

La sclérose en plaques (SEP) est une maladie inflammatoire neurodégénérative auto-
immune chronique du système nerveux central (SNC). Il n'existe pas de traitement efficace …

مقدمه: مطالعات انجام شده نشان می‌دهد که احتمال ابتلا به مالتیپل اسکلروزیس (Multiple sclerosis یا
MS) در افراد دارای سابقه‌ی خانوادگی بیشتر است. هدف از انجام پژوهش حاضر، بررسی ارتباط بین …‎

Multiple sclerosis (MS) is common inflammatory disease of the central nervous system
(CNS) and the hallmark is demyelination of the axons. Demyelination affects the cerebrum …