Sentence examples for multiple sclerosis gender from inspiring English sources

In relapsing onset multiple sclerosis, gender influenced disability progression during Phase 1 only.

There were no restrictions on subtype of Multiple Sclerosis, gender, ethnicity or frequency of use of health care.

In relapsing onset multiple sclerosis, gender, age at onset, residual deficit after the first relapse and relapses during the first 2 years of multiple sclerosis were found to be independent predictive factors of disability progression, but only during Phase 1.

One of these studies (Confavreux et al., 2003) also showed that in the whole multiple sclerosis population, gender influenced the time from multiple sclerosis clinical onset to DSS 4, but not the time from DSS 4 to DSS 6 or 7. Our data demonstrated that only the relapsing onset phenotype accounted for this observation.

This gender disparity is particularly marked for autoimmune diseases, especially multiple sclerosis (MS) where the gender ratio is 2 3:1 [ 2, 3].

Prior reviews have suggested a female prevalence similar to that seen in classic forms of multiple sclerosis (Comi, 2004), however, no gender predilection was observed in the current series.

These comprised gender, age at multiple sclerosis onset and relapse history (relapses within the first 2 years, and residual deficit after the first relapse).

Average raw Cycle threshold values (Ct-avg), standard deviation (SD), coefficient of variability (CV) and sample size (n) for the qRT-PCR analyses of RNA samples from 20 patients with multiple sclerosis compared to 20 age and gender matched control subjects.

The 10 best candidate control genes, as well as commonly used house-keeping controls and PPIB, were validated with independent samples of whole-blood RNA from both patients with multiple sclerosis (MS) and age- and gender-matched controls by qRT-PCR.

Four cohorts of ethnically Danish patients, with verified multiple sclerosis [9], were identified together with controls of similar ethnicity and gender from the same part of the country.

Thus, our findings are robust, and characteristics such as gender distribution, age of onset and type of multiple sclerosis distribution of our cohort are similar to those reported in most other multiple sclerosis cohorts.