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Titlebook: Early Indicators Early Treatments Neuroprotection in Multiple Sclerosis; Otto R. Hommes,Giancarlo Comi Book 2004 Springer-Verlag Italia 20

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Antibody Mediated Demyelination, laboratory marker supporting the diagnosis of this disease. The intrathecal IgG fractions contain Abs with many different specificities, including myelin-specific Abs. Reports on anti-myelin Abs in cerebrospinal (CSF) and sera are controversial [1-7]. Several reports describe the presence of anti-m
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Sunlight, Vitamin D, and Multiple Sclerosis, progression of the disease [1]. Compared with unrelated individuals, biological first-degree relatives of MS patients show a 20- to 40-fold increased risk of disease, and this increased risk is attributable to genetic factors, rather than a transmissible agent [2]. However, 70% of monozygotic twin
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The Yin and Yang of Inflammation in Multiple Sclerosis,by attacks of neurological dysfunction due to focal central nervous system (CNS) inflammation, followed by recovery and a period of remission, and on the other side is primary progressive (PP) disease, which is progressive from the outset with no clinical relapses. Between these two extremes are pat
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https://doi.org/10.1007/978-3-8274-2676-5 relapse, for instance, or the transition from relapsing-remitting disease to progressive accumulation of disability. Here, we report observation from the close study of a small number of patients treated with an experimental agent, Campath-1H, that cast some light on these issues.
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https://doi.org/10.1007/978-3-7091-4484-8 to ten genes theoretically having a major impact on disease susceptibility [1-3]. This is supported by epidemiological data demonstrating a considerable lowering of concordance rates from monozygotic to dizygotic twins [4]. It has been known for approximately 30 years that certain haplotypes of the
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Weiterempfehlungen mit Service-Recoveryedness was the natural result of blood vessel physiology. Now we know that the blood vessels are only one of the many factors involved in inflammation, a process in which immune cells of various types and their molecular products interact with signal molecules produced by the injured tissue.
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