|
|
|
|
LEADER |
04313nma a2200913 u 4500 |
001 |
EB002039083 |
003 |
EBX01000000000000001182749 |
005 |
00000000000000.0 |
007 |
cr||||||||||||||||||||| |
008 |
220822 ||| eng |
020 |
|
|
|a books978-3-0365-3097-0
|
020 |
|
|
|a 9783036530970
|
020 |
|
|
|a 9783036530963
|
100 |
1 |
|
|a Rivera, Víctor M.
|
245 |
0 |
0 |
|a Multiple Sclerosis
|h Elektronische Ressource
|b Diagnosis and Treatment
|
260 |
|
|
|a Basel
|b MDPI - Multidisciplinary Digital Publishing Institute
|c 2022
|
300 |
|
|
|a 1 electronic resource (192 p.)
|
653 |
|
|
|a genetics
|
653 |
|
|
|a Rituxan
|
653 |
|
|
|a innate immune system
|
653 |
|
|
|a neuronal
|
653 |
|
|
|a cognitive impairment
|
653 |
|
|
|a outcome measures
|
653 |
|
|
|a anti-CD20
|
653 |
|
|
|a monoclonal antibodies
|
653 |
|
|
|a remyelination
|
653 |
|
|
|a autologous hematopoietic
|
653 |
|
|
|a induced pluripotent
|
653 |
|
|
|a Medicine / bicssc
|
653 |
|
|
|a NADPH oxidase
|
653 |
|
|
|a stem cells
|
653 |
|
|
|a multiple sclerosis
|
653 |
|
|
|a mitochondria
|
653 |
|
|
|a oligodendrocyte
|
653 |
|
|
|a autoimmunity
|
653 |
|
|
|a pregnancy
|
653 |
|
|
|a demyelinating diseases
|
653 |
|
|
|a neurodegeneration
|
653 |
|
|
|a aquaporin 4-IgG
|
653 |
|
|
|a interleukin-2
|
653 |
|
|
|a biomarkers
|
653 |
|
|
|a CD25
|
653 |
|
|
|a reactive oxygen species
|
653 |
|
|
|a myelin
|
653 |
|
|
|a relapsing multiple sclerosis
|
653 |
|
|
|a Tysabri
|
653 |
|
|
|a disease modifying therapies
|
653 |
|
|
|a progressive multiple sclerosis
|
653 |
|
|
|a DRESS
|
653 |
|
|
|a drug reaction with eosinophilia systemic symptoms
|
653 |
|
|
|a post-partum
|
653 |
|
|
|a treatment
|
653 |
|
|
|a demyelination
|
653 |
|
|
|a disease modifying therapy
|
653 |
|
|
|a clinical trial
|
653 |
|
|
|a association study
|
653 |
|
|
|a Ocrevus
|
653 |
|
|
|a cortex
|
653 |
|
|
|a neuromyelitis optica spectrum disorders
|
653 |
|
|
|a mesenchymal
|
653 |
|
|
|a axon
|
653 |
|
|
|a anti-MOG syndrome
|
653 |
|
|
|a cognitive dysfunction
|
653 |
|
|
|a CYBB
|
653 |
|
|
|a human embryonic
|
653 |
|
|
|a generic medicines
|
653 |
|
|
|a daclizumab
|
653 |
|
|
|a myelin oligodendrocyte glycoprotein
|
700 |
1 |
|
|a Rivera, Víctor M.
|
041 |
0 |
7 |
|a eng
|2 ISO 639-2
|
989 |
|
|
|b DOAB
|a Directory of Open Access Books
|
500 |
|
|
|a Creative Commons (cc), https://creativecommons.org/licenses/by/4.0/
|
028 |
5 |
0 |
|a 10.3390/books978-3-0365-3097-0
|
856 |
4 |
2 |
|u https://directory.doabooks.org/handle/20.500.12854/78841
|z DOAB: description of the publication
|
856 |
4 |
0 |
|u https://www.mdpi.com/books/pdfview/book/4935
|7 0
|x Verlag
|3 Volltext
|
082 |
0 |
|
|a 610
|
082 |
0 |
|
|a 140
|
082 |
0 |
|
|a 700
|
520 |
|
|
|a Multiple sclerosis (MS) offers important challenges to understanding its complex genetics and molecular and immunological mechanisms, which eventually lead to relapsing and progressive clinical forms and a constellation of clinical manifestations. Along with the progress in knowledge, disease-modifying treatments and new therapeutic molecules have made an impact on the prognosis of the disease. Essential in the diagnostic identification process of MS is the differentiation of this major demyelinating disease with other inflammatory CNS disorders, including Neuromyelitis Optica and MOG antibody disease. MS is more prevalent in women; therefore, pregnancy and post-partum hormonal and immunological changes typically affect the clinical behavior of the disease. This Special Issue of Biomedicines addresses recent advances in the mechanistic genetic and immunological processes of MS, opening more options to future studies and to the consideration of further therapeutic possibilities. The issue discusses the application of modern therapies, including monoclonal antibodies, some still in the process of complete development, and the current strategies managing progressive MS. The aim of this issue is to stimulate basic and clinical research and promote observations on the ever-expanding and complex field of MS. Advancement in the understanding of the mechanisms and the clinical characterizations of this disease should result in improved therapeutic outcomes that reduce neurological and cognitive disability commonly associated with progressive disease.
|