منابع مشابه
The age of single-gene neurological disorders is not dead.
term follow up of patients with clinically isolated syndromes, relapsing-remitting and secondary progressive multiple sclerosis. et al. Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation. microarrays identify key mediators of autoimmune brain inflammation. The natural history of mult...
متن کاملStem Cell Therapy in Pediatric Neurological Disorders
Pediatric neurological disorders including muscular dystrophy, cerebral palsy, and spinal cord injury are defined as a heterogenous group of diseases, of which some are known to be genetic. The two significant features represented for stem cells, leading to distinguish them from other cell types are addressed as below: they can renew themselves besides the ability to differentiate into cells wi...
متن کاملNeurological Disorders
Historically, policy makers and researchers have used mortality statistics as the principal measure of the seriousness of diseases, based on which countries and organizations have launched disease control programs. Mortality statistics alone, however, underestimate the suffering caused by diseases that may be nonfatal but cause substantial disability. Many neurological and psychiatric condition...
متن کاملGenetics of neurological disorders.
Neurological diseases are defined as an inappropriate function of the peripheral or central nervous system due to impaired electrical impulses throughout the brain and/or nervous system that may present with heterogeneous symptoms according to the parts of the system involved in these pathologic processes. Growing evidence on genetic components of neurological disease have been collected during...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Australian Journal of Physiotherapy
سال: 1963
ISSN: 0004-9514
DOI: 10.1016/s0004-9514(14)60790-x