MUS : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 5 페이지: 8

Muscular Atrophy, Spinal - 새창 A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)
Synonyms : Adult Spinal Muscular Atrophy, Bulbo-Spinal Atrophy, X-Linked, Distal Spinal Muscular Atrophy, Myelopathic Muscular Atrophy, Myelopathic Muscular Atrophy, Progressive, Progressive Myelopathic Muscular Atrophy, Spinal Muscular Atrophy, Distal
Muscular Diseases - 새창 Acquired, familial, and congenital disorders of skeletal muscle (MUSCLE, SKELETAL) and smooth muscle (MUSCLE, SMOOTH).
Synonyms : Myopathic Conditions, Muscle Disorder, Muscular Disease, Myopathic Condition, Myopathy
Muscular Disorders, Atrophic - 새창 Disorders characterized by an abnormal reduction in muscle volume due to a decrease in the size or number of muscle fibers. Atrophy may result from diseases intrinsic to muscle tissue (e.g., MUSCULAR DYSTROPHY) or secondary to PERIPHERAL NERVOUS SYSTEM DISEASES that impair innervation to muscle tissue (e.g., MUSCULAR ATROPHY, SPINAL).
Synonyms : Atrophic Muscular Disorders, Spinobulbar Atrophy, Spinopontine Atrophy, Atrophic Muscular Disorder, Atrophies, Disuse, Atrophies, Spinobulbar, Atrophies, Spinobulbar Muscular, Atrophies, Spinopontine, Atrophy, Spinobulbar, Atrophy, Spinobulbar Muscular
Muscular Dystrophies - 새창 A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS.
Synonyms : Myodystrophica, Myodystrophy, Dystrophies, Muscular, Dystrophy, Muscular, Myodystrophicas, Myodystrophies
Muscular Dystrophies, Limb-Girdle - 새창 A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).
Synonyms : Limb-Girdle Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Muscular Dystrophy, Limb-Girdle, Limb Girdle Muscular Dystrophies, Limb Girdle Muscular Dystrophy, Muscular Dystrophies, Limb Girdle, Muscular Dystrophy, Limb Girdle