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MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 3
  • Amyloidosis - »õâ A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits.
    Synonyms : Amyloidoses
  • Amyloidosis, Familial - »õâ Diseases in which there is a familial pattern of AMYLOIDOSIS.
    Synonyms : Amyloidoses, Familial, Amyloidoses, Hereditary, Familial Amyloidoses, Familial Amyloidosis, Hereditary Amyloidoses, Hereditary Amyloidosis
  • Amylopectin - »õâ A highly branched glucan in starch.
    Synonyms :
  • Amylose - »õâ An unbranched glucan in starch.
    Synonyms :
  • Amyotrophic Lateral Sclerosis - »õâ A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
    Synonyms : ALS (Amyotrophic Lateral Sclerosis), Amyotrophic Lateral Sclerosis With Dementia, Amyotrophic Lateral Sclerosis, Guam Form, Dementia With Amyotrophic Lateral Sclerosis, Gehrig's Disease, Guam Form of Amyotrophic Lateral Sclerosis, Lou Gehrig's Disease
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MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 3
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