OP : 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

Opsoclonus-Myoclonus Syndrome - 새창 A neurological condition that is characterized by uncontrolled rapid irregular movements of the eye (OPSOCLONUS) and the muscle (MYOCLONUS) causing unsteady, trembling gait. It is also known as dancing eyes-dancing feet syndrome and is often associated with neoplasms, viral infections, or autoimmune disorders involving the nervous system.
Synonyms : Dancing Eyes-Dancing Feet Syndrome, Kinsbourne Syndrome, Opsoclonus Myoclonus Ataxia, Dancing Eyes Dancing Feet Syndrome, Opsoclonus Myoclonus Syndrome, Paraneoplastic Opsoclonus Myoclonus Ataxia
Opsonin Proteins - 새창 Proteins that bind to particles and cells to increase susceptibility to PHAGOCYTOSIS, especially ANTIBODIES bound to EPITOPES that attach to FC RECEPTORS. COMPLEMENT C3B may also participate.
Synonyms : Proteins, Opsonin
Optic Atrophies, Hereditary - 새창 Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER).
Synonyms : Optic Atrophy, Hereditary, Atrophies, Hereditary Optic, Atrophy, Hereditary Optic, Hereditary Optic Atrophies
Optic Atrophy - 새창 Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition.
Synonyms : Atrophy, Optic
Optic Atrophy, Autosomal Dominant - 새창 Dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity, color vision deficits, a centrocecal scotoma, and optic nerve pallor (Hum. Genet. 1998; 102: 79-86). Mutations leading to this condition have been mapped to the OPA1 gene at chromosome 3q28-q29. OPA1 codes for a dynamin-related GTPase that localizes to mitochondria.
Synonyms : Autosomal Dominant Optic Atrophy, Optic Atrophy Type 1, Optic Atrophy, Kjer Type, Dominant Optic Atrophies, Optic Atrophies, Dominant, Optic Atrophy, Dominant