| PFKL | phosphofructokinase, liver type; 6-phosphofructo-2-kinase, liver type |
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| PFKP | phosphofructokinase, platelet type; 6-phosphofructo-2-kinase, platelet type |
| AFB | Acid-Fast Bacillus(Type that causes Tuberculosis) |
| DMD | Duchenne type Muscular Dystrophy; 악성형 Duchenne형 근이영양증 |
| EA | 1) Esophageal Atresia Types 1. Esophageal Atresia with Dis... |
| communicating branch of otic ganglion with meningeal branch of mandibular nerve | <anatomy, nerve> A branch of otic ganglion to the meningeal branch of mandibular nerve conveying postsynaptic parasympathetic fibres which run back to the main stem of the mandibular nerve for distribution to the parotid gland via the auriculotemporal nerve. Synonym: ramus communicans ganglii otici cum ramo meningeo nervi mandibularis. (05 Mar 2000) |
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| posterior meningeal artery | <anatomy, artery> Origin, ascending pharyngeal; distribution, dura mater of posterior cranial fossa; anastomoses, branches of middle meningeal and vertebral. Synonym: arteria meningea posterior. (05 Mar 2000) |
| orbital branch of middle meningeal artery | <anatomy, artery> Branch of middle meningeal artery traversing superior orbital fissure and running toward lacrimal gland. See: anastomotic branch of middle meningeal artery to lacrimal artery. Synonym: ramus orbitalis arteriae meningeae mediae. (05 Mar 2000) |
| tuberculosis, meningeal | Tuberculous meningitis. The causative agent is mycobacterium tuberculosis. (12 Dec 1998) |
| acrocephalosyndactyly type 1 | <paediatrics> An inherited disease (autosomal dominant) or a spontaneously occurring disease characterised by a peaked head and unusual facial appearance, due to the premature closure of the cranial sutures. A skull X-ray can confirm the diagnosis and treatment is surgical. Inheritance: autosomal dominant. (27 Sep 1997) |
| Alzheimer type I astrocyte | Enlarged frequently multinucleated astrocytes, seen in progressive multifocal leukoencephalopathy. (05 Mar 2000) |
| Alzheimer type II astrocyte | Enlarged astrocytes with vesicular nuclei and one or more small basophilic nucleoli, seen in hepatocerebral disease and Wilson's disease. (05 Mar 2000) |
| American Type Culture Collection | <cell culture> A key resource for cultured cells, located in Rockville, USA. (12 Dec 1998) |
| Antoni type A neurilemoma | <tumour> Relatively solid or compact arrangement of neoplastic tissue that consists of Schwann cells arranged in twisting bundles and associated with delicate reticulin fibres; the nuclei of the Schwann cells are frequently grouped in parallel rows (so-called palisades), and the nuclei and fibres sometimes form exaggerated tactile corpuscles, called Verocay bodies. (05 Mar 2000) |
| Antoni type B neurilemoma | <tumour> Relatively soft or loose arrangement of neoplastic tissue that consists of Schwann cells in a haphazard or nondescript type of arrangement among reticulin fibres and tiny cystlike foci; fat-laden macrophages may be observed in some of the larger neoplasms. (05 Mar 2000) |
| arthus-type reaction's | Reaction's in man and other species that result from the same basic immunologic (allergic) mechanism which evokes, in the rabbit, the typical Arthus phenomenon. See: immune complex disease. (05 Mar 2000) |
| avian adenovirus type 1 proteinase | <enzyme> 206 aa residues of which 66% are homologous to human ad2 emzyme embl/genbank l13161 Registry number: EC 3.4.22.- Synonym: aavl proteinase, aavl endopeptidase (26 Jun 1999) |
| basic personality type | An individual's unique, covert, or underlying personality propensities, whether or not they are behaviourally manifest or overt, personality characteristics of an individual which are also shared by a majority of the members of a social group. (05 Mar 2000) |
| Becker type muscular dystrophy | A muscular dystrophy that has many of the clinical features of Duchenne muscular dystrophy e.g., symmetrical involvement of first the pelvicrural muscles and then the pectoral girdle and proximal upper extremity muscles; pseudohypertrophy, especially of the calf muscles but with a much later age of onset (35-45 years), and more benign course. X-linked inheritance. (05 Mar 2000) |
| Becker type tardive muscular dystrophy | Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal. Compare: Duchenne dystrophy. Synonym: Becker type tardive muscular dystrophy. (05 Mar 2000) |