| FC | fasciculus cuneatus; fast component [of a neuron]; febrile convulsions; feline conjunctivitis; ferri... |
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| GCN | geometric constraint network; giant cerebral neuron |
| GSCN | giant serotonin-containing neuron |
| GSN | gelsonin; giant serotonin-containing neuron |
| HN | head and neck; head nurse; hemagglutinin neuraminidase; hematemesis neonatorum; hemorrhage of newbor... |
| upper motor neuron | Clinical term indicating those neuron's of the motor cortex that contribute to the formation of the pyramidal or corticospinal and corticobulbar tracts, as distinguished from the lower motor neuron's innervating the skeletal muscles. Although not motor neuron's in the strict sense, these cortical neuron's became colloquially classified as motor neuron's because their stimulation produces movement and their destruction causes severe disorders of movement. See: motor neuron, motor cortex. (05 Mar 2000) |
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| upper motor neuron lesion | Injury to cerebral descending (corticonuclear) fibres above the brainstem or spinal motor nerve nucleus. Synonym: upper motor neuron lesion. (05 Mar 2000) |
| lower motor neuron | Clinical term used to indicate the final motor neuron's that innervate the skeletal muscles; distinguished from upper motor neuron's of the motor cortex that contribute to the pyramidal or corticospinal tract. See: motor neuron. (05 Mar 2000) |
| lower motor neuron dysarthria | Dysarthria caused by dysfunction of the motor nuclei and the lower pons or medulla, or other neural connections, central and peripheral to the muscles of articulation. (05 Mar 2000) |
| lower motor neuron lesion | Injury to motor cells in the brainstem or spinal cord, or of the axons derived from them. (05 Mar 2000) |
| 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) |