| NF | Neuro-Fibromatosis = Von Recklinghausen's Disease NF 1; Neuro-Fibroma... |
|---|---|
| PFKL | phosphofructokinase, liver type; 6-phosphofructo-2-kinase, liver type |
| PFKP | phosphofructokinase, platelet type; 6-phosphofructo-2-kinase, platelet type |
| SADS | Schedule for Affective Disorders & Schizophrenia; 미국 고안 |
| SPR | Schizophrenia |
| schizophrenia, paranoid | A chronic form of schizophrenia characterised primarily by the presence of persecutory or grandiose delusions, often associated with hallucination. (12 Dec 1998) |
|---|---|
| pseudoneurotic schizophrenia | Schizophrenia in which the underlying psychotic process is masked by complaints ordinarily regarded as neurotic. (05 Mar 2000) |
| psychosis, schizophrenia | The most chronic and disabling of the major mental illnesses. Schizophrenia may be one disorder, or it may be many disorders, with different causes. Because of the disorder's complexity, few generalisations hold true for all people who are diagnosed as schizophrenic. (12 Dec 1998) |
| simple schizophrenia | Schizophrenia characterised by withdrawal, apathy, indifference, and impoverishment of human relationships without overt psychotic features. (05 Mar 2000) |
| disorganised schizophrenia | A severe form of schizophrenia characterised by the predominance of incoherence, blunted, inappropriate or silly affect, and the absence of systematised delusions. Synonym: hebephrenic schizophrenia. (05 Mar 2000) |
| latent schizophrenia | A preexisting susceptibility for developing overt schizophrenia under strong emotional stress. (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) |