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排序方式: 共有2322条查询结果,搜索用时 46 毫秒
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S A Edlavitch R Crow G L Burke J Huber R Prineas H Blackburn 《Journal of clinical epidemiology》1990,43(1):93-99
One method used to control costs in community cardiovascular disease surveillance is to limit the number of electrocardiograms (ECGs) used to validate acute myocardial infarction (AMI). The Minnesota Heart Survey investigated the impact of decreasing the maximum number of ECGs analyzed on classification of ECG pattern and final AMI diagnosis (definite, probable, none). A 50% sample of all 1980 acute CHD hospital discharge records (ICD-9 code 410 or 411) from 30 of 31 Twin Cities hospitals were abstracted. Comparing results using all available ECGs in the record (maximum of 12) with those obtained using up to 4 ECGs showed little differences in the ECG classification or final AMI diagnosis. 相似文献
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Leonidas JC; Berdon WE; Valderrama E; Neveling U; Schuval S; Weiss SJ; Hilfer C; Godine L 《Radiology》1996,198(2):377
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F. Okada T. J. Crow G. W. Roberts 《Journal of neural transmission (Vienna, Austria : 1996)》1991,84(1-2):147-153
Summary We have measured the amount of Gi (the inhibitory G-protein) or Go (a similar G-protein of unknown function) in 5 areas of the medial temporal lobe of control and schizophrenic brains utilizing pertussis toxin-catalyzed ADP ribosylation. The material used has previously been shown to have asymmetrical structural abnormalities of the ventricular system. The amount of Gi or Go was reduced on the left side in the hippocampus, amygdala and parahippocampal gyrus, the difference reaching significance in the hippocampus. This data is the first report of a neurochemical correlate of the structural change in the brains of patients with schizophrenia. Decreased Gi or Go in hippocampus may relate to other reported neurochemical deficits or other transmembrane signalling abnormalities. Further investigations of these indices of secondary messenger function in relation to structural changes are indicated. 相似文献
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Y J Crow S M Zuberi R McWilliam J L Tolmie A Hollman K Pohl J B Stephenson 《Journal of medical genetics》1998,35(2):94-98
The Coffin-Lowry syndrome is a rare cause of mental retardation recognised by its distinctive facial and digital features. We have observed an unusual, non-epileptic, cataplexy-like phenomenon in three subjects with the syndrome and we speculate that this feature may go unrecognised. We also provide evidence of neuromuscular dysfunction as part of the phenotype by showing abnormalities on muscle ultrasound in four gene carriers. 相似文献
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Kaufmann SJ; Sharif K; Sharma V; McVerry BA 《Human reproduction (Oxford, England)》1998,13(2):498-499
The patient was diagnosed in childhood as having severe congenital
neutropenia and had recurrent admissions with severe infections. In 1987,
prior to getting married, she was sterilized. She continued to require i.v.
antibiotics when she contracted a severe infection. On one occasion, she
was treated with growth colony stimulating factor (G- CSF). Her increased
neutrophil count was sustained following this treatment. In June 1993, she
wished to start a family and underwent in- vitro fertilization (IVF)
treatment. G-CSF was given prior to oocyte retrieval. She conceived on her
first cycle and an ultrasound scan revealed a singleton pregnancy.
Throughout the course of the pregnancy, her white cell count was monitored
closely and remained at <1.0x10(9)/l. The pregnancy progressed
uneventfully and at 37 weeks gestation she was admitted for G-CSF
injections. At 38 weeks she was delivered of a boy weighing 3350 g, by
elective Caesarean section. His white cell count was normal. This is the
first case of G-CSF being used before conception and during pregnancy in a
patient with congenital neutropenia. It shows that advances in cytokine
therapy and close interdisciplinary liaison can lead to a successful
outcome and help patients, who would otherwise remain childless, to achieve
a family.
相似文献