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排序方式: 共有275条查询结果,搜索用时 687 毫秒
81.
EA Mitchell KP Nelson JMD Thompson AW Stewart BJ Taylor RPK Ford R Scragg DMO Becroft EA Allen IB Hassall A Roberts 《Acta paediatrica (Oslo, Norway : 1992)》1994,83(8):815-818
We investigated the relationship between travel and changes in routine and the sudden infant death syndrome (SIDS) among 485 SIDS cases compared with 1800 randomly selected control infants. There was no increased risk of SIDS with travel. Special events, such as christenings, were not associated with an increased risk of SIDS. However, visits to and by friends or relatives were associated with a significantly reduced risk of SIDS after controlling for potential confounders (odds ratios = 0.70; 95% confidence interval = 0.52, 0.96). These findings may indicate less social support in SIDS cases. 相似文献
82.
A 13-year-old girl with Turner's syndrome and bleeding from intestinal venous ectasia is reported. The various types of vascular anomaly of the bowel associated with Turner's syndrome are discussed. Awareness of these anomalies may help prevent unnecessary laparotomy in children with this syndrome. 相似文献
83.
84.
Gender and the sudden infant death syndrome 总被引:1,自引:0,他引:1
Abstract A nationwide case-control study compared the prevalence and magnitude of risk factors for sudden infant death syndrome (SIDS) in male and female infants. The risk factors of SIDS and their magnitude for males and females are very similar. After adjustment for potential confounders male infants had a 1.42-fold (95% CI = 1.04, 1.94) increased risk of SIDS compared with females. Risk factors identified in most epidemiological studies are not the reason for the increased SIDS mortality seen in male infants. 相似文献
85.
86.
RP Ford EA Mitchell AW Stewart R Scragg BJ Taylor 《Archives of disease in childhood》1997,77(1):54-55
One component of the Back to Sleep campaign to reduce the risk of sudden infant death syndrome (SIDS) is the recommendation that parents seek medical attention if their infant is unwell. The aim of this study was to investigate of SIDS could in part be explained by sick infants not getting appropriate medical care. Data on symptoms of illness and on acute medical contacts made for infants dying from SIDS (n = 390) within two weeks of their death were compared with those from a randomly selected group of control infants (n = 1592). SIDS cases had more severe illness than controls (odds ratio (OR) = 3.43; 95% confidence interval (CI) = 1.69 to 5.38), and were more likely to have seen a general practitioner (OR = 1.37; 95% CI = 1.09 to 1.73) or attended hospital (OR = 3.43, 95% CI = 1.09 to 1.73). Only 1.3% of all SIDS cases had symptoms suggesting severe illness and had not seen a general practitioner. A lack of medical contacts in the two weeks before death does not contribute to the risk of SIDS. 相似文献
87.
88.
AW Craft PJ Hamilton J McQuillin DJ Scott W Walker 《Journal of clinical pathology》1981,34(9):1047-1051
The clinical course and necropsy findings are described of an 11-year-old child found to have active cytomegalovirus infection at the time of bone marrow transplantation for acute lymphoblastic leukaemia. Attention is drawn to the presence of primitive mononuclear cells of uncertain origin in the regenerating bone marrow. 相似文献
89.
勃乐斯治疗肝硬化腹水30例 总被引:2,自引:0,他引:2
1 对象和方法1.1 对象 2 0 0 0 - 0 3/ 2 0 0 0 - 0 96 0例肝硬化腹水住院患者 ,经B超、肝功能、胃镜、实验室检查证实为肝硬化引起的腹水患者 6 0 (男 48,女 12 )例 ,平均年龄 42 .5 (2 9~ 80 )岁 ;其中肝炎后肝硬化 47例 (78.3% ) ,乙醇性肝硬化 3例 (5 .0 % ) ,心源性肝硬化 3例 (5 .0 % ) ,原因不明者 7例 (11.7% ) ;随机分成治疗组和对照组各 30例 ,按 Child- pugh改良分级法 :治疗组肝功能 A级 2例 ,B级 11例 ,C级 17例 ;对照组肝功能 A级 2例 ,B级 12例 ,C级 16例 ,两组间无明显差异 (P>0 .0 5 ) ;6 0例患者自首次确诊肝硬… 相似文献
90.
Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23 总被引:8,自引:1,他引:8
Temple IK; Gardner RJ; Robinson DO; Kibirige MS; Ferguson AW; Baum JD; Barber JC; James RS; Shield JP 《Human molecular genetics》1996,5(8):1117-1121
Transient neonatal diabetes mellitus (TNDM) is a rare form of childhood
diabetes which usually resolves in the first 6 months of life but which
predisposes to type 2 diabetes of adult onset. We recently reported
paternal uniparental isodisomy of chromosome 6 (UPD6) in two children with
TNDM and proposed that there may be an imprinted gene important in the
aetiology of diabetes on chromosome 6. We now describe two unrelated
families which independently suggest that the gene is imprinted, is
paternally expressed and maps to 6q22-q23. One family has a duplication
while the other, with familial TNDM, shows linkage to a marker in this
region.
相似文献