全文获取类型
收费全文 | 1752篇 |
免费 | 145篇 |
国内免费 | 714篇 |
专业分类
安全科学 | 91篇 |
废物处理 | 116篇 |
环保管理 | 104篇 |
综合类 | 1749篇 |
基础理论 | 182篇 |
污染及防治 | 330篇 |
评价与监测 | 29篇 |
社会与环境 | 5篇 |
灾害及防治 | 5篇 |
出版年
2023年 | 12篇 |
2022年 | 29篇 |
2021年 | 44篇 |
2020年 | 46篇 |
2019年 | 63篇 |
2018年 | 52篇 |
2017年 | 53篇 |
2016年 | 71篇 |
2015年 | 99篇 |
2014年 | 110篇 |
2013年 | 116篇 |
2012年 | 160篇 |
2011年 | 184篇 |
2010年 | 162篇 |
2009年 | 164篇 |
2008年 | 114篇 |
2007年 | 200篇 |
2006年 | 175篇 |
2005年 | 139篇 |
2004年 | 108篇 |
2003年 | 99篇 |
2002年 | 91篇 |
2001年 | 71篇 |
2000年 | 31篇 |
1999年 | 24篇 |
1998年 | 33篇 |
1997年 | 22篇 |
1996年 | 11篇 |
1995年 | 40篇 |
1994年 | 34篇 |
1993年 | 19篇 |
1992年 | 3篇 |
1991年 | 7篇 |
1990年 | 4篇 |
1989年 | 2篇 |
1988年 | 4篇 |
1987年 | 2篇 |
1986年 | 2篇 |
1985年 | 2篇 |
1984年 | 4篇 |
1983年 | 3篇 |
1982年 | 1篇 |
1981年 | 1篇 |
排序方式: 共有2611条查询结果,搜索用时 15 毫秒
251.
Ronald J. Wapner Thomas M. Jenkins Neil Silverman Marion Kaufmann Cheryl Hannau Peter McCue 《黑龙江环境通报》2001,21(4):256-261
The diagnosis of congenital nephrosis is difficult during the antepartum period. The combination of an elevated amniotic fluid alpha-fetoprotein, a negative acetylcholinesterase, and a negative ultrasound examination is highly indicative of congenital nephrosis; however, these findings can also be associated with a normal gestation. This is the first report of pathologic confirmation of congenital nephrosis from an in utero fetal kidney biopsy. Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
252.
Trish Chudleigh 《黑龙江环境通报》2001,21(11):936-941
Mild pyelectasis is a common finding which is often incidental, with no significant long term sequelae. However, there is a small association with aneuploidy and postnatal renal pathology. In this paper the aetiology and prognosis are discussed and the management strategies described. Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
253.
254.
255.
256.
257.
258.
Gisela Enders Ursula Bäder Lisa Lindemann Gunnar Schalasta Anja Daiminger 《黑龙江环境通报》2001,21(5):362-377
An Erratum has been published for this article in Prenatal Diagnosis 21(7) 2001, 605. Prenatal diagnosis (PD) of fetal cytomegalovirus (CMV) infection was performed in 242 pregnancies, with known outcome in 189 cases. In 141/189 pregnancies, PD was carried out on account of suspicious maternal CMV serology up to gestational week (WG) 23, and in 48 cases on account of abnormal ultrasonic findings detected between WG 18 and 39. Chorionic villus samples (n=6), amniotic fluid (AF, n=176) and/or fetal blood specimens (n=80) were investigated for detection of virus by cell culture, shell vial assay, PCR and/or CMV-specific IgM antibodies. Of 189 fetuses correctly evaluated by CMV detection either in fetal tissue following therapeutic abortion/stillbirth (n=24) or in urine of neonates within the first 2 weeks of life (n=33), 57 were congenitally infected. In women with proven or suspected primary infection, the intrauterine transmission rates were 20.6% (7/34) and 24.4% (10/41), respectively. Of the congenitally infected live-born infants, 57.6% (19/33) had symptoms of varying degree. The overall sensitivity of PD in the serologic and ultrasound risk groups was 89.5% (51/57). A sensitivity of 100% was achieved by combining detection of CMV-DNA and CMV-specific IgM in fetal blood or by combined testing of AF and fetal blood for CMV-DNA or IgM antibodies. There was no instance of intrauterine death following the invasive procedure. The predictive value of PD for fetal infection was 95.7% (132/138) for negative results and 100% (51/51) for positive results. Correct results for congenital CMV infection by testing AF samples can be expected with samples obtained after WG 21 and after a time interval of at least 6 weeks between first diagnosis of maternal infection and PD. In case of negative findings in AF or fetal blood and the absence of ultrasound abnormalities at WG 22–23, fetal infection and neonatal disease could be excluded with high confidence. Positive findings for CMV infection in AF and/or fetal blood in combination with CMV suspicious ultrasound abnormalities predicted a high risk of cytomegalic inclusion disease (CID). Furthermore, detection of specific IgM antibodies in fetal blood was significantly correlated with severe outcome for the fetus or the newborn (p=0.0224). However, normal ultrasound of infected fetuses at WG 22–23 can neither completely exclude an abnormal ultrasound at a later WG and the birth of a severely damaged child nor the birth of neonates which are afflicted by single manifestations at birth or later and of the kind which are not detectable by currently available ultrasonographic techniques. Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
259.
Lower urinary tract obstruction has a significant impact on neonatal and child health. Pulmonary hyperplasia and renal impairment could be direct or indirect consequences of this condition leading to significant morbidity and mortality. Evaluation of fetuses with suspected lower urinary tract obstruction is performed not only to confirm the diagnosis but also to assess renal prognosis. Ultrasound examination and urinary analysis aid in the evaluation of these fetuses. The decision to perform fetal intervention in these cases is a difficult one. Vesico‒amniotic fetal shunting, open fetal surgery and more recently endoscopic fetal surgery for this condition are available as possible modalities of fetal intervention. Case selection for fetal intervention is extremely important in order to both avoid unnecessary intervention in those unlikely to survive, and also to avoid procedure related complications in fetuses likely to do well without intervention. Vesico‒amniotic shunting has the advantage of bypassing the obstruction, however it is often associated with complications. Open fetal surgery is not usually recommended because of the complications and high fetal loss rate. Endoscopic surgery to visualise and treat the cause of lower urinary tract obstruction has been tried. Fetal endoscopic surgery is in its infancy and endoscopic procedures are limited to a few groups. This current review addresses evaluation, case selection and therapeutic options for lower urinary tract obstruction in utero. It also discusses the limited data against which the efficacy of the various options can be assessed. The current state of fetal intervention is detailed in the present review. Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
260.