Published in Anesth Analg on July 01, 1997
Assessment of hemostatic changes after crystalloid and colloid fluid preloading in trauma patients using standard coagulation parameters and thromboelastography. Saudi J Anaesth (2013) 0.77
Comparing effects of low and high-flow anesthesia on hemorheology and coagulation factors. Pak J Med Sci (2015) 0.75
Randomised controlled trial of genetic amniocentesis in 4606 low-risk women. Lancet (1986) 4.71
Randomised study of risk of fetal loss related to early amniocentesis versus chorionic villus sampling. Lancet (1997) 2.72
Care of the dying cancer patient in the emergency department: findings from a National survey of Australian emergency department clinicians. Intern Med J (2014) 2.64
Randomised comparison of amniocentesis and transabdominal and transcervical chorionic villus sampling. Lancet (1992) 2.15
An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study. Hum Hered (1973) 1.64
Criminality in XYY and XXY men. Science (1976) 1.57
European Guidelines for Quality Assurance in Cervical Cancer Screening. Europe against cancer programme. Eur J Cancer (1993) 1.52
Should the indications for prenatal chromosome analysis be changed? Br Med J (1977) 1.45
Larvae in the mouth. Br Dent J (2007) 1.45
Biopsy of the breast. Br J Hosp Med (1981) 1.42
Comparative genomic hybridization reveals a recurrent pattern of chromosomal aberrations in severe dysplasia/carcinoma in situ of the cervix and in advanced-stage cervical carcinoma. Genes Chromosomes Cancer (1999) 1.40
Sampling success and risk by transabdominal chorionic villus sampling, transcervical chorionic villus sampling and amniocentesis: a randomized study. Ultrasound Obstet Gynecol (1991) 1.40
Between a rock and a hard place: exploring the conflict between respecting the privacy of patients and informing their carers. Intern Med J (2009) 1.39
Breast self-examination: clinical results from a population-based prospective study. Br J Cancer (1984) 1.17
Comparative genomic hybridization in clinical cytogenetics. Am J Hum Genet (1995) 1.15
Synthesis, spectral, optical and thermal studies of 1-methyl-2,6-dimethyl-4-hydroxypyridinium chloride monohydrate and bromide monohydrate. Spectrochim Acta A Mol Biomol Spectrosc (2007) 1.08
Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency. Am J Hum Genet (1992) 1.06
Clinical measures to assess the practice and efficiency of breast self-examination. Cancer (1986) 1.05
Comparative genomic hybridization reveals non-random chromosomal aberrations in early preinvasive cervical lesions. Cancer Genet Cytogenet (2001) 1.04
Screening for Down's syndrome using an iso-risk curve based on maternal age and serum alpha-fetoprotein level. Br J Obstet Gynaecol (1987) 1.03
Health Belief Model variables as predictors of screening mammography utilization. J Behav Med (1994) 1.03
Enlarged chromosome No. 1 in a patient with primary amenorrhoea. Cytogenetics (1965) 1.00
Assessment of changes in coagulation in parturients with preeclampsia using thromboelastography. Anesthesiology (1999) 0.99
The frequency of chromosome aberrations in tall men with special reference to 47, XYY and 47, XXY. Am J Hum Genet (1976) 0.99
A clinical and cytogenetical study of XX male. Hereditas (1969) 0.98
Simultaneous confocal recording of multiple fluorescent labels with improved channel separation. J Microsc (1994) 0.98
Dignity in dying: a preliminary study of patients in the last three days of life. J Palliat Care (1996) 0.97
Nephrobronchial fistula - a case report. Int Urol Nephrol (2007) 0.95
Relationship between infant birth weight </=2000 g and maternal zinc levels at Muhimbili National Hospital, Dar Es Salaam, Tanzania. J Trop Pediatr (2005) 0.95
LSD in mice: abnormalities in meiotic chromosomes. Science (1968) 0.94
Studies on meiotic chromosomes in infertile men and controls with normak karyotypes. J Reprod Fertil (1973) 0.94
A familial, balanced 2-5 translocation associated with trisomy 21 in one individual. Hum Hered (1974) 0.93
Stimulation of amniotic fluid cells by fibroblast growth factor. Clin Genet (1978) 0.93
Semiautomated chromosome analysis. A clinical test. Clin Genet (1985) 0.93
Primary amenorrhea. A study of 101 cases. Fertil Steril (1966) 0.92
Is screening for ovarian cancer worthwhile? J Med Screen (1994) 0.91
Prevention of hypotension during spinal anesthesia: a comparison of intravascular administration of hetastarch versus lactated Ringer's solution. Anesth Analg (1997) 0.91
Assessing platelet and fibrinogen contribution to clot strength using modified thromboelastography in pregnant women. Anesth Analg (1999) 0.90
Y-22 translocation in a YY male. Cytogenet Cell Genet (1973) 0.90
Administration of nitrous oxide in normal subjects. Evaluation of systems of gas delivery for their clinical use and hemodynamic effects. Chest (1977) 0.90
Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridization. Prenat Diagn (1992) 0.90
A culture vessel for amniotic fluid cells allowing faster preparation of chromosome slides. Prenat Diagn (1985) 0.89
InJection adaptable fine ionization source ('JaFIS') for continuous flow nano-electrospray. Rapid Commun Mass Spectrom (1998) 0.89
Colour vision deficiency in on of two presumably monozygotic twins with secondary amenorrhoea. Ann Hum Genet (1969) 0.89
A randomized, controlled trial comparing lidocaine periprostatic nerve block, diclofenac suppository and both for transrectal ultrasound guided biopsy of prostate. J Urol (2005) 0.86
Thromboelastographic changes in healthy parturients and postpartum women. Anesth Analg (1997) 0.85
Patient reporting and doctor recognition of dyspnoea in a comprehensive cancer centre. Intern Med J (2006) 0.84
Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH. Am J Hum Genet (1996) 0.84
Public interest warning: should we ban wooden/ornamental toilet seats for male infants? BJU Int (2008) 0.84
Microspectrophotometry of trypsin-Leishman-stained human chromosomes. Nature (1973) 0.84
New rapid test for prenatal detection of trisomy 21 (Down's syndrome): preliminary report. BMJ (1992) 0.83
Prenatal detection of chromosome aneuploidies by fluorescence in situ hybridization: experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trial. Prenat Diagn (1997) 0.82
Outcome of pregnancy after amniocentesis for chromosome analysis. Br Med J (1978) 0.82
45,XO Turner's syndrome without evidence of mosaicism in a patient with two pregnancies. Acta Obstet Gynecol Scand (1976) 0.82
Cytogenetic investigations in male infertility. Acta Obstet Gynecol Scand (1970) 0.82
Detection of chromosomal aberrations in seminomatous germ cell tumours using comparative genomic hybridization. Genes Chromosomes Cancer (1997) 0.82
The effect of dydrogesterone on premenstrual symptoms. A double-blind, randomized, placebo-controlled study in general practice. Scand J Prim Health Care (1988) 0.81
Intrathecal sufentanil compared to epidural bupivacaine for labor analgesia. Anesthesiology (1994) 0.81
Quantification of human seminiferous epithelium. 3. Histological studies in 44 infertile men with normal chromosome complements. Acta Pathol Microbiol Scand A (1973) 0.81
MULTISCAN--a Scandinavian multicenter second trimester obstetric ultrasound and serum screening study. Acta Obstet Gynecol Scand (1999) 0.80
Use of hormone replacement therapy among Danish nurses in 1993. Acta Obstet Gynecol Scand (2000) 0.80
Concurrence of turner's syndrome and anorexia nervosa. Acta Psychiatr Scand (1975) 0.80
Squamous cell carcinoma arising at the site of an underlying bullet. J R Coll Surg Edinb (1982) 0.80
Increased risk of abortion after genetic amniocentesis in twin pregnancies. Prenat Diagn (1983) 0.80
[Prenatal diagnosis of anencephaly and spina bifida. Determination of alphafetoprotein in amniotic fluid and serum in the 16th-24th gestational week]. Ugeskr Laeger (1975) 0.80
Citrullinaemia: the possibility of prenatal diagnosis. J Inherit Metab Dis (1980) 0.79
Coexistence of ferromagnetism and superconductivity in Ni/Bi bilayers. Phys Rev Lett (2005) 0.79
Comparison of transabdominal and transcervical CVS and amniocentesis: sampling success and risk. Prenat Diagn (1991) 0.79
Cell adhesion mechanisms: modeling using derivatized beads and sea urchin cell systems. Acta Histochem (1996) 0.79
Studies on the isolation and identification of fetal nucleated red blood cells in the circulation of pregnant women before and after chorion villus sampling. Fetal Diagn Ther (2003) 0.79
Quantification of human seminiferous epithelium. IV. Histological studies in 17 men with numerical and structural autosomal aberrations. Acta Pathol Microbiol Scand A (1973) 0.79
Fluorescence in situ hybridization with a chromosome 21-specific cosmid contig: 1-day detection of trisomy 21 in uncultured mesenchymal chorionic villus cells. Prenat Diagn (1994) 0.78
Ideal care and the realities of practice: interdisciplinary relationships in the management of advanced cancer patients in Australian emergency departments. Support Care Cancer (2013) 0.78
Transabdominal chorionic villus sampling in the second and third trimesters of pregnancy: chromosome quality, reporting time, and feto-maternal bleeding. Prenat Diagn (1993) 0.78
Early prenatal chromosome analysis of 604 fetuses. Acta Obstet Gynecol Scand (1977) 0.78
Rapid detection of numerical aberrations of chromosomes 13, 18 and 21 in chorionic mesenchymal cells. Prenat Diagn (1993) 0.78
Comparison of cell cultures, chromosome quality and karyotypes obtained after chorionic villus sampling and early amniocentesis with filter technique. Prenat Diagn (1999) 0.78
Prenatal diagnosis of chronic granulomatous disease. Lancet (1982) 0.78
Cold haemagglutinin disease in systemic lupus erythematosus. Yonsei Med J (1997) 0.78
Health-related quality of life in rheumatoid arthritis patients in South India. Singapore Med J (2009) 0.77
Incidence of fetal chromosome abnormalities in 2264 low-risk women. Prenat Diagn (1987) 0.77
Spinal anesthesia for cesarean section following inadequate labor epidural analgesia: a retrospective audit. Int J Obstet Anesth (2004) 0.77
Amniocentesis with increased cell yield, obtained by filtration and reinjection of the amniotic fluid. Ultrasound Obstet Gynecol (1991) 0.77
Antenatal and perinatal conditions correlated to handicap among 4-year-old children. Am J Perinatol (1989) 0.77
Adverse events arising from a palliative care survey. Palliat Med (2009) 0.77
Inadvertent development of subatmospheric airway pressure during cardiopulmonary bypass. Anesthesiology (1989) 0.77
[Randomized comparison of transabdominal, transcervical chorionic villi sampling and amniocentesis]. Ugeskr Laeger (1993) 0.77
Prenatal diagnosis by fluorescence in situ hybridization on chorionic villus cells: nonsignificance of maternal cell contamination. Fetal Diagn Ther (1994) 0.77
Prevalence and predictors of fatigue in haemo-oncological patients. Intern Med J (2014) 0.76
Cytogenetic analysis of 2928 CVS samples and 1075 amniocenteses from randomized studies. Prenat Diagn (1993) 0.76
Evidence from in vitro and in vivo studies showing that nuclear factor-κB within the pituitary folliculostellate cells and corticotrophs regulates adrenocorticotrophic hormone secretion in experimental endotoxaemia. J Neuroendocrinol (2012) 0.76
Chromosome analysis of fetuses in risk pregnancies. Acta Obstet Gynecol Scand Suppl (1974) 0.76
Meiotic chromosomes in Klinefelter's syndrome. Nature (1969) 0.76
Trisomy 8 syndrome. A psychological and somatic study of a mentally non-retarded male with 46,XY/47,XY,+8 chromosome constitution. Clin Genet (1977) 0.76
Needle size and risk of miscarriage after amniocentesis. Lancet (1988) 0.76
Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples. Acta Obstet Gynecol Scand (2000) 0.76
Subserosal appendicular stripping. Int J Surg (2006) 0.76
Haemophilia A and B--two years experience of genetic counselling and prenatal diagnosis. Clin Genet (1982) 0.76
[Myelomeningocele in Denmark]. Ugeskr Laeger (1988) 0.75