Published in Anesthesiology on August 01, 1994
The difficult airway with recommendations for management--part 2--the anticipated difficult airway. Can J Anaesth (2013) 1.42
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Predicting difficult intubation: a multivariable analysis. Can J Anaesth (2000) 2.41
In vivo and in vitro chromosomal damage induced by LSD-25. N Engl J Med (1967) 2.39
Testing the raters: inter-rater reliability of standardized anaesthesia simulator performance. Can J Anaesth (1997) 2.37
Craniosynostoses: phenotypic/molecular correlations. Am J Med Genet (1995) 2.35
The postoperative interview: assessing risk factors for nausea and vomiting. Anesth Analg (1994) 2.28
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Testing internal consistency and construct validity during evaluation of performance in a patient simulator. Anesth Analg (1998) 1.95
A newly recognized hamartomatous syndrome. Birth Defects Orig Artic Ser (1979) 1.89
Laparoscopic loop ileostomy for temporary fecal diversion. Dis Colon Rectum (1993) 1.88
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The Saethre-Chotzen syndrome. Birth Defects Orig Artic Ser (1975) 1.72
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Inter-observer reliability of ten tests used for predicting difficult tracheal intubation. Can J Anaesth (1996) 1.71
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Craniosynostosis and syndromes with craniosynostosis: incidence, genetics, penetrance, variability, and new syndrome updating. Birth Defects Orig Artic Ser (1979) 1.67
The incidence of airway problems depends on the definition used. Can J Anaesth (1996) 1.65
Holoprosencephaly and cytogenetic findings: further information. Am J Med Genet (1989) 1.63
Frontonasal dysplasia. J Pediatr (1970) 1.62
An etiologic and nosologic overview of craniosynostosis syndromes. Birth Defects Orig Artic Ser (1975) 1.62
The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography. Ann Genet (1971) 1.61
Bayes factor of model selection validates FLMP. Psychon Bull Rev (2001) 1.55
Tests of auditory-visual integration efficiency within the framework of the fuzzy logical model of perception. J Acoust Soc Am (2000) 1.55
Chromosomal damage in human leukocytes induced by lysergic acid diethylamide. Science (1967) 1.54
Pericentric inversion in a group D chromosome (13-15) associated with amenorrhea and gonadal dysgenesis. Ann Hum Genet (1967) 1.51
Perception of asynchronous and conflicting visual and auditory speech. J Acoust Soc Am (1996) 1.51
The premature infant: anesthesia for cesarean delivery. Anesth Analg (1994) 1.50
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome. Nat Genet (1996) 1.49
Variations in hysterectomy rates in Ontario: does the indication matter? CMAJ (1994) 1.48
Two human X-autosome translocations identified by autoradiography and fluorescence. Am J Hum Genet (1972) 1.48
Planned and unplanned postoperative admissions to critical care for mechanical ventilation. Can J Anaesth (1996) 1.48
Hypotension during cemented arthroplasty. Relationship to cardiac output and fat embolism. J Bone Joint Surg Br (1993) 1.46
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Stimulation of mucus and nonparietal cell secretion by the E2 prostaglandins. Am J Dig Dis (1978) 1.39
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Wiedemann-Beckwith syndrome, imprinting, IGF2, and H19: implications for hemihyperplasia, associated neoplasms, and overgrowth. Am J Med Genet (1994) 1.38
Chorionic villus sampling: the University of Maryland experience. Md Med J (1992) 1.38
Human dicentric Y chromosomes. Case report and review of the literature. J Med Genet (1973) 1.32
Fetal risk of anesthesia and surgery during pregnancy. Anesthesiology (1986) 1.31
The quest for meaningful outcomes. Anesthesiology (1993) 1.30
DNA content measurements and an improved idiogram for the Indian muntjac. Cytometry (1993) 1.30
Accuracy of common hapatic duct size in the evaluation of extrahepatic biliary obstruction. Radiology (1980) 1.30
An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15. Ann Genet (1975) 1.28
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The oral manifestations of Apert syndrome. J Craniofac Genet Dev Biol (1992) 1.23
An update on the holoprosencephalic disorders. J Pediatr (1982) 1.22
A prospective study of the risk of developing multiple sclerosis in uncomplicated optic neuritis. Neurology (1979) 1.22
A multivariable model for predicting the need for blood transfusion in patients undergoing first-time elective coronary bypass graft surgery. Transfusion (2001) 1.21
Clinical differentiation between Proteus syndrome and hemihyperplasia: description of a distinct form of hemihyperplasia. Am J Med Genet (1998) 1.21
Racial differences in the length of the human Y chromosome. Cytogenetics (1966) 1.19
Genetic perspectives on craniosynostosis and syndromes with craniosynostosis. J Neurosurg (1977) 1.19
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Holoprosencephaly and facial dysmorphia: nosology, etiology and pathogenesis. Birth Defects Orig Artic Ser (1971) 1.17
Langer-Giedion syndrome. Birth Defects Orig Artic Ser (1974) 1.17
Chromatin-positive Klinefelter's syndrome with undetectable peripheral FSH levels. Am J Med (1975) 1.16
Further delineation of Weaver syndrome. J Pediatr (1986) 1.15
Case report and delineation of the congenital hypothalamic hamartoblastoma syndrome (Pallister-Hall syndrome). Am J Med Genet (1989) 1.14
The prevalence of Campylobacter pylori gastritis among asymptomatic adults. CMAJ (1989) 1.14
Paresthesias and motor dysfunction after labor and delivery. Anesth Analg (1987) 1.13
The Canadian four-centre study of anaesthetic outcomes: III. Are anaesthetic complications predictable in day surgical practice? Can J Anaesth (1992) 1.13
Down's syndrome associated with a familial (21q-; 22q+) translocation. Cytogenetics (1967) 1.13
An autosomal-dominant form of juvenile periodontitis: its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc. J Craniofac Genet Dev Biol (1986) 1.12
Letter: The demise of the Marshall syndrome. J Pediatr (1974) 1.11
Effect of cigarette smoking on human gastric secretory responses. Gut (1971) 1.11
Frontometaphyseal dysplasia. A new syndrome. Am J Dis Child (1969) 1.10
Craniofrontonasal syndrome: study of 41 patients. Am J Med Genet (1996) 1.10
Robin sequences and complexes: causal heterogeneity and pathogenetic/phenotypic variability. Am J Med Genet (1999) 1.10
Saethre-Chotzen syndrome with familial translocation at chromosome 7p22. Am J Med Genet (1993) 1.09
A comparison of outcome and cost of open vs. laparoscopic cholecystectomy. J Laparoendosc Surg (1992) 1.09
PTEN mutations and proteus syndrome. Lancet (2001) 1.09
The validity of performance assessments using simulation. Anesthesiology (2001) 1.08
Genetic approaches to understanding brain development: holoprosencephaly as a model. Ment Retard Dev Disabil Res Rev (2000) 1.08
Protection against aspirin-induced antral and duodenal damage with enprostil. A double-blind endoscopic study. Gastroenterology (1985) 1.08
Craniosynostosis-radial aplasia: Baller-Gerold syndrome. Am J Dis Child (1979) 1.08
Treatment and mortality of perforated peptic ulcer: a survey of 852 cases. Can Med Assoc J (1971) 1.07
Holoprosencephaly survival and performance. Am J Med Genet (1999) 1.07
Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes. J Craniomaxillofac Surg (1993) 1.06
Cigarette smoking reduces human gastric luminal prostaglandin E2. Gut (1985) 1.05
Confirmation of an oroacral pattern of anomalies: a disruption? Am J Med Genet (1992) 1.05