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BMC Medical Informatics and Decision Making|April 23, 2022
Environmental and clinical data utility in pediatric asthma exacerbation risk prediction modelsJillian H Hurst, Congwen Zhao, Haley P Hostetler, et al.
American Journal of Human Genetics|October 12, 2000
Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9A K Lalwani, J A Goldstein, M J Kelley, et al.
Pediatric Research|July 1, 1980
Effect of chemical sympathectomy on myocardial cell division in the newborn ratJ D Kugler, P C Gillette, S P Graham, et al.
Journal of Vascular and Interventional Radiology : JVIR|August 31, 2010
Occupational health hazards in the interventional laboratory: progress report of the Multispecialty Occupational Health GroupDonald L Miller, Lloyd W Klein, Stephen Balter, et al.
The Spine Journal : Official Journal of the North American Spine Society|May 19, 2009
Effect of intervertebral disc height on postoperative motion and clinical outcomes after Prodisc-C cervical disc replacementChan W B Peng, Martin Quirno, Martin Quirnoa, et al.
The Journal of Bone and Joint Surgery. American Volume|March 15, 2011
Prospective, randomized, multicenter Food and Drug Administration investigational device exemption study of the ProDisc-L total disc replacement compared with circumferential arthrodesis for the treatment of two-level lumbar degenerative disc disease: results at twenty-four monthsRick Delamarter, Jack E Zigler, Richard A Balderston, et al.
Cancer Medicine|May 7, 2020
The concordance of treatment decision guided by OncotypeDX and the PREDICT tool in real-world early-stage breast cancerDaniel A Goldstein, Chen Mayer, Tzippy Shochat, et al.
American Journal of Nephrology|January 1, 1982
Autonomic nervous system dysfunction and impotence in uremiaV M Campese, W R Procci, D Levitan, et al.
AJR. American Journal of Roentgenology|March 1, 1997
Imaging of pelvic postpartum complicationsJ Zuckerman, D Levine, M M McNicholas, et al.
Molecular Pharmacology|October 1, 1994
Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in JapaneseS M De Morais, G R Wilkinson, J Blaisdell, et al.
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