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The American Journal of Cardiology|June 1, 1983
Subxyphoid 2-dimensional echocardiographic identification of left ventricular papillary muscle anomalies in complete common atrioventricular canalA J Chin, F Z Bierman, S P Sanders, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|June 1, 1991
Is adrenaline released by sympathetic nerves in man?M Esler, G Eisenhofer, J Chin, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1982
Appearance of crystalloid endoplasmic reticulum in compactin-resistant Chinese hamster cells with a 500-fold increase in 3-hydroxy-3-methylglutaryl-coenzyme A reductaseD J Chin, K L Luskey, R G Anderson, et al.
Cytopathology : Official Journal of the British Society for Clinical Cytology|April 2, 2004
A review of post-trachelectomy isthmic and vaginal smear cytologyN Singh, E Titmuss, J Chin Aleong, et al.
British Journal of Hospital Medicine|June 2, 1993
Transjugular intrahepatic portosystemic stent-shuntP A McCormick, R Dick, J Chin, et al.
The Annals of Thoracic Surgery|June 1, 1993
Changes in right ventricular geometry and heart rate early after hemi-Fontan procedureM A Seliem, J M Baffa, J M Vetter, et al.
Anesthesia and Analgesia|June 29, 2001
Hyperbaric spinal ropivacaine for cesarean delivery: a comparison to hyperbaric bupivacaineC J Chung, S R Choi, K H Yeo, et al.
Circulation|September 1, 1986
Analysis of potential anatomic or physiologic determinants of outcome of palliative surgery for hypoplastic left heart syndromeJ G Helton, B A Aglira, A J Chin, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|December 4, 2016
Is Ultrasound a Valid and Reliable Imaging Modality for Airway Evaluation?: An Observational Computed Tomographic Validation Study Using Submandibular Scanning of the Mouth and OropharynxFaraj W Abdallah, Eugene Yu, Phantila Cholvisudhi, et al.
Human Genetics|September 10, 1999
A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotypeM A Maxwell, P V Nelson, S J Chin, et al.
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