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American Heart Journal|November 13, 1998
Relation between impedance and electrode temperature during radiofrequency catheter ablation of accessory pathways and atrioventricular nodal reentrant tachycardiaE Nsah, R Berger, L Rosenthal, et al.
The American Journal of Cardiology|November 5, 1997
Safety and effectiveness of placement of pacemaker and defibrillator leads in the axillary vein guided by contrast venographyB M Ramza, L Rosenthal, R Hui, et al.
Vox Sanguinis|January 3, 2008
Transfusion support for a patient with McLeod phenotype without chronic granulomatous disease and with antibodies to Kx and KmI Bansal, H-R Jeon, S R Hui, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 11, 2001
A malignant phenotype of hypertrophic cardiomyopathy caused by Arg719Gln cardiac beta-myosin heavy-chain mutation in a Chinese familyX Huang, L Song, A Q Ma, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 29, 2000
INK4a gene expression and methylation in primary breast cancer: overexpression of p16INK4a messenger RNA is a marker of poor prognosisR Hui, R D Macmillan, F S Kenny, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 1, 1996
Cyclin D1 and estrogen receptor messenger RNA levels are positively correlated in primary breast cancerR Hui, A L Cornish, R A McClelland, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 3, 1999
Overexpression of cyclin D1 messenger RNA predicts for poor prognosis in estrogen receptor-positive breast cancerF S Kenny, R Hui, E A Musgrove, et al.
Cell Death and Differentiation|November 15, 2014
MicroRNA-221 inhibits autophagy and promotes heart failure by modulating the p27/CDK2/mTOR axisM Su, J Wang, C Wang, et al.
Oncogene|October 31, 1997
EMS1 amplification can occur independently of CCND1 or INT-2 amplification at 11q13 and may identify different phenotypes in primary breast cancerR Hui, D H Campbell, C S Lee, et al.
Clinical Genetics|March 25, 2000
Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German familiesW Pei, H Baron, B Müller-Myhsok, et al.
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