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M-K Chung

Showing results (91-100 of 119) with videos related to

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Regulatory Toxicology and Pharmacology : RTP|November 18, 2004
Subacute toxicity evaluation of a new camptothecin anticancer agent CKD-602 administered by intravenous injection to ratsJ C Kim, D H Shin, S H Kim, et al.
Journal of the American College of Cardiology|July 21, 1998
Is hospital admission for initiation of antiarrhythmic therapy with sotalol for atrial arrhythmias required? Yield of in-hospital monitoring and prediction of risk for significant arrhythmia complicationsM K Chung, R A Schweikert, B L Wilkoff, et al.
Journal of Dental Research|February 12, 2024
Murine IRF8 Mutation Offers New Insight into Osteoclast and Root ResorptionA Das, S K Yesupatham, D Allison, et al.
Heart (British Cardiac Society)|June 1, 2005
Preimplantation B-type natriuretic peptide concentration is an independent predictor of future appropriate implantable defibrillator therapiesA Verma, F Kilicaslan, D O Martin, et al.
American Journal of Human Genetics|March 1, 2008
Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23Kate V Everett, Barry A Chioza, Christina Georgoula, et al.
Clinical Genetics|April 19, 2003
KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden deathS Chen, L Zhang, R M Bryant, et al.
The European Respiratory Journal|February 23, 2018
Primary ciliary dyskinesia with normal ultrastructure: three-dimensional tomography detects absence of DNAH11Amelia Shoemark, Thomas Burgoyne, Robert Kwan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2002
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesiaLucia Bartoloni, Jean-Louis Blouin, Yanzhen Pan, et al.
Nature Genetics|March 6, 2012
Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesiaHannah M Mitchison, Miriam Schmidts, Niki T Loges, et al.
Nature Genetics|January 15, 2002
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetryHeike Olbrich, Karsten Häffner, Andreas Kispert, et al.
Pageof 12

Showing results (91-100 of 119) with videos related to

Sort By:
Pageof 12
Regulatory Toxicology and Pharmacology : RTP|November 18, 2004
Subacute toxicity evaluation of a new camptothecin anticancer agent CKD-602 administered by intravenous injection to ratsJ C Kim, D H Shin, S H Kim, et al.
Journal of the American College of Cardiology|July 21, 1998
Is hospital admission for initiation of antiarrhythmic therapy with sotalol for atrial arrhythmias required? Yield of in-hospital monitoring and prediction of risk for significant arrhythmia complicationsM K Chung, R A Schweikert, B L Wilkoff, et al.
Journal of Dental Research|February 12, 2024
Murine IRF8 Mutation Offers New Insight into Osteoclast and Root ResorptionA Das, S K Yesupatham, D Allison, et al.
Heart (British Cardiac Society)|June 1, 2005
Preimplantation B-type natriuretic peptide concentration is an independent predictor of future appropriate implantable defibrillator therapiesA Verma, F Kilicaslan, D O Martin, et al.
American Journal of Human Genetics|March 1, 2008
Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23Kate V Everett, Barry A Chioza, Christina Georgoula, et al.
Clinical Genetics|April 19, 2003
KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden deathS Chen, L Zhang, R M Bryant, et al.
The European Respiratory Journal|February 23, 2018
Primary ciliary dyskinesia with normal ultrastructure: three-dimensional tomography detects absence of DNAH11Amelia Shoemark, Thomas Burgoyne, Robert Kwan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2002
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesiaLucia Bartoloni, Jean-Louis Blouin, Yanzhen Pan, et al.
Nature Genetics|March 6, 2012
Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesiaHannah M Mitchison, Miriam Schmidts, Niki T Loges, et al.
Nature Genetics|January 15, 2002
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetryHeike Olbrich, Karsten Häffner, Andreas Kispert, et al.
Pageof 12