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Annals of Internal Medicine
|
June 1, 1978
Inherited deficiency of second component of complement and HLA haplotype A10,B18 associated with inflammatory bowel disease
J D Slade, A T Luskin, H Gewurz, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
March 14, 2009
Organization of the amplified type I interferon gene cluster and associated chromosome regions in the interphase nucleus of human osteosarcoma cells
Michael J Zeitz, Narasimharao V Marella, Kishore S Malyavantham, et al.
Journal of the American Academy of Dermatology
|
March 1, 1985
Fatal panniculitis
I K Aronson, D P West, D Variakojis, et al.
International Journal of Cardiology
|
June 30, 2018
Clinical and coronary haemodynamic determinants of recurrent chest pain in patients without obstructive coronary artery disease - A pilot study
Abdul R Sheikh, Christopher J Zeitz, Sharmalar Rajendran, et al.
JAMA
|
November 2, 1994
Rote learning in medical school
M G Regan-Smith, S S Obenshain, C Woodward, et al.
International Journal of Cardiology
|
May 26, 2015
Clinical determinants of acetylcholine-induced coronary artery spasm in Australian patients
David P Di Fiore, Christopher J Zeitz, Margaret A Arstall, et al.
Journal of Cardiovascular Pharmacology
|
March 10, 2000
The positive inotropic effects of milrinone but not of digoxin are attenuated at short cycle lengths
C J Zeitz, R H Ritchie, R G Jarrett, et al.
The Medical Journal of Australia
|
June 19, 2014
A framework for overcoming disparities in management of acute coronary syndromes in the Australian Aboriginal and Torres Strait Islander population. A consensus statement from the National Heart Foundation of Australia
Marcus K Ilton, Warren F Walsh, Alex D H Brown, et al.
International Journal of Clinical Practice
|
September 23, 2009
Unperceived treatment gaps in acute coronary syndromes
L T Huynh, D P B Chew, R M Sladek, et al.
The New England Journal of Medicine
|
July 4, 1985
The molecular basis for genetic deficiency of the second component of human complement
F S Cole, A S Whitehead, H S Auerbach, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 95) with videos related to
Sort By:
Page
of 10
Annals of Internal Medicine
|
June 1, 1978
Inherited deficiency of second component of complement and HLA haplotype A10,B18 associated with inflammatory bowel disease
J D Slade, A T Luskin, H Gewurz, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
March 14, 2009
Organization of the amplified type I interferon gene cluster and associated chromosome regions in the interphase nucleus of human osteosarcoma cells
Michael J Zeitz, Narasimharao V Marella, Kishore S Malyavantham, et al.
Journal of the American Academy of Dermatology
|
March 1, 1985
Fatal panniculitis
I K Aronson, D P West, D Variakojis, et al.
International Journal of Cardiology
|
June 30, 2018
Clinical and coronary haemodynamic determinants of recurrent chest pain in patients without obstructive coronary artery disease - A pilot study
Abdul R Sheikh, Christopher J Zeitz, Sharmalar Rajendran, et al.
JAMA
|
November 2, 1994
Rote learning in medical school
M G Regan-Smith, S S Obenshain, C Woodward, et al.
International Journal of Cardiology
|
May 26, 2015
Clinical determinants of acetylcholine-induced coronary artery spasm in Australian patients
David P Di Fiore, Christopher J Zeitz, Margaret A Arstall, et al.
Journal of Cardiovascular Pharmacology
|
March 10, 2000
The positive inotropic effects of milrinone but not of digoxin are attenuated at short cycle lengths
C J Zeitz, R H Ritchie, R G Jarrett, et al.
The Medical Journal of Australia
|
June 19, 2014
A framework for overcoming disparities in management of acute coronary syndromes in the Australian Aboriginal and Torres Strait Islander population. A consensus statement from the National Heart Foundation of Australia
Marcus K Ilton, Warren F Walsh, Alex D H Brown, et al.
International Journal of Clinical Practice
|
September 23, 2009
Unperceived treatment gaps in acute coronary syndromes
L T Huynh, D P B Chew, R M Sladek, et al.
The New England Journal of Medicine
|
July 4, 1985
The molecular basis for genetic deficiency of the second component of human complement
F S Cole, A S Whitehead, H S Auerbach, et al.
Page
of 10