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Heart (British Cardiac Society)
|
October 16, 2004
Lack of association between baseline plasma homocysteine concentrations and restenosis rates after a first elective percutaneous coronary intervention without stenting
C-K Wong, C J K Hammett, R The, et al.
Journal of the American College of Cardiology
|
April 24, 2007
Polymer-based, paclitaxel-eluting TAXUS Liberté stent in de novo lesions: the pivotal TAXUS ATLAS trial
Mark A Turco, John A Ormiston, Jeffrey J Popma, et al.
JACC. Cardiovascular Interventions
|
April 20, 2010
Monitoring in vivo absorption of a drug-eluting bioabsorbable stent with intravascular ultrasound-derived parameters a feasibility study
Nico Bruining, Sebastiaan de Winter, Jos R T C Roelandt, et al.
Brain Communications
|
February 25, 2021
Magnetic resonance imaging pattern recognition in childhood bilateral basal ganglia disorders
Shekeeb S Mohammad, Rajeshwar Reddy Angiti, Andrew Biggin, et al.
Marine Genomics
|
March 3, 2018
Performance and precision of double digestion RAD (ddRAD) genotyping in large multiplexed datasets of marine fish species
F Maroso, J E J Hillen, B G Pardo, et al.
Pain
|
May 3, 2019
Antibodies binding the head domain of P2X4 inhibit channel function and reverse neuropathic pain
Wendy A Williams, John E Linley, Clare A Jones, et al.
Addiction (Abingdon, England)
|
March 21, 2000
Gender differences in alcohol consumption and adverse drinking consequences: cross-cultural patterns
R W Wilsnack, N D Vogeltanz, S C Wilsnack, et al.
Nature Communications
|
July 8, 2015
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III
Isabelle Thiffault, Nicole I Wolf, Diane Forget, et al.
Neurology
|
April 1, 2016
Delineation of the movement disorders associated with FOXG1 mutations
Apostolos Papandreou, Ruth B Schneider, Erika F Augustine, et al.
Journal of Inherited Metabolic Disease
|
March 18, 2021
ALG13 X-linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes
Hind Alsharhan, Miao He, Andrew C Edmondson, et al.
Page
of 20
Search research articles
Search
Showing results (181-190 of 198) with videos related to
Sort By:
Page
of 20
Heart (British Cardiac Society)
|
October 16, 2004
Lack of association between baseline plasma homocysteine concentrations and restenosis rates after a first elective percutaneous coronary intervention without stenting
C-K Wong, C J K Hammett, R The, et al.
Journal of the American College of Cardiology
|
April 24, 2007
Polymer-based, paclitaxel-eluting TAXUS Liberté stent in de novo lesions: the pivotal TAXUS ATLAS trial
Mark A Turco, John A Ormiston, Jeffrey J Popma, et al.
JACC. Cardiovascular Interventions
|
April 20, 2010
Monitoring in vivo absorption of a drug-eluting bioabsorbable stent with intravascular ultrasound-derived parameters a feasibility study
Nico Bruining, Sebastiaan de Winter, Jos R T C Roelandt, et al.
Brain Communications
|
February 25, 2021
Magnetic resonance imaging pattern recognition in childhood bilateral basal ganglia disorders
Shekeeb S Mohammad, Rajeshwar Reddy Angiti, Andrew Biggin, et al.
Marine Genomics
|
March 3, 2018
Performance and precision of double digestion RAD (ddRAD) genotyping in large multiplexed datasets of marine fish species
F Maroso, J E J Hillen, B G Pardo, et al.
Pain
|
May 3, 2019
Antibodies binding the head domain of P2X4 inhibit channel function and reverse neuropathic pain
Wendy A Williams, John E Linley, Clare A Jones, et al.
Addiction (Abingdon, England)
|
March 21, 2000
Gender differences in alcohol consumption and adverse drinking consequences: cross-cultural patterns
R W Wilsnack, N D Vogeltanz, S C Wilsnack, et al.
Nature Communications
|
July 8, 2015
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III
Isabelle Thiffault, Nicole I Wolf, Diane Forget, et al.
Neurology
|
April 1, 2016
Delineation of the movement disorders associated with FOXG1 mutations
Apostolos Papandreou, Ruth B Schneider, Erika F Augustine, et al.
Journal of Inherited Metabolic Disease
|
March 18, 2021
ALG13 X-linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes
Hind Alsharhan, Miao He, Andrew C Edmondson, et al.
Page
of 20