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Scandinavian Cardiovascular Journal : SCJ
|
May 25, 2011
Age and gender differences in the association between Nt-proBNP and glucometabolic disturbances
Margret Leosdottir, Ronnie Willenheimer, Christian Hall, et al.
Journal of the American Heart Association
|
June 19, 2019
Impact of Cardiovascular Neurohormones on Onset of Vasovagal Syncope Induced by Head-up Tilt
Parisa Torabi, Fabrizio Ricci, Viktor Hamrefors, et al.
Open Heart
|
July 5, 2017
Syndromes of orthostatic intolerance and syncope in young adults
Viktor Hamrefors, Jasmina Medic Spahic, David Nilsson, et al.
Cell
|
November 16, 2007
RNF8 ubiquitylates histones at DNA double-strand breaks and promotes assembly of repair proteins
Niels Mailand, Simon Bekker-Jensen, Helene Faustrup, et al.
Journal of Hypertension
|
August 14, 2008
Determinants of kidney function in Swedish families: role of heritable factors
Cristiano Fava, Martina Montagnana, Philippe Burri, et al.
Diabetes
|
July 30, 2002
Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels
Marju Orho-Melander, Mia Klannemark, Malin K Svensson, et al.
Journal of Lipid Research
|
March 28, 2012
Intake levels of dietary long-chain PUFAs modify the association between genetic variation in FADS and LDL-C
S Hellstrand, E Sonestedt, U Ericson, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 9, 2012
Genetic variation in the glucose-dependent insulinotropic polypeptide receptor modifies the association between carbohydrate and fat intake and risk of type 2 diabetes in the Malmo Diet and Cancer cohort
Emily Sonestedt, Valeriya Lyssenko, Ulrika Ericson, et al.
Journal of Internal Medicine
|
March 14, 2013
Chromosome 9p21 genetic variation explains 13% of cardiovascular disease incidence but does not improve risk prediction
K Gränsbo, P Almgren, M Sjögren, et al.
BMC Medical Genetics
|
June 27, 2013
A genetic variant of the atrial natriuretic peptide gene is associated with left ventricular hypertrophy in a non-diabetic population--the Malmö preventive project study
Amra Jujić, Margret Leosdottir, Gerd Östling, et al.
Page
of 171
Search research articles
Search
Showing results (881-890 of 1,704) with videos related to
Sort By:
Page
of 171
Scandinavian Cardiovascular Journal : SCJ
|
May 25, 2011
Age and gender differences in the association between Nt-proBNP and glucometabolic disturbances
Margret Leosdottir, Ronnie Willenheimer, Christian Hall, et al.
Journal of the American Heart Association
|
June 19, 2019
Impact of Cardiovascular Neurohormones on Onset of Vasovagal Syncope Induced by Head-up Tilt
Parisa Torabi, Fabrizio Ricci, Viktor Hamrefors, et al.
Open Heart
|
July 5, 2017
Syndromes of orthostatic intolerance and syncope in young adults
Viktor Hamrefors, Jasmina Medic Spahic, David Nilsson, et al.
Cell
|
November 16, 2007
RNF8 ubiquitylates histones at DNA double-strand breaks and promotes assembly of repair proteins
Niels Mailand, Simon Bekker-Jensen, Helene Faustrup, et al.
Journal of Hypertension
|
August 14, 2008
Determinants of kidney function in Swedish families: role of heritable factors
Cristiano Fava, Martina Montagnana, Philippe Burri, et al.
Diabetes
|
July 30, 2002
Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels
Marju Orho-Melander, Mia Klannemark, Malin K Svensson, et al.
Journal of Lipid Research
|
March 28, 2012
Intake levels of dietary long-chain PUFAs modify the association between genetic variation in FADS and LDL-C
S Hellstrand, E Sonestedt, U Ericson, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 9, 2012
Genetic variation in the glucose-dependent insulinotropic polypeptide receptor modifies the association between carbohydrate and fat intake and risk of type 2 diabetes in the Malmo Diet and Cancer cohort
Emily Sonestedt, Valeriya Lyssenko, Ulrika Ericson, et al.
Journal of Internal Medicine
|
March 14, 2013
Chromosome 9p21 genetic variation explains 13% of cardiovascular disease incidence but does not improve risk prediction
K Gränsbo, P Almgren, M Sjögren, et al.
BMC Medical Genetics
|
June 27, 2013
A genetic variant of the atrial natriuretic peptide gene is associated with left ventricular hypertrophy in a non-diabetic population--the Malmö preventive project study
Amra Jujić, Margret Leosdottir, Gerd Östling, et al.
Page
of 171