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Showing results (1221-1230 of 1,983) with videos related to
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Journal of Cardiac Failure
|
September 19, 2001
Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease
P M Jakobs, E L Hanson, K A Crispell, et al.
American Journal of Obstetrics and Gynecology
|
October 1, 1995
Underlying disorders associated with severe early-onset preeclampsia
G A Dekker, J I de Vries, P M Doelitzsch, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
January 28, 1998
Hyperhomocysteinemia is associated with an increased risk of cardiovascular disease, especially in non-insulin-dependent diabetes mellitus: a population-based study
E K Hoogeveen, P J Kostense, P J Beks, et al.
Die Rehabilitation
|
March 3, 2025
[Operational integration management (OIM) in the school setting: Aims and experiences of employees at schools in Rhineland-Palatinate, Germany - Results of a qualitative study]
Merle Riechmann-Wolf, Silvia Benkler, Kathrin Bogner, et al.
Clinical Chemistry and Laboratory Medicine
|
July 10, 2007
Global DNA methylation measured by liquid chromatography-tandem mass spectrometry: analytical technique, reference values and determinants in healthy subjects
Robert M Kok, Desirée E C Smith, Rob Barto, et al.
American Journal of Physiology. Renal Physiology
|
July 24, 2004
Homocysteine clearance and methylation flux rates in health and end-stage renal disease: association with S-adenosylhomocysteine
Frank Stam, Coen van Guldener, Piet M ter Wee, et al.
Journal of Biology
|
December 25, 2007
Dynamic rerouting of the carbohydrate flux is key to counteracting oxidative stress
Markus Ralser, Mirjam M Wamelink, Axel Kowald, et al.
Neurobiology of Disease
|
August 1, 2006
Binding of copper is a mechanism of homocysteine toxicity leading to COX deficiency and apoptosis in primary neurons, PC12 and SHSY-5Y cells
Michael Linnebank, Holger Lutz, Eva Jarre, et al.
Journal of Medical Genetics
|
May 4, 2007
L-2-hydroxyglutaric aciduria: characterisation of the molecular defect in a spontaneous canine model
Jacques Penderis, Jacqui Calvin, Carley Abramson, et al.
Journal of Inherited Metabolic Disease
|
January 7, 2010
A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy
Megumi Tsuji, Noriko Aida, Takayuki Obata, et al.
Page
of 199
Search research articles
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Showing results (1221-1230 of 1,983) with videos related to
Sort By:
Page
of 199
Journal of Cardiac Failure
|
September 19, 2001
Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease
P M Jakobs, E L Hanson, K A Crispell, et al.
American Journal of Obstetrics and Gynecology
|
October 1, 1995
Underlying disorders associated with severe early-onset preeclampsia
G A Dekker, J I de Vries, P M Doelitzsch, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
January 28, 1998
Hyperhomocysteinemia is associated with an increased risk of cardiovascular disease, especially in non-insulin-dependent diabetes mellitus: a population-based study
E K Hoogeveen, P J Kostense, P J Beks, et al.
Die Rehabilitation
|
March 3, 2025
[Operational integration management (OIM) in the school setting: Aims and experiences of employees at schools in Rhineland-Palatinate, Germany - Results of a qualitative study]
Merle Riechmann-Wolf, Silvia Benkler, Kathrin Bogner, et al.
Clinical Chemistry and Laboratory Medicine
|
July 10, 2007
Global DNA methylation measured by liquid chromatography-tandem mass spectrometry: analytical technique, reference values and determinants in healthy subjects
Robert M Kok, Desirée E C Smith, Rob Barto, et al.
American Journal of Physiology. Renal Physiology
|
July 24, 2004
Homocysteine clearance and methylation flux rates in health and end-stage renal disease: association with S-adenosylhomocysteine
Frank Stam, Coen van Guldener, Piet M ter Wee, et al.
Journal of Biology
|
December 25, 2007
Dynamic rerouting of the carbohydrate flux is key to counteracting oxidative stress
Markus Ralser, Mirjam M Wamelink, Axel Kowald, et al.
Neurobiology of Disease
|
August 1, 2006
Binding of copper is a mechanism of homocysteine toxicity leading to COX deficiency and apoptosis in primary neurons, PC12 and SHSY-5Y cells
Michael Linnebank, Holger Lutz, Eva Jarre, et al.
Journal of Medical Genetics
|
May 4, 2007
L-2-hydroxyglutaric aciduria: characterisation of the molecular defect in a spontaneous canine model
Jacques Penderis, Jacqui Calvin, Carley Abramson, et al.
Journal of Inherited Metabolic Disease
|
January 7, 2010
A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy
Megumi Tsuji, Noriko Aida, Takayuki Obata, et al.
Page
of 199