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American Journal of Hypertension
|
January 13, 2012
Association of left ventricular mass with the AGTR1 A1166C polymorphism
Yu Jin, Tatiana Kuznetsova, Lut Thijs, et al.
The Journal of Allergy and Clinical Immunology
|
November 22, 2025
Autonomic dysfunction and vasoregulation in long COVID-19 are linked to anti-GPCR autoantibodies
Boris Schmitz, René Garbsch, Hendrik Schäfer, et al.
Plos One
|
February 10, 2016
Baseline Characteristics and Prescription Patterns of Standard Drugs in Patients with Angiographically Determined Coronary Artery Disease and Renal Failure (CAD-REF Registry)
Holger Reinecke, Günter Breithardt, Christiane Engelbertz, et al.
International Journal of Cardiology
|
May 21, 2017
Two-year outcome and risk factors for mortality in patients with coronary artery disease and renal failure: The prospective, observational CAD-REF Registry
Christiane Engelbertz, Holger Reinecke, Günter Breithardt, et al.
Journal of Hypertension
|
September 18, 2015
Differential response to endothelial epithelial sodium channel inhibition ex vivo correlates with arterial stiffness in humans
Malte Lenders, Verena Hofschröer, Boris Schmitz, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
May 26, 2021
Sex-specific differences and long-term outcome of patients with coronary artery disease and chronic kidney disease: the Coronary Artery Disease and Renal Failure (CAD-REF) Registry
Christiane Engelbertz, Hans O Pinnschmidt, Eva Freisinger, et al.
Journal of Medical Genetics
|
April 24, 2019
Mutation-specific Fabry disease patient-derived cell model to evaluate the amenability to chaperone therapy
Malte Lenders, Franciska Stappers, Christoph Niemietz, et al.
Scientific Reports
|
February 28, 2019
Genome-wide association study suggests impact of chromosome 10 rs139401390 on kidney function in patients with coronary artery disease
Boris Schmitz, Marcus E Kleber, Malte Lenders, et al.
Orphanet Journal of Rare Diseases
|
November 27, 2014
Cryptogenic stroke and small fiber neuropathy of unknown etiology in patients with alpha-galactosidase A -10T genotype
Michael Schelleckes, Malte Lenders, Katrin Guske, et al.
American Journal of Hypertension
|
August 19, 2011
Are retinal microvascular phenotypes associated with the 1675G/A polymorphism in the angiotensin II type-2 receptor gene?
Yan-Ping Liu, Tatiana Kuznetsova, Lutgarde Thijs, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 90) with videos related to
Sort By:
Page
of 9
American Journal of Hypertension
|
January 13, 2012
Association of left ventricular mass with the AGTR1 A1166C polymorphism
Yu Jin, Tatiana Kuznetsova, Lut Thijs, et al.
The Journal of Allergy and Clinical Immunology
|
November 22, 2025
Autonomic dysfunction and vasoregulation in long COVID-19 are linked to anti-GPCR autoantibodies
Boris Schmitz, René Garbsch, Hendrik Schäfer, et al.
Plos One
|
February 10, 2016
Baseline Characteristics and Prescription Patterns of Standard Drugs in Patients with Angiographically Determined Coronary Artery Disease and Renal Failure (CAD-REF Registry)
Holger Reinecke, Günter Breithardt, Christiane Engelbertz, et al.
International Journal of Cardiology
|
May 21, 2017
Two-year outcome and risk factors for mortality in patients with coronary artery disease and renal failure: The prospective, observational CAD-REF Registry
Christiane Engelbertz, Holger Reinecke, Günter Breithardt, et al.
Journal of Hypertension
|
September 18, 2015
Differential response to endothelial epithelial sodium channel inhibition ex vivo correlates with arterial stiffness in humans
Malte Lenders, Verena Hofschröer, Boris Schmitz, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society
|
May 26, 2021
Sex-specific differences and long-term outcome of patients with coronary artery disease and chronic kidney disease: the Coronary Artery Disease and Renal Failure (CAD-REF) Registry
Christiane Engelbertz, Hans O Pinnschmidt, Eva Freisinger, et al.
Journal of Medical Genetics
|
April 24, 2019
Mutation-specific Fabry disease patient-derived cell model to evaluate the amenability to chaperone therapy
Malte Lenders, Franciska Stappers, Christoph Niemietz, et al.
Scientific Reports
|
February 28, 2019
Genome-wide association study suggests impact of chromosome 10 rs139401390 on kidney function in patients with coronary artery disease
Boris Schmitz, Marcus E Kleber, Malte Lenders, et al.
Orphanet Journal of Rare Diseases
|
November 27, 2014
Cryptogenic stroke and small fiber neuropathy of unknown etiology in patients with alpha-galactosidase A -10T genotype
Michael Schelleckes, Malte Lenders, Katrin Guske, et al.
American Journal of Hypertension
|
August 19, 2011
Are retinal microvascular phenotypes associated with the 1675G/A polymorphism in the angiotensin II type-2 receptor gene?
Yan-Ping Liu, Tatiana Kuznetsova, Lutgarde Thijs, et al.
Page
of 9