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Hypertension Research : Official Journal of the Japanese Society of Hypertension
|
March 6, 2009
Left ventricular structure in relation to the human SAH gene in the European Project on Genes in Hypertension
Yu Jin, Tatiana Kuznetsova, Valérie Tikhonoff, et al.
Trials
|
June 2, 2022
PragmaTic, prospEctive, randomized, controlled, double-blind, mulTi-centre, multinational study on the safety and efficacy of a 6% HydroxYethyl Starch (HES) solution versus an electrolyte solution in trauma patients: study protocol for the TETHYS study
Clementina Duran Palma, Musawenkosi Mamba, Johan Geldenhuys, et al.
Journal of Hypertension
|
February 7, 2007
SAH gene variants are associated with obesity-related hypertension in Caucasians: the PEGASE Study
Ralph Telgmann, Eva Brand, Viviane Nicaud, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]
|
February 6, 2023
Position statement on the definition, incidence, diagnosis and outcome of acute on chronic pancreatitis
Tiago Bouça-Machado, Stefan A W Bouwense, Martin Brand, et al.
Diabetes
|
July 18, 2008
G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes
David-Alexandre Trégouet, Per-Henrik Groop, Steven McGinn, et al.
Clinical Pharmacology and Therapeutics
|
March 22, 2020
Treatment of Fabry's Disease With Migalastat: Outcome From a Prospective Observational Multicenter Study (FAMOUS)
Malte Lenders, Peter Nordbeck, Christine Kurschat, et al.
European Heart Journal. Cardiovascular Pharmacotherapy
|
May 5, 2022
Treatment of Fabry Disease management with migalastat-outcome from a prospective 24 months observational multicenter study (FAMOUS)
Malte Lenders, Peter Nordbeck, Christine Kurschat, et al.
American Journal of Human Genetics
|
March 16, 2010
A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1
Pierre-Emmanuel Morange, Irene Bezemer, Noémie Saut, et al.
Nature
|
September 13, 2011
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
, Georg B Ehret, Patricia B Munroe, et al.
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of 11
Search research articles
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Showing results (101-110 of 109) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 109 results.
Hypertension Research : Official Journal of the Japanese Society of Hypertension
|
March 6, 2009
Left ventricular structure in relation to the human SAH gene in the European Project on Genes in Hypertension
Yu Jin, Tatiana Kuznetsova, Valérie Tikhonoff, et al.
Trials
|
June 2, 2022
PragmaTic, prospEctive, randomized, controlled, double-blind, mulTi-centre, multinational study on the safety and efficacy of a 6% HydroxYethyl Starch (HES) solution versus an electrolyte solution in trauma patients: study protocol for the TETHYS study
Clementina Duran Palma, Musawenkosi Mamba, Johan Geldenhuys, et al.
Journal of Hypertension
|
February 7, 2007
SAH gene variants are associated with obesity-related hypertension in Caucasians: the PEGASE Study
Ralph Telgmann, Eva Brand, Viviane Nicaud, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]
|
February 6, 2023
Position statement on the definition, incidence, diagnosis and outcome of acute on chronic pancreatitis
Tiago Bouça-Machado, Stefan A W Bouwense, Martin Brand, et al.
Diabetes
|
July 18, 2008
G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes
David-Alexandre Trégouet, Per-Henrik Groop, Steven McGinn, et al.
Clinical Pharmacology and Therapeutics
|
March 22, 2020
Treatment of Fabry's Disease With Migalastat: Outcome From a Prospective Observational Multicenter Study (FAMOUS)
Malte Lenders, Peter Nordbeck, Christine Kurschat, et al.
European Heart Journal. Cardiovascular Pharmacotherapy
|
May 5, 2022
Treatment of Fabry Disease management with migalastat-outcome from a prospective 24 months observational multicenter study (FAMOUS)
Malte Lenders, Peter Nordbeck, Christine Kurschat, et al.
American Journal of Human Genetics
|
March 16, 2010
A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1
Pierre-Emmanuel Morange, Irene Bezemer, Noémie Saut, et al.
Nature
|
September 13, 2011
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
, Georg B Ehret, Patricia B Munroe, et al.
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of 11