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Los conectores contraargumentativos y la enseñanza de español como lengua adicional

Caracol (São Paulo, Brazil), 2020-06 (19), p.510-535

Esteve, Cristina Corral

2020

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Characterization and proteomic profile of extracellular vesicles from peritoneal dialysis efflux

PloS one, 2017-05, Vol.12 (5), p.e0176987-e0176987

2017

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Caesarean delivery is associated with an absolute increase in the prevalence of overweight in the offspring: The SENDO project

Journal of paediatrics and child health, 2021-06, Vol.57 (6), p.819-825

2021

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Structure–activity relationships (SAR) and structure–kinetic relationships (SKR) of bicyclic heteroaromatic acetic acids as potent CRTh2 antagonists III: The role of a hydrogen-bond acceptor in long receptor residence times

Bioorganic & medicinal chemistry letters, 2014-11, Vol.24 (21), p.5127-5133

2014

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Design, application and evaluation of a cricothyrotomy model for a multidisciplinary simulation. An observational single centre study

Educación médica, 2021-07, Vol.22, p.305-310

2021

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Design, Synthesis, and Structure−Activity Relationships of 1-,3-,8-, and 9-Substituted-9-deazaxanthines at the Human A2B Adenosine Receptor

Journal of medicinal chemistry, 2006-01, Vol.49 (1), p.282-299

2006

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Prediction of Difficult Tracheal Intubation

Anesthesiology (Philadelphia), 2012-12, Vol.117 (6), p.1223-1233

2012

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Prediction of Difficult Tracheal Intubation: Time for a Paradigm Change

Anesthesiology (Philadelphia), 2012-12, Vol.117 (6), p.1223-1233

2012

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FP558A LONGITUDINAL PILOT STUDY OF EXTRACELLULAR VESICLES FROM EFFLUENT OF PERITONEAL DIALYSIS FLUID IN MAINTENANCE PERITONEAL DIALYSIS PATIENTS

Nephrology, dialysis, transplantation, 2019-06, Vol.34 (Supplement_1)

2019

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Proteomic profiling of peritoneal dialysis effluent-derived extracellular vesicles: a longitudinal study

Journal of nephrology, 2019-12, Vol.32 (6), p.1021-1031

2019

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Discovery of LAS101057: A Potent, Selective, and Orally Efficacious A2B Adenosine Receptor Antagonist

ACS medicinal chemistry letters, 2011-03, Vol.2 (3), p.213-218

2011

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Discovery of 7-azaindole derivatives as potent Orai inhibitors showing efficacy in a preclinical model of asthma

Bioorganic & medicinal chemistry letters, 2015-03, Vol.25 (6), p.1217-1222

2015

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Structure-activity relationships (SAR) and structure-kinetic relationships (SKR) of sulphone-based CRTh2 antagonists

European journal of medicinal chemistry, 2016-05, Vol.113, p.102-133

2016

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First synthesis of pyrrolothiadiazinones. An alternative core ring for xanthine based structures

Tetrahedron letters, 2006-08, Vol.47 (33), p.5875-5877

2006

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Novel triazolopyridylbenzamides as potent and selective p38α inhibitors

Bioorganic & medicinal chemistry letters, 2012-05, Vol.22 (10), p.3431-3436

2012

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In Reply

Anesthesiology (Philadelphia), 2013-08, Vol.119 (2), p.491-492

2013

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In Reply

Anesthesiology (Philadelphia), 2013-08, Vol.119 (2), p.491-492

2013

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OP-ECHO-03 - Intraoperative transoesophageal echocardiography: Impact on cardiac surgery decision-making

Journal of cardiothoracic and vascular anesthesia, 2018-08, Vol.32, p.S41-S41

2018

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Intraoperative transoesophageal echocardiography: Impact on cardiac surgery decision-making

Journal of cardiothoracic and vascular anesthesia, 2018-08, Vol.32, p.S41

2018

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Pyrazine-based Syk kinase inhibitors

Bioorganic & medicinal chemistry letters, 2012-04, Vol.22 (8), p.2784-2788

2012

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Design, Synthesis, and Structure−Activity Relationships of Aminopyridine N-Oxides, a Novel Scaffold for the Potent and Selective Inhibition of p38 Mitogen Activated Protein Kinase

Journal of medicinal chemistry, 2009-09, Vol.52 (17), p.5531-5545

2009

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Structure–activity relationships (SAR) and structure–kinetic relationships (SKR) of bicyclic heteroaromatic acetic acids as potent CRTh2 antagonists I

Bioorganic & medicinal chemistry letters, 2014-11, Vol.24 (21), p.5118-5122

2014

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Effect of glucose-insulin-potassium in severe acute heart failure after brain death

Critical care medicine, 2008-10, Vol.36 (10), p.2740-2745

2008

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Structure–activity relationships (SAR) and structure–kinetic relationships (SKR) of bicyclic heteroaromatic acetic acids as potent CRTh2 antagonists II: Lead optimization

Bioorganic & medicinal chemistry letters, 2014-11, Vol.24 (21), p.5123-5126

2014

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Characterization and proteomic profile of extracellular vesicles from peritoneal dialysis efflux

Journal of extracellular vesicles, 2018-01, Vol.7, p.146-146

2018

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Los conectores contraargumentativos y la enseñanza de español como lengua adicional

Characterization and proteomic profile of extracellular vesicles from peritoneal dialysis efflux

Caesarean delivery is associated with an absolute increase in the prevalence of overweight in the offspring: The SENDO project

Structure–activity relationships (SAR) and structure–kinetic relationships (SKR) of bicyclic heteroaromatic acetic acids as potent CRTh2 antagonists III: The role of a hydrogen-bond acceptor in long receptor residence times

Design, application and evaluation of a cricothyrotomy model for a multidisciplinary simulation. An observational single centre study

Design, Synthesis, and Structure−Activity Relationships of 1-,3-,8-, and 9-Substituted-9-deazaxanthines at the Human A2B Adenosine Receptor

Prediction of Difficult Tracheal Intubation

Prediction of Difficult Tracheal Intubation: Time for a Paradigm Change

FP558A LONGITUDINAL PILOT STUDY OF EXTRACELLULAR VESICLES FROM EFFLUENT OF PERITONEAL DIALYSIS FLUID IN MAINTENANCE PERITONEAL DIALYSIS PATIENTS

Proteomic profiling of peritoneal dialysis effluent-derived extracellular vesicles: a longitudinal study

Discovery of LAS101057: A Potent, Selective, and Orally Efficacious A2B Adenosine Receptor Antagonist

Discovery of 7-azaindole derivatives as potent Orai inhibitors showing efficacy in a preclinical model of asthma

Structure-activity relationships (SAR) and structure-kinetic relationships (SKR) of sulphone-based CRTh2 antagonists

First synthesis of pyrrolothiadiazinones. An alternative core ring for xanthine based structures

Novel triazolopyridylbenzamides as potent and selective p38α inhibitors

In Reply

In Reply

OP-ECHO-03 - Intraoperative transoesophageal echocardiography: Impact on cardiac surgery decision-making

Intraoperative transoesophageal echocardiography: Impact on cardiac surgery decision-making

Pyrazine-based Syk kinase inhibitors

Design, Synthesis, and Structure−Activity Relationships of Aminopyridine N-Oxides, a Novel Scaffold for the Potent and Selective Inhibition of p38 Mitogen Activated Protein Kinase

Structure–activity relationships (SAR) and structure–kinetic relationships (SKR) of bicyclic heteroaromatic acetic acids as potent CRTh2 antagonists I

Effect of glucose-insulin-potassium in severe acute heart failure after brain death

Structure–activity relationships (SAR) and structure–kinetic relationships (SKR) of bicyclic heteroaromatic acetic acids as potent CRTh2 antagonists II: Lead optimization

Characterization and proteomic profile of extracellular vesicles from peritoneal dialysis efflux

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