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1. Full Text Temporal Trends in Transcatheter Aortic Valve Replacement in France: FRANCE 2 to FRANCE TAVI
by Auffret, Vincent and Lefevre, Thierry and Van Belle, Eric and Eltchaninoff, Hélène and Iung, Bernard and Koning, René and Motreff, Pascal and Leprince, Pascal and Verhoye, Jean Philippe and Manigold, Thibaut and Souteyrand, Geraud and Boulmier, Dominique and Joly, Patrick and Pinaud, Frédéric and Himbert, Dominique and Collet, Jean Philippe and Rioufol, Gilles and Ghostine, Said and Bar, Olivier and Dibie, Alain and Champagnac, Didier and Leroux, Lionel and Collet, Frédéric and Teiger, Emmanuel and Darremont, Olivier and Folliguet, Thierry and Leclercq, Florence and Lhermusier, Thibault and Olhmann, Patrick and Huret, Bruno and Lorgis, Luc and Drogoul, Laurent and Bertrand, Bernard and Spaulding, Christian and Quilliet, Laurent and Cuisset, Thomas and Delomez, Maxence and Beygui, Farzin and Claudel, Jean-Philippe and Hepp, Alain and Jegou, Arnaud and Gommeaux, Antoine and Mirode, Anfani and Christiaens, Luc and Christophe, Charles and Cassat, Claude and Metz, Damien and Mangin, Lionel and Isaaz, Karl and Jacquemin, Laurent and Guyon, Philippe and Pouillot, Christophe and Makowski, Serge and Bataille, Vincent and Rodés-Cabau, Josep and Gilard, Martine and Le Breton, Hervé and Le Breton, Hervé and Eltchaninoff, Hélène and Gilard, Martine and Iung, Bernard and Le Breton, Hervé and Lefevre, Thierry and Van Belle, Eric and Laskar, Marc and Leprince, Pascal and Iung, Bernard and Bataille, Vincent and Chevalier, Bernard and Garot, Philippe and Hovasse, Thomas and Lefevre, Thierry and Donzeau Gouge, Patrick and Farge, Arnaud and Romano, Mauro and Cormier, Bertrand and Bouvier, Erik and Bauchart, Jean-Jacques and Bodart, Jean-Christophe and Delhaye, Cédric and Houpe, David and Lallemant, Robert and Leroy, Fabrice and Sudre, Arnaud and Van Belle, Eric and Juthier, Francis and Koussa, Mohamed and Modine, Thomas and Rousse, Natacha and Auffray, Jean-Luc and Richardson, Marjorie and Berland, Jacques and Eltchaninoff, Hélène and Godin, Mathieu and Koning, René and Bessou, Jean-Paul and Letocart, Vincent and Manigold, Thibaut and Roussel, Jean-Christian and Jaafar, Philippe and ... and FRANCE TAVI Investigators
Journal of the American College of Cardiology, ISSN 0735-1097, 07/2017, Volume 70, Issue 1, pp. 42 - 55
Background Transcatheter aortic valve replacement (TAVR) is standard therapy for patients with severe aortic stenosis who are at high surgical risk. However,... 
national registry | pacemaker | outcomes | transfemoral | CARDIAC & CARDIOVASCULAR SYSTEMS | STENOSIS | LONG-TERM OUTCOMES | TRANSFEMORAL TRANSCATHETER | TRIAL | HIGH-RISK PATIENTS | IMPLANTATION | PREDICTORS | PROSTHESIS | CLINICAL-OUTCOMES | REGISTRY | France - epidemiology | Echocardiography, Transesophageal | Prognosis | Prospective Studies | Survival Rate - trends | Follow-Up Studies | Humans | Male | Aortic Valve Stenosis - diagnosis | Incidence | Aortic Valve Stenosis - epidemiology | Time Factors | Transcatheter Aortic Valve Replacement - trends | Aged, 80 and over | Female | Registries | Aortic Valve Stenosis - surgery | Heart valve diseases | Valves | Analysis | Heart | Therapy | Heart surgery | Stenosis | Clinical outcomes | Tamponade | Consortia | Risk assessment | Surgery | Electrocardiography | Aorta | Trends | Cardiology | Heart diseases | Dissection | Age | Stroke | Echocardiography | Complications | Mortality | Rupture | Medical instruments | Implantation | Patients | Coronary vessels | Men | Aortic valve | Life Sciences | Human health and pathology | Cardiology and cardiovascular system
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2. AT THE ORIGINS OF MATHEMATICAL ECONOMICS: THE ECONOMICS OF A.N. ISNARD. (1748-1803)
by VAN DEN BERG, RICHARD
2006, ROUTLEDGE STUDIES IN THE HISTORY OF ECONOMICS; 76., ISBN 9780415306492, Volume 76, 480
Achille Nicolas Isnard (1749-1803) an engineer with a keen interest in political economy, is best known for demonstrating the concept of market equilibrium... 
History of Economic Thought | Operator Theory | Economic Theory & Philosophy | Economists | Economics, Mathematical
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3. Full Text The Genetic Bases of Cardiomyopathies
by Richard, Pascale and Villard, Eric and Charron, Philippe and Isnard, Richard
Journal of the American College of Cardiology, ISSN 0735-1097, 11/2006, Volume 48, Issue 9, pp. A79 - A89
The Genetic Bases of Cardiomyopathies Pascale Richard, Eric Villard, Philippe Charron, Richard Isnard Cardiomyopathies are characterized by a great genetic... 
BINDING-PROTEIN-C | CONVERTING ENZYME GENE | CARDIAC & CARDIOVASCULAR SYSTEMS | FAMILIAL HYPERTROPHIC CARDIOMYOPATHY | IDIOPATHIC DILATED CARDIOMYOPATHY | CARDIAC TROPONIN-T | LAMIN A/C GENE | ANGIOTENSIN-ALDOSTERONE SYSTEM | CONGESTIVE-HEART-FAILURE | MYOSIN HEAVY-CHAIN | LEFT-VENTRICULAR HYPERTROPHY | Coenzymes | Gene mutations | Muscle proteins | Adenosine triphosphate | Membrane proteins | Proteins | Confidence intervals | Heart failure | Disease | Cardiomyopathy | Genes | Mortality | Mutation
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4. Full Text Left bundle branch block-induced cardiomyopathy: Myth or reality?
by Isnard, Richard and Pousset, Françoise
International journal of cardiology, ISSN 0167-5273, 08/2019
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5. Full Text Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
by Richard, Pascale and Charron, Philippe and Carrier, Lucie and Ledeuil, Céline and Cheav, Theary and Pichereau, Claire and Benaiche, Abdelaziz and Isnard, Richard and Dubourg, Olivier and Burban, Marc and Gueffet, Jean-Pierre and Millaire, Alain and Desnos, Michel and Schwartz, Ketty and Hainque, Bernard and Komajda, Michel and EUROGENE Heart Failure Project
Circulation, ISSN 0009-7322, 05/2003, Volume 107, Issue 17, pp. 2227 - 2232
Background - Hypertrophic cardiomyopathy is an autosomal-dominant disorder in which 10 genes and numerous mutations have been reported. The aim of the present... 
Genetics | Prognosis | Cardiomyopathy | Hypertrophy | POPULATION | CARDIAC & CARDIOVASCULAR SYSTEMS | hypertrophy | IDENTIFICATION | prognosis | MYOSIN HEAVY-CHAIN | PATHOGENESIS | genetics | MISSENSE MUTATION | PERIPHERAL VASCULAR DISEASE | TROPONIN-T | cardiomyopathy | HEMATOLOGY | BINDING | Cardiomyopathy, Hypertrophic, Familial - diagnosis | Carrier Proteins - genetics | Genetic Predisposition to Disease | Molecular Diagnostic Techniques | Cardiomyopathy, Hypertrophic, Familial - genetics | Humans | Myosin Heavy Chains - genetics | Genotype | Mutation
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6. Full Text Adult intensive-care patients with 2009 pandemic influenza A(H1N1) infection
by FUHRMAN, C and BONMARIN, I and BITAR, D and CARDOSO, T and DUPORT, N and HERIDA, M and ISNARD, H and GUIDET, B and MIMOZ, O and RICHARD, J. C. M and BRUN-BUISSON, C and BROCHARD, L and MAILLES, A and PATY, A. C and SAURA, C and LÉVY-BRUHL, D
Epidemiology and Infection, ISSN 0950-2688, 8/2011, Volume 139, Issue 8, pp. 1202 - 1209
In France, the surveillance of hospitalized cases of pandemic influenza was implemented in July 2009 and restricted to intensive-care unit (ICU) patients in... 
Intensive care units | Obesity | Pandemics | Mortality | Respiratory diseases | Predisposing factors | Antivirals | Disease risk | Death | Viruses | influenza | outbreaks | surveillance | Infectious disease epidemiology | MORTALITY | INFECTIOUS DISEASES | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | H1N1 INFLUENZA | ENGLAND | Influenza, Human - pathology | Age Factors | Obesity - complications | Humans | Middle Aged | Risk Factors | Male | Hospitalization | Antiviral Agents - administration & dosage | Pregnancy | Young Adult | Influenza A Virus, H1N1 Subtype - isolation & purification | Time Factors | Adolescent | Aged, 80 and over | Influenza, Human - mortality | Adult | Critical Care | Female | Influenza, Human - virology | Aged | Influenza, Human - drug therapy | France
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7. Full Text Effect of aliskiren on post-discharge outcomes among diabetic and non-diabetic patients hospitalized for heart failure: Insights from the ASTRONAUT trial
by Maggioni, Aldo P and Greene, Stephen J and Fonarow, Gregg C and Böhm, Michael and Zannad, Faiez and Solomon, Scott D and Lewis, Eldrin F and Baschiera, Fabio and Hua, Tsushung A and Gimpelewicz, Claudio R and Lesogor, Anastasia and Gheorghiade, Mihai and ASTRONAUT Investigators and ASTRONAUT Investigators and Coordinators and for the ASTRONAUT Investigators and Coordinators
European Heart Journal, ISSN 0195-668X, 10/2013, Volume 34, Issue 40, pp. 3117 - 3127
AIM The objective of the Aliskiren Trial on Acute Heart Failure Outcomes (ASTRONAUT) was to determine whether aliskiren, a direct renin inhibitor, would... 
Aliskiren | Diabetes | Post-discharge | Outcomes | MORTALITY | DIAGNOSIS | MULTICENTER | DESIGN | CARDIAC & CARDIOVASCULAR SYSTEMS | RATIONALE | RANDOMIZED-TRIAL | EVEREST TRIAL | DOUBLE-BLIND | ASSOCIATION | Prospective Studies | Diabetic Cardiomyopathies - drug therapy | Double-Blind Method | Administration, Oral | Diabetic Cardiomyopathies - mortality | Humans | Middle Aged | Kaplan-Meier Estimate | Hospitalization - statistics & numerical data | Fumarates - administration & dosage | Male | Treatment Outcome | Death, Sudden, Cardiac - etiology | Heart Failure - drug therapy | Cardiotonic Agents - administration & dosage | Renin - antagonists & inhibitors | Female | Amides - administration & dosage | Heart Failure - mortality | Esc Fasttrack
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8. Full Text A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy
by Friedrich, Felix W and Bausero, Pedro and Sun, Yuli and Treszl, Andras and Krämer, Elisabeth and Juhr, Denise and Richard, Pascale and Wegscheider, Karl and Schwartz, Ketty and Brito, Dulce and Arbustini, Eloisa and Waldenström, Anders and Isnard, Richard and Komajda, Michel and Eschenhagen, Thomas and Carrier, Lucie and EUROGENE Heart Failure Project and for the EUROGENE Heart Failure Project and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
European Heart Journal, ISSN 0195-668X, 7/2009, Volume 30, Issue 13, pp. 1648 - 1655
Aims Familial hypertrophic cardiomyopathy (FHC) is caused by mutations in genes encoding sarcomeric proteins. Incomplete penetrance suggests the existence of... 
Myocardium | Genetics | Calcium | Cardiomyopathy | Hypertrophy | CARDIAC & CARDIOVASCULAR SYSTEMS | PROTEIN-C GENE | STRUCTURAL ORGANIZATION | CARDIAC-HYPERTROPHY | BINDING PROTEINS | MUTATION | DISEASE | CALCIUM-BINDING | HOT-SPOT | EXPRESSION | ALPHA-TROPOMYOSIN | Calmodulin - genetics | Age Distribution | Calmodulin - metabolism | Cardiomyopathy, Hypertrophic, Familial - genetics | Gene Frequency | Humans | Middle Aged | Molecular Sequence Data | Rats | Cardiomyopathy, Hypertrophic, Familial - metabolism | Genotype | Male | Promoter Regions, Genetic - genetics | Polymorphism, Genetic | Animals | Transfection | Base Sequence | Myocytes, Cardiac - metabolism | Adult | Female | Heterozygote | Aged
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9. Full Text External validation of risk factors for malignant ventricular arrhythmias in lamin A/C mutation carriers
by Thuillot, Marine and Maupain, Carole and Gandjbakhch, Estelle and Waintraub, Xavier and Hidden‐Lucet, Françoise and Isnard, Richard and Ader, Flavie and Rouanet, Stephanie and Richard, Pascale and Charron, Philippe
European Journal of Heart Failure, ISSN 1388-9842, 02/2019, Volume 21, Issue 2, pp. 253 - 254
CARDIAC & CARDIOVASCULAR SYSTEMS | Life Sciences | Human health and pathology | Cardiology and cardiovascular system
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10. Full Text Evidence of isotopic fractionation of natural uranium in cultured human cells
by Eduardo Paredes and Emilie Avazeri and Véronique Malard and Claude Vidaud and Pascal E. Reiller and Richard Ortega and Anthony Nonell and Hélène Isnard and Frédéric Chartier and Carole Bresson
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2016, Volume 113, Issue 49, pp. 14007 - 14012
The study of the isotopic fractionation of endogen elements and toxic heavy metals in living organisms for biomedical applications, and for metabolic and... 
Microsamples | Isotopic fractionation | Neuronal cells | Uranium | Analytical procedure development | isotopic fractionation | MULTIDISCIPLINARY SCIENCES | U-238/U-235 | HEAVY-ELEMENTS | STABILITY-CONSTANTS | MASS-SPECTROMETRY | SIDE-CHAINS | analytical procedure development | URANYL | REDUCTION | AMINO-ACIDS | neuronal cells | uranium | METAL-COMPLEXES | microsamples | Cell Line - metabolism | Uranium - analysis | Humans | Neurons - metabolism | Cell Culture Techniques | Uranium - metabolism | Chemical Fractionation - methods | Isotopes | Biological Sciences | Physical Sciences
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11. Full Text Isotopic variations of copper at the protein fraction level in neuronal human cells exposed in vitro to uranium
by Paredes, Eduardo and Malard, Véronique and Vidaud, Claude and Avazeri, Emilie and Ortega, Richard and Nonell, Anthony and Isnard, Hélène and Chartier, Frédéric and Bresson, Carole
The Analyst, ISSN 0003-2654, 10/2019, Volume 144, Issue 2, pp. 5928 - 5933
The study of isotopic variations of endogenous and toxic metals in fluids and tissues is a recent research topic with an outstanding potential in biomedical... 
Mass balance | Proteins | Bulk sampling | Size exclusion chromatography | Toxicology | Inductively coupled plasma | Uranium | Biomarkers | Biocompatibility | Copper | Metabolism | Mass spectrometry | Index Medicus
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12. Full Text Prevalence of Memory Disorders in Ambulatory Patients Aged ≥70 Years With Chronic Heart Failure (from the EFICARE Study)
by Hanon, Olivier, MD, PhD and Vidal, Jean-Sébastien, MD, PhD and de Groote, Pascal, MD, PhD and Galinier, Michel, MD, PhD and Isnard, Richard, MD, PhD and Logeart, Damien, MD, PhD and Komajda, Michel, MD
American Journal of Cardiology, The, ISSN 0002-9149, 2014, Volume 113, Issue 7, pp. 1205 - 1210
The aim of this multicenter observational study conducted in France was to determine the prevalence of memory impairment in ambulatory patients aged ≥70 years... 
Cardiovascular | CARDIAC & CARDIOVASCULAR SYSTEMS | DEMENTIA | OLDER-ADULTS | COGNITIVE IMPAIRMENT | HEALTH | EXERCISE | DECLINE | Heart Failure - complications | Memory Disorders - epidemiology | Memory Disorders - physiopathology | Risk Assessment - methods | France - epidemiology | Prevalence | Age Factors | Ventricular Function, Left | Humans | Risk Factors | Heart Failure - physiopathology | Male | Stroke Volume | Memory Disorders - etiology | Outpatients | Aged, 80 and over | Cognition - physiology | Female | Aged | Retrospective Studies | Heart failure | Strategic planning (Business) | Memory | Depression, Mental | Prevalence studies (Epidemiology) | Hypertension | Cardiovascular disease | Secondary schools | Confidence intervals | Heart rate | Variables | Higher education | Older people | Diuretics | Cardiology | Age
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13. Full Text A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy
by Villard, Eric and Perret, Claire and Gary, Françoise and Proust, Carole and Dilanian, Gilles and Hengstenberg, Christian and Ruppert, Volker and Arbustini, Eloisa and Wichter, Thomas and Germain, Marine and Dubourg, Olivier and Tavazzi, Luigi and Aumont, Marie-Claude and De Groote, Pascal and Fauchier, Laurent and Trochu, Jean-Noël and Gibelin, Pierre and Aupetit, Jean-François and Stark, Klaus and Erdmann, Jeanette and Hetzer, Roland and Roberts, Angharad M and Barton, Paul J.R and Regitz-Zagrosek, Vera and Consortium, Cardiogenics and Aslam, Uzma and Duboscq-Bidot, Laëtitia and Meyborg, Matthias and Maisch, Bernhard and Madeira, Hugo and Waldenström, Anders and Galve, Enrique and Cleland, John G and Dorent, Richard and Roizes, Gerard and Zeller, Tanja and Blankenberg, Stefan and Goodall, Alison H and Cook, Stuart and Tregouet, David A and Tiret, Laurence and Isnard, Richard and Komajda, Michel and Charron, Philippe and Cambien, François and Cardiogenics Consortium and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
European Heart Journal, ISSN 0195-668X, 05/2011, Volume 32, Issue 9, pp. 1065 - 1076
Aims Dilated cardiomyopathy (DCM) is a major cause of heart failure with a high familial recurrence risk. So far, the genetics of DCM remains largely... 
Heart failure | CLCNKA | Dilated cardiomyopathy | Genome wide association study | BAG3 | HSPB7 | CARDIAC & CARDIOVASCULAR SYSTEMS | VARIANTS | CANDIDATE GENES | RISK | POPULATIONS | DISEASES | DNA | MUTATION | COMMON | Cardiomyopathy, Dilated - genetics | Genome-Wide Association Study | Humans | Middle Aged | Genetic Loci - genetics | Heart Failure - genetics | Male | Chloride Channels - genetics | Mutation, Missense - genetics | HSP27 Heat-Shock Proteins - genetics | Apoptosis Regulatory Proteins | Adaptor Proteins, Signal Transducing - genetics | Polymorphism, Single Nucleotide - genetics | Adult | Female | Heterozygote | Chromosomes, Human, Pair 10 - genetics | Chromosomes, Human, Pair 1 - genetics | Life Sciences | Genetics | Fasttrack Clinical | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
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