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2008, ISBN 9782846541305, 390
Book
Digestive and Liver Disease, ISSN 1590-8658, 2015, Volume 48, Issue 3, pp. 242 - 247
Journal Article
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
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 02/2007, Volume 356, Issue 5, pp. 469 - 478
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2016, Volume 11, Issue 4, pp. e0153176 - e0153176
Journal Article
Nature, ISSN 0028-0836, 06/2018, Volume 558, Issue 7711, pp. 540 - 546
CLOVES syndrome (congenital lipomatous overgrowth, vascular malformations, epidermal naevi, scoliosis/skeletal and spinal syndrome) is a genetic disorder that... 
CRITERIA | PIK3CA(H1047R) MUTATION | NVP-BYL719 | INHIBITION | PHOSPHATIDYLINOSITOL 3-KINASE | MULTIDISCIPLINARY SCIENCES | SPECTRUM | EXPRESSION | DISCOVERY | Vascular Neoplasms - complications | Class I Phosphatidylinositol 3-Kinases - metabolism | Humans | Vascular Malformations - enzymology | Male | Thiazoles - therapeutic use | Molecular Targeted Therapy | Nevus - enzymology | Scoliosis - drug therapy | Adult | Female | Nevus - drug therapy | Musculoskeletal Abnormalities - enzymology | Vascular Malformations - drug therapy | Child | Disease Models, Animal | Heart Failure - complications | Sirolimus - therapeutic use | Class I Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Syndrome | Heart Failure - drug therapy | Lipoma - drug therapy | Lipoma - enzymology | Musculoskeletal Abnormalities - drug therapy | Phenotype | Scoliosis - complications | Animals | Mice | HeLa Cells | Vascular Neoplasms - drug therapy | Molecular targeted therapy | Care and treatment | Genetic disorders | Analysis | Methods | Senescence | Nuclear magnetic resonance--NMR | Congenital defects | Medical services | Clinical trials | Congestive heart failure | Kinases | Patients | Cancer therapies | Side effects | Cell growth | Scoliosis | Cell cycle | Mutation | Tumors | Apoptosis | Index Medicus | Life Sciences | Human health and pathology
Journal Article
Kidney International, ISSN 0085-2538, 03/2018, Volume 93, Issue 3, pp. 716 - 726
Intracranial aneurysm rupture is a dramatic complication of autosomal dominant polycystic kidney disease (ADPKD). It remains uncertain whether screening should... 
cardiovascular disease | ADPKD | intracranial aneurysms | cost-utility analysis | costutility analysis | EMPHASIS | SUBARACHNOID HEMORRHAGE | UROLOGY & NEPHROLOGY | PREVALENCE | OUTCOMES | CEREBRAL ANEURYSMS | REGISTRY | AGE | Predictive Value of Tests | Intracranial Aneurysm - diagnostic imaging | Prognosis | Humans | Middle Aged | Magnetic Resonance Angiography - economics | Male | Aneurysm, Ruptured - economics | Aneurysm, Ruptured - etiology | Cerebral Angiography - methods | Mass Screening - methods | Cerebral Angiography - economics | Patient Selection | Intracranial Aneurysm - therapy | Time Factors | Clinical Decision-Making | Aneurysm, Ruptured - therapy | Adult | Female | Retrospective Studies | Aneurysm, Ruptured - diagnostic imaging | Quality-Adjusted Life Years | Reproducibility of Results | Mass Screening - economics | Risk Factors | Intracranial Aneurysm - etiology | Health Care Costs | Intracranial Aneurysm - economics | Polycystic Kidney, Autosomal Dominant - economics | Polycystic Kidney, Autosomal Dominant - diagnosis | Cost-Benefit Analysis | Program Evaluation | Polycystic Kidney, Autosomal Dominant - complications | Nephrology | Medical imaging | Kidneys | Angiography | Polycystic kidney | Aneurysm | Rupture | Aneurysms | Family medical history | Medical screening | Patients | Carotid arteries | Risk factors | Motivation | Tomography | Population | Kidney diseases | Age | Veins & arteries | Index Medicus
Journal Article
by Jacquemont, S and Reymond, A and Zufferey, F and Harewood, L and Walters, R.G and Kutalik, Z and Martinet, D and Shen, Y and Valsesia, A and Beckmann, N.D and Thorleifsson, G and Belfiore, M and Bouquillon, S and Campion, D and Leeuw, N. de and Vries, L.B.A. de and Esko, T and Fernandez, B.A and Fernandez-Aranda, F and Fernandez-Real, J.M and Gratacos, M and Guilmatre, A and Hoyer, J and Jarvelin, M.R and Kooy, R.F and Kurg, A and Caignec, C. Le and Mannik, K and Platt, O.S and Sanlaville, D and Haelst, M.M. van and Villatoro Gomez, S and Walha, F and Wu, B.L and Yu, Y and Aboura, A and Addor, M.C and Alembik, Y and Antonarakis, S.E and Arveiler, B and Barth, M and Bednarek, N and Bena, F and Bergmann, S and Beri, M and Bernardini, L and Blaumeiser, B and Bonneau, D and Bottani, A and Boute, O and Brunner, H.G and Cailley, D and Callier, P and Chiesa, J and Chrast, J and Coin, L and Coutton, C and Cuisset, J.M and Cuvellier, J.C and David, A and Freminville, B. de and Delobel, B and Delrue, M.A and Demeer, B and Descamps, D and Didelot, G and Dieterich, K and Disciglio, V and Doco-Fenzy, M and nat, S and Duban-Bedu, B and Dubourg, C and El-Sayed Moustafa, J.S and Elliott, P and Faas, B.H.W and Faivre, L and Faudet, A and Fellmann, F and Ferrarini, A and Fisher, R and Flori, E and Forer, L and Gaillard, D and Gerard, M and Gieger, C and Gimelli, S and Gimelli, G and Grabe, H.J and Guichet, A and Guillin, O and Hartikainen, A.L and Heron, D and Hippolyte, L and Holder, M and Homuth, G and Isidor, B and Jaillard, S and Jaros, Z and Jimenez-Murcia, S and Helas, G.J and ...
Nature, ISSN 0028-0836, 2011, Volume 478, Issue 7367, pp. 97 - 102
Both obesity and being underweight have been associated with increased mortality. Underweight, defined as a body mass index (BMI) DEPENDENT PROBE AMPLIFICATION | FAILURE-TO-THRIVE | METABOLIC SYNDROME | RELATIVE QUANTIFICATION | SNP GENOTYPING DATA | HIDDEN-MARKOV MODEL | MULTIDISCIPLINARY SCIENCES | BODY-MASS INDEX | TIME QUANTITATIVE PCR | COPY NUMBER VARIATION | CIRCULAR BINARY SEGMENTATION | Humans | Middle Aged | Child, Preschool | RNA, Messenger - analysis | Head - anatomy & histology | Infant | Male | Developmental Disabilities - genetics | Gene Expression Profiling | North America | Obesity - genetics | Case-Control Studies | Young Adult | Mental Disorders - genetics | Aging | Gene Duplication - genetics | Adult | Female | Transcription, Genetic | Energy Metabolism - genetics | Child | Infant, Newborn | Chromosomes, Human, Pair 16 - genetics | Body Mass Index | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Europe | RNA, Messenger - genetics | Mutation - genetics | Body Height - genetics | Thinness - genetics | Phenotype | Comparative Genomic Hybridization | Adolescent | Heterozygote | Aged | Cohort Studies | Sequence Deletion - genetics | Obesity | Chromosome mapping | Usage | Genetic variation | Genetic aspects | Cognition disorders | Research | Risk factors | Schizophrenia | Gender | Behavior | Gene expression | Bias | Index Medicus | Life Sciences | Human health and pathology | Genetics | Endocrinology and metabolism | Gene Duplication | Developmental Disabilities | Sequence Deletion | Thinness | genetics | Genetic Predisposition to Disease | Head | Gene Dosage | analysis | Energy Metabolism | Mental Disorders | Chromosomes, Human, Pair 16 | Body Height | Mutation | anatomy & histology | RNA, Messenger
Journal Article