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1. Full Text 10-year follow-up of diabetes incidence and weight loss in the Diabetes Prevention Program Outcomes Study
by Diabetes Prevention Program Research Group and Diabet Prevention Program Res Grp and Diabetes Prevention Program Research Group
The Lancet (British edition), ISSN 0140-6736, 2009, Volume 374, Issue 9702, pp. 1677 - 1686
Internal Medicine | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Public health. Hygiene-occupational medicine | Public health. Hygiene | General aspects | Diabetes. Impaired glucose tolerance | Biological and medical sciences | Endocrinopathies | Etiopathogenesis. Screening. Investigations. Target tissue resistance | Medical sciences | Epidemiology | Endocrine pancreas. Apud cells (diseases) | United States - epidemiology | Life Style | Overweight - complications | Metformin - therapeutic use | Follow-Up Studies | Cardiovascular Diseases - prevention & control | Humans | Middle Aged | Male | Weight Loss - drug effects | Exercise Therapy | Diabetes Mellitus, Type 2 - epidemiology | Incidence | Statistics, Nonparametric | Cardiovascular Diseases - epidemiology | Female | Diabetes Mellitus, Type 2 - complications | Diabetes, Gestational - etiology | Patient Education as Topic | Hypoglycemic Agents - therapeutic use | Cardiovascular Diseases - etiology | Double-Blind Method | Risk Reduction Behavior | Diabetes Mellitus, Type 2 - prevention & control | Treatment Outcome | Overweight - prevention & control | Pregnancy | Regression Analysis | Analysis of Variance | Aged | Prevention | Forecasts and trends | Diabetes | Patient outcomes | Intervention | Diabetic retinopathy | Plasma | Mortality | Educational materials | Cardiovascular disease | Minority & ethnic groups | Risk factors | Clinical outcomes | Studies | Prevention programs | Behavior | Asian Americans | Index Medicus | Abridged Index Medicus
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2. Full Text Efficacy and safety of tenecteplase in combination with enoxaparin, abciximab, or unfractionated heparin: the ASSENT-3 randomised trial in acute myocardial infarction
by Armstrong, P.W and Wallentin, L and Adgey, A.A.J and Binbrek, A.S and Califf, R and Cassim, S and Diaz, R and Fioretti, P.M and Huber, K and López-Sendón, J.L and Mäkijärvi, M and Navarro Robles, J and Pfisterer, M and Seabra-Gomes, R and Soares-Piegas, L and Sugrue, D and Tendera, M and Toutouzas, P and Danays, T and Houbracken, K and Kaye, J and Hacke, W and von Kummer, R and Brower, R and Hirsh, J and Maggioni, A and Tijssen, J and Weaver, D and Beernaert, A and Beysen, N and Broos, K and D’hollander, K and Fransen, A and Genesse, D and Goffin, L and Hendrickx, R and Jorissen, F and Marschal, C and Moreira, M and Munsters, K and Schoovaerts, C and Sinnaeve, P and Schildermans, C and Van Gucht, H and Van Rompaey, P and Vlassak, S and Wittockx, H and Humeniuk, L and Seidel, A and Molina, M and Alexander, J and Pascual, A and Bestilny, S and Bassani Arrieta, C.A and Cagnolatti, A and Cartasegna, L.R and Chekerdemian, S and Covelli, G and Cuello, J.L and Ferro-Queirel, E and Gambarte, A and Garcia-Duran, R and Hrabar, A and Marinig, A and Muntaner, J and Orlandini, A.D and Piombo, A.C and Amerena, J and Aroney, G and Buckmaster, N and Fitzpatrick, M and Newman, R and Rowe, M and Singh, B and Eber, B and Gaul, G.B and Klein, W and Leisch, F and Mayr, H and Niessner, H and Pachinger, O and Pichler, M and Traindl, O and Zenker, G and Berthe, C and Bodur, G and Carpentier, J and Charlier, F and Clement, A and Coenen, A and De Keyser, F and Dendale, P and Dhooghe, G and Elshot, S and Emmerechts, C and Foret, F and Gatera, E and Gerardy, A.C and Gysbrechts, M and Hellemans, S and ... and The Assessment of the Safety and Efficacy of a New Thrombolytic Regimen (ASSENT)-3 Investigators and Assessment Safety Efficacy New Thr and Assessment of the Safety and Efficacy of a New Thrombolytic Regimen (ASSENT)-3 Investigators
The Lancet (British edition), ISSN 0140-6736, 08/2001, Volume 358, Issue 9282, pp. 605 - 613
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Cardiovascular system | Cardiology. Vascular system | Heart | Miscellaneous | Pharmacology. Drug treatments | Biological and medical sciences | Medical sciences | Coronary heart disease | Recurrence | Humans | Middle Aged | Heparin - administration & dosage | Male | Tissue Plasminogen Activator - administration & dosage | Treatment Outcome | Chi-Square Distribution | Enoxaparin - administration & dosage | Immunoglobulin Fab Fragments - administration & dosage | Injections | Myocardial Infarction - drug therapy | Antibodies, Monoclonal - administration & dosage | Platelet Aggregation Inhibitors - administration & dosage | Survival Analysis | Female | Aged | Fibrinolytic Agents - administration & dosage | Drug Therapy, Combination | Dosage and administration | Thrombolytic drugs | Research | Tenecteplase | Drug therapy | Heart attack | Prevention | Evaluation | Ischemia | Enoxaparin | Reperfusion (Physiology) | Drug therapy, Combination | Heparin | Health aspects | Clinical trials | Heart attacks | Myocardial infarction | Coagulation | Hemorrhage | Evidence-based medicine | Bleeding | Infusion | Randomization | Reperfusion | Motivation | Blood platelets | Safety | Anticoagulants | Stroke | Effectiveness | Complications | Mortality | Pharmacology | Glycoproteins | Patients | Trauma | Molecular chains | Studies | Fibrin | Monoclonal antibodies | Infarction | Index Medicus | Abridged Index Medicus
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3. Full Text Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
by O’Donnell-Luria, Anne H and Pais, Lynn S and Faundes, Víctor and Wood, Jordan C and Sveden, Abigail and Luria, Victor and Abou Jamra, Rami and Accogli, Andrea and Amburgey, Kimberly and Anderlid, Britt Marie and Azzarello-Burri, Silvia and Basinger, Alice A and Bianchini, Claudia and Bird, Lynne M and Buchert, Rebecca and Carre, Wilfrid and Ceulemans, Sophia and Charles, Perrine and Cox, Helen and Culliton, Lisa and Currò, Aurora and McRae, Jeremy F and Clayton, Stephen and Fitzgerald, Tomas W and Kaplanis, Joanna and Prigmore, Elena and Rajan, Diana and Sifrim, Alejandro and Aitken, Stuart and Akawi, Nadia and Alvi, Mohsan and Ambridge, Kirsty and Barrett, Daniel M and Bayzetinova, Tanya and Jones, Philip and Jones, Wendy D and King, Daniel and Krishnappa, Netravathi and Mason, Laura E and Singh, Tarjinder and Tivey, Adrian R and Ahmed, Munaza and Anjum, Uruj and Archer, Hayley and Armstrong, Ruth and Awada, Jana and Balasubramanian, Meena and Banka, Siddharth and Baralle, Diana and Barnicoat, Angela and Batstone, Paul and Baty, David and Bennett, Chris and Berg, Jonathan and Bernhard, Birgitta and Bevan, A. Paul and Bitner-Glindzicz, Maria and Blair, Edward and Blyth, Moira and Bohanna, David and Bourdon, Louise and Bourn, David and Bradley, Lisa and Brady, Angela and Brent, Simon and Brewer, Carole and Brunstrom, Kate and Bunyan, David J and Burn, John and Canham, Natalie and Castle, Bruce and Chandler, Kate and Chatzimichali, Elena and Cilliers, Deirdre and Clarke, Angus and Clasper, Susan and Clayton-Smith, Jill and Clowes, Virginia and Coates, Andrea and Cole, Trevor and Colgiu, Irina and Collins, Amanda and Collinson, Morag N and Connell, Fiona and Cooper, Nicola and Cox, Helen and Cresswell, Lara and Cross, Gareth and Crow, Yanick and D’Alessandro, Mariella and Dabir, Tabib and Davidson, Rosemarie and Davies, Sally and de Vries, Dylan and Dean, John and Deshpande, Charu and Devlin, Gemma and Dixit, Abhijit and Dobbie, Angus and Donaldson, Alan and ... and Deciphering Developmental Disorders (DDD) Study and Deciphering Dev Disorders DDD
American journal of human genetics, ISSN 0002-9297, 06/2019, Volume 104, Issue 6, pp. 1210 - 1222
KMT2E | epilepsy | H3K4 methylation | global developmental delay | neurodevelopmental disorder | intellectual disability | epileptic encephalopathy | autism | yes | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Child, Preschool | Infant | Male | DNA-Binding Proteins - genetics | Epilepsy - etiology | Neurodevelopmental Disorders - pathology | Haploinsufficiency | Genetic Variation | Young Adult | Phenotype | Pedigree | Adolescent | Adult | Female | Heterozygote | Child | Epilepsy - pathology | Neurodevelopmental Disorders - etiology | Genetic variation | Epilepsy | Nervous system | Genetic aspects | Degeneration | Research | Risk factors | Index Medicus | Life Sciences | Genetics | Human genetics | Report | Medicin och hälsovetenskap
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4. Full Text Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between
by Jarvik, Gail P and Amendola, Laura M and Berg, Jonathan S and Brothers, Kyle and Clayton, Ellen W and Chung, Wendy and Evans, Barbara J and Evans, James P and Fullerton, Stephanie M and Gallego, Carlos J and Garrison, Nanibaa’ A and Gray, Stacy W and Holm, Ingrid A and Kullo, Iftikhar J and Lehmann, Lisa Soleymani and McCarty, Cathy and Prows, Cynthia A and Rehm, Heidi L and Sharp, Richard R and Salama, Joseph and Sanderson, Saskia and Van Driest, Sara L and Williams, Marc S and Wolf, Susan M and Wolf, Wendy A and Harley, John and Myers, Melanie and Namjou, Bahram and Vinks, Sander and Connolly, John and Keating, Brendan and Gerhard, Glenn and Sundaresan, Agnes and Tromp, Gerard and Crosslin, David and Leppig, Kathy and Wicklund, Cathy and Chute, Christopher and Lynch, John and De Andrade, Mariza and Heit, John and McCormick, Jen and Brilliant, Murray and Kitchner, Terrie and Ritchie, Marylyn and Böttinger, Erwin and Peter, Inga and Persell, Stephen and Rasmussen-Torvik, Laura and McGregor, Tracy and Roden, Dan and Antommaria, Armand and Chiavacci, Rosetta and Faucett, Andy and Ledbetter, David and Williams, Janet and Hartzler, Andrea and Vitek, Carolyn R. Rohrer and Frost, Norm and Ferryman, Kadija and Horowitz, Carol and Rhodes, Rosamond and Zinberg, Randi and Aufox, Sharon and Pan, Vivian and Long, Rochelle and Ramos, Erin and Odgis, Jackie and Wise, Anastasia and Hull, Sara and Gitlin, Jonathan and Green, Robert and Metterville, Danielle and McGuire, Amy and Kong, Sek Won and Trinidad, Sue and Veenstra, David and Roche, Myra and Skinner, Debra and Raspberry, Kelly and O’Daniel, Julianne and Parsons, Will and Eng, Christine and Hilsenbeck, Susan and Karavite, Dean and Conlin, Laura and Spinner, Nancy and Krantz, Ian and Falk, Marni and Santani, Avni and Dechene, Elizabeth and Dulik, Matthew and Bernhardt, Barbara and Schuetze, Scott and Everett, Jessica and Gornick, Michele Caroline and Wilfond, Ben and Tabor, Holly and Lemke, Amy A and Richards, Sue and ... and eMERGE Act-ROR Committee and CERC Committee and CSER Act-ROR Working Group and CERC Comm and CSER Act-ROR Working Grp and eMERGE Act-ROR Comm
American journal of human genetics, ISSN 0002-9297, 06/2014, Volume 94, Issue 6, pp. 818 - 826
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Biomedical Research - ethics | Genetics, Medical - ethics | Patient Access to Records - ethics | Genetic Privacy | Humans | Societies, Scientific | Population Groups | High-Throughput Nucleotide Sequencing | Disclosure | Genome, Human | Genomics - ethics | Genetic research | Research | Nucleotide sequencing | Population genetics | DNA sequencing | Health care industry | Morality | Mutation | Genomics | Medical ethics | Index Medicus
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5. Full Text Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)
by Blok, Lot Snijders and Rousseau, Justine and Twist, Joanna and Ehresmann, Sophie and Takaku, Motoki and Venselaar, Hanka and Rodan, Lance H and Nowak, Catherine B and Douglas, Jessica and Swoboda, Kathryn J and Steeves, Marcie A and Sahai, Inderneel and Stumpel, Connie T R M and Stegmann, Alexander P A and Wheeler, Patricia and Willing, Marcia and Fiala, Elise and Kochhar, Aaina and Gibson, William T and Cohen, Ana S A and Agbahovbe, Ruky and Innes, A Micheil and Au, P Y Billie and Rankin, Julia and Anderson, Ilse J and Skinner, Steven A and Louie, Raymond J and Warren, Hannah E and Afenjar, Alexandra and Keren, Boris and Nava, Caroline and Buratti, Julien and Isapof, Arnaud and Rodriguez, Diana and Lewandowski, Raymond and Propst, Jennifer and van Essen, Ton and Choi, Murim and Lee, Sangmoon and Chae, Jong H and Price, Susan and Schnur, Rhonda E and Douglas, Ganka and Wentzensen, Ingrid M and Zweier, Christiane and Reis, André and Bialer, Martin G and Moore, Christine and Koopmans, Marije and Brilstra, Eva H and Monroe, Glen R and van Gassen, Koen L I and van Binsbergen, Ellen and Newbury-Ecob, Ruth and Bownass, Lucy and Bader, Ingrid and Mayr, Johannes A and Wortmann, Saskia B and Jakielski, Kathy J and Strand, Edythe A and Kloth, Katja and Bierhals, Tatjana and Roberts, John D and Petrovich, Robert M and Machida, Shinichi and Kurumizaka, Hitoshi and Lelieveld, Stefan and Pfundt, Rolph and Jansen, Sandra and Deriziotis, Pelagia and Faivre, Laurence and Thevenon, Julien and Assoum, Mirna and Shriberg, Lawrence and Kleefstra, Tjitske and Brunner, Han G and Wade, Paul A and Fisher, Simon E and Campeau, Philippe M and DDD study and The DDD study
Nature communications, ISSN 2041-1723, 02/2019, Volume 10, Issue 1, pp. 1 - 4
DNA helicase | Neurodevelopmental disorders | Mutation
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