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1. Full Text What is eHealth (6)? Development of a Conceptual Model for eHealth: Qualitative Study with Key Informants
by Shaw, Tim and McGregor, Deborah and Brunner, Melissa and Keep, Melanie and Janssen, Anna and Barnet, Stewart
Journal of medical Internet research, ISSN 1438-8871, 10/2017, Volume 19, Issue 10, pp. e324 - e324
qualitative research | interview | eHealth | health care | models, theoretical | Health Care Sciences & Services | Life Sciences & Biomedicine | Medical Informatics | Science & Technology | Qualitative Research | Delivery of Health Care - methods | Humans | Telemedicine - methods | Hypothesis testing | Medical personnel | Health care | Qualitative research | Medical research | Translation | Taxonomy | Semistructured interviews | Respondents | Health education | Governance | Care delivery | Conceptual development | Information technology | Conceptual models | Health care delivery | Health information | Service delivery | Classification | Communications technology | Sampling | Index Medicus
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2. Full Text Risk thresholds for alcohol consumption: combined analysis of individual-participant data for 599 912 current drinkers in 83 prospective studies
by Wood, Angela M and Kaptoge, Stephen and Butterworth, Adam S and Willeit, Peter and Warnakula, Samantha and Bolton, Thomas and Paige, Ellie and Paul, Dirk S and Sweeting, Michael and Burgess, Stephen and Bell, Steven and Astle, William and Stevens, David and Koulman, Albert and Selmer, Randi M and Verschuren, W M Monique and Sato, Shinichi and Njølstad, Inger and Woodward, Mark and Salomaa, Veikko and Nordestgaard, Børge G and Yeap, Bu B and Fletcher, Astrid and Melander, Olle and Kuller, Lewis H and Balkau, Beverley and Marmot, Michael and Koenig, Wolfgang and Casiglia, Edoardo and Cooper, Cyrus and Arndt, Volker and Franco, Oscar H and Wennberg, Patrik and Gallacher, John and de la Cámara, Agustín Gómez and Völzke, Henry and Dahm, Christina C and Dale, Caroline E and Bergmann, Manuela M and Crespo, Carlos J and van der Schouw, Yvonne T and Kaaks, Rudolf and Simons, Leon A and Lagiou, Pagona and Schoufour, Josje D and Boer, Jolanda M A and Key, Timothy J and Rodriguez, Beatriz and Moreno-Iribas, Conchi and Davidson, Karina W and Taylor, James O and Sacerdote, Carlotta and Wallace, Robert B and Quiros, J Ramon and Tumino, Rosario and Blazer, Dan G and Linneberg, Allan and Daimon, Makoto and Panico, Salvatore and Howard, Barbara and Skeie, Guri and Strandberg, Timo and Weiderpass, Elisabete and Nietert, Paul J and Psaty, Bruce M and Kromhout, Daan and Salamanca-Fernandez, Elena and Kiechl, Stefan and Krumholz, Harlan M and Grioni, Sara and Palli, Domenico and Huerta, José M and Price, Jackie and Sundström, Johan and Arriola, Larraitz and Arima, Hisatomi and Travis, Ruth C and Panagiotakos, Demosthenes B and Karakatsani, Anna and Trichopoulou, Antonia and Kühn, Tilman and Grobbee, Diederick E and Barrett-Connor, Elizabeth and van Schoor, Natasja and Boeing, Heiner and Overvad, Kim and Kauhanen, Jussi and Wareham, Nick and Langenberg, Claudia and Forouhi, Nita and Wennberg, Maria and Després, Jean-Pierre and Cushman, Mary and Cooper, Jackie A and Rodriguez, Carlos J and Sakurai, Masaru and Shaw, Jonathan E and Knuiman, Matthew and Voortman, Trudy and Meisinger, Christa and ... and Emerging Risk Factors Collaboration/EPIC-CVD/UK Biobank Alcohol Study Group and Emerging Risk Factors Collabora and Emerging Risk Factors Collaboration
The Lancet (British edition), ISSN 0140-6736, 04/2018, Volume 391, Issue 10129, pp. 1513 - 1523
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Cardiovascular Diseases - etiology | Prospective Studies | Humans | Middle Aged | Female | Male | Alcohol Drinking - adverse effects | Alcohol Drinking - mortality | Drinking of alcoholic beverages | Myocardial infarction | Heart attacks | Sex | Income | Cardiovascular disease | Dosage | Risk factors | Guidelines | Alcohol use | Aorta | Heart diseases | Age | Consumption | Medical research | Cerebral infarction | Data analysis | Stroke | Life expectancy | Thresholds | Drinking behavior | Mortality | Diabetes mellitus | Health risks | Data processing | Risk analysis | Disease control | Cholesterol | Studies | Lipoproteins | Life span | Collaboration | Alcoholic beverages | Infarction | Diabetes | Cardiovascular diseases | Health risk assessment | Smoking | Index Medicus | Abridged Index Medicus | Community medicine, Social medicine: 801 | Samfunnsmedisin, sosialmedisin: 801 | VDP | Helsefag: 800 | Health sciences: 800 | Medisinske Fag: 700 | Medical disciplines: 700 | Arbetsmedicin och miljömedicin | Hälsovetenskap | Medical and Health Sciences | Medicin och hälsovetenskap | Health Sciences | Environmental Health and Occupational Health | Human Nutrition & Health | Human Nutrition | Afdeling Humane voeding | Humane Voeding | Humane Voeding & Gezondheid | Human Nutrition (HNE)
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3. Full Text NBEA: Developmental disease gene with early generalized epilepsy phenotypes
by Mulhern, Maureen S and Stumpel, C and Stong, N and Brunner, H.G and Bier, Louise and Lippa, Natalie and Kempers, M.J.E and Pfundt, R.P and Snijders Blok, L and Stevens, S.J.C and Sands, Tristan T and EuroEPINOMICS-RES-MAE Working Grp and CAUSES Study and CAUSES study and EuroEPINOMICS-RES-MAE working group and for the CAUSES study and for the EuroEPINOMICS‐RES‐MAE working group
Annals of neurology, ISSN 0364-5134, 2018, Volume 84, Issue 5, pp. 788 - 795
Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Epilepsy, Generalized - genetics | Humans | Child, Preschool | Genotype | Male | Neurodevelopmental Disorders - genetics | Nerve Tissue Proteins - genetics | Carrier Proteins - genetics | Phenotype | Adolescent | Female | Mutation | Child | Autism | Phenotypes | Neurodevelopmental disorders | Patients | Epilepsy | Seizures | Life Sciences | Genetics | Human genetics
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4. Full Text Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
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 (London), ISSN 0028-0836, 2011, Volume 478, Issue 7367, pp. 97 - 102
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Human | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | 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 | Medicin och hälsovetenskap
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5. Full Text Efficacy and safety of tocilizumab in patients with polyarticular-course juvenile idiopathic arthritis: results from a phase 3, randomised, double-blind withdrawal trial
by Brunner, Hermine I and Ruperto, Nicolino and Zuber, Zbigniew and Keane, Caroline and Harari, Olivier and Kenwright, Andrew and Lu, Peng and Cuttica, Ruben and Keltsev, Vladimir and Xavier, Ricardo M and Calvo, Inmaculada and Nikishina, Irina and Rubio-Pérez, Nadina and Alexeeva, Ekaterina and Chasnyk, Vyacheslav and Horneff, Gerd and Opoka-Winiarska, Violetta and Quartier, Pierre and Silva, Clovis A and Silverman, Earl and Spindler, Alberto and Baildam, Eileen and Gámir, M Luz and Martin, Alan and Rietschel, Christoph and Siri, Daniel and Smolewska, Elzbieta and Lovell, Daniel and Martini, Alberto and De Benedetti, Fabrizio and Paediat Rheumatology Int Trials and PRCSG and Paediatric Rheumatology International Trials Organisation PRINTO and Pediatric Rheumatology Collaborative Study Group (PRCSG) and for the Paediatric Rheumatology International Trials Organisation (PRINTO) and the Pediatric Rheumatology Collaborative Study Group (PRCSG)
Annals of the rheumatic diseases, ISSN 0003-4967, 06/2015, Volume 74, Issue 6, pp. 1110 - 1117
Life Sciences & Biomedicine | Rheumatology | Science & Technology | Bronchitis - chemically induced | Antibodies, Monoclonal, Humanized - therapeutic use | Double-Blind Method | Humans | Child, Preschool | Male | Treatment Outcome | Receptors, Interleukin-6 - antagonists & inhibitors | Methotrexate - therapeutic use | Adrenal Cortex Hormones - therapeutic use | Disease Progression | Arthritis, Juvenile - drug therapy | Cellulitis - chemically induced | Maintenance Chemotherapy - methods | Pneumonia - chemically induced | Adolescent | Female | Remission Induction - methods | Drug Therapy, Combination | Child | Antirheumatic Agents - therapeutic use | Treatment outcome | Usage | Care and treatment | Rheumatoid arthritis | Analysis | Clinical trials | Risk factors | Arthritis | Low density lipoprotein | Cholesterol | Index Medicus | DMARDs (biologic) | Clinical and Epidemiological Research | Treatment | 1506 | Juvenile Idiopathic Arthritis
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6. Full Text Dependence of flood peaks and volumes in modeled discharge time series: Effect of different uncertainty sources
by Brunner, Manuela I and Sikorska-Senoner, Anna E
Journal of hydrology (Amsterdam), ISSN 0022-1694, 05/2019, Volume 572, pp. 620 - 629
Bivariate flood frequency analysis | Data resolution | Uncertainty assessment | HBV | Precipitation distribution | Geosciences, Multidisciplinary | Engineering | Physical Sciences | Geology | Technology | Engineering, Civil | Water Resources | Science & Technology
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7. Full Text The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
by Redin, C and Brand, H and Collins, R.L and Kammin, T and Mitchell, E and Hodge, J.C and Hanscom, C and Pillalamarri, V and Seabra, C.M and Abbott, M.-A and Abdul-Rahman, Omar and Aberg, E and Adley, R and Alcaraz-Estrada, S.L and Alkuraya, Fowzan S and An, Y and Anderson, M.-A and Antolik, C and Anyane-Yeboa, K and Atkin, Joan and Bartell, T and Bernstein, J.A and Beyer, E and Blumenthal, I and Bongers, Ernie and Brilstra, E.H and Brown, C.W and Brüggenwirth, Hennie and Callewaert, L and Chiang, C and Corning, K and Cox, H and Cuppen, Edwin and Currall, B.B and Cushing, Tom and David, D and Deardorff, Matthew and Dheedene, Annelies and D'Hooghe, Marc and Vries, Boukje and Earl, D.L and Ferguson, H.L and Fisher, H and Fitzpatrick, David R and Gerrol, P and Giachino, D and Glessner, J.T and Gliem, T and Grady, M and Graham, B.H and Griffis, C and Gripp, Karen and Gropman, A.L and Hanson-Kahn, A and Harris, D.J and Hayden, M.A and Hill, R and Hochstenbach, R and Hoffman, J.D and Hopkin, R and Hubshman, M.W and Innes, M and Irons, M and Irving, M and Jacobsen, J.C and Janssens, Sana and Jewett, T and Johnson, J.P and Jongmans, Marjolijn and Kahler, Stephen G and Koolen, David and Korzelius, J and Kroisel, Peter and Lacassie, Y and Lawless, W and Lemyre, E and Leppig, Kathy and Levin, A.V and Li, H and Liao, E.C and Lim, C and Lose, E.J and Lucente, D and MacEra, M.J and Manavalan, P and Manile, G and Marcelis, Carlo and Margolin, L and Mason, T and Masser-Frye, Diane and McClellan, M.W and Zepeda Mendoza, C.J and Menten, B and Middelkamp, S and Mikami, L.R and Moe, E and Mohammed, Shabaz and Mononen, T and Mortenson, M.E and Moya, G and ...
Nature genetics, ISSN 1061-4036, 01/2017, Volume 49, Issue 1, pp. 36 - 45
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Congenital Abnormalities - genetics | Gene Rearrangement | Genetic Markers - genetics | Humans | Chromosome Aberrations | Female | Male | Cytogenetics | Nucleotide sequencing | Analysis | Genomics | DNA sequencing | Studies | Medical research | Genetic counseling | Congenital diseases | Intellectual disabilities | Genomes | Mutation | Grants | Localization | Index Medicus | structural variation | MEF2C | translocation | inversion | Hi-C | chromothripsis | topologically associated domain (TAD) | congenital anomaly | intellectual disability | autism | balanced chromosomal abnormality
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