Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (24) 24
humans (21) 21
inflammatory bowel disease (18) 18
crohn's disease (15) 15
gastroenterology & hepatology (15) 15
ulcerative colitis (13) 13
crohn disease - genetics (11) 11
gastroenterology and hepatology (11) 11
genetics (11) 11
female (10) 10
genetic predisposition to disease (10) 10
male (10) 10
adult (9) 9
genome-wide association (9) 9
genome-wide association study (9) 9
inflammatory-bowel-disease (9) 9
colitis, ulcerative - genetics (8) 8
genomes (8) 8
inflammatory bowel diseases (8) 8
inflammatory bowel diseases - genetics (8) 8
ulcerative-colitis (8) 8
case-control studies (7) 7
crohns-disease (7) 7
genetic aspects (7) 7
intestine (7) 7
polymorphism, single nucleotide (7) 7
risk factors (7) 7
gastroenterology (6) 6
pathogenesis (6) 6
susceptibility loci (6) 6
abridged index medicus (5) 5
genetics & heredity (5) 5
genotype (5) 5
loci (5) 5
middle aged (5) 5
research (5) 5
risk (5) 5
association (4) 4
celiac disease (4) 4
cohort studies (4) 4
crohn’s disease (4) 4
disease control (4) 4
gene expression (4) 4
genetic variation (4) 4
netherlands (4) 4
patients (4) 4
phenotype (4) 4
susceptibility (4) 4
variants (4) 4
young adult (4) 4
alleles (3) 3
article (3) 3
colitis, ulcerative - therapy (3) 3
colon (3) 3
digestive system diseases (3) 3
disease (3) 3
european continental ancestry group - genetics (3) 3
genetic association studies (3) 3
genetic variance (3) 3
identification (3) 3
management (3) 3
medicine (3) 3
medicine, general & internal (3) 3
meta-analysis (3) 3
multiple (3) 3
nod2 signaling adaptor protein - genetics (3) 3
phenotypes (3) 3
population (3) 3
risk loci (3) 3
sequence variants (3) 3
severity of illness index (3) 3
studies (3) 3
activation (2) 2
active crohns-disease (2) 2
adolescent (2) 2
aged (2) 2
aged, 80 and over (2) 2
association analysis (2) 2
biochemistry & molecular biology (2) 2
care and treatment (2) 2
celiac disease - genetics (2) 2
classification (2) 2
colitis, ulcerative - pathology (2) 2
complex traits (2) 2
crohn disease - therapy (2) 2
crohns disease (2) 2
diet (2) 2
digestive system (2) 2
disease susceptibility (2) 2
environmental factors (2) 2
extraintestinal manifestations (2) 2
gastroenterology and hepatology/inflammatory bowel disease (2) 2
gastrointestinal diseases (2) 2
gene frequency (2) 2
gene loci (2) 2
genetic loci (2) 2
genetic loci - genetics (2) 2
genetic predisposition to disease - genetics (2) 2
genetic research (2) 2
genetic susceptibility (2) 2
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
by Franke, Ane and McGovern, Dermot P. B and Barrett, Jeffrey C and Wang, Kai and Radford-Smith, Graham L and Ahmad, Tariq and Lees, Charlie W and Balschun, Tobias and Lee, James and Roberts, Rebecca and Anderson, Carl A and Bis, Joshua C and Bumpstead, Suzanne and Ellinghaus, David and Festen, Eleonora M and Georges, Michel and Green, Todd and Haritunians, Talin and Jostins, Luke and Latiano, Anna and Mathew, Christopher G and Montgomery, Grant W and Prescott, Natalie J and Raychaudhuri, Soumya and Rotter, Jerome I and Schumm, Philip and Sharma, Yashoda and Simms, Lisa A and Taylor, Kent D and Whiteman, David and Wijmenga, Cisca and Baldassano, Robert N and Barclay, Murray and Bayless, Theodore M and Brand, Stephan and Büning, Carsten and Cohen, Albert and Colombel, Jean-Frederick and Cottone, Mario and Stronati, Laura and Denson, Ted and de Vos, Martine and D'Inca, Renata and Dubinsky, Marla and Edwards, Cathryn and Florin, Tim and Franchimont, Denis and Gearry, Richard and Glas, Jürgen and van Gossum, Ane and Guthery, Stephen L and Halfvarson, Jonas and Verspaget, Hein W and Hugot, Jean-Pierre and Karban, Amir and Laukens, Debby and Lawrance, Ian and Lemann, Marc and Levine, Arie and Libioulle, Cecile and Louis, Edouard and Mowat, Craig and Newman, William and Panés, Julián and Phillips, Anne and Proctor, Deborah D and Regueiro, Miguel and Russell, Richard and Rutgeerts, Paul and Sanderson, Jeremy and Sans, Miquel and Seibold, Frank and Steinhart, A. Hillary and Stokkers, Pieter C. F and Torkvist, Leif and Kullak-Ublick, Gerd and Wilson, David and Walters, Thomas and Targan, Stephan R and Brant, Steven R and Rioux, John D and D'Amato, Mauro and Weersma, Rinse K and Kugathasan, Subra and Griffiths, Anne M and Mansfield, John C and Vermeire, Severine and Duerr, Richard H and Silverberg, Mark S and Satsangi, Jack and Schreiber, Stefan and Cho, Judy H and Annese, Vito and Hakonarson, Hakon and Daly, Mark J and Parkes, Miles and Hälsoakademin and Örebro universitet
Nature genetics, ISSN 1061-4036, 2010, Volume 42, Issue 12, pp. 1118 - 1125
We undertook a meta-analysis of six Crohn's disease genome-wide association studies (GWAS) comprising 6,333 affected individuals (cases) and 15,056 controls... 
COMMON VARIANTS | ACTIVATION | INFLAMMATORY-BOWEL-DISEASE | PROTEIN | NEDD4 FAMILY | GENE | GENETICS & HEREDITY | SEQUENCE VARIANTS | RECEPTOR | IDENTIFICATION | ASSOCIATION | Genetic Variation | Crohn Disease - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Reproducibility of Results | Humans | Computational Biology | Genetic Loci - genetics | Crohn Disease - etiology | Genome, Human - genetics | Genetic Linkage | Care and treatment | Methyltransferases | Physiological aspects | Disease susceptibility | Genetic aspects | Crohn's disease | Research | Risk factors | Inflammatory bowel disease | Genetics | Genomics | Meta-analysis | Index Medicus | Medicine | Medicin | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Interplay of host genetics and gut microbiota underlying the onset and clinical presentation of inflammatory bowel disease
by Imhann, Floris and Vich Vila, Arnau and Bonder, Marc Jan and Fu, Jingyuan and Gevers, Dirk and Visschedijk, Marijn C and Spekhorst, Lieke M and Alberts, Rudi and Franke, Lude and van Dullemen, Hendrik M and Ter Steege, Rinze W F and Huttenhower, Curtis and Dijkstra, Gerard and Xavier, Ramnik J and Festen, Eleonora A M and Wijmenga, Cisca and Zhernakova, Alexandra and Weersma, Rinse K
Gut, ISSN 0017-5749, 01/2018, Volume 67, Issue 1, pp. 108 - 119
ObjectivePatients with IBD display substantial heterogeneity in clinical characteristics. We hypothesise that individual differences in the complex interaction... 
BACTERIAL INTERACTIONS | INFLAMMATORY BOWEL DISEASE | GENETICS | INTESTINAL BACTERIA | CROHNS | RISK | BACTERIA | LOCI | RARE | GASTROENTEROLOGY & HEPATOLOGY | Severity of Illness Index | Crohn Disease - genetics | Risk Assessment - methods | Genetic Predisposition to Disease | Humans | Middle Aged | Colitis, Ulcerative - genetics | Male | Colitis, Ulcerative - pathology | Dysbiosis - complications | Dysbiosis - microbiology | Gastrointestinal Microbiome - genetics | Case-Control Studies | Feces - microbiology | Colitis, Ulcerative - microbiology | Dysbiosis - genetics | Host-Pathogen Interactions - genetics | Crohn Disease - pathology | Inflammatory Bowel Diseases - pathology | Inflammatory Bowel Diseases - genetics | Adult | Crohn Disease - microbiology | Female | Inflammatory Bowel Diseases - microbiology | Inflammatory bowel diseases | Care and treatment | Genetic aspects | Research | Microbiota (Symbiotic organisms) | Genetic variation | Phenotypes | Bacterial infections | Breastfeeding & lactation | rRNA 16S | Pathogenesis | Genomes | Inflammation | Crohn's disease | Family medical history | Crohns disease | Inflammatory bowel disease | Genetic variance | Microbiota | Antibiotics | Intestine | Gastroenterology | Peripheral blood | Genetics | Gene loci | Colon | Endoscopy | Acetic acid | NOD2 protein | Index Medicus | Abridged Index Medicus | Gut microbiota | Healthy controls | Host genetics
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease
by Festen, Eleonora A. M and Goyette, Philippe and Green, Todd and Boucher, Gabrielle and Beauchamp, Claudine and Trynka, Gosia and Dubois, Patrick C and Lagacé, Caroline and Stokkers, Pieter C. F and Hommes, Daan W and Barisani, Donatella and Palmieri, Orazio and Annese, Vito and van Heel, David A and Weersma, Rinse K and Daly, Mark J and Wijmenga, Cisca and Rioux, John D
PLoS genetics, ISSN 1553-7390, 2011, Volume 7, Issue 1, pp. e1001283 - e1001283
Crohn's disease (CD) and celiac disease (CelD) are chronic intestinal inflammatory diseases, involving genetic and environmental factors in their pathogenesis.... 
IMPUTATION | INFLAMMATORY-BOWEL-DISEASE | ULCERATIVE-COLITIS | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | GENETIC-VARIANTS | MULTIPLE | Crohn Disease - genetics | Interleukin-18 Receptor beta Subunit - genetics | Data Interpretation, Statistical | Genetic Predisposition to Disease | Genome-Wide Association Study | Celiac Disease - genetics | Humans | Risk Factors | GTPase-Activating Proteins - genetics | Hydro-Lyases - genetics | Protein Tyrosine Phosphatase, Non-Receptor Type 2 - genetics | Celiac disease | Genetic susceptibility | Interleukins | Crohn's disease | Genetic aspects | Research | Risk factors | Interferon gamma | Index Medicus | Medical research | Diet | Genetics | Genomes | Small intestine | Meta-analysis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text SLC39A8 missense variant is associated with Crohn's disease but does not have a major impact on gut microbiome composition in healthy subjects
by Collij, V and Imhann, F and Vila, AV and Fu, JY and Dijkstra, G and Festen, EAM and Voskuil, MD and Daly, MJ and Xavier, RJ and Wijmenga, C and Zhernakova, A and Weersma, RK
PLOS ONE, ISSN 1932-6203, 01/2019, Volume 14, Issue 1, pp. e0211328 - e0211328
Background Gene-microbiome interactions are important in aetiology and pathogenesis of inflammatory bowel disease, a chronic inflammatory disorder of the... 
INFLAMMATORY-BOWEL-DISEASE | MULTIDISCIPLINARY SCIENCES | GENOME | ZINC | Crohn's disease | Genetic aspects | Research | Microbiota (Symbiotic organisms) | Pediatrics | Inflammatory bowel diseases | rRNA 16S | Control methods | Pathogenesis | Microbiomes | Genomes | Gene sequencing | Microorganisms | Microbiota | Intestine | Hepatology | Gastroenterology | Peripheral blood | Population | Genetics | Digestive tract | Phenotypes | Composition | Digestive system | Health risks | Gastrointestinal tract | Disease control | Patients | Variance analysis | Zinc | Carriers | Inflammatory bowel disease | Studies | Biological warfare | Gastrointestinal system | Alleles | Sampling methods | Ulcerative colitis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis
by Alberts, Rudi and de Vries, Elisabeth M G and Goode, Elizabeth C and Jiang, Xiaojun and Sampaziotis, Fotis and Rombouts, Krista and Böttcher, Katrin and Folseraas, Trine and Weismüller, Tobias J and Mason, Andrew L and Wang, Weiwei and Alexander, Graeme and Alvaro, Domenico and Bergquist, Annika and Björkström, Niklas K and Beuers, Ulrich and Björnsson, Einar and Boberg, Kirsten Muri and Bowlus, Christopher L and Bragazzi, Maria C and Carbone, Marco and Chazouillères, Olivier and Cheung, Angela and Dalekos, Georgios and Eaton, John and Eksteen, Bertus and Ellinghaus, David and Färkkilä, Martti and Festen, Eleonora A M and Floreani, Annarosa and Franceschet, Irene and Gotthardt, Daniel Nils and Hirschfield, Gideon M and Hoek, Bart van and Holm, Kristian and Hohenester, Simon and Hov, Johannes Roksund and Imhann, Floris and Invernizzi, Pietro and Juran, Brian D and Lenzen, Henrike and Lieb, Wolfgang and Liu, Jimmy Z and Marschall, Hanns-Ulrich and Marzioni, Marco and Melum, Espen and Milkiewicz, Piotr and Müller, Tobias and Pares, Albert and Rupp, Christian and Rust, Christian and Sandford, Richard N and Schramm, Christoph and Schreiber, Stefan and Schrumpf, Erik and Silverberg, Mark S and Srivastava, Brijesh and Sterneck, Martina and Teufel, Andreas and Vallier, Ludovic and Verheij, Joanne and Vila, Arnau Vich and Vries, Boudewijn de and Zachou, Kalliopi and Chapman, Roger W and Manns, Michael P and Pinzani, Massimo and Rushbrook, Simon M and Lazaridis, Konstantinos N and Franke, Andre and Anderson, Carl A and Karlsen, Tom H and Ponsioen, Cyriel Y and Weersma, Rinse K and PSC Study Grp and UK PSC Consortium and International PSC Study Group, The UK PSC Consortium and Sahlgrenska akademin and Institute of Medicine, Department of Molecular and Clinical Medicine and Institutionen för medicin, avdelningen för molekylär och klinisk medicin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy
Gut, ISSN 0017-5749, 08/2018, Volume 67, Issue 8, pp. 1517 - 1524
ObjectivePrimary sclerosing cholangitis (PSC) is a genetically complex, inflammatory bile duct disease of largely unknown aetiology often leading to liver... 
Primary sclerosing cholangitis | liver transplantation | genetics | RISK LOCI | ACTIVATION | MALIGNANCY | HEPATIC STELLATE CELLS | CIRRHOSIS | ULCERATIVE-COLITIS | LIVER FIBROSIS | GASTROENTEROLOGY & HEPATOLOGY | MULTIPLE | EPIDEMIOLOGY | GENOME-WIDE ASSOCIATION | Animal models | Transplants & implants | Disease | Syngeneic grafts | Association analysis | Effector cells | Genomes | Single-nucleotide polymorphism | Allografts | Etiology | Gastroenterology | Genetic analysis | Gallbladder | Antigens | Stellate cells | Liver diseases | Cholangitis | Regression analysis | Gene expression | Bile duct | Inflammatory bowel disease | Genetic variance | Hepatocytes | Quality control | Liver cirrhosis | Bile | Liver transplantation | Index Medicus | Abridged Index Medicus | Genetics | Genètica | Trasplantament hepàtic | Bilious diseases and biliousness | Hepatic transplantation | Malalties del tracte biliar | Gastroenterology and Hepatology | Gastroenterologi
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Drug Repositioning in Inflammatory Bowel Disease Based on Genetic Information
by Collij, Valerie and Festen, Eleonora A. M and Alberts, Rudi and Weersma, Rinse K
INFLAMMATORY BOWEL DISEASES, ISSN 1078-0998, 11/2016, Volume 22, Issue 11, pp. 2562 - 2570
Background:Currently, 200 genetic risk loci have been identified for inflammatory bowel disease (IBD). Although these findings have significantly advanced our... 
Crohn's disease | ulcerative colitis | drug identification | drug repositioning | candidate genes | inflammatory bowel disease | CROHNS-DISEASE | ULCERATIVE-COLITIS | SUSCEPTIBILITY LOCI | POPULATIONS | PATHOGENESIS | TRIAL | METABOLISM | TOFACITINIB | GASTROENTEROLOGY & HEPATOLOGY | GENOME-WIDE ASSOCIATION | Inflammatory Bowel Diseases - drug therapy | Genetic Association Studies | Humans | Drug Repositioning - methods | Gastrointestinal Agents - therapeutic use | Inflammatory Bowel Diseases - genetics | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease
by Fransen, Karin and Visschedijk, Marijn C and van Sommeren, Suzanne and Fu, Jinyuan Y and Franke, Lude and Festen, Eleonora A. M and Stokkers, Pieter C. F and van Bodegraven, Aiaan A and Crusius, J. Bart A and Hommes, Daniel W and Zanen, Pieter and de Jong, Dirk J and Wijmenga, Cisca and van Diemen, Cleo C and Weersma, Rinse K
Human molecular genetics, ISSN 0964-6906, 2010, Volume 19, Issue 17, pp. 3482 - 3488
Genome-wide association studies (GWAS) for Crohn's disease (CD) have identified loci explaining approximately 20% of the total genetic risk of CD. Part of the... 
PATHOGENESIS | INFLAMMATORY-BOWEL-DISEASE | VARIANTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | GENOME-WIDE ASSOCIATION | Crohn Disease - genetics | European Continental Ancestry Group - genetics | Gene Expression | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | Male | Proto-Oncogene Proteins - genetics | Ubiquitin-Conjugating Enzymes - genetics | Transcription Factors - genetics | Case-Control Studies | Female | Polymorphism, Single Nucleotide | Cohort Studies | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Association of Genetic Variants in NUDT15 with Thiopurine-Induced Myelosuppression in Patients with Inflammatory Bowel Disease
by Walker, Gareth J and Harrison, James W and Heap, Graham A and Voskuil, Michiel D and Andersen, Vibeke and Anderson, Carl A and Ananthakrishnan, Ashwin N and Barrett, Jeffrey C and Beaugerie, Laurent and Bewshea, Claire M and Cole, Andy T and Cummings, Fraser R and Daly, Mark J and Ellul, Pierre and Fedorak, Richard N and Festen, Eleonora A. M and Florin, Timothy H and Gaya, Daniel R and Halfvarson, Jonas and Hart, Ailsa L and Heerasing, Neel M and Hendy, Peter and Irving, Peter and Jones, Samuel E and Koskela, Jukka and Lindsay, James O and Mansfield, John C and McGovern, Dermot and Parkes, Miles and Pollok, Richard C. G and Ramakrishnan, Subramaniam and Rampton, David S and Rivas, Manuel A and Russell, Richard K and Schultz, Michael and Sebastian, Shaji and Seksik, Philippe and Singh, Abhey and So, Kenji and Sokol, Harry and Subramaniam, Kavitha and Todd, Anthony and Annese, Vito and Weersma, Rinse K and Xavier, Ramnik and Ward, Rebecca and Weedon, Michael N and Goodhand, James R and Kennedy, Nicholas A and Ahmad, Tariq and Holden, Arthur L and Andrews, Jane and Auth, Marcus and Babu, Sathish and Bampton, Peter and Banim, Paul and Barnes, Theresa and Basude, Dharam and Beckly, John and Bell, Andy and Bell, Sally and Bhandari, Pradeep and Bloom, Stuart and Border, Dave and Bredin, Francesca and Brookes, Matthew J and Brown, Matthew and Calvert, Chris and Campbell, David and Chanchlani, Neil and Chaudhary, Basant and Chaudhary, Rakesh and Chung-Faye, Guy and Colleypriest, Ben and Connor, Susan and Cooney, Rachel and Cooper, Sheldon and Creed, Tom J and Croft, Nick and Cullen, Sue and D'Amato, Mauro and D'Inca, Renata and Dalal, Helen and Daneshmend, Tawfique K and Das, Debasish and Delaney, Michael and DeSilva, Shanika and Dhar, Anjan and Dharmasiri, Suranga and Direkze, Natalie and Dunckley, Paul and Elphick, David and Everett, Simon M and Feeney, Mark and Fell, John and Foley, Stephen and Franke, Andre and Gavin, Daniel and Gee, Ian and Ghosh, Deb and ... and IBD Pharmacogenetics Study Grp and IBD Pharmacogenetics Study Group and for the IBD Pharmacogenetics Study Group
JAMA - Journal of the American Medical Association, ISSN 0098-7484, 02/2019, Volume 321, Issue 8, pp. 753 - 761
IMPORTANCE Use of thiopurines may be limited by myelosuppression. TPMT pharmacogenetic testing identifies only 25% of at-risk patients of European ancestry.... 
MEDICINE, GENERAL & INTERNAL | S-METHYLTRANSFERASE | POLYMORPHISMS | MANAGEMENT | PREDICTOR | THERAPY | ACUTE LYMPHOBLASTIC-LEUKEMIA | SUSCEPTIBILITY | AZATHIOPRINE | MERCAPTOPURINE INTOLERANCE | CHILDREN | Haplotypes | Crohn Disease - genetics | Genome-Wide Association Study | Colitis, Ulcerative - metabolism | Humans | Methyltransferases - metabolism | Colitis, Ulcerative - genetics | Methyltransferases - genetics | Pyrophosphatases - genetics | Crohn Disease - metabolism | European Continental Ancestry Group | Male | Case-Control Studies | Methyltransferases - therapeutic use | Exome | Young Adult | Crohn Disease - drug therapy | Adolescent | Adult | Female | Leukocyte Count | Polymorphism, Single Nucleotide | Colitis, Ulcerative - drug therapy | Sequence Analysis, DNA - methods | Antimitotic agents | Complications and side effects | Inflammatory bowel diseases | Genetic variation | Myelosuppression | Dosage and administration | Genetic aspects | Research | Antineoplastic agents | Drug therapy | Health aspects | Chromosome 6 | Risk | Genomes | Chromosome deletion | Pharmacology | Gene deletion | Disease control | Patients | Inflammatory bowel disease | White blood cells | Genetic variance | Genotyping | Clonal deletion | Intestine | Deletion | Chromosome 13 | Genetic testing | Genotypes | Index Medicus | Abridged Index Medicus | Original Investigation
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Prevalence of-and risk factors for work disability in Dutch patients with inflammatory bowel disease
by Lieke M Spekhorst Bas Oldenburg Ad A van Bodegraven Dirk J de Jong Floris Imhann Andrea E van der Meulen-de Jong Marieke J Pierik Janneke C van der Woude Gerard Dijkstra Geert D’Haens Mark L?wenberg Rinse K Weersma Eleonora AM Festen Parelsnoer Institute and the Dutch Initiative on Crohn and Colitis and Parelsnoer Inst Dutch Initiative C and Parelsnoer Institute and the Dutch Initiative on Crohn and Colitis
世界胃肠病学杂志：英文版, ISSN 1007-9327, 2017, Volume 23, Issue 46, pp. 8182 - 8192
AIM To determine the prevalence of work disability in inflammatory bowel disease(IBD), and to assess risk factors associated with work disability.METHODS For... 
Inflammatory bowel disease | Health care costs | Crohn's disease | Work disability | Ulcerative colitis | POPULATION | CROHNS-DISEASE | ULCERATIVE-COLITIS | PROCTOCOLECTOMY | SICK LEAVE | THERAPY | QUALITY-OF-LIFE | GASTROENTEROLOGY & HEPATOLOGY | EMPLOYMENT | UNEMPLOYMENT | PARTICIPATION | Index Medicus | Retrospective Cohort Study | Crohn’s disease
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10.