Found: 43
Select item for more details and to access through your institution.
Phase II study of preoperative radiotherapy and concomitant weekly intravenous oxaliplatin combined with oral capecitabine for stages II-III rectal cancer.
- Published in:
- Clinical & Translational Oncology, 2012, v. 14, n. 8, p. 592, doi. 10.1007/s12094-012-0846-7
- By:
- Publication type:
- Article
Factores pronósticos e indicaciones quirÚrgicas en las metástasis hepáticas de carcinoma colorrectal.
- Published in:
- Clinical & Translational Oncology, 2000, v. 2, n. 6, p. 309, doi. 10.1007/BF02979594
- By:
- Publication type:
- Article
Two consecutive studies using oral UFT-based chemotherapy regimens in elderly patients with advanced colorectal cancer.
- Published in:
- Clinical & Translational Oncology, 2000, v. 2, n. 3, p. 154, doi. 10.1007/BF02979483
- By:
- Publication type:
- Article
Characteristics of Adrenocortical Carcinoma Associated With Lynch Syndrome.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2021, v. 106, n. 2, p. 318, doi. 10.1210/clinem/dgaa833
- By:
- Publication type:
- Article
Caspase-3 activity, response to chemotherapy and clinical outcome in patients with colon cancer.
- Published in:
- International Journal of Colorectal Disease, 2008, v. 23, n. 1, p. 21, doi. 10.1007/s00384-007-0362-3
- By:
- Publication type:
- Article
A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscape.
- Published in:
- Scientific Reports, 2017, p. 39348, doi. 10.1038/srep39348
- By:
- Publication type:
- Article
Erratum: Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis.
- Published in:
- Scientific Reports, 2016, p. 23880, doi. 10.1038/srep23880
- By:
- Publication type:
- Article
Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis.
- Published in:
- Scientific Reports, 2016, p. 20697, doi. 10.1038/srep20697
- By:
- Publication type:
- Article
Longer Telomeres Are Associated with Cancer Risk in MMR-Proficient Hereditary Non-Polyposis Colorectal Cancer.
- Published in:
- PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0086063
- By:
- Publication type:
- Article
Telomere Length and Genetic Anticipation in Lynch Syndrome.
- Published in:
- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0061286
- By:
- Publication type:
- Article
Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Lessons learnt from a population-based pilot programme for colorectal cancer screening in Catalonia (Spain).
- Published in:
- Journal of Medical Screening, 2007, v. 14, n. 2, p. 81, doi. 10.1258/096914107781261936
- By:
- Publication type:
- Article
Non-Lynch Familial and Early-Onset Colorectal Cancer Explained by Accumulation of Low-Risk Genetic Variants.
- Published in:
- Cancers, 2021, v. 13, n. 15, p. 3857, doi. 10.3390/cancers13153857
- By:
- Publication type:
- Article
Correction: Dueñas et al. Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals. Cancers 2020, 12 , 3419.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals.
- Published in:
- Cancers, 2020, v. 12, n. 11, p. 3419, doi. 10.3390/cancers12113419
- By:
- Publication type:
- Article
Complete Loss of EPCAM Immunoexpression Identifies EPCAM Deletion Carriers in MSH2-Negative Colorectal Neoplasia.
- Published in:
- Cancers, 2020, v. 12, n. 10, p. 2803, doi. 10.3390/cancers12102803
- By:
- Publication type:
- Article
Comprehensive Constitutional Genetic and Epigenetic Characterization of Lynch-Like Individuals.
- Published in:
- Cancers, 2020, v. 12, n. 7, p. 1799, doi. 10.3390/cancers12071799
- By:
- Publication type:
- Article
Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 5, p. 511, doi. 10.1038/ejhg.2012.204
- By:
- Publication type:
- Article
MLH1 methylation screening is effective in identifying epimutation carriers.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 12, p. 1256, doi. 10.1038/ejhg.2012.136
- By:
- Publication type:
- Article
Furosemide test in stage III-chronic kidney disease and kidney transplant patients on tacrolimus.
- Published in:
- International Urology & Nephrology, 2013, v. 45, n. 5, p. 1471, doi. 10.1007/s11255-012-0351-5
- By:
- Publication type:
- Article
Mitomycin-C and Vinblastine in Advanced Breast Cancer.
- Published in:
- Oncology, 1989, v. 46, n. 3, p. 137, doi. 10.1159/000226702
- By:
- Publication type:
- Article
Tumor analysis of MMR genes in Lynch‐like syndrome: Challenges associated with results interpretation.
- Published in:
- Cancer Medicine, 2024, v. 13, n. 7, p. 1, doi. 10.1002/cam4.7041
- By:
- Publication type:
- Article
NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-45281-1
- By:
- Publication type:
- Article
COMPARISON BETWEEN TWO URINE DILUTION TESTS: THEIR ADVANTAGES AND DISADVANTAGES.
- Published in:
- Electronic Journal of Biomedicine, 2015, n. 2, p. 1
- By:
- Publication type:
- Article
OBSTRUCTIVE NEPHROPATHY: ITS PHYSIOPATHOLOGY.
- Published in:
- Electronic Journal of Biomedicine, 2011, n. 3, p. 1
- By:
- Publication type:
- Article
NEFROPATÍA OBSTRUCTIVA: SU FISIOPATOLOGÍA.
- Published in:
- Electronic Journal of Biomedicine, 2011, n. 2, p. 48
- By:
- Publication type:
- Article
Mutations in TP53 are a prognostic factor in colorectal hepatic metastases undergoing surgical resection.
- Published in:
- Carcinogenesis, 2007, v. 28, n. 6, p. 1241, doi. 10.1093/carcin/bgm012
- By:
- Publication type:
- Article
Polymorphisms in sulfotransferases SULT1A1 and SULT1A2 are not related to colorectal cancer.
- Published in:
- International Journal of Cancer, 2005, v. 113, n. 4, p. 683, doi. 10.1002/ijc.20613
- By:
- Publication type:
- Article
Primary constitutional MLH1 epimutations: a focal epigenetic event.
- Published in:
- 2018
- By:
- Publication type:
- journal article
UFT-induced haemolytic anaemia.
- Published in:
- Cancer Chemotherapy & Pharmacology, 2001, v. 47, n. 3, p. 280, doi. 10.1007/s002800000195
- By:
- Publication type:
- Article
New insights into POLE and POLD1 germline mutations in familial colorectal cancer and polyposis.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 13, p. 3506, doi. 10.1093/hmg/ddu058
- By:
- Publication type:
- Article
Breast Cancer Patient with Li-Fraumeni Syndrome: A Case Report Highlighting the Importance of Multidisciplinary Management.
- Published in:
- Case Reports in Oncology, 2020, v. 13, n. 1, p. 130, doi. 10.1159/000505684
- By:
- Publication type:
- Article
Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteria.
- Published in:
- Familial Cancer, 2017, v. 16, n. 4, p. 501, doi. 10.1007/s10689-017-9981-1
- By:
- Publication type:
- Article
Comprehensive analysis and ACMG‐based classification of CHEK2 variants in hereditary cancer patients.
- Published in:
- Human Mutation, 2020, v. 41, n. 12, p. 2128, doi. 10.1002/humu.24110
- By:
- Publication type:
- Article
Candidate genes for hereditary colorectal cancer: Mutational screening and systematic review.
- Published in:
- Human Mutation, 2020, v. 41, n. 9, p. 1563, doi. 10.1002/humu.24057
- By:
- Publication type:
- Article
Contribution to colonic polyposis of recently proposed predisposing genes and assessment of the prevalence of NTHL1‐ and MSH3‐associated polyposes.
- Published in:
- Human Mutation, 2019, v. 40, n. 11, p. 1910, doi. 10.1002/humu.23853
- By:
- Publication type:
- Article
Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis.
- Published in:
- Human Mutation, 2018, v. 39, n. 9, p. 1214, doi. 10.1002/humu.23564
- By:
- Publication type:
- Article
GALNT12 is Not a Major Contributor of Familial Colorectal Cancer Type X.
- Published in:
- Human Mutation, 2014, v. 35, n. 1, p. 50, doi. 10.1002/humu.22454
- By:
- Publication type:
- Article
Comprehensive Functional Assessment of MLH1 Variants of Unknown Significance.
- Published in:
- Human Mutation, 2013, v. 34, n. 1, p. 274, doi. 10.1002/humu.22246
- By:
- Publication type:
- Article
Comprehensive functional assessment of MLH1 variants of unknown significance.
- Published in:
- Human Mutation, 2012, v. 33, n. 11, p. 1576, doi. 10.1002/humu.22142
- By:
- Publication type:
- Article
HIDDEN CLOTTED VASCULAR ACCESS INFECTION DIAGNOSED BY FLUORODEOXYGLUCOSE POSITRON EMISSION TOMOGRAPHY.
- Published in:
- Nephrology, 2008, v. 13, n. 3, p. 264, doi. 10.1111/j.1440-1797.2007.00837.x
- By:
- Publication type:
- Article
Impaired Urine Dilution Capability in HIV Stable Patients.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Impaired Urine Dilution Capability in HIV Stable Patients.
- Published in:
- International Journal of Nephrology, 2014, p. 1, doi. 10.1155/2014/381985
- By:
- Publication type:
- Article