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1Academic Journal
المؤلفون: Vasen, Hans F A, Velthuizen, Mary E, Kleibeuker, Jan H, Menko, Fred H, Nagengast, Fokke M, Cats, Annemieke, van der Meulen-de Jong, Andrea E, Breuning, Martijn H, Roukema, Anne J, van Leeuwen-Cornelisse, Inge, de Vos Tot Nederveen Cappel, Wouter H, Wijnen, Juul T
المصدر: Vasen , H F A , Velthuizen , M E , Kleibeuker , J H , Menko , F H , Nagengast , F M , Cats , A , van der Meulen-de Jong , A E , Breuning , M H , Roukema , A J , van Leeuwen-Cornelisse , I , de Vos Tot Nederveen Cappel , W H & Wijnen , J T 2016 , ' Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer : contributions from the Dutch Lynch syndrome registry ' , Familial Cancer , vol. 15 , ....
مصطلحات موضوعية: Hereditary cancer, Registry, Follow-up system, Identification, Lynch syndrome, Cancer risk, Surveillance, NONPOLYPOSIS COLORECTAL-CANCER, ENDOMETRIAL CANCER, MUTATION CARRIERS, CLINICAL MANAGEMENT, SYNDROME FAMILIES, GEOLYNCH COHORT, TUMOR SPECTRUM, RISK, HNPCC
وصف الملف: application/pdf
الاتاحة: https://hdl.handle.net/11370/4dadd914-14c5-462f-8bd6-6a71a1d33a4e
https://research.rug.nl/en/publications/4dadd914-14c5-462f-8bd6-6a71a1d33a4e
https://doi.org/10.1007/s10689-016-9897-1
https://pure.rug.nl/ws/files/41717756/Hereditary_cancer_registries_improve_the_care_of_patients_with_a_genetic_predisposition_to_cancer.pdf -
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المؤلفون: Maartje Nielsen, Marjolijn J. L. Ligtenberg, Yvonne Tiersma, Juul T. Wijnen, Maran J. W. Olderode-Berends, Encarna Gomez Garcia, B. Redeker, José B. M. Zonneveld, Sanne W. ten Broeke, Frederik J. Hes, Carli M. J. Tops, Peter Devilee, Theo A. M. van Os, Christi J. van Asperen, Hans J. J. P. Gille, Niels de Wind, Heleen M. van der Klift, Arjen R. Mensenkamp, Tom G.W. Letteboer, Yvonne J. Vos, Elsa C. Bik, Mark Drost, S. Verhoef, Liselotte P. van Hest, Anja Wagner
المساهمون: Human Genetics, Human genetics, CCA - Cancer biology, RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Polikliniek (9), Klinische Genetica, Medical Genetics, Clinical Genetics
المصدر: Human mutation, 37(11), 1162-1179. Wiley-Liss Inc.
Human Mutation, 37(11), 1162-1179. Wiley-Liss Inc.
Human Mutation, 37(11), 1162–1179. Wiley-Liss Inc.
Human Mutation, 37(11), 1162-1179. Wiley
Human Mutation, 37(11), 1162-1179
Human Mutation, 37, 11, pp. 1162-1179
Human Mutation, 37, 1162-1179
van der Klift, H M, Mensenkamp, A R, Drost, M, Bik, E C, Vos, Y J, Gille, H J J P, Redeker, B E J W, Tiersma, Y, Zonneveld, J B M, Garcia, E G, Letteboer, T G W, Olderode-Berends, M J W, van Hest, L P, van Os, T A, Verhoef, S, Wagner, A, van Asperen, C J, Ten Broeke, S W, Hes, F J, de Wind, N, Nielsen, M, Devilee, P, Ligtenberg, M J L, Wijnen, J T & Tops, C M J 2016, ' Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome ', Human Mutation, vol. 37, no. 11, pp. 1162-1179 . https://doi.org/10.1002/humu.23052مصطلحات موضوعية: 0301 basic medicine, DNA Mutational Analysis, pseudogenes, COLORECTAL-CANCER, Cohort Studies, 0302 clinical medicine, Mutation Carrier, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], PMS2, Missense mutation, Genetics (clinical), Mismatch Repair Endonuclease PMS2, Netherlands, Medicine(all), Genetics, Brain Neoplasms, MLH1, Neoplastic Syndromes, Hereditary/genetics, Lynch syndrome, CMMRD, missense variants, immunohistochemistry, mismatch repair, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), DNA mismatch repair, Microsatellite Instability, Colorectal Neoplasms, EUROPEAN CONSORTIUM CARE, PSEUDOGENE INTERFERENCE, congenital, hereditary, and neonatal diseases and abnormalities, DNA Mutational Analysis/methods, Biology, 03 medical and health sciences, Germline mutation, Neoplastic Syndromes, Hereditary, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, SYNDROME FAMILIES, CFR PARTICIPANTS, medicine, Journal Article, Humans, Genetic Predisposition to Disease, Germ-Line Mutation, Brain Neoplasms/genetics, Microsatellite instability, Genetic Variation, Mismatch Repair Endonuclease PMS2/genetics, medicine.disease, Colorectal Neoplasms/genetics, Colorectal Neoplasms, Hereditary Nonpolyposis, GENE, digestive system diseases, 030104 developmental biology, PROMOTER HYPERMETHYLATION, 3' DELETIONS, Cancer research, NONPOLYPOSIS COLON-CANCER
وصف الملف: image/pdf
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المؤلفون: Silvia Sanduleanu, Jasmijn F. Haanstra, Elisabeth M. H. Mathus-Vliegen, Hans F. A. Vasen, Roeland A. Veenendaal, Monique E. van Leerdam, Jan J. Koornstra, Abdulbaqi Al-toma, Evelien Dekker, Jan H. Kleibeuker, Steven A L W Vanhoutvin, Fokko M. Nagengast, Wouter H. de Vos tot Nederveen Cappel, Annemieke Cats
المساهمون: Molecular Genetics, Gastroenterology & Hepatology, Guided Treatment in Optimal Selected Cancer Patients (GUTS), Promovendi NTM, RS: GROW - Oncology, RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, CCA -Cancer Center Amsterdam, Gastroenterology and Hepatology
المصدر: Gut, 64(10), 1578-1583. BMJ Publishing Group
Gut, 64, 10, pp. 1578-83
Gut, 64, 1578-83
Gut, 64(10), 1578-1583. BMJ PUBLISHING GROUP
Gut, 64(10), 1578-1583مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adenoma, Duodenum, Gene mutation, Asymptomatic, Gastroenterology, Capsule Endoscopy, RECOMMENDATIONS, Diagnosis, Differential, SDG 3 - Good Health and Well-being, Internal medicine, Double-balloon enteroscopy, SYNDROME FAMILIES, SURVEILLANCE, Intestine, Small, MANAGEMENT, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Prevalence, Medicine, Humans, Prospective Studies, METAANALYSIS, Aged, Netherlands, LESIONS, medicine.diagnostic_test, business.industry, Middle Aged, medicine.disease, CANCER, TUMORS, Colorectal Neoplasms, Hereditary Nonpolyposis, Lynch syndrome, digestive system diseases, Endoscopy, Adenocarcinoma, MR ENTEROCLYSIS, Female, DOUBLE-BALLOON ENTEROSCOPY, medicine.symptom, Duodenal cancer, business, Follow-Up Studies
وصف الملف: application/pdf
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المؤلفون: Wouter H. de Vos tot Nederveen Cappel, Inge van Leeuwen-Cornelisse, Fokke M Nagengast, Annemieke Cats, Fred H. Menko, Mary E. Velthuizen, Juul T. Wijnen, Martijn H. Breuning, Anne J. Roukema, Hans F. A. Vasen, Jan H. Kleibeuker, Andrea E. van der Meulen-de Jong
المساهمون: Guided Treatment in Optimal Selected Cancer Patients (GUTS), Medical and Clinical Psychology
المصدر: Familial Cancer, 15(3), 429-435. SPRINGER
Familial Cancer, 15(3), 429-435. Springer
Familial Cancerمصطلحات موضوعية: Cancer Research, Identification, Colorectal cancer, DNA Mismatch Repair, Cancer risk, 0302 clinical medicine, Epidemiology, Genetics(clinical), Registries, Genetics (clinical), Early Detection of Cancer, Netherlands, RISK, GEOLYNCH COHORT, Surveillance, medicine.diagnostic_test, Mortality rate, Incidence, NONPOLYPOSIS COLORECTAL-CANCER, Colonoscopy, Lynch syndrome, Oncology, 030220 oncology & carcinogenesis, 030211 gastroenterology & hepatology, Original Article, medicine.medical_specialty, Registry, Follow-up system, HNPCC, MUTATION CARRIERS, 03 medical and health sciences, Meta-Analysis as Topic, SYNDROME FAMILIES, medicine, Genetic predisposition, Genetics, Humans, Genetic Predisposition to Disease, Genetic Testing, Genetic testing, Gynecology, business.industry, Endometrial cancer, Cancer, ENDOMETRIAL CANCER, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Hereditary cancer, DNA Repair Enzymes, TUMOR SPECTRUM, Family medicine, Mutation, CLINICAL MANAGEMENT, business
وصف الملف: application/pdf
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المصدر: Lancet Oncology. 10(4):400-408
مصطلحات موضوعية: URINARY-TRACT CANCER, MUIR-TORRE-SYNDROME, SYNDROME FAMILIES, NONPOLYPOSIS COLORECTAL-CANCER, MSH6 GERMLINE MUTATIONS, SYNDROME-II, ENDOMETRIAL CANCER, TRANSITIONAL-CELL CARCINOMA, SMALL-BOWEL CANCER, GASTRIC-CANCER
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المؤلفون: Jan J. Koornstra, Hans F. A. Vasen, Jan H. Kleibeuker
المساهمون: Guided Treatment in Optimal Selected Cancer Patients (GUTS)
المصدر: Lancet Oncology, 9(9), 901-905. ELSEVIER SCIENCE INC
مصطلحات موضوعية: Adult, Male, Pediatrics, medicine.medical_specialty, MICROSATELLITE INSTABILITY, Colorectal cancer, Cost-Benefit Analysis, Population, UNITED-STATES, Gene mutation, Capsule Endoscopy, Gastroenterology, Endoscopy, Gastrointestinal, PROGNOSTIC-FACTORS, Double-balloon enteroscopy, Internal medicine, SYNDROME FAMILIES, Intestinal Neoplasms, Intestine, Small, medicine, Humans, Mass Screening, education, Mass screening, Aged, Aged, 80 and over, SMALL-INTESTINE, education.field_of_study, medicine.diagnostic_test, business.industry, Cancer, Microsatellite instability, NONPOLYPOSIS COLORECTAL-CANCER, ADENOCARCINOMA, Middle Aged, VIDEO CAPSULE ENDOSCOPY, medicine.disease, TUMORS, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, Lynch syndrome, Oncology, Population Surveillance, Disease Progression, Female, DOUBLE-BALLOON ENTEROSCOPY, business
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المصدر: Lancet Oncology. 9(9):901-905
مصطلحات موضوعية: SMALL-INTESTINE, PROGNOSTIC-FACTORS, MICROSATELLITE INSTABILITY, SYNDROME FAMILIES, UNITED-STATES, NONPOLYPOSIS COLORECTAL-CANCER, ADENOCARCINOMA, DOUBLE-BALLOON ENTEROSCOPY, VIDEO CAPSULE ENDOSCOPY, TUMORS
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8Academic Journal
المؤلفون: Haanstra, Jasmijn F., Al-Toma, Abdul, Dekker, Evelien, Vanhoutvin, Steven A. L. W., Nagengast, Fokko M., Mathus-Vliegen, Elisabeth M., van Leerdam, Monique E., Cappel, Wouter H. de Vos tot Nederveen, Sanduleanu, Silvia, Veenendaal, Roeland A., Cats, Annemieke, Vasen, Hans F. A., Kleibeuker, Jan H., Koornstra, Jan J.
المصدر: Haanstra , J F , Al-Toma , A , Dekker , E , Vanhoutvin , S A L W , Nagengast , F M , Mathus-Vliegen , E M , van Leerdam , M E , Cappel , W H D V T N , Sanduleanu , S , Veenendaal , R A , Cats , A , Vasen , H F A , Kleibeuker , J H & Koornstra , J J 2015 , ' Prevalence of small-bowel neoplasia in Lynch syndrome assessed by video capsule endoscopy ' , Gut , vol. 64 , no. 10 , pp. ....
مصطلحات موضوعية: DOUBLE-BALLOON ENTEROSCOPY, SYNDROME FAMILIES, MR ENTEROCLYSIS, SURVEILLANCE, LESIONS, CANCER, RECOMMENDATIONS, METAANALYSIS, MANAGEMENT, TUMORS
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9Academic Journal
المؤلفون: Koornstra, Jan J, Mourits, Marian Je, Sijmons, Rolf H, Leliveld-Kors, Anna, Hollema, Harry, Kleibeuker, Jan H
المصدر: Koornstra , J J , Mourits , M J , Sijmons , R H , Leliveld-Kors , A , Hollema , H & Kleibeuker , J H 2009 , ' Management of extracolonic tumours in patients with Lynch syndrome ' , Lancet Oncology , vol. 10 , no. 4 , pp. 400-408 . https://doi.org/10.1016/S1470-2045(09)70041-5
مصطلحات موضوعية: NONPOLYPOSIS COLORECTAL-CANCER, SMALL-BOWEL CANCER, MUIR-TORRE-SYNDROME, TRANSITIONAL-CELL CARCINOMA, MSH6 GERMLINE MUTATIONS, URINARY-TRACT CANCER, ENDOMETRIAL CANCER, GASTRIC-CANCER, SYNDROME FAMILIES, SYNDROME-II
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10Academic Journal
المؤلفون: Koornstra, Jan J., Kleibeuker, Jan H., Vasen, Hans F. A.
المصدر: Koornstra , J J , Kleibeuker , J H & Vasen , H F A 2008 , ' Small-bowel cancer in Lynch syndrome : is it time for surveillance? ' , Lancet Oncology , vol. 9 , no. 9 , pp. 901-905 .
مصطلحات موضوعية: NONPOLYPOSIS COLORECTAL-CANCER, DOUBLE-BALLOON ENTEROSCOPY, VIDEO CAPSULE ENDOSCOPY, PROGNOSTIC-FACTORS, MICROSATELLITE INSTABILITY, SYNDROME FAMILIES, SMALL-INTESTINE, UNITED-STATES, ADENOCARCINOMA, TUMORS
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المؤلفون: Rolf H. Sijmons, Harry Hollema, Annemarie M Leliveld, Jan H. Kleibeuker, Marian J.E. Mourits, Jan J. Koornstra
المصدر: The Lancet. Oncology. 10(4)
مصطلحات موضوعية: Oncology, Male, medicine.medical_specialty, MUIR-TORRE-SYNDROME, Colorectal cancer, medicine.medical_treatment, MSH6 GERMLINE MUTATIONS, URINARY-TRACT CANCER, Muir–Torre syndrome, Internal medicine, Neoplasms, SYNDROME FAMILIES, medicine, Humans, TRANSITIONAL-CELL CARCINOMA, Hysterectomy, business.industry, Endometrial cancer, Cancer, NONPOLYPOSIS COLORECTAL-CANCER, SYNDROME-II, ENDOMETRIAL CANCER, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, Lynch syndrome, Pedigree, Transitional cell carcinoma, Female, Skin cancer, business, SMALL-BOWEL CANCER, GASTRIC-CANCER
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13Academic Journal
المؤلفون: Crosnier, Cécile, Driancourt, Cathrine, Raynaud, Nicolas, Pollet, Sophie, Pollet, Nicolas, Bernard, Olivier, Hadchouel, Michèle, Meunier-Rotival, Michelle
المساهمون: Institut National de la Santé et de la Recherche Médicale (INSERM), AP-HP Hôpital Bicêtre (Le Kremlin-Bicêtre)
المصدر: ISSN: 0016-5085 ; Gastroenterology ; https://hal.inrae.fr/hal-02698837 ; Gastroenterology, WB Saunders, 1999, 116 (5), pp.1141-1148. ⟨10.1016/s0016-5085(99)70017-x⟩.
مصطلحات موضوعية: arteriohepatic dysplasia, deletion, nomenclature, syndrome families, [SDV]Life Sciences [q-bio]
Relation: info:eu-repo/semantics/altIdentifier/pmid/10220506; hal-02698837; https://hal.inrae.fr/hal-02698837; PRODINRA: 480971; PUBMED: 10220506; WOS: 000079947900020
الاتاحة: https://hal.inrae.fr/hal-02698837
https://doi.org/10.1016/s0016-5085(99)70017-x -
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المؤلفون: Nicole Raynaud, Sophie Dhorne–Pollet, Catherine Driancourt, Michèle Meunier–Rotival, Michelle Hadchouel, Nicolas Pollet, Cécile Crosnier, Olivier Bernard
المساهمون: Institut National de la Santé et de la Recherche Médicale (INSERM), AP-HP Hôpital Bicêtre (Le Kremlin-Bicêtre)
المصدر: Gastroenterology
Gastroenterology, WB Saunders, 1999, 116 (5), pp.1141-1148. ⟨10.1016/s0016-5085(99)70017-x⟩مصطلحات موضوعية: Male, Genotype, [SDV]Life Sciences [q-bio], Nonsense mutation, DNA Mutational Analysis, arteriohepatic dysplasia, Biology, medicine.disease_cause, Polymerase Chain Reaction, 03 medical and health sciences, Exon, 0302 clinical medicine, Gene Frequency, Alagille syndrome, medicine, Missense mutation, Humans, Serrate-Jagged Proteins, deletion, Genetic Testing, Gene, Polymorphism, Single-Stranded Conformational, 030304 developmental biology, Genetics, 0303 health sciences, Mutation, Polymorphism, Genetic, Hepatology, Calcium-Binding Proteins, Gastroenterology, Membrane Proteins, Proteins, Single-strand conformation polymorphism, medicine.disease, 3. Good health, Alagille Syndrome, Phenotype, syndrome families, Intercellular Signaling Peptides and Proteins, nomenclature, 030211 gastroenterology & hepatology, Female, Jagged-1 Protein