نتائج البحث - "van Leeuwen-Cornelisse"

1

دورية أكاديمية

Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer:Contributions from the Dutch Lynch syndrome registry

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, J.A., 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 , J A , 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 , ....

وصف الملف: application/pdf

العلاقة: https://research.tilburguniversity.edu/en/publications/7d212e11-8753-4ab6-b15e-94acfa145c6bTest

الإتاحة: https://doi.org/10.1007/s10689-016-9897-1Test
https://research.tilburguniversity.edu/en/publications/7d212e11-8753-4ab6-b15e-94acfa145c6bTest
https://pure.uvt.nl/ws/files/12532956/MCP_Roukema_hereditary_cancer_FC_open_access_2016.pdfTest

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2

دورية أكاديمية

Hereditary Nonpolyposis Colorectal Cancer Families Not Complying with the Amsterdam Criteria Show Extremely Low Frequency of Mismatch-Repair-Gene Mutations

المؤلفون: Wijnen, Juul, Khan, P. Meera, Vasen, Hans, van der Klift, Heleen, Mulder, Adri, van Leeuwen-Cornelisse, Inge, Bakker, Bert, Losekoot, Monique, Møller, Pål, Fodde, Riccardo

المصدر: The American Journal of Human Genetics ; volume 61, issue 2, page 329-335 ; ISSN 0002-9297

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1086/514847Test
https://api.elsevier.com/content/article/PII:S0002929707640580?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0002929707640580?httpAccept=text/plainTest

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3

Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry

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 Cancer

مصطلحات 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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40bacf63aa38d0795b9fc825b496be6bTest
https://hdl.handle.net/1887/117207Test

4

Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis

المؤلفون: Rob. B. van der Luijt, P. Meera Khan, Hans F.A. Vasen, Carli M.J. Tops, Inge S.J. van Leeuwen‐Cornelisse, Juul Th. Wijnen, Heleen M. van der Klift, Rob J. Plug, Gerrit Griffioen, Riccardo Fodde

المصدر: Human Mutation. 9:7-16

مصطلحات موضوعية: Genetics, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::cfdb1bfca9c3b8c6fe001f8e56bc4da9Test
https://doi.org/10.1002Test/(sici)1098-1004(1997)9:1<7::aid-humu2>3.3.co;2-7

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Molecular, cytogenetic, and phenotypic studies of a constitutional reciprocal translocation t(5; I0)(q22; q25) responsible for familial adenomatous polyposis in a Dutch pedigree

المؤلفون: Cor Breukel, Heleen M. van der Klift, Rob B. van der Luijt, P. Meera Khan, Hans F. A. Vasen, Riccardo Fodde, Pleun Snel, Carli M. J. Tops, Inge van Leeuwen-Cornelisse, Frederik J. M. Slors, Ellen Van Noort, Geoffrey C. Beverstock, Hans G. Dauwerse

المصدر: Genes, Chromosomes and Cancer. 13:192-202

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, biology, Adenomatous polyposis coli, Translocation Breakpoint, Chromosomal translocation, Gene rearrangement, medicine.disease, Null allele, Molecular biology, Germline, Familial adenomatous polyposis, Germline mutation, Genetics, biology.protein, medicine

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::278e61cd478b28d09303dfe2e2811144Test
https://doi.org/10.1002/gcc.2870130309Test

6

The value of screening and central registration of families with familial adenomatous polyposis

المؤلفون: I. S. J. van Leeuwen-Cornelisse, F. C. A. den Hartog Jager, P. Meera Khan, E. A. van Slooten, G. J. A. Offerhaus, Gerrit Griffioen, Hans F. A. Vasen, Cornelis B.H.W. Lamers

المساهمون: Other departments

المصدر: Diseases of the colon and rectum, 33(3), 227-230. Lippincott Williams and Wilkins

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Pediatrics, Adolescent, Colorectal cancer, Late onset, Gastroenterology, Group B, Familial adenomatous polyposis, Internal medicine, Epidemiology, medicine, Carcinoma, Humans, Mass Screening, Registries, Risk factor, Aged, Netherlands, business.industry, Age Factors, Cancer, General Medicine, Middle Aged, medicine.disease, Adenomatous Polyposis Coli, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f12e73add6737f5503e4479c6476af3Test
https://doi.org/10.1007/bf02134185Test

7

دورية أكاديمية

Clinical findings with implications for genetic testing in families with clustering of colorectal cancer

المصدر: Wijnen , JT , Vasen , HFA , Khan , PM , Zwinderman , AH , van der Klift , H , Mulder , A , Tops , C , Moller , P , Fodde , R , Menko , F , Taal , B , Nagengast , F , Brunner , H , Kleibeuker , J , Sijmons , R , Griffioen , G , Brocker-Vriends , A , Bakker , E , van Leeuwen-Cornelisse , N V , Meijers-Heijboer , A , Lindhout , D , Breuning , M , Post , J , Schaap , C ....

مصطلحات موضوعية: GRADIENT-GEL-ELECTROPHORESIS, MICROSATELLITE INSTABILITY, COLON-CANCER, MUTATION ANALYSIS, APC GENE, HNPCC, POLYPOSIS, MAJORITY, RECEPTOR, HOMOLOG

العلاقة: https://research.rug.nl/en/publications/5cf5bbce-d21c-4327-befc-ec49d1d1b78eTest

الإتاحة: https://hdl.handle.net/11370/5cf5bbce-d21c-4327-befc-ec49d1d1b78eTest
https://research.rug.nl/en/publications/5cf5bbce-d21c-4327-befc-ec49d1d1b78eTest

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8

Clinical findings with implications for genetic testing in families with clustering of colorectal cancer

المساهمون: Other departments, Faculteit Medische Wetenschappen/UMCG, Guided Treatment in Optimal Selected Cancer Patients (GUTS)

المصدر: ResearcherID
New England journal of medicine, 339(8), 511-518. Massachussetts Medical Society
New England Journal of Medicine, 339(8), 511-518. MASSACHUSETTS MEDICAL SOC

مصطلحات موضوعية: Oncology, Male, APC GENE, DNA Repair, Colorectal cancer, MICROSATELLITE INSTABILITY, DNA Mutational Analysis, MUTATION ANALYSIS, medicine.disease_cause, Neoplasms, Multiple Primary, PMS2, Cluster Analysis, Genetics, Mutation, medicine.diagnostic_test, COLON-CANCER, Age Factors, GRADIENT-GEL-ELECTROPHORESIS, Nuclear Proteins, General Medicine, Middle Aged, Electrophoresis, Gel, Pulsed-Field, Neoplasm Proteins, DNA-Binding Proteins, POLYPOSIS, MutS Homolog 2 Protein, Female, Colorectal Neoplasms, MutL Protein Homolog 1, Adult, medicine.medical_specialty, Amsterdam criteria, congenital, hereditary, and neonatal diseases and abnormalities, HNPCC, MLH1, Internal medicine, Proto-Oncogene Proteins, medicine, Humans, Genetic Testing, neoplasms, Genetic testing, Adaptor Proteins, Signal Transducing, Aged, RECEPTOR, business.industry, nutritional and metabolic diseases, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, Endometrial Neoplasms, MSH6, HOMOLOG, Logistic Models, MSH2, Multivariate Analysis, MAJORITY, business, Carrier Proteins

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bca113090b3a1a1d7c066d495ccb1c0Test
https://pubmed.ncbi.nlm.nih.gov/9709044Test

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Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations

المؤلفون: Heleen M. van der Klift, Bert Bakker, Monique Losekoot, Riccardo Fodde, Juul T. Wijnen, Pål Møller, Hans F. A. Vasen, Inge van Leeuwen-Cornelisse, Adri Mulder, P. Meera Khan

المصدر: ResearcherID
Scopus-Elsevier

مصطلحات موضوعية: Amsterdam criteria, congenital, hereditary, and neonatal diseases and abnormalities, Protein Denaturation, DNA Repair, Colorectal cancer, Denmark, Biology, Gene mutation, medicine.disease_cause, Germline mutation, Proto-Oncogene Proteins, Genetics, medicine, Humans, Genetics(clinical), Genetics (clinical), Germ-Line Mutation, Genetic testing, Adaptor Proteins, Signal Transducing, Czech Republic, Netherlands, Mutation, medicine.diagnostic_test, Nucleic Acid Heteroduplexes, Microsatellite instability, nutritional and metabolic diseases, Nuclear Proteins, Reference Standards, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, Neoplasm Proteins, DNA-Binding Proteins, MutS Homolog 2 Protein, Italy, Case-Control Studies, DNA mismatch repair, Electrophoresis, Polyacrylamide Gel, Carrier Proteins, MutL Protein Homolog 1, Research Article, Microsatellite Repeats

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ee841f503524d3b14b4d9012b555134Test
https://europepmc.org/articles/PMC1715907Test/

10

Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis

المؤلفون: R B, van der Luijt, P M, Khan, H F, Vasen, C M, Tops, I S, van Leeuwen-Cornelisse, J T, Wijnen, H M, van der Klift, R J, Plug, G, Griffioen, R, Fodde

المصدر: Human mutation. 9(1)

مصطلحات موضوعية: Gene Rearrangement, Male, Blotting, Southern, Genes, APC, Adenomatous Polyposis Coli, Humans, Electrophoresis, Polyacrylamide Gel, Female, Exons, Germ-Line Mutation, Netherlands, Pedigree

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::44ab5f06327b1bd3c54e3a6f0d3da04eTest
https://pubmed.ncbi.nlm.nih.gov/8990002Test

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