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1
المؤلفون: Bernadette P M van Nesselrooij, Olaf M. Dekkers, Gerlof D. Valk, Medard F M van den Broek, Wouter W. de Herder, Annemarie A. Verrijn Stuart, Peter H. Bisschop, Bas Havekes, Carolina R. C. Pieterman, Michiel N. Kerstens, Annenienke C van de Ven, Madeleine L. Drent
المساهمون: Internal Medicine, Interne Geneeskunde, MUMC+: MA Endocrinologie (9), RS: NUTRIM - R1 - Obesity, diabetes and cardiovascular health, Guided Treatment in Optimal Selected Cancer Patients (GUTS), Endocrinology, AGEM - Endocrinology, metabolism and nutrition, AMS - Ageing & Morbidty, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam Movement Sciences, AMS - Ageing & Vitality, Internal medicine, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep
المصدر: van den Broek, M F M, van Nesselrooij, B P M, Pieterman, C R C, Verrijn Stuart, A A, van de Ven, A C, de Herder, W W, Dekkers, O M, Drent, M L, Havekes, B, Kerstens, M N, Bisschop, P H & Valk, G D 2020, ' Clues For Genetic Anticipation In Multiple Endocrine Neoplasia Type 1 ', The Journal of clinical endocrinology and metabolism, vol. 105, no. 7, dgaa257 . https://doi.org/10.1210/clinem/dgaa257Test
Journal of Clinical Endocrinology and Metabolism, 105, 7
Journal of Clinical Endocrinology and Metabolism, 105(7). Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 105(7), E2491-E2500. ENDOCRINE SOC
Journal of Clinical Endocrinology & Metabolism, 105(7), E2491-E2500. Oxford University Press
Journal of Clinical Endocrinology and Metabolism, 105
Journal of Clinical Endocrinology and Metabolism, 105(7):dgaa257, E2491-E2500. ENDOCRINE SOC
Journal of clinical endocrinology and metabolism, 105(7):dgaa257. The Endocrine Society
The Journal of clinical endocrinology and metabolism, 105(7):dgaa257. The Endocrine Societyمصطلحات موضوعية: Male, 0301 basic medicine, guide, endocrine system diseases, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Disease, Neuroendocrine tumors, Bioinformatics, Biochemistry, 0302 clinical medicine, Endocrinology, Multiple endocrine neoplasia, Genetic anticipation, Netherlands, Aged, 80 and over, men1, Surveillance, Age Factors, Middle Aged, families, Penetrance, CANCER, 030220 oncology & carcinogenesis, ascertainment bias, Multiple endocrine neoplasia type 1, Female, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9], Adult, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, endocrine system, Age of onset, Context (language use), Young Adult, 03 medical and health sciences, AGE, Proto-Oncogene Proteins, Internal medicine, medicine, Humans, MEN1, Aged, Anticipation, Genetic, business.industry, Biochemistry (medical), Pituitary tumors, medicine.disease, 030104 developmental biology, Mutation, TELOMERE LENGTH, business
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الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2ac70101856ed2321ef91474b5d06b3Test
https://doi.org/10.1210/clinem/dgaa257Test -
2
المؤلفون: Frederik J. Hes, Jan Maarten Cobben, Hans Morreau, Romana T. Netea-Maier, Bruce H. R. Wolffenbuttel, Gerlof D. Valk, Karin van der Tuin, Fred H. Menko, Muriel A. Adank, Bernadette P M van Nesselrooij, Neveen A. T. Hamdy, Carli M. J. Tops, Jan C. Oosterwijk, Marjolijn C.J. Jongmans
المساهمون: Medical Genetics, ANS - Cellular & Molecular Mechanisms, Paediatric Genetics, Human genetics, ACS - Atherosclerosis & ischemic syndromes, Damage and Repair in Cancer Development and Cancer Treatment (DARE), Targeted Gynaecologic Oncology (TARGON), Lifestyle Medicine (LM), Center for Liver, Digestive and Metabolic Diseases (CLDM)
المصدر: Journal of Clinical Endocrinology and Metabolism, 102, 4534-4540
Journal of clinical endocrinology and metabolism, 102(12), 4534-4540. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 102, 12, pp. 4534-4540
Journal of Clinical Endocrinology and Metabolism, 102(12), 4534-4540
van der Tuin, K, Tops, C M J, Adank, M A, Cobben, J M, Hamdy, N A T, Jongmans, M C, Menko, F H, van Nesselrooij, B P M, Netea-Maier, R T, Oosterwijk, J C, Valk, G D, Wolffenbuttel, B H R, Hes, F J & Morreau, H 2017, ' CDC73-Related Disorders : Clinical Manifestations and Case Detection in Primary Hyperparathyroidism ', The Journal of clinical endocrinology and metabolism, vol. 102, no. 12, pp. 4534-4540 . https://doi.org/10.1210/jc.2017-01249Test
The Journal of clinical endocrinology and metabolism, 102(12), 4534-4540. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 102(12), 4534-4540. ENDOCRINE SOCمصطلحات موضوعية: Male, Pediatrics, Hyperparathyroidism, Primary/genetics, endocrine system diseases, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Penetrance, Jaw Neoplasms/genetics, Biochemistry, 0302 clinical medicine, Endocrinology, Child, Parathyroid adenoma, Netherlands, Medicine(all), FAMILIAL ISOLATED HYPERPARATHYROIDISM, JAW TUMOR SYNDROME, Parathyroid Neoplasms/genetics, Middle Aged, Hyperparathyroidism, Primary, CANCER, Jaw Neoplasms, Parathyroid Neoplasms, Parathyroid carcinoma, HRPT2 GENE, 030220 oncology & carcinogenesis, Cohort studies, young adult, Female, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9], GENETIC ANALYSES, Adult, medicine.medical_specialty, Heterozygote, Adolescent, Mutation/genetics, Genetic counseling, 030209 endocrinology & metabolism, Context (language use), Rare cancers Radboud Institute for Molecular Life Sciences [Radboudumc 9], Tumor Suppressor Proteins/genetics, 03 medical and health sciences, Germline mutation, All institutes and research themes of the Radboud University Medical Center, Internal medicine, GERMLINE, medicine, PARATHYROID CARCINOMA, MANAGEMENT, Humans, Germ-Line Mutation, Aged, Retrospective Studies, Hyperparathyroidism, business.industry, MUTATIONS, Tumor Suppressor Proteins, Biochemistry (medical), medicine.disease, PARAFIBROMIN, Mutation, business, aged, 80 and over, Primary hyperparathyroidism
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الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dca8796cb0daf1fb908879827070461aTest
https://doi.org/10.1210/jc.2017-01249Test -
3Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
المؤلفون: Tsun Leung Chan, Eugène T P Verwiel, Irma Kluijt, Diana Eccles, Rolf H. Sijmons, Egbert J.W. Redeker, Rachel S. van der Post, Encarna B. Gomez Garcia, Reinhard Büttner, Cora M. Aalfs, Roland P. Kuiper, Johan J.P. Gille, Bernadette P M van Nesselrooij, Frans B. L. Hogervorst, Marjolijn J L Ligtenberg, Tracy Graham, Julie O. Culver, Edith Olah, Monique Goossens, Carli M. J. Tops, Elke Holinski-Feder, David J. Bunyan, Marielle E. van Gijn, Frederik J. Hes, Suet Yi Leung, Pierre O. Chappuis, Monika Morak, Edward M Leter, Nils Rahner, Lea Velsher, János Papp, Renee C. Niessen, J. Han van Krieken, Lambertus A. Kiemeney, Ad Geurts van Kessel, Charlotte W. Ockeloen, Nicoline Hoogerbrugge, Marlies Kempers, Iris D. Nagtegaal, Verena Steinke, Hans K. Schackert, Matthias Kloor, Melanie R. Palomares, Sapna Syngal, Pierre Hutter, Elena M. Stoffel
المساهمون: Genetica & Celbiologie, RS: GROW - School for Oncology and Reproduction, Clinical sciences, Human Genetics, ACS - Amsterdam Cardiovascular Sciences, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Other Research, Guided Treatment in Optimal Selected Cancer Patients (GUTS), Human genetics, CCA - Oncogenesis
المصدر: Kempers, M J E, Kuiper, R P, Ockeloen, C W, Chappuis, P O, Hutter, P, Rahner, N, Schackert, H K, Steinke, V, Holinski-Feder, E, Morak, M, Kloor, M, Buttner, R, Verwiel, E T P, van Krieken, J H, Nagtegaal, I D, Goossens, M, van der Post, R S, Niessen, R C, Sijmons, RH, Kluijt, I, Hogervorst, F B L, Leter, E M, Gille, J J P, Aalfs, C M, Redeker, E J W, Hes, F J, Tops, C M J, van Nesselrooij, B P M, van Gijn, M E, Garcia, E B G, Eccles, D M, Bunyan, D J, Syngal, S, Stoffel, E M, Culver, J O, Palomares, M R, Graham, T, Velsher, L, Papp, J, Olah, E, Chan, T L, Leung, S Y, van Kessel, A G, Kiemeney, L A L M, Hoogerbrugge, N & Ligtenberg, M J L 2011, ' Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study ', Lancet Oncology, vol. 12, no. 1, pp. 49-55 . https://doi.org/10.1016/S1470-2045Test(10)70265-5
The Lancet Oncology, 49-55
STARTPAGE=49;ENDPAGE=55;TITLE=The Lancet Oncology
Lancet Oncology, 12, 1, pp. 49-55
Lancet oncology, 12(1), 49-55. Elsevier Science
Lancet Oncology, 12, 49-55
lancet oncology, 12(1), 49-55. Lancet Publishing Group
Lancet Oncology, 12(1), 49-55. ELSEVIER SCIENCE INC
Lancet Oncology, 12(1), 49-55. Lancet Publishing Groupمصطلحات موضوعية: Male, Oncology, Genetics and epigenetic pathways of disease [NCMLS 6], REPAIR GENE HMSH2, Colorectal cancer, FAMILIES, chemistry.chemical_compound, Promoter Regions, Genetic, Colorectal Neoplasms/etiology, risk, Sequence Deletion, Medicine(all), METHYLATION, Epithelial cell adhesion molecule, Middle Aged, Epithelial Cell Adhesion Molecule, Translational research Tissue engineering and pathology [ONCOL 3], Lynch syndrome, Antigens, Neoplasm/genetics, Endometrial Neoplasms/etiology, MutS Homolog 2 Protein, Cohort studies, Female, Duodenal cancer, Colorectal Neoplasms, Cell Adhesion Molecules/genetics, STEM-CELLS, MutS Homolog 2 Protein/genetics, Adult, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, TACSTD1, Hereditary cancer and cancer-related syndromes Genetics and epigenetic pathways of disease [ONCOL 1], MUTATION CARRIERS, MLH1, Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular epidemiology [NCEBP 1], Antigens, Neoplasm, Translational research [ONCOL 3], Internal medicine, SURVEILLANCE, medicine, MANAGEMENT, Humans, Genetics and epigenetic pathways of disease Translational research [NCMLS 6], neoplasms, Aged, Molecular epidemiology Aetiology, screening and detection [NCEBP 1], Gynecology, Hereditary cancer and cancer-related syndromes [ONCOL 1], business.industry, Endometrial cancer, Cancer, nutritional and metabolic diseases, medicine.disease, HYPERMETHYLATION, digestive system diseases, Endometrial Neoplasms, MSH2, MSH6, chemistry, business, Cell Adhesion Molecules, Gene Deletion
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الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85f4a39c0f97e31d38f52cdcda56a8a1Test
https://hdl.handle.net/2066/97324Test