المؤلفون: Carolijn J. M. de Bresser, Bart-Jeroen Petri, Arthur J. A. T. Braat, Bart de Keizer, Mark J. C. van Treijen, Jan Willem Dankbaar, Frank A. Pameijer, Marius G. J. Kok, Mischa de Ridder, Bernadette P. M. van Nesselrooij, Remco de Bree, Gert J. de Borst, Johannes A. Rijken

المصدر: Cancers, Vol 16, Iss 5, p 986 (2024)

مصطلحات موضوعية: head and neck paraganglioma, [68Ga]Ga-DOTATOC PET/CT, MRI, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2072-6694/16/5/986Test; https://doaj.org/toc/2072-6694Test

الوصول الحر: https://doaj.org/article/5472e51753c14c9babd69480cf5c32cbTest

المؤلفون: Medard F. M. van den Broek, Bernadette P. M. van Nesselrooij, Annemarie A. Verrijn Stuart, Rachel S. van Leeuwaarde, Gerlof D. Valk

المصدر: Frontiers in Endocrinology, Vol 10 (2019)

مصطلحات موضوعية: pituitary adenoma, germline mutation, genetic analysis, mutation, screening, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/article/10.3389/fendo.2019.00837/fullTest; https://doaj.org/toc/1664-2392Test

الوصول الحر: https://doaj.org/article/f2c5d1c2173f4bb38a9112169179ca39Test

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 Society

مصطلحات 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

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2ac70101856ed2321ef91474b5d06b3Test
https://doi.org/10.1210/clinem/dgaa257Test

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 SOC

مصطلحات 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

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dca8796cb0daf1fb908879827070461aTest
https://doi.org/10.1210/jc.2017-01249Test

المؤلفون: Medard F. M. van den Broek, Bernadette P. M. van Nesselrooij, Annemarie A. Verrijn Stuart, Rachel S. van Leeuwaarde, Gerlof D. Valk

مصطلحات موضوعية: Endocrinology, Reproduction, Cell Metabolism, pituitary adenoma, germline mutation, genetic analysis, mutation, screening

العلاقة: https://figshare.com/articles/dataset/Data_Sheet_4_Clinical_Relevance_of_Genetic_Analysis_in_Patients_With_Pituitary_Adenomas_A_Systematic_Review_docx/11345150Test

الإتاحة: https://doi.org/10.3389/fendo.2019.00837.s004Test
https://figshare.com/articles/dataset/Data_Sheet_4_Clinical_Relevance_of_Genetic_Analysis_in_Patients_With_Pituitary_Adenomas_A_Systematic_Review_docx/11345150Test

المؤلفون: Ad R. M. M. Hermus, Gerlof D. Valk, Joanne M. de Laat, Wouter W. de Herder, Madeleine L. Drent, Carolina R. C. Pieterman, Menno R. Vriens, Olaf M. Dekkers, Peter H. Bisschop, Anouk N A van der Horst-Schrivers, Bas Havekes, Bernadette P M van Nesselrooij, Rachel S van Leeuwaarde

المساهمون: Clinical Neuropsychology, IBBA, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam Movement Sciences, Endocrinology, Internal Medicine, Interne Geneeskunde, MUMC+: MA Endocrinologie (9), RS: NUTRIM - R1 - Metabolic Syndrome, Internal medicine, Guided Treatment in Optimal Selected Cancer Patients (GUTS)

المصدر: Journal of Clinical Endocrinology and Metabolism, 101, 3, pp. 1159-65
Journal of Clinical Endocrinology and Metabolism, 101(3), 1159-65. Oxford University Press
Journal of Clinical Endocrinology and Metabolism, 101, 1159-65
Van Leeuwaarde, R S, Van Nesselrooij, B P M, Hermus, A R, Dekkers, O M, De Herder, W W, Van Der Horst-Schrivers, A N, Drent, M L, Bisschop, P H, Havekes, B, Vriens, M R, De Laat, J M, Pieterman, C R C & Valk, G D 2016, ' Impact of delay in diagnosis in outcomes in MEN1 : Results from the Dutch MEN1 study group ', Journal of Clinical Endocrinology and Metabolism, vol. 101, no. 3, pp. 1159-1165 . https://doi.org/10.1210/jc.2015-3766Test
Journal of clinical endocrinology and metabolism, 101(3), 1159-1165. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 101(3), 1159. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 101(3), 1159-1165. Endocrine Society
Journal of Clinical Endocrinology & Metabolism, 101(3), 1159-1165. Oxford University Press
van Leeuwaarde, R S, Hermus, A R, Dekkers, O M, de Herder, W W, van der Horst-Schrivers, A N, Drent, M L, Bisschop, P H, Havekes, B, Vriens, M R, de Laat, J M, Pieterman, C R C & Valk, G D 2016, ' Impact of Delay in Diagnosis in Outcomes in MEN1 : Results From the Dutch MEN1 Study Group ', Journal of Clinical Endocrinology and Metabolism, vol. 101, no. 3, pp. 1159-65 . https://doi.org/10.1210/jc.2015-3766Test
Journal of Clinical Endocrinology and Metabolism, 101(3), 1159-1165
Journal of Clinical Endocrinology and Metabolism, 101(3), 1159-1165. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 101(3), 1159-1165. ENDOCRINE SOC

مصطلحات موضوعية: Male, Delayed Diagnosis, endocrine system diseases, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Vascular damage Radboud Institute for Health Sciences [Radboudumc 16], GUIDELINES, Biochemistry, 0302 clinical medicine, Endocrinology, IMPLEMENTATION, Medicine, Young adult, Non-U.S. Gov't, Child, Index case, ENDOCRINE NEOPLASIA TYPE-1, Netherlands, education.field_of_study, medicine.diagnostic_test, Research Support, Non-U.S. Gov't, Middle Aged, Prognosis, MANIFESTATIONS, 030220 oncology & carcinogenesis, Female, Cohort study, Adult, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, endocrine system, Adolescent, Genetic counseling, Population, 030209 endocrinology & metabolism, Research Support, 03 medical and health sciences, Young Adult, Germline mutation, SDG 3 - Good Health and Well-being, Internal medicine, Proto-Oncogene Proteins, Journal Article, Multiple Endocrine Neoplasia Type 1, Humans, Family, Genetic Testing, education, Survival analysis, Germ-Line Mutation, Genetic testing, Aged, business.industry, Biochemistry (medical), CARE, Survival Analysis, Morbidity, business, NEUROENDOCRINE TUMORS

وصف الملف: image/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7d34e6fdb741cd3c7ff4ccd3d95b08eTest
https://cris.maastrichtuniversity.nl/en/publications/b8bc352b-1c62-49c4-a3c1-6ea0a692ce93Test

المؤلفون: Inne H.M. Borel Rinkes, Anouk N A van der Horst-Schrivers, Marc Timmers, Bernadette P M van Nesselrooij, Rob B. van der Luijt, Jo W.M. Höppener, Gerlof D. Valk, Cornelis J.M. Lips, Koen M.A. Dreijerink, Menno R. Vriens, Thera P. Links

المصدر: Genetic Diagnosis of Endocrine Disorders ISBN: 9780128008928

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, endocrine system, Pathology, medicine.medical_specialty, endocrine system diseases, Medullary cavity, business.industry, Multiple endocrine neoplasia type 2, Neuroendocrine tumors, medicine.disease, Pheochromocytoma, Thyroid carcinoma, medicine.anatomical_structure, Anterior pituitary, medicine, MEN1, Multiple endocrine neoplasia, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::bb07e444425b56d14b57514639c99d8fTest
https://doi.org/10.1016/b978-0-12-800892-8.00024-5Test

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 Group

مصطلحات 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

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85f4a39c0f97e31d38f52cdcda56a8a1Test
https://hdl.handle.net/2066/97324Test

المؤلفون: Saskia C.M. Bakker, Bernadette P M van Nesselrooij, Mark van Roosmalen, Wigard P. Kloosterman, Martin Poot, Victor Guryev, Karen Duran, Edwin Cuppen, Ewart de Bruijn, Tom G.W. Letteboer, Ron Hochstenbach

المساهمون: Hubrecht Institute for Developmental Biology and Stem Cell Research

المصدر: Human Molecular Genetics, 20(10), 1916-1924. Oxford University Press

مصطلحات موضوعية: Male, Molecular Sequence Data, Biology, Genome, Germline, Structural variation, Gene Order, Genetics, Humans, Child, Molecular Biology, Genetics (clinical), Chromosome Aberrations, Gene Rearrangement, Chromothripsis, Base Sequence, Models, Genetic, Chromosomes, Human, Pair 10, Breakpoint, Computational Biology, Chromosome Breakage, Sequence Analysis, DNA, General Medicine, Gene rearrangement, Germ Cells, Chromosomes, Human, Pair 1, Female, Human genome, Chromosomes, Human, Pair 4, Chromosome breakage

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b27717c70d9fd455877247ed1720cbfTest
https://doi.org/10.1093/hmg/ddr073Test

المؤلفون: Koen M.A. Dreijerink, Cornelis J.M. Lips, Jo W.M. Höppener, Bernadette P M van Nesselrooij, Rob B. van der Luijt

المساهمون: Internal medicine

المصدر: Genetic Diagnosis of Endocrine Disorders, 261-270
STARTPAGE=261;ENDPAGE=270;TITLE=Genetic Diagnosis of Endocrine Disorders
Lips, C J M, Dreijerink, K M A, van der Luijt, R B, van Nesselrooij, B P M & Höppener, J W M 2010, Multiple Endocrine Neoplasia Type 1 (MEN1) . in Genetic Diagnosis of Endocrine Disorders . Elsevier Inc., pp. 261-270 . https://doi.org/10.1016/B978-0-12-374430-2.00023-7Test

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, endocrine system, endocrine system diseases, Adenoma, Biology, Neuroendocrine tumors, medicine.disease, Exon, Germline mutation, Cancer research, medicine, MEN1 Gene Mutation, MEN1, Multiple endocrine neoplasia, Gene

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a365bc0e8f8533a8554b964284c3664aTest
https://doi.org/10.1016/b978-0-12-374430-2.00023-7Test