المؤلفون: Debra M Gordon, Pablo Beckers, Emilie Castermans, Sebastian J C M M Neggers, Liliya Rostomyan, Vincent Bours, Patrick Petrossians, Vinciane Dideberg, Albert Beckers, Adrian F Daly

المصدر: Endocrine Connections, Vol 11, Iss 1, Pp 1-8 (2022)

مصطلحات موضوعية: sdhb, founder mutation, paraganglioma, pheochromocytoma, south africa, dutch, netherlands, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

Relation: https://ec.bioscientifica.com/view/journals/ec/11/1/EC-21-0560.xml; https://doaj.org/toc/2049-3614

URL الوصول: https://doaj.org/article/fdb326be44f14b8796f6d3b5360ca482

المؤلفون: Adrian F Daly, David A Cano, Eva Venegas-Moreno, Patrick Petrossians, Elena Dios, Emilie Castermans, Alvaro Flores-Martínez, Vincent Bours, Albert Beckers, Alfonso Soto-Moreno

المصدر: Endocrine Connections, Vol 8, Iss 4, Pp 338-348 (2019)

مصطلحات موضوعية: AIP, FIPA, acromegaly, somatostatin analog, resistance, MEN1, pituitary adenoma, pasireotide, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

Relation: https://ec.bioscientifica.com/view/journals/ec/8/4/EC-19-0027.xml; https://doaj.org/toc/2049-3614

URL الوصول: https://doaj.org/article/5ba297d7db284cefb8f6d3bcf79c86e7

المؤلفون: Emilie Castermans, Muriel Hannon, Jacques Dutrieux, Stéphanie Humblet-Baron, Laurence Seidel, Rémi Cheynier, Evelyne Willems, André Gothot, Jean-François Vanbellinghen, Vincent Geenen, Brenda M. Sandmaier, Rainer Storb, Yves Beguin, Frédéric Baron

المصدر: Haematologica, Vol 96, Iss 2 (2011)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

Relation: https://haematologica.org/article/view/5879; https://doaj.org/toc/0390-6078; https://doaj.org/toc/1592-8721

URL الوصول: https://doaj.org/article/7f62437f09c74fc5ab29af62d287f66e

المؤلفون: Emilie Castermans, Frédéric Baron, Evelyne Willems, Nicole Schaaf-Lafontaine, Nathalie Meuris, André Gothot, Jean-François Vanbellighen, Christian Herens, Laurence Seidel, Vincent Geenen, Remi Cheynier, Yves Beguin

المصدر: Haematologica, Vol 93, Iss 2 (2008)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

Relation: https://haematologica.org/article/view/4745; https://doaj.org/toc/0390-6078; https://doaj.org/toc/1592-8721

URL الوصول: https://doaj.org/article/0ccc9401e7764b74a0686f7a27ba3930

المؤلفون: Debra M Gordon, Pablo Beckers, Emilie Castermans, Sebastian J C M M Neggers, Liliya Rostomyan, Vincent Bours, Patrick Petrossians, Vinciane Dideberg, Albert Beckers, Adrian F Daly

المساهمون: Internal Medicine

المصدر: Endocrine Connections, 11(1):e210560. Bioscientifica Ltd
Endocrine Connections, Vol 11, Iss 1, Pp 1-8 (2022)

مصطلحات موضوعية: south africa, Endocrinology, Diabetes and Metabolism, netherlands, SDG 10 - Reduced Inequalities, RC648-665, pheochromocytoma, Diseases of the endocrine glands. Clinical endocrinology, paraganglioma, Endocrinology, sdhb, SDG 3 - Good Health and Well-being, Internal Medicine, founder mutation, dutch

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a928f5e2e20ab2efbc0ade1c6f46521f
https://pubmed.ncbi.nlm.nih.gov/34939938

المؤلفون: Vinciane Dideberg, Esther Korpershoek, Sandrine Petignot, Vincent Bours, Emilie Castermans, Pablo Beckers, Adrian Daly, Albert Beckers, Vincent Rohmer, Irène Scagnol

المساهمون: Pathology

المصدر: Hormone & Metabolic Research, 52(11), 784-787. Georg Thieme Verlag

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, Pathology, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Biochemistry, Pheochromocytoma, Loss of heterozygosity, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, Internal medicine, Biopsy, Medicine, Humans, MEN1, Genetic Predisposition to Disease, Genetic Testing, Multiple endocrine neoplasia, Germ-Line Mutation, medicine.diagnostic_test, business.industry, Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, Biochemistry (medical), General Medicine, Middle Aged, medicine.disease, Prognosis, Uniparental disomy, Pedigree, Pancreatic Neuroendocrine Neoplasm, Pancreatic Neoplasms, Neuroendocrine Tumors, 030104 developmental biology, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Female, business, Pancreas, Gene Deletion

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46b0773a2b22897bbe9969de28e5fdc2
https://doi.org/10.1055/a-1186-0790

المؤلفون: Emilie Castermans, Iulia Potorac, Wouter W. de Herder, Vincent Bours, Pablo Beckers, Aart-Jan van der Lely, Albert Beckers, Adrian Daly, Lindsey Oudijk, Mirtha Guitelman, Sebastian J C M M Neggers, Nathalie Sacre

المساهمون: Pathology, Internal Medicine

المصدر: Endocrine-Related Cancer, 25(5), L37-L42. Bioscientifica Ltd

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, business.industry, Endocrinology, Diabetes and Metabolism, 030209 endocrinology & metabolism, 03 medical and health sciences, Exon, 030104 developmental biology, 0302 clinical medicine, Endocrinology, Oncology, Cancer research, Medicine, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88777072c3c70cbd22b61a473205e2c0
https://doi.org/10.1530/erc-18-0065

المؤلفون: Alvaro Flores-Martínez, Patrick Petrossians, David A. Cano, Vincent Bours, Emilie Castermans, Adrian Daly, Albert Beckers, Eva Venegas-Moreno, Alfonso Soto-Moreno, Elena Dios

المساهمون: Centre Hospitalier Universitaire de Liège, JABBS Foundation, Instituto de Salud Carlos III, European Commission, Junta de Andalucía

المصدر: Digital.CSIC. Repositorio Institucional del CSIC
instname
Endocrine Connections
Endocrine Connections, Vol 8, Iss 4, Pp 338-348 (2019)

مصطلحات موضوعية: Oncology, medicine.medical_specialty, endocrine system diseases, Endocrinology, Diabetes and Metabolism, Resistance, lcsh:Diseases of the endocrine glands. Clinical endocrinology, FIPA, Somatostatin analog, chemistry.chemical_compound, Endocrinology, Germline mutation, Pituitary adenoma, Internal medicine, Acromegaly, Internal Medicine, medicine, MEN1, Multiplex ligation-dependent probe amplification, AIP, Prolactinoma, lcsh:RC648-665, business.industry, Research, medicine.disease, Pasireotide, chemistry, Immunohistochemistry, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1023a57dd8250b8f3daadfde31ba9c07
http://hdl.handle.net/10261/203531

المؤلفون: Ann Verhaegen, Olivier Van Caenegem, Raymond Kacenelenbogen, Michel Guillaume, Fabian Demeure, Caroline Wallemacq, Olivier Vanakker, Anna A.H. Mertens, Michel Hermans, Antoine Bondue, Anne De Leener, Stephane Carlier, Walter Desmet, Pieter Vermeersch, Ernst Rietzschel, Ivan Elegeert, Fabien Chenot, Jean-Louis Vanoverschelde, Emilie Castermans, Christophe Beauloye, Olivier S. Descamps, Antoine De Meester, E. Hoffer, Christophe De Block, Marc J. Claeys, Jean-Luc Balligand, Nicolas Paquot, Attilio Leone, Michel Langlois, Herbert De Raedt, Patrizio Lancellotti

المساهمون: BAS, BSC, RBSLM, Clinical sciences, Vrije Universiteit Brussel, Faculty of Arts and Philosophy, UCL - SSS/IREC/FATH - Pôle de Pharmacologie et thérapeutique, UCL - SSS/IREC/MONT - Pôle Mont Godinne, UCL - SSS/IREC/CARD - Pôle de recherche cardiovasculaire, UCL - SSS/IREC/EDIN - Pôle d'endocrinologie, diabète et nutrition, UCL - SSS/IREC/SLUC - Pôle St.-Luc, UCL - (SLuc) Service de pathologie cardiovasculaire, UCL - (SLuc) Service de pathologies cardiovasculaires intensives, UCL - (SLuc) Service de soins intensifs, UCL - (SLuc) Service d'endocrinologie et de nutrition, UCL - (SLuc) Service de médecine interne générale, UCL - (SLuc) Centre de génétique médicale UCL, UCL - (MGD) Service de cardiologie

المصدر: Atherosclerosis
Atherosclerosis, 277
Atherosclerosis, Vol. 277, p. 369-376 (2018)

مصطلحات موضوعية: Cardiac & Cardiovascular Systems, Cardiologie et circulation, IMPACT, CHILDREN, Disease, 030204 cardiovascular system & hematology, Workflow, 0302 clinical medicine, Belgium, Risk Factors, Prevalence, CRITERIA, 030212 general & internal medicine, Myocardial infarction, CARDIOLOGY, education.field_of_study, Autosomal dominant lipoprotein disorder, Prognosis, Cardiovascular disease, Phenotype, Cardiovascular Diseases, Critical Pathways, Lipoprotein disorder, Cardiology and Cardiovascular Medicine, Familial hypercholesterolaemia, Life Sciences & Biomedicine, Algorithms, Genetic Markers, Coronary care unit, medicine.medical_specialty, Consensus, Clinical Decision-Making, Population, Cascade screening, DIAGNOSIS, Risk Assessment, Significant elevation, Decision Support Techniques, Hyperlipoproteinemia Type II, 03 medical and health sciences, Predictive Value of Tests, EUROPEAN ATHEROSCLEROSIS SOCIETY, medicine, MANAGEMENT, Humans, Genetic Predisposition to Disease, Low-density lipoprotein cholesterol, Intensive care medicine, education, Alirocumab, Science & Technology, business.industry, Coronary Care Units, ALIROCUMAB, Cholesterol, LDL, medicine.disease, Peripheral Vascular Disease, MYOCARDIAL-INFARCTION, Mutation, Cardiovascular System & Cardiology, Human medicine, business, Biomarkers, GENETIC-DEFECTS

وصف الملف: Print; 2 full-text file(s): application/pdf; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fa7fe6a13da8ba1575f688d75a2eeb4
https://lirias.kuleuven.be/handle/123456789/629864

المؤلفون: Paraskevi Xekouki, Natalia Strebkova, Eva Szarek, Leonor Palmeira, Isaac Levy, James R. Lupski, William E. Farrell, Mauricette Jamar, Peter Kamenický, Catherine S. Choong, Maria Chiara Zatelli, Stanko S. Stojilkovic, Emanuele Ferrante, Rodrigo Bertollo de Alexandre, Stefano Costanzi, Leticia F Leal, Darwin O. Larco, Aggeliki Dimopoulos, Emilie Castermans, Philippe Chanson, Giampaolo Trivellin, Albert Beckers, Luciana Ansaneli Naves, Wouter Coppieters, Allison D. Manning, Jérôme Bertherat, Liliya Rostomyan, Maria de la Luz Sierra, Vincent Bours, Bo Yuan, Constantine A. Stratakis, Nadia Mazerkina, Martha Quezado, Prashant Chittiboina, Anne Barlier, Chiara Villa, T. John Wu, Jürgen Wess, Anelia Horvath, Michel Georges, Fabio R. Faucz, Daniel Metzger, Philippe A. Lysy, Ivana Bjelobaba, Jean-Hubert Caberg, Adrian Daly, Pengfei Liu, Marie Helene Schernthaner-Reiter, Margaret F. Keil, Maya Lodish, Nalini S. Shah

المصدر: New England Journal of Medicine. 371:2363-2374

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, Protein Conformation, Gigantism, Receptors, G-Protein-Coupled, Internal medicine, Chromosome Duplication, Acromegaly, Gene duplication, Humans, Medicine, Age of Onset, Child, Receptor, Gene, Chromosomes, Human, X, Human Growth Hormone, business.industry, Infant, Chromosome, General Medicine, medicine.disease, Phenotype, Endocrinology, Child, Preschool, Mutation, Female, Age of onset, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::038c6565b6bb63d4bb071b5a48c0829b
https://doi.org/10.1056/nejmoa1408028