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1. Full Text Correction to: Eosinophilic myenteric ganglionitis as a cause of chronic intestinal pseudo-obstruction
by Ooms, Ariadne H. A. G and Verheij, Joanne and Hulst, Jessie M and Vlot, John and van der Starre, Cynthia and de Ridder, Lissy and de Krijger, Ronald R
Virchows Archiv, ISSN 0945-6317, 10/2019, Volume 475, Issue 4, pp. 533 - 533
It has been identified that one of the dosages listed within the above article was incorrectly abbreviated during the production process. This is now presented... 
Medicine & Public Health | Pathology | Intestine | Leukocytes (eosinophilic)
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2. Full Text Inhibin alpha-subunit (INHA) expression in adrenocortical cancer is linked to genetic and epigenetic INHA promoter variation
by Hofland, Johannes and Steenbergen, Jacobie and Voorsluijs, Jacoba and Verbiest, Michael and Krijger, Ronald and Hofland, Leo and Herder, Wouter and Uitterlinden, Ané and Feelders, Richard and Jong, Frank
PLoS ONE, ISSN 1932-6203, 08/2014, Volume 9, Issue 8, p. e104944
textabstractAdrenocortical carcinoma (ACC) is a rare, but highly malignant tumor of unknown origin. Inhibin α-subunit (Inha) knockout mice develop ACCs... 
ACTIVATION | CORTEX | MULTIDISCIPLINARY SCIENCES | DEFICIENT MICE | SECRETION | COMPARATIVE GENOMIC HYBRIDIZATION | ADRENAL-CORTICAL CARCINOMA | PROGNOSTIC VALUE | TUMORS | CHILDHOOD | ACTIVIN | Adrenocortical Carcinoma - genetics | Epigenesis, Genetic | Humans | Middle Aged | RNA, Messenger - genetics | Child, Preschool | Male | DNA Methylation - genetics | Promoter Regions, Genetic - genetics | Sequence Analysis, DNA | Adrenal Cortex Neoplasms - genetics | Inhibins - biosynthesis | Base Sequence | Adrenocortical Carcinoma - metabolism | Adult | Female | Aged | Biomarkers, Tumor - genetics | Genetic Variation - genetics | Inhibins - blood | Inhibins - genetics | Adrenal Cortex Neoplasms - metabolism | Tumor markers | Adrenal glands | Inhibin | INHA gene | Genetic diversity | Gene expression | Human performance | Animal tissues | Genetic analysis | DNA methylation | Epigenetics | Methylation | Variation | Genotypes | Gonadectomy | CpG islands | Tumors
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3. Full Text Somatic SDHB Mutation in an Extraadrenal Pheochromocytoma
by de Krijger, Ronald R and Lenders, Jacques W.M and van Nederveen, Francien H and Korpershoek, Esther and Dinjens, Winand N.M
The New England Journal of Medicine, ISSN 0028-4793, 07/2007, Volume 357, Issue 3, pp. 306 - 308
To the Editor: As many as 25% of pheochromocytomas — catecholamine-producing tumors located along the sympathetic nervous system, including the adrenals —... 
GERM-LINE MUTATIONS | GENE | MEDICINE, GENERAL & INTERNAL | Succinate Dehydrogenase - genetics | Urinary Bladder Neoplasms - genetics | DNA Mutational Analysis | Humans | Iron-Sulfur Proteins - genetics | Adult | Female | Pheochromocytoma - genetics | Loss of Heterozygosity
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4. Full Text Publisher Correction: The UMBRELLA SIOP-RTSG 2016 Wilms tumour pathology and molecular biology protocol
by Vujanić, Gordan M and Gessler, Manfred and Ooms, Ariadne H A G and Collini, Paola and Coulomb-l'Hermine, Aurore and D'Hooghe, Ellen and de Krijger, Ronald R and Perotti, Daniela and Pritchard-Jones, Kathy and Vokuhl, Christian and van den Heuvel-Eibrink, Marry M and Graf, Norbert and International Society of Paediatric Oncology–Renal Tumour Study Group (SIOP–RTSG) and on behalf of the International Society of Paediatric Oncology–Renal Tumour Study Group (SIOP–RTSG)
Nature reviews. Urology, ISSN 1759-4812, 09/2019, Volume 16, Issue 9, pp. 563 - 563
In the version of this article initially published online it was not open access, this has now been corrected. 
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5. European Society of Endocrinology Clinical Practice Guidelines on the management of adrenocortical carcinoma in adults, in collaboration with the European Network for the Study of Adrenal Tumors
by Martin Fassnacht and Olaf M Dekkers and Tobias Else and Eric Baudin and Alfredo Berruti and Ronald R de Krijger and Harm R Haak and Radu Mihai and Guillaume Assie and Massimo Terzolo
European Journal of Endocrinology, ISSN 0804-4643, 10/2018, Volume 179, Issue 4, p. G1
Adrenocortical carcinoma (ACC) is a rare and in most cases steroid hormone-producing tumor with variable prognosis. The purpose of these guidelines is to... 
Histopathology | Surgery | Etoposide | Radiation measurement | Radiation therapy | Metastasis | Management | Doxorubicin | Patients | Cisplatin | Tumors | Metastases
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6. False-positive findings on 6-[^sup 18^F]fluor-L-3,4-dihydroxyphenylalanine PET (18F-FDOPA-PET) performed for imagingof neuroendocrine tumors
by Annika M A Berends and Michiel N Kerstens and Janne W Bolt and Thera P Links and Esther Korpershoek and Ronald R de Krijger and Annemiek M E Walenkamp and Walter Noordzij and Boudewijn van Etten and Gursah Kats-Ugurlu and Adrienne H Brouwers and Anouk N A van der Horst-Schrivers
European Journal of Endocrinology, ISSN 0804-4643, 08/2018, Volume 179, Issue 2, p. 125
Background/aim PET with 6-[18F]fluor-L-3,4-dihydroxyphenylalanine (18F-FDOPA) has been shown to be a useful imaging tool with a high sensitivity for the... 
Dihydroxyphenylalanine | Squamous cell carcinoma | Chondrosarcoma | Schwann cells | Multiple myeloma | Hepatocellular carcinoma | Scintigraphy | Cervix | Pathology | Nets | Levodopa | Positron emission tomography | Neuroendocrine tumors
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7. Full Text SDHA Immunohistochemistry Detects Germline SDHA Gene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas
by Korpershoek, Esther and Favier, Judith and Gaal, José and Burnichon, Nelly and van Gessel, Bram and Oudijk, Lindsey and Badoual, Cécile and Gadessaud, Noémie and Venisse, Annabelle and Bayley, Jean-Pierre and van Dooren, Marieke F and de Herder, Wouter W and Tissier, Frédérique and Plouin, Pierre-François and van Nederveen, Francien H and Dinjens, Winand N. M and Gimenez-Roqueplo, Anne-Paule and de Krijger, Ronald R
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 09/2011, Volume 96, Issue 9, pp. E1472 - E1476
Context: Pheochromocytoma-paraganglioma syndrome is caused by mutations in SDHB, SDHC, and SDHD, encoding subunits of succinate dehydrogenase (SDH), and in... 
SUCCINATE-DEHYDROGENASE | CHAIN COMPLEX-II | LEIGH-SYNDROME | FLAVOPROTEIN GENE | ENDOCRINOLOGY & METABOLISM | PATIENT | SUBUNIT | Immunohistochemistry | Pheochromocytoma - metabolism | Electron Transport Complex II - genetics | Paraganglioma - genetics | Humans | Loss of Heterozygosity | DNA Mutational Analysis | Electron Transport Complex II - metabolism | Paraganglioma - metabolism | Alleles | Adrenal Gland Neoplasms - metabolism | Germ-Line Mutation | Pheochromocytoma - genetics | Adrenal Gland Neoplasms - genetics
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8. Full Text Integrated genomic characterization of adrenocortical carcinoma
by Assié, Guillaume and Letouzé, Eric and Fassnacht, Martin and Jouinot, Anne and Luscap, Windy and Barreau, Olivia and Omeiri, Hanin and Rodriguez, Stéphanie and Perlemoine, Karine and René-Corail, Fernande and Elarouci, Nabila and Sbiera, Silviu and Kroiss, Matthias and Allolio, Bruno and Waldmann, Jens and Quinkler, Marcus and Mannelli, Massimo and Mantero, Franco and Papathomas, Thomas and De Krijger, Ronald and Tabarin, Antoine and Kerlan, Véronique and Baudin, Eric and Tissier, Frédérique and Dousset, Bertrand and Groussin, Lionel and Amar, Laurence and Clauser, Eric and Bertagna, Xavier and Ragazzon, Bruno and Beuschlein, Felix and Libé, Rossella and De Reyniès, Aurélien and Bertherat, Jérôme
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 6, pp. 607 - 612
Adrenocortical carcinomas (ACCs) are aggressive cancers originating in the cortex of the adrenal gland(1). Despite overall poor prognosis, ACC outcome is... 
MOLECULAR CLASSIFICATION | COPY-NUMBER CHANGES | MANAGEMENT | LONG NONCODING RNAS | GENE | GENETICS & HEREDITY | TUMOR-SUPPRESSOR | MUTATIONS | EXPRESSION | HUMAN CANCER | MICRORNA | Multigene Family | Prognosis | Telomere - ultrastructure | Genomics | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Male | MicroRNAs - metabolism | Gene Expression Profiling | Loss of Heterozygosity | Exome | Young Adult | DNA Methylation | DNA Mutational Analysis | Aged, 80 and over | Adult | Female | Adrenocortical Carcinoma - genetics | Ubiquitin-Protein Ligases - metabolism | beta Catenin - metabolism | Adrenal Cortex Neoplasms - genetics | Adolescent | Aged | Polymorphism, Single Nucleotide | Mutation | Cohort Studies | Single nucleotide polymorphisms | Identification and classification | Methods | Exome sequencing | Genomes | Gene expression | Experiments | Cancer therapies | Medical prognosis | Software | Arrays | Charitable foundations | Chromosomes | Bioinformatics | Deoxyribonucleic acid--DNA | Tumors | Cancer | Life Sciences | Human health and pathology
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9. Een appendectomie gevolgd door een pancreaticoduodenectomie: Solide pseudopapillair neoplasma van het pancreas
by Fest, Jesse and Van Den Boom, Anne Loes and De Krijger, Ronald R and Roos, Daphne
Nederlands Tijdschrift voor Geneeskunde, ISSN 0028-2162, 2015, Volume 159, Issue 46
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10. Full Text EANM 2012 guidelines for radionuclide imaging of phaeochromocytoma and paraganglioma
by Taieb, D and Timmers, H.J.L.M and Hindie, E and Guillet, B.A and Neumann, H.P and Walz, M.K and Opocher, G and de Herder, W.W and Boedeker, C.C and de Krijger, R.R and Chiti, A and Al-Nahhas, A and Pacak, K and Rubello, D and European Association of Nuclear Medicine
European Journal of Nuclear Medicine and Molecular Imaging, ISSN 1619-7070, 2012, Volume 39, Issue 12, pp. 1977 - 1995
PURPOSE: Radionuclide imaging of phaeochromocytomas (PCCs) and paragangliomas (PGLs) involves various functional imaging techniques and approaches for accurate... 
Medicine & Public Health | Review literature | Orthopedics | Phaeochromocytoma | Paraganglioma | Oncology | Nuclear Medicine | Imaging / Radiology | Cardiology | Guidelines | Radionuclide imaging | METASTATIC PHEOCHROMOCYTOMA | I-123 METAIODOBENZYLGUANIDINE | F-18-DOPA PET-CT | POSITRON-EMISSION-TOMOGRAPHY | NECK PARAGANGLIOMAS | MALIGNANT PHEOCHROMOCYTOMA | IN-111-PENTETREOTIDE SCINTIGRAPHY | I-131/I-123-METAIODOBENZYLGUANIDINE MIBG SCINTIGRAPHY | SOMATOSTATIN RECEPTOR SCINTIGRAPHY | OCTREOTIDE SCINTIGRAPHY | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Nervous System Neoplasms - diagnostic imaging | Paraganglioma - diagnostic imaging | Europe | Humans | Positron-Emission Tomography - standards | Adrenal Gland Neoplasms - diagnostic imaging | Pheochromocytoma - diagnostic imaging | Tomography, Emission-Computed, Single-Photon - standards | Radiopharmaceuticals - standards | Tomography | Nuclear medicine | Medical diagnosis | Cancer
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11. Full Text Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations
by Katherine A. Janeway and Su Young Kim and Maya Lodish and Vânia Nosé and Pierre Rustin and José Gaal and Patricia L. M. Dahia and Bernadette Liegl and Evan R. Ball and Margarita Raygada and Angela H. Lai and Lorna Kelly and Jason L. Hornick and NIH Pediatric and Wild-Type GIST Clinic and Maureen O'Sullivan and Ronald R. de Krijger and Winand N. M. Dinjens and George D. Demetri and Cristina R. Antonescu and Jonathan A. Fletcher and Lee Helman and Constantine A. Stratakis and Stuart H. Orkin and NIH Pediat Wild Type GIST Clinic and NIH Pediatric and Wild-Type GIST Clinic
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2011, Volume 108, Issue 1, pp. 314 - 318
Carney-Stratakis syndrome, an inherited condition predisposing affected individuals to gastrointestinal stromal tumor (GIST) and paraganglioma, is caused by... 
Pediatrics | Gastrointestinal stromal tumors | Germ cells | Dehydrogenases | Medical genetics | Paraganglioma | Germline mutation | Genetic mutation | Summarization | Tumors | Genetic predisposition | Sarcoma | Pediatric | RESPIRATORY-CHAIN | GIST | sarcoma | VARIANTS | SDHD GENE | MULTIDISCIPLINARY SCIENCES | PHENOTYPE | PARAGANGLIOMA | MECHANISMS | APPARENTLY SPORADIC PHEOCHROMOCYTOMAS | pediatric | COMPLEX-II | genetic predisposition | GERMLINE MUTATIONS | Gastrointestinal Stromal Tumors - enzymology | Immunohistochemistry | Genetic Predisposition to Disease - genetics | Paraganglioma - enzymology | Electron Transport Complex II - genetics | Humans | Germ-Line Mutation - genetics | Blotting, Western | Syndrome | Succinate Dehydrogenase - genetics | Cell Respiration - genetics | DNA Mutational Analysis | Electron Transport Complex II - metabolism | Receptor, Platelet-Derived Growth Factor alpha - genetics | Adolescent | Cell Respiration - physiology | Proto-Oncogene Proteins c-kit - genetics | Succinate Dehydrogenase - metabolism | Polymorphism, Single Nucleotide | Protein Subunits - genetics | Physiological aspects | Succinate dehydrogenase complex | Platelet-derived growth factor | Gene mutations | Biological Sciences
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12. Full Text An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC , or SDHD gene mutations: a retrospective and prospective analysis
by van Nederveen, Francien H, MD and Gaal, José, MD and Favier, Judith, PhD and Korpershoek, Esther, BSc and Oldenburg, Rogier A, MD and de Bruyn, Elly MCA, BSc and Sleddens, Hein FBM, BSc and Derkx, Pieter, BSc and Rivière, Julie, BSc and Dannenberg, Hilde, MD and Petri, Bart-Jeroen, MD and Komminoth, Paul, Prof and Pacak, Karel, Prof and Hop, Wim CJ, PhD and Pollard, Patrick J, MD and Mannelli, Massimo, Prof and Bayley, Jean-Pierre, PhD and Perren, Aurel, MD and Niemann, Stephan, PhD and Verhofstad, Albert A, MD and de Bruïne, Adriaan P, Prof and Maher, Eamonn R, Prof and Tissier, Frédérique, MD and Méatchi, Tchao, MD and Badoual, Cécile, MD and Bertherat, Jérôme, Prof and Amar, Laurence, MD and Alataki, Despoina, MD and Van Marck, Eric, Prof and Ferrau, Francesco, MD and François, Jerney, BSc and de Herder, Wouter W, MD and Peeters, Mark-Paul FM Vrancken, MD and van Linge, Anne, MD and Lenders, Jacques WM, Prof and Gimenez-Roqueplo, Anne-Paule, Prof and de Krijger, Ronald R, MD and Dinjens, Winand NM, Dr
Lancet Oncology, The, ISSN 1470-2045, 2009, Volume 10, Issue 8, pp. 764 - 771
Summary Background Phaeochromocytomas and paragangliomas are neuro-endocrine tumours that occur sporadically and in several hereditary tumour syndromes,... 
Hematology, Oncology and Palliative Medicine | MALIGNANT PHEOCHROMOCYTOMAS | MITOCHONDRIAL RESPIRATORY-CHAIN | COMPLEX-II | ONCOLOGY | LINE MUTATIONS | DISEASE | SUCCINATE | UPDATE | ENZYMATIC-ACTIVITY | HYPOXIA | FEATURES | Membrane Proteins - genetics | Paraganglioma - genetics | Pheochromocytoma - diagnosis | Humans | Middle Aged | Male | Paraganglioma - diagnosis | Blotting, Western | Syndrome | Adrenal Gland Neoplasms - diagnosis | Immunohistochemistry - methods | Young Adult | Succinate Dehydrogenase - genetics | DNA Mutational Analysis | Adolescent | Germ-Line Mutation | Adult | Female | Pheochromocytoma - genetics | Aged | Adrenal Gland Neoplasms - genetics | Child | Immunohistochemistry | Hypertension | Molecular genetics | Gene mutations | Developmental biology | Genetic research | Genetic aspects | Universities and colleges | Human genetics | Tumors
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13. Full Text MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma
by Burnichon, Nelly and Cascoń, Alberto and Schiavi, Francesca and Morales, NicolePaes and Comino-Méndez, Iñaki and Abermil, Nasséra and Inglada-Pérez, Lucía and Cubas, Aguirre and Amar, Laurence and Barontini, Marta and Quiroś, Sana Bernaldo and Bertherat, Jerome and Bignon, Yves-Jean and Blok, Marinus and Bobisse, Sara and Borrego, Salud and Castellano, Maurizio and Chanson, Philippe and Chiara, A and Corssmit, Eleonora and Giacchè, Mara and Krijger, Ronald and Ercolino, Tonino and Girerd, Xavier and Gómez García, Encarna and Gómez-Graña, Álvaro and Guilhem, Isabelle and Hes, Frederik and Honrado, Emiliano and Korpershoek, Esther and Lenders, Jacques and Letón, Rocío and Mensenkamp, Arjen and Merlo, Anna and Mori, Luigi and Murat, Arnaud and Pierre, Peggy and Plouin, Pierre-Franco̧is and Prodanov, Tamara and Quesada-Charneco, Miguel and Qin, Nan and Rapizzi, Elena and Raymond, Eric and Reisch, Nicole and Roncador, Giovanna and Ruiz-Ferrer, Macarena and Schillo, Frank and Stegmann, Sander and Suarez, Carlos and Taschin, Elisa and Timmers, H.J.L.M and Tops, Carli and Urioste, Miguel and Beuschlein, Felix and Pacak, Karel and Mannelli, Massimo and Dahia, Patricia and Opocher, Giuseppe and Eisenhofer, Graeme and Gimenez-Roqueplo, A.P and Robledo, Mercedes
Clinical Cancer Research, ISSN 1078-0432, 05/2012, Volume 18, Issue 10, pp. 2828 - 2837
textabstractPurpose: Pheochromocytomas (PCC) and paragangliomas (PGL) are genetically heterogeneous neural crest-derived neoplasms. Recently we identified... 
GENE-MUTATIONS | SUCCINATE-DEHYDROGENASE | GERM-LINE MUTATIONS | ONCOLOGY | DNA | LINDAU DISEASE | SUSCEPTIBILITY | SDHB | FAMILIAL PHEOCHROMOCYTOMA | Genetic Predisposition to Disease | Paraganglioma - genetics | Humans | Middle Aged | Child, Preschool | Male | Young Adult | Adolescent | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - genetics | Aged, 80 and over | Germ-Line Mutation | Adult | Female | Pheochromocytoma - genetics | Aged | Adrenal Gland Neoplasms - genetics | Child | Pheochromocytoma | Paraganglioma | Life Sciences | Human health and pathology | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors | Adrenal Gland Neoplasms
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14. Full Text Pheochromocytomas and Paragangliomas: New Developments with Regard to Classification, Genetics, and Cell of Origin
by Koopman, K and Gaal, J and de Krijger, RR
CANCERS, ISSN 2072-6694, 08/2019, Volume 11, Issue 8, p. 1070
Pheochromocytomas (PCC) and paragangliomas (PGL) are rare neuroendocrine tumors that arise in the adrenal medulla and in extra-adrenal locations, such as the... 
pheochromocytoma | MARKERS | SDHB | paraganglioma | scoring system | MAX MUTATIONS | SPORADIC PHEOCHROMOCYTOMA | tumor classification | H-RAS | PASS | HEREDITARY | ONCOLOGY | PREDISPOSITION | GERMLINE MUTATIONS | GAPP | SPECTRUM | IMMUNOHISTOCHEMISTRY
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15. Neoadjuvant Treatment of Nonfunctioning Pancreatic Neuroendocrine Tumors with [^sup 177^Lu-DOTA^sup 0^,Tyr^sup 3^]Octreotate
by Esther I van Vliet and Casper H van Eijck and Ronald R de Krijger and Elisabeth J Nieveen van Dijkum and Jaap J Teunissen and Boen L Kam and Wouter W de Herder and Richard A Feelders and Bert A Bonsing and Tessa Brabander and Eric P Krenning and Dik J Kwekkeboom
The Journal of Nuclear Medicine, ISSN 0161-5505, 11/2015, Volume 56, Issue 11, p. 1647
  Pancreatic neuroendocrine tumors (NETs) are rare neoplasms for which surgery has almost the only potential for cure. When surgery is not possible because of... 
Nuclear medicine | Medical treatment | Metastasis | Pancreas | Tumors
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16. Full Text Pathology of pheochromocytoma and paraganglioma
by Tischler, Arthur S and De Krijger, Ronald R
Endocrine-Related Cancer, ISSN 1351-0088, 08/2015, Volume 22, Issue 4, pp. T123 - T133
Pathologists using their routine diagnostic tools can contribute both to the care of patients with pheochromocytoma/paraganglioma and to understanding the... 
Immunohistochemistry | Pathology | PASS | Oncology | Cancer Research | Histology | GAPP | Endocrinology, Diabetes and Metabolism | Endocrinology | pathology | NEUROENDOCRINE | CLINICAL-FEATURES | SDHD | TUMORS | SUSTENTACULAR CELLS | histology | GENE | ONCOLOGY | ENDOCRINOLOGY & METABOLISM | immunohistochemistry | MUTATIONS | NEUROFIBROMATOSIS TYPE-1 | S100 PROTEIN
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17. Full Text IGF and mTOR pathway expression and in vitro effects of linsitinib and mTOR inhibitors in adrenocortical cancer
by De Martino, Maria Cristina and van Koetsveld, Peter M and Feelders, Richard A and de Herder, Wouter W and Dogan, Fadime and Janssen, Joseph A. M. J. L and Hofste op Bruinink, Davine and Pivonello, Claudia and Waaijers, A Marlijn and Colao, Annamaria and de Krijger, Ronald R and Pivonello, Rosario and Hofland, Leo J
Endocrine, ISSN 1355-008X, 6/2019, Volume 64, Issue 3, pp. 673 - 684
The IGF and mTOR-pathways are considered as potential targets for therapy in patients with adrenocortical carcinoma (ACC). This study aims to describe the IGF... 
Adrenocortical cancer | Medicine & Public Health | Science, Humanities and Social Sciences, multidisciplinary | Linsitinib | Internal Medicine | IGF | Diabetes | Adrenal | Insulin receptor | Endocrinology | GROWTH-FACTOR-II | FACTOR RECEPTOR | TUMORS | LOCUS | INSULIN | MOLECULAR CLASSIFICATION | GENETICS | ENDOCRINOLOGY & METABOLISM | BINDING PROTEIN-2 | FACTOR SYSTEM | CARCINOMA | Antimitotic agents | Insulin-like growth factors | Cellular signal transduction | Antineoplastic agents | Health aspects | Immunosuppressive agents | Testing | Original
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18. Full Text SDHB immunohistochemistry: A useful tool in the diagnosis of Carney-Stratakis and Carney triad gastrointestinal stromal tumors
by Gaal, José and Stratakis, Constantine and Carney, J. Aidan and Ball, Evan and Korpershoek, Esther and Lodish, Maya Beth and Levy, Isaac and Xekouki, Paraskevi and Nederveen, Francien and Bakker, Michael and O'Sullivan, Maureen and Dinjens, Winand and Krijger, Ronald
Modern Pathology, ISSN 0893-3952, 01/2011, Volume 24, Issue 1, pp. 147 - 151
textabstractMutations in the tumor suppressor genes SDHB, SDHC, and SDHD (or collectively SDHx) cause the inherited paraganglioma syndromes, characterized by... 
Carney triad | Carney-Stratakis syndrome | immunohistochemistry | gastrointestinal stromal tumor | SDHB | GENE-MUTATIONS | ANGIOGENESIS | PARAGANGLIOMA | PATHOLOGY | PHEOCHROMOCYTOMA | GERMLINE MUTATIONS | SUCCINATE | EXPRESSION | STOMACH | Immunohistochemistry | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Humans | Proto-Oncogene Proteins c-kit - metabolism | Syndrome | Epithelioid Cells - metabolism | Succinate Dehydrogenase - genetics | Gastrointestinal Stromal Tumors - diagnosis | DNA Mutational Analysis | Receptor, Platelet-Derived Growth Factor alpha - genetics | Carney Complex - genetics | Biomarkers, Tumor - metabolism | Gastrointestinal Stromal Tumors - metabolism | Proto-Oncogene Proteins c-kit - genetics | Succinate Dehydrogenase - metabolism | Mutation | Carney Complex - metabolism | Carney Complex - diagnosis | Gastrointestinal Stromal Tumors - genetics | Epithelioid Cells - pathology | Carney–Stratakis syndrome
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