Search Results - "Krijger, Ronald R de"

Overview of the 2022 WHO Classification of Paragangliomas and Pheochromocytomas by Mete, Ozgur, Asa, Sylvia L., Gill, Anthony J., Kimura, Noriko, de Krijger, Ronald R., Tischler, Arthur

“…This review summarizes the classification of tumors of the adrenal medulla and extra-adrenal paraganglia as outlined in the 5th series of the WHO…”
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Overview of the 2022 WHO Classification of Adrenal Cortical Tumors by Mete, Ozgur, Erickson, Lori A., Juhlin, C. Christofer, de Krijger, Ronald R., Sasano, Hironobu, Volante, Marco, Papotti, Mauro G.

“…The new WHO classification of adrenal cortical proliferations reflects translational advances in the fields of endocrine pathology, oncology and molecular…”
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Familial Male-limited Precocious Puberty (FMPP) and Testicular Germ Cell Tumors by Kooij, Cezanne D, Mavinkurve-Groothuis, Annelies M.C, Hovinga, Idske C.L. Kremer, Looijenga, Leendert H.J, Rinne, Tuula, Giltay, Jacques C, Kort, Laetitia M.O. de, Klijn, Aart J, Krijger, Ronald R. de, Stuart, Annemarie A. Verrijn

“…Objective: The purpose of this study is to report development of a malignant testicular germ cell tumor (GCT) in 2 young adult males with familial male-limited…”
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Renal Tumors of Childhood-A Histopathologic Pattern-Based Diagnostic Approach by Ooms, Ariadne H A G, Vujanić, Gordan M, D'Hooghe, Ellen, Collini, Paola, L'Herminé-Coulomb, Aurore, Vokuhl, Christian, Graf, Norbert, Heuvel-Eibrink, Marry M van den, de Krijger, Ronald R

“…Renal tumors comprise approximately 7% of all malignant pediatric tumors. This is a highly heterogeneous group of tumors, each with its own therapeutic…”
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Chorioamnionitis Alters the Response to Surfactant in Preterm Infants by Been, Jasper V., MD, Rours, Ingrid G., MD, Kornelisse, René F., MD, PhD, Jonkers, Femke, MD, de Krijger, Ronald R., MD, PhD, Zimmermann, Luc J., MD, PhD

“…Objective To study the association between antenatal exposure to chorioamnionitis and the neonatal response to surfactant. Study design Prospective…”
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MRI Characteristics of Pediatric and Young-Adult Renal Cell Carcinoma: A Single-Center Retrospective Study and Literature Review by Beek, Justine N van der, Krijger, Ronald R de, Nievelstein, Rutger A J, Bex, Axel, Klijn, Aart J, Heuvel-Eibrink, Marry M van den, Littooij, Annemieke S

“…Pediatric renal cell carcinoma (RCC) is a rare malignancy. Magnetic resonance imaging (MRI) is the preferred imaging modality for assessment of these tumors…”
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An organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity by Calandrini, Camilla, Schutgens, Frans, Oka, Rurika, Margaritis, Thanasis, Candelli, Tito, Mathijsen, Luka, Ammerlaan, Carola, van Ineveld, Ravian L., Derakhshan, Sepide, de Haan, Sanne, Dolman, Emmy, Lijnzaad, Philip, Custers, Lars, Begthel, Harry, Kerstens, Hindrik H. D., Visser, Lindy L., Rookmaaker, Maarten, Verhaar, Marianne, Tytgat, Godelieve A. M., Kemmeren, Patrick, de Krijger, Ronald R., Al-Saadi, Reem, Pritchard-Jones, Kathy, Kool, Marcel, Rios, Anne C., van den Heuvel-Eibrink, Marry M., Molenaar, Jan J., van Boxtel, Ruben, Holstege, Frank C. P., Clevers, Hans, Drost, Jarno

“…Kidney tumours are among the most common solid tumours in children, comprising distinct subtypes differing in many aspects, including cell-of-origin, genetics,…”
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Pathology and genetics of phaeochromocytoma and paraganglioma by Turchini, John, Cheung, Veronica K Y, Tischler, Arthur S, De Krijger, Ronald R, Gill, Anthony J

“…Phaeochromocytoma and paraganglioma (PHEO/PGL) are rare tumours with an estimated annual incidence of 3 per million. Advances in molecular understanding have…”
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Histologic chorioamnionitis, fetal involvement, and antenatal steroids: effects on neonatal outcome in preterm infants by Been, Jasper V., MD, Rours, Ingrid G.I.J.G., MD, Kornelisse, René F., MD, PhD, Lima Passos, Valéria, PhD, Kramer, Boris W., MD, PhD, Schneider, Tom A.J., MD, de Krijger, Ronald R., MD, PhD, Zimmermann, Luc J.I., MD, PhD

“…Objective The objective of the study was to study the effects of histologic chorioamnionitis (HC) with or without fetal involvement and antenatal steroid (AS)…”
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Incidence of pheochromocytoma and sympathetic paraganglioma in the Netherlands: A nationwide study and systematic review by Berends, Annika M.A., Buitenwerf, Edward, de Krijger, Ronald R., Veeger, Nic J.G.M., van der Horst-Schrivers, Anouk N.A., Links, Thera P., Kerstens, Michiel N.

“…Recent years have seen major changes in clinical practice which may have affected the incidence rates of pheochromocytoma(PCC)/sympathetic paraganglioma(sPGL)…”
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SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T) by Papathomas, Thomas G, Oudijk, Lindsey, Persu, Alexandre, Gill, Anthony J, van Nederveen, Francien, Tischler, Arthur S, Tissier, Frédérique, Volante, Marco, Matias-Guiu, Xavier, Smid, Marcel, Favier, Judith, Rapizzi, Elena, Libe, Rosella, Currás-Freixes, Maria, Aydin, Selda, Huynh, Thanh, Lichtenauer, Urs, van Berkel, Anouk, Canu, Letizia, Domingues, Rita, Clifton-Bligh, Roderick J, Bialas, Magdalena, Vikkula, Miikka, Baretton, Gustavo, Papotti, Mauro, Nesi, Gabriella, Badoual, Cécile, Pacak, Karel, Eisenhofer, Graeme, Timmers, Henri J, Beuschlein, Felix, Bertherat, Jérôme, Mannelli, Massimo, Robledo, Mercedes, Gimenez-Roqueplo, Anne-Paule, Dinjens, Winand NM, Korpershoek, Esther, de Krijger, Ronald R

“…Despite the established role of SDHB/SDHA immunohistochemistry as a valuable tool to identify patients at risk for familial succinate dehydrogenase-related…”
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Somatic mutations and single-cell transcriptomes reveal the root of malignant rhabdoid tumours by Custers, Lars, Khabirova, Eleonora, Coorens, Tim H. H., Oliver, Thomas R. W., Calandrini, Camilla, Young, Matthew D., Vieira Braga, Felipe A., Ellis, Peter, Mamanova, Lira, Segers, Heidi, Maat, Arie, Kool, Marcel, Hoving, Eelco W., van den Heuvel-Eibrink, Marry M., Nicholson, James, Straathof, Karin, Hook, Liz, de Krijger, Ronald R., Trayers, Claire, Allinson, Kieren, Behjati, Sam, Drost, Jarno

“…Malignant rhabdoid tumour (MRT) is an often lethal childhood cancer that, like many paediatric tumours, is thought to arise from aberrant fetal development…”
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SDHA Immunohistochemistry Detects Germline SDHA Gene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas by Korpershoek, Esther, Favier, Judith, Gaal, José, Burnichon, Nelly, van Gessel, Bram, Oudijk, Lindsey, Badoual, Cécile, Gadessaud, Noémie, Venisse, Annabelle, Bayley, Jean-Pierre, van Dooren, Marieke F, de Herder, Wouter W, Tissier, Frédérique, Plouin, Pierre-François, van Nederveen, Francien H, Dinjens, Winand N. M, Gimenez-Roqueplo, Anne-Paule, de Krijger, Ronald R

“…Context: Pheochromocytoma-paraganglioma syndrome is caused by mutations in SDHB, SDHC, and SDHD, encoding subunits of succinate dehydrogenase (SDH), and in…”
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Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants by Taïeb, David, Wanna, George B, Ahmad, Maleeha, Lussey-Lepoutre, Charlotte, Perrier, Nancy D, Nölting, Svenja, Amar, Laurence, Timmers, Henri J L M, Schwam, Zachary G, Estrera, Anthony L, Lim, Michael, Pollom, Erqi Liu, Vitzthum, Lucas, Bourdeau, Isabelle, Casey, Ruth T, Castinetti, Frédéric, Clifton-Bligh, Roderick, Corssmit, Eleonora P M, de Krijger, Ronald R, Del Rivero, Jaydira, Eisenhofer, Graeme, Ghayee, Hans K, Gimenez-Roqueplo, Anne-Paule, Grossman, Ashley, Imperiale, Alessio, Jansen, Jeroen C, Jha, Abhishek, Kerstens, Michiel N, Kunst, Henricus P M, Liu, James K, Maher, Eamonn R, Marchioni, Daniele, Mercado-Asis, Leilani B, Mete, Ozgur, Naruse, Mitsuhide, Nilubol, Naris, Pandit-Taskar, Neeta, Sebag, Frédéric, Tanabe, Akiyo, Widimsky, Jiri, Meuter, Leah, Lenders, Jacques W M, Pacak, Karel

“…Patients with germline SDHD pathogenic variants (encoding succinate dehydrogenase subunit D; ie, paraganglioma 1 syndrome) are predominantly affected by head…”
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MR imaging in discriminating between benign and malignant paediatric ovarian masses: a systematic review by van Nimwegen, Lotte W. E., Mavinkurve-Groothuis, Annelies M. C., de Krijger, Ronald R., Hulsker, Caroline C. C., Goverde, Angelique J., Zsiros, József, Littooij, Annemieke S.

“…Objectives The use of magnetic resonance (MR) imaging in differentiation between benign and malignant adnexal masses in children and adolescents might be of…”
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Porphyromonas gingivalis within Placental Villous Mesenchyme and Umbilical Cord Stroma Is Associated with Adverse Pregnancy Outcome by Vanterpool, Sizzle F, Been, Jasper V, Houben, Michiel L, Nikkels, Peter G J, De Krijger, Ronald R, Zimmermann, Luc J I, Kramer, Boris W, Progulske-Fox, Ann, Reyes, Leticia

“…Intrauterine presence of Porphyromonas gingivalis (Pg), a common oral pathobiont, is implicated in preterm birth. Our aim was to determine if the location of…”
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Mass spectrometry imaging identifies metabolic patterns associated with malignant potential in pheochromocytoma and paraganglioma by Murakami, Masanori, Sun, Na, Greunke, Christian, Feuchtinger, Annette, Kircher, Stefan, Deutschbein, Timo, Papathomas, Thomas, Bechmann, Nicole, William Wallace, Paal, Peitzsch, Mirko, Korpershoek, Esther, Friemel, Juliane, Gimenez-Roqueplo, Anne-Paule, Robledo, Mercedes, J L M Timmers, Henri, Canu, Letizia, Weber, Achim, R de Krijger, Ronald, Fassnacht, Martin, Knösel, Thomas, Kirchner, Thomas, Reincke, Martin, Karl Walch, Axel, Kroiss, Matthias, Beuschlein, Felix

“…Objective Within the past decade, important genetic drivers of pheochromocytoma and paraganglioma (PPGLs) development have been identified. The…”
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Organoid-based drug screening reveals neddylation as therapeutic target for malignant rhabdoid tumors by Calandrini, Camilla, van Hooff, Sander R., Paassen, Irene, Ayyildiz, Dilara, Derakhshan, Sepide, Dolman, M. Emmy M., Langenberg, Karin P.S., van de Ven, Marieke, de Heus, Cecilia, Liv, Nalan, Kool, Marcel, de Krijger, Ronald R., Tytgat, Godelieve A.M., van den Heuvel-Eibrink, Marry M., Molenaar, Jan J., Drost, Jarno

“…Malignant rhabdoid tumors (MRTs) represent one of the most aggressive childhood malignancies. No effective treatment options are available, and prognosis is,…”
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Data set for the reporting of pheochromocytoma and paraganglioma: explanations and recommendations of the guidelines from the International Collaboration on Cancer Reporting by Thompson, Lester D.R., Gill, Anthony J., Asa, Sylvia L., Clifton-Bligh, Roderick J., de Krijger, Ronald R., Kimura, Noriko, Komminoth, Paul, Lack, Ernest E., Lenders, Jacques W.M., Lloyd, Ricardo V., Papathomas, Thomas G., Sadow, Peter M., Tischler, Arthur S.

“…The International Collaboration on Cancer Reporting (ICCR) is a not-for-profit to develop evidence-based, internationally agreed-upon standardized data sets…”
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SDHB immunohistochemistry: a useful tool in the diagnosis of Carney-Stratakis and Carney triad gastrointestinal stromal tumors by Gaal, José, Stratakis, Constantine A, Carney, J Aidan, Ball, Evan R, Korpershoek, Esther, Lodish, Maya B, Levy, Isaac, Xekouki, Paraskevi, van Nederveen, Francien H, den Bakker, Michael A, O'Sullivan, Maureen, Dinjens, Winand NM, de Krijger, Ronald R

“…Mutations in the tumor suppressor genes SDHB , SDHC , and SDHD (or collectively SDHx ) cause the inherited paraganglioma syndromes, characterized by…”
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