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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 2
1994 2
1998 4
1999 5
2000 6
2001 6
2002 7
2003 6
2004 12
2005 6
2006 18
2007 12
2008 9
2009 19
2010 15
2011 18
2012 20
2013 16
2014 15
2015 13
2016 8
2017 4
2018 11
2019 12
2020 17
2021 16
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245 results
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Page 1
The UMBRELLA SIOP-RTSG 2016 Wilms tumour pathology and molecular biology protocol.
Vujanić GM, Gessler M, Ooms AHAG, Collini P, Coulomb-l'Hermine A, D'Hooghe E, de Krijger RR, Perotti D, Pritchard-Jones K, Vokuhl C, van den Heuvel-Eibrink MM, Graf N; International Society of Paediatric Oncology–Renal Tumour Study Group (SIOP–RTSG). Vujanić GM, et al. Among authors: de krijger rr. Nat Rev Urol. 2018 Nov;15(11):693-701. doi: 10.1038/s41585-018-0100-3. Nat Rev Urol. 2018. PMID: 30310143 Free PMC article.
A common classification framework for neuroendocrine neoplasms: an International Agency for Research on Cancer (IARC) and World Health Organization (WHO) expert consensus proposal.
Rindi G, Klimstra DS, Abedi-Ardekani B, Asa SL, Bosman FT, Brambilla E, Busam KJ, de Krijger RR, Dietel M, El-Naggar AK, Fernandez-Cuesta L, Klöppel G, McCluggage WG, Moch H, Ohgaki H, Rakha EA, Reed NS, Rous BA, Sasano H, Scarpa A, Scoazec JY, Travis WD, Tallini G, Trouillas J, van Krieken JH, Cree IA. Rindi G, et al. Among authors: de krijger rr. Mod Pathol. 2018 Dec;31(12):1770-1786. doi: 10.1038/s41379-018-0110-y. Epub 2018 Aug 23. Mod Pathol. 2018. PMID: 30140036 Free PMC article.
Pathology and genetics of phaeochromocytoma and paraganglioma.
Turchini J, Cheung VKY, Tischler AS, De Krijger RR, Gill AJ. Turchini J, et al. Among authors: de krijger rr. Histopathology. 2018 Jan;72(1):97-105. doi: 10.1111/his.13402. Histopathology. 2018. PMID: 29239044 Review.
An organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity.
Calandrini C, Schutgens F, Oka R, Margaritis T, Candelli T, Mathijsen L, Ammerlaan C, van Ineveld RL, Derakhshan S, de Haan S, Dolman E, Lijnzaad P, Custers L, Begthel H, Kerstens HHD, Visser LL, Rookmaaker M, Verhaar M, Tytgat GAM, Kemmeren P, de Krijger RR, Al-Saadi R, Pritchard-Jones K, Kool M, Rios AC, van den Heuvel-Eibrink MM, Molenaar JJ, van Boxtel R, Holstege FCP, Clevers H, Drost J. Calandrini C, et al. Among authors: de krijger rr. Nat Commun. 2020 Mar 11;11(1):1310. doi: 10.1038/s41467-020-15155-6. Nat Commun. 2020. PMID: 32161258 Free PMC article.
Association of PDGFRB Mutations With Pediatric Myofibroma and Myofibromatosis.
Dachy G, de Krijger RR, Fraitag S, Théate I, Brichard B, Hoffman SB, Libbrecht L, Arts FA, Brouillard P, Vikkula M, Limaye N, Demoulin JB. Dachy G, et al. Among authors: de krijger rr. JAMA Dermatol. 2019 Aug 1;155(8):946-950. doi: 10.1001/jamadermatol.2019.0114. JAMA Dermatol. 2019. PMID: 31017643 Free PMC article.
Renal Tumors of Childhood-A Histopathologic Pattern-Based Diagnostic Approach.
Ooms AHAG, Vujanić GM, D'Hooghe E, Collini P, L'Herminé-Coulomb A, Vokuhl C, Graf N, Heuvel-Eibrink MMVD, de Krijger RR. Ooms AHAG, et al. Among authors: de krijger rr. Cancers (Basel). 2020 Mar 19;12(3):729. doi: 10.3390/cancers12030729. Cancers (Basel). 2020. PMID: 32204536 Free PMC article. Review.
Pheochromocytoma.
Eisenhofer G, Pacak K, Maher ER, Young WF, de Krijger RR. Eisenhofer G, et al. Among authors: de krijger rr. Clin Chem. 2013 Mar;59(3):466-72. doi: 10.1373/clinchem.2012.182246. Epub 2012 Dec 3. Clin Chem. 2013. PMID: 23209036 Free PMC article. No abstract available.
Metabolomics, machine learning and immunohistochemistry to predict succinate dehydrogenase mutational status in phaeochromocytomas and paragangliomas.
Wallace PW, Conrad C, Brückmann S, Pang Y, Caleiras E, Murakami M, Korpershoek E, Zhuang Z, Rapizzi E, Kroiss M, Gudziol V, Timmers HJ, Mannelli M, Pietzsch J, Beuschlein F, Pacak K, Robledo M, Klink B, Peitzsch M, Gill AJ, Tischler AS, de Krijger RR, Papathomas T, Aust D, Eisenhofer G, Richter S. Wallace PW, et al. Among authors: de krijger rr. J Pathol. 2020 Aug;251(4):378-387. doi: 10.1002/path.5472. Epub 2020 Jul 1. J Pathol. 2020. PMID: 32462735 Free PMC article.
MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma.
Burnichon N, Cascón A, Schiavi F, Morales NP, Comino-Méndez I, Abermil N, Inglada-Pérez L, de Cubas AA, Amar L, Barontini M, de Quirós SB, Bertherat J, Bignon YJ, Blok MJ, Bobisse S, Borrego S, Castellano M, Chanson P, Chiara MD, Corssmit EP, Giacchè M, de Krijger RR, Ercolino T, Girerd X, Gómez-García EB, Gómez-Graña A, Guilhem I, Hes FJ, Honrado E, Korpershoek E, Lenders JW, Letón R, Mensenkamp AR, Merlo A, Mori L, Murat A, Pierre P, Plouin PF, Prodanov T, Quesada-Charneco M, Qin N, Rapizzi E, Raymond V, Reisch N, Roncador G, Ruiz-Ferrer M, Schillo F, Stegmann AP, Suarez C, Taschin E, Timmers HJ, Tops CM, Urioste M, Beuschlein F, Pacak K, Mannelli M, Dahia PL, Opocher G, Eisenhofer G, Gimenez-Roqueplo AP, Robledo M. Burnichon N, et al. Among authors: de krijger rr. Clin Cancer Res. 2012 May 15;18(10):2828-37. doi: 10.1158/1078-0432.CCR-12-0160. Epub 2012 Mar 27. Clin Cancer Res. 2012. PMID: 22452945 Free article.
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