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Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomas.
López-Jiménez E, Gómez-López G, Leandro-García LJ, Muñoz I, Schiavi F, Montero-Conde C, de Cubas AA, Ramires R, Landa I, Leskelä S, Maliszewska A, Inglada-Pérez L, de la Vega L, Rodríguez-Antona C, Letón R, Bernal C, de Campos JM, Diez-Tascón C, Fraga MF, Boullosa C, Pisano DG, Opocher G, Robledo M, Cascón A. López-Jiménez E, et al. Among authors: de la vega l, de campos jm, de cubas aa. Mol Endocrinol. 2010 Dec;24(12):2382-91. doi: 10.1210/me.2010-0256. Epub 2010 Oct 27. Mol Endocrinol. 2010. PMID: 20980436 Free PMC article.
SDHC mutation in an elderly patient without familial antecedents.
López-Jiménez E, de Campos JM, Kusak EM, Landa I, Leskelä S, Montero-Conde C, Leandro-García LJ, Vallejo LA, Madrigal B, Rodríguez-Antona C, Robledo M, Cascón A. López-Jiménez E, et al. Among authors: de campos jm. Clin Endocrinol (Oxf). 2008 Dec;69(6):906-10. doi: 10.1111/j.1365-2265.2008.03368.x. Epub 2008 Aug 4. Clin Endocrinol (Oxf). 2008. PMID: 18681855
Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2.
Boedeker CC, Erlic Z, Richard S, Kontny U, Gimenez-Roqueplo AP, Cascon A, Robledo M, de Campos JM, van Nederveen FH, de Krijger RR, Burnichon N, Gaal J, Walter MA, Reschke K, Wiech T, Weber J, Rückauer K, Plouin PF, Darrouzet V, Giraud S, Eng C, Neumann HP. Boedeker CC, et al. Among authors: de campos jm, de krijger rr. J Clin Endocrinol Metab. 2009 Jun;94(6):1938-44. doi: 10.1210/jc.2009-0354. Epub 2009 Mar 31. J Clin Endocrinol Metab. 2009. PMID: 19336503 Free PMC article. Review.
Chromosomal patterns in human malignant astrocytomas.
Rey JA, Bello MJ, de Campos JM, Kusak ME, Ramos C, Benitez J. Rey JA, et al. Among authors: de campos jm. Cancer Genet Cytogenet. 1987 Dec;29(2):201-21. doi: 10.1016/0165-4608(87)90232-9. Cancer Genet Cytogenet. 1987. PMID: 2824025
Characterization of endolymphatic sac tumors and von Hippel-Lindau disease in the International Endolymphatic Sac Tumor Registry.
Bausch B, Wellner U, Peyre M, Boedeker CC, Hes FJ, Anglani M, de Campos JM, Kanno H, Maher ER, Krauss T, Sansó G, Barontini M, Letizia C, Hader C, Schiavi F, Zanoletti E, Suárez C, Offergeld C, Malinoc A, Zschiedrich S, Glasker S, Bobin S, Sterkers O, Ba Huy PT, Giraud S, Links T, Eng C, Opocher G, Richard S, Neumann HP; International Endolymphatic Sac Tumor (ELST) Consortium. Bausch B, et al. Among authors: de campos jm. Head Neck. 2016 Apr;38 Suppl 1:E673-9. doi: 10.1002/hed.24067. Epub 2015 Jul 14. Head Neck. 2016. PMID: 25867206
Six novel mutations in the NF2 tumor suppressor gene.
Leone PE, Bello MJ, Mendiola M, Vaquero J, Sarasa JL, Kusak ME, De Campos JM, Pestana A, Rey JA. Leone PE, et al. Among authors: de campos jm. Int J Oncol. 1998 Apr;12(4):935-8. doi: 10.3892/ijo.12.4.935. Int J Oncol. 1998. PMID: 9499458
Cytogenetic clones in a recurrent neurofibroma.
Rey JA, Bello MJ, de Campos JM, Benítez J, Sarasa JL, Boixados JR, Sánchez Cascos A. Rey JA, et al. Among authors: de campos jm. Cancer Genet Cytogenet. 1987 May;26(1):157-63. doi: 10.1016/0165-4608(87)90142-7. Cancer Genet Cytogenet. 1987. PMID: 3103906
113 results