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Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients.
Pena-Couso L, Ercibengoa M, Mercadillo F, Gómez-Sánchez D, Inglada-Pérez L, Santos M, Lanillos J, Gutiérrez-Abad D, Hernández A, Carbonell P, Letón R, Robledo M, Rodríguez-Antona C, Perea J, Urioste M; PHTS Working Group. Pena-Couso L, et al. Among authors: robledo m. Orphanet J Rare Dis. 2022 Feb 28;17(1):85. doi: 10.1186/s13023-021-02079-7. Orphanet J Rare Dis. 2022. PMID: 35227301 Free PMC article.
[Molecular analysis in 23 patients with T-lymphomas].
Santos M, Robledo M, Echezarreta G, Rivas C, Santón A, Benítez J. Santos M, et al. Among authors: robledo m. Sangre (Barc). 1991 Apr;36(2):113-6. Sangre (Barc). 1991. PMID: 1866650 Spanish.
Malignant degeneration of presacral teratoma in the Currarino anomaly.
Urioste M, Garcia-Andrade Mdel C, Valle L, Robledo M, González-Palacios F, Méndez R, Ferreirós J, Nuño J, Benítez J. Urioste M, et al. Among authors: robledo m. Am J Med Genet A. 2004 Jul 30;128A(3):299-304. doi: 10.1002/ajmg.a.30028. Am J Med Genet A. 2004. PMID: 15216552
Succinate dehydrogenase D variants do not constitute a risk factor for developing C cell hyperplasia or sporadic medullary thyroid carcinoma.
Cascon A, Cebrian A, Pollan M, Ruiz-Llorente S, Montero-Conde C, Leton R, Gutierrez R, Lesueur F, Milne RL, Gonzalez-Albarran O, Lucas-Morante T, Benitez J, Ponder BA, Robledo M. Cascon A, et al. Among authors: robledo m. J Clin Endocrinol Metab. 2005 Apr;90(4):2127-30. doi: 10.1210/jc.2004-2059. Epub 2004 Dec 28. J Clin Endocrinol Metab. 2005. PMID: 15623805
Cowden disease in a family: a clinical and genetic diagnosis.
Mangas C, Hilari JM, Ribera M, Robledo M, Urioste M, Benítez J, Fuente MJ, Ferrándiz C. Mangas C, et al. Among authors: robledo m. J Am Acad Dermatol. 2005 Aug;53(2):359-60. doi: 10.1016/j.jaad.2005.03.044. J Am Acad Dermatol. 2005. PMID: 16021145 No abstract available.
367 results