Cascón A - Search Results

1

A Novel Approach for the Identification of Pharmacogenetic Variants in MT-RNR1 through Next-Generation Sequencing Off-Target Data.

Lanillos J, Santos M, Carcajona M, Roldan-Romero JM, Martinez AM, Calsina B, Monteagudo M, Leandro-García LJ, Montero-Conde C, Cascón A, Maietta P, Alvarez S, Robledo M, Rodriguez-Antona C. Lanillos J, et al. Among authors: cascon a. J Clin Med. 2020 Jul 2;9(7):2082. doi: 10.3390/jcm9072082. J Clin Med. 2020. PMID: 32630724 Free PMC article.

2

Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.

Cascon A, Ruiz-Llorente S, Cebrian A, Telleria D, Rivero JC, Diez JJ, Lopez-Ibarra PJ, Jaunsolo MA, Benitez J, Robledo M. Cascon A, et al. Eur J Hum Genet. 2002 Aug;10(8):457-61. doi: 10.1038/sj.ejhg.5200829. Eur J Hum Genet. 2002. PMID: 12111639

3

A rapid and easy method for multiple endocrine neoplasia type 1 mutation detection using conformation-sensitive gel electrophoresis.

Arancha C, Ruíz-Llorente S, Cascón A, Osorio A, Martínez-Delgado B, Benítez J, Robledo M. Arancha C, et al. Among authors: cascon a. J Hum Genet. 2002;47(4):190-5. doi: 10.1007/s100380200022. J Hum Genet. 2002. PMID: 12166655

4

SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation.

Cascón A, Cebrián A, Ruiz-Llorente S, Tellería D, Benítez J, Robledo M. Cascón A, et al. J Med Genet. 2002 Oct;39(10):E64. doi: 10.1136/jmg.39.10.e64. J Med Genet. 2002. PMID: 12362046 Free PMC article. No abstract available.

5

Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients.

Cebrián A, Ruiz-Llorente S, Cascón A, Pollán M, Díez JJ, Picó A, Tellería D, Benítez J, Robledo M. Cebrián A, et al. Among authors: cascon a. J Med Genet. 2003 May;40(5):e72. doi: 10.1136/jmg.40.5.e72. J Med Genet. 2003. PMID: 12746426 Free PMC article. No abstract available.

6

Genetic characterization and structural analysis of VHL Spanish families to define genotype-phenotype correlations.

Ruiz-Llorente S, Bravo J, Cebrián A, Cascón A, Pollan M, Tellería D, Letón R, Urioste M, Rodríguez-López R, de Campos JM, Muñoz MJ, Lacambra C, Benítez J, Robledo M. Ruiz-Llorente S, et al. Among authors: cascon a. Hum Mutat. 2004 Feb;23(2):160-169. doi: 10.1002/humu.10309. Hum Mutat. 2004. PMID: 14722919

7

Expression profiling of T-cell lymphomas differentiates peripheral and lymphoblastic lymphomas and defines survival related genes.

Martinez-Delgado B, Meléndez B, Cuadros M, Alvarez J, Castrillo JM, Ruiz De La Parte A, Mollejo M, Bellas C, Diaz R, Lombardía L, Al-Shahrour F, Domínguez O, Cascon A, Robledo M, Rivas C, Benitez J. Martinez-Delgado B, et al. Among authors: cascon a. Clin Cancer Res. 2004 Aug 1;10(15):4971-82. doi: 10.1158/1078-0432.CCR-04-0269. Clin Cancer Res. 2004. PMID: 15297397

8

A novel candidate region linked to development of both pheochromocytoma and head/neck paraganglioma.

Cascón A, Ruiz-Llorente S, Rodríguez-Perales S, Honrado E, Martínez-Ramírez A, Letón R, Montero-Conde C, Benítez J, Dopazo J, Cigudosa JC, Robledo M. Cascón A, et al. Genes Chromosomes Cancer. 2005 Mar;42(3):260-8. doi: 10.1002/gcc.20139. Genes Chromosomes Cancer. 2005. PMID: 15609347

9

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. 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

10

About the origin and development of hereditary conventional renal cell carcinoma in a four-generation t(3;8)(p14.1;q24.23) family.

Valle L, Cascón A, Melchor L, Otero I, Rodríguez-Perales S, Sánchez L, Cruz Cigudosa J, Robledo M, Weber B, Urioste M, Benítez J. Valle L, et al. Among authors: cascon a. Eur J Hum Genet. 2005 May;13(5):570-8. doi: 10.1038/sj.ejhg.5201371. Eur J Hum Genet. 2005. PMID: 15756303

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