Badenas C - Search Results

1

Role of the CDKN2A locus in patients with multiple primary melanomas.

Puig S, Malvehy J, Badenas C, Ruiz A, Jimenez D, Cuellar F, Azon A, Gonzàlez U, Castel T, Campoy A, Herrero J, Martí R, Brunet-Vidal J, Milà M. Puig S, et al. Among authors: badenas c. J Clin Oncol. 2005 May 1;23(13):3043-51. doi: 10.1200/JCO.2005.08.034. J Clin Oncol. 2005. PMID: 15860862

2

A female compound heterozygote (pre- and full mutation) for the CGG FMR1 expansion.

Milà M, Castellví-Bel S, Giné R, Vazquez C, Badenas C, Sánchez A, Estivill X. Milà M, et al. Among authors: badenas c. Hum Genet. 1996 Oct;98(4):419-21. doi: 10.1007/s004390050232. Hum Genet. 1996. PMID: 8792815

3

Maternal transmission in sporadic Huntington's disease.

Sánchez A, Milà M, Castellví-Bel S, Rosich M, Jiménez D, Badenas C, Estivill X. Sánchez A, et al. Among authors: badenas c. J Neurol Neurosurg Psychiatry. 1997 May;62(5):535-7. doi: 10.1136/jnnp.62.5.535. J Neurol Neurosurg Psychiatry. 1997. PMID: 9153618 Free PMC article.

4

Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation.

Milà M, Sànchez A, Badenas C, Brun C, Jiménez D, Villa MP, Castellví-Bel S, Estivill X. Milà M, et al. Among authors: badenas c. Hum Genet. 1997 Oct;100(5-6):503-7. doi: 10.1007/s004390050542. Hum Genet. 1997. PMID: 9341861

5

Mutational analysis within the 3' region of the PKD1 gene.

Badenas C, Torra R, San Millán JL, Lucero L, Milà M, Estivill X, Darnell A. Badenas C, et al. Kidney Int. 1999 Apr;55(4):1225-33. doi: 10.1046/j.1523-1755.1999.00368.x. Kidney Int. 1999. PMID: 10200984 Free article.

6

Single-strand conformation polymorphism analysis in the FMR1 gene.

Castellví-Bel S, Sánchez A, Badenas C, Mallolas J, Barceló A, Jiménez D, Villa M, Estivill X, Milà M. Castellví-Bel S, et al. Among authors: badenas c. Am J Med Genet. 1999 May 28;84(3):262-5. Am J Med Genet. 1999. PMID: 10331603

7

A loss-of-function model for cystogenesis in human autosomal dominant polycystic kidney disease type 2.

Torra R, Badenas C, San Millán JL, Pérez-Oller L, Estivill X, Darnell A. Torra R, et al. Among authors: badenas c. Am J Hum Genet. 1999 Aug;65(2):345-52. doi: 10.1086/302501. Am J Hum Genet. 1999. PMID: 10417277 Free PMC article.

8

Influence of the ACE gene polymorphism in the progression of renal failure in autosomal dominant polycystic kidney disease.

Pérez-Oller L, Torra R, Badenas C, Milà M, Darnell A. Pérez-Oller L, et al. Among authors: badenas c. Am J Kidney Dis. 1999 Aug;34(2):273-8. doi: 10.1016/s0272-6386(99)70355-0. Am J Kidney Dis. 1999. PMID: 10430974

9

Rare variants in the promoter of the fragile X syndrome gene (FMR1).

Milà M, Castellví-Bel S, Sánchez A, Barceló A, Badenas C, Mallolas J, Estivill X. Milà M, et al. Among authors: badenas c. Mol Cell Probes. 2000 Apr;14(2):115-9. doi: 10.1006/mcpr.2000.0293. Mol Cell Probes. 2000. PMID: 10799273

10

Increased prevalence of polycystic kidney disease type 2 among elderly polycystic patients.

Torra R, Badenas C, Pérez-Oller L, Luis J, Millán S, Nicolau C, Oppenheimer F, Milà M, Darnell A. Torra R, et al. Among authors: badenas c. Am J Kidney Dis. 2000 Oct;36(4):728-34. doi: 10.1053/ajkd.2000.17619. Am J Kidney Dis. 2000. PMID: 11007674

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