Pereira L - Search Results

1

A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndrome.

Pereira L, Levran O, Ramirez F, Lynch JR, Sykes B, Pyeritz RE, Dietz HC. Pereira L, et al. N Engl J Med. 1994 Jul 21;331(3):148-53. doi: 10.1056/NEJM199407213310302. N Engl J Med. 1994. PMID: 8008028 Free article.

2

The fibrillin-Marfan syndrome connection.

Ramirez F, Pereira L, Zhang H, Lee B. Ramirez F, et al. Among authors: pereira l. Bioessays. 1993 Sep;15(9):589-94. doi: 10.1002/bies.950150904. Bioessays. 1993. PMID: 8240311 Review.

3

Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome.

Pereira L, D'Alessio M, Ramirez F, Lynch JR, Sykes B, Pangilinan T, Bonadio J. Pereira L, et al. Hum Mol Genet. 1993 Jul;2(7):961-8. doi: 10.1093/hmg/2.7.961. Hum Mol Genet. 1993. PMID: 8364578

4

Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome.

Pereira L, Andrikopoulos K, Tian J, Lee SY, Keene DR, Ono R, Reinhardt DP, Sakai LY, Biery NJ, Bunton T, Dietz HC, Ramirez F. Pereira L, et al. Nat Genet. 1997 Oct;17(2):218-22. doi: 10.1038/ng1097-218. Nat Genet. 1997. PMID: 9326947

5

The fibrillins.

Ramirez F, Pereira L. Ramirez F, et al. Among authors: pereira l. Int J Biochem Cell Biol. 1999 Feb;31(2):255-9. doi: 10.1016/s1357-2725(98)00109-5. Int J Biochem Cell Biol. 1999. PMID: 10216958 Review.

6

Mutations of extracellular matrix components in vascular disease.

Ramirez F, Pereira L. Ramirez F, et al. Among authors: pereira l. Ann Thorac Surg. 1999 Jun;67(6):1857-8; discussion 1868-70. doi: 10.1016/s0003-4975(99)00437-3. Ann Thorac Surg. 1999. PMID: 10391325

7

Marfan syndrome: new clues to genotype-phenotype correlations.

Ramirez F, Gayraud B, Pereira L. Ramirez F, et al. Among authors: pereira l. Ann Med. 1999 Jun;31(3):202-7. doi: 10.3109/07853899909115979. Ann Med. 1999. PMID: 10442675 Review.

8

Fifteen novel FBN1 mutations causing Marfan syndrome detected by heteroduplex analysis of genomic amplicons.

Nijbroek G, Sood S, McIntosh I, Francomano CA, Bull E, Pereira L, Ramirez F, Pyeritz RE, Dietz HC. Nijbroek G, et al. Among authors: pereira l. Am J Hum Genet. 1995 Jul;57(1):8-21. Am J Hum Genet. 1995. PMID: 7611299 Free PMC article.

9

Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome.

Pereira L, D'Alessio M, Ramirez F, Lynch JR, Sykes B, Pangilinan T, Bonadio J. Pereira L, et al. Hum Mol Genet. 1993 Oct;2(10):1762. doi: 10.1093/hmg/2.10.1762. Hum Mol Genet. 1993. PMID: 8268958 No abstract available.

10

Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1.

Pereira L, Lee SY, Gayraud B, Andrikopoulos K, Shapiro SD, Bunton T, Biery NJ, Dietz HC, Sakai LY, Ramirez F. Pereira L, et al. Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):3819-23. doi: 10.1073/pnas.96.7.3819. Proc Natl Acad Sci U S A. 1999. PMID: 10097121 Free PMC article.

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