Giraldo A - Search Results

1

Mutation spectrum in South American Lynch syndrome families.

Dominguez-Valentin M, Nilbert M, Wernhoff P, López-Köstner F, Vaccaro C, Sarroca C, Palmero EI, Giraldo A, Ashton-Prolla P, Alvarez K, Ferro A, Neffa F, Caris J, Carraro DM, Rossi BM. Dominguez-Valentin M, et al. Among authors: giraldo a. Hered Cancer Clin Pract. 2013 Dec 18;11(1):18. doi: 10.1186/1897-4287-11-18. Hered Cancer Clin Pract. 2013. PMID: 24344984 Free PMC article.

2

MLH1 and MSH2 mutations in Colombian families with hereditary nonpolyposis colorectal cancer (Lynch syndrome)--description of four novel mutations.

Giraldo A, Gómez A, Salguero G, García H, Aristizábal F, Gutiérrez O, Angel LA, Padrón J, Martínez C, Martínez H, Malaver O, Flórez L, Barvo R. Giraldo A, et al. Fam Cancer. 2005;4(4):285-90. doi: 10.1007/s10689-005-4523-7. Fam Cancer. 2005. PMID: 16341804

3

[Detection mutations in the DNA mismatch repair genes of hMLH1 and hMSH2 genes in Colombian families with suspicion of hereditary non-polyposis colorectal carcinoma (Lynch syndrome)].

Gómez A, Salguero G, García H, Aristizábal F, Gutiérrez O, Angel LA, Padrón J, Martínez C, Martínez H, Malaver O, Barvo R, Giraldo A. Gómez A, et al. Among authors: giraldo a. Biomedica. 2005 Sep;25(3):315-24. Biomedica. 2005. PMID: 16276679 Spanish.

4

[Frequency of congenital anomalies at the Instituto Materno Infantil, Bogota, Colombia].

García H, Salguero GA, Moreno J, Arteaga C, Giraldo A. García H, et al. Among authors: giraldo a. Biomedica. 2003 Jun;23(2):161-72. Biomedica. 2003. PMID: 12872555 Spanish.

5

Allele frequencies for 13 STR's from two Colombian populations: Bogotá and Boyacá.

Rey M, Gutiérrez A, Schroeder B, Usaquén W, Carracedo A, Bustos I, Giraldo A. Rey M, et al. Among authors: giraldo a. Forensic Sci Int. 2003 Sep 9;136(1-3):83-5. doi: 10.1016/s0379-0738(03)00221-4. Forensic Sci Int. 2003. PMID: 12969625

6

[Basic standards for Colombian paternity testing laboratories, 2005].

Giraldo A, Bermúdez A, Jiménez M, Lizarazo R. Giraldo A, et al. Rev Salud Publica (Bogota). 2006 May-Aug;8(2):229-37. doi: 10.1590/s0124-00642006000200011. Rev Salud Publica (Bogota). 2006. PMID: 17191607 Free article. Spanish.

7

[Identification of point mutations in the 21-hydroxylase gene in patients affected with congenital adrenal hyperplasia].

Fonseca D, Gutiérrez A, Silva C, Coll M, Malo G, Orjuela C, Arteaga C, Giraldo A. Fonseca D, et al. Among authors: giraldo a. Biomedica. 2005 Jun;25(2):220-30. Biomedica. 2005. PMID: 16022377 Spanish.

8

Multiplex ligation-dependent probe amplification to subtelomeric rearrangements in idiopathic intellectual disability in Colombia.

Medina A, Piñeros L, Arteaga C, Velasco H, Izquierdo A, Giraldo A, Espinosa E. Medina A, et al. Among authors: giraldo a. Pediatr Neurol. 2014 Mar;50(3):250-4. doi: 10.1016/j.pediatrneurol.2013.10.017. Epub 2013 Oct 30. Pediatr Neurol. 2014. PMID: 24412240

9

Genetic services in Colombia.

Giraldo A. Giraldo A. Community Genet. 2004;7(2-3):126-9. doi: 10.1159/000080782. Community Genet. 2004. PMID: 15539828

10

Thalidomide, a current teratogen in South America.

Castilla EE, Ashton-Prolla P, Barreda-Mejia E, Brunoni D, Cavalcanti DP, Correa-Neto J, Delgadillo JL, Dutra MG, Felix T, Giraldo A, Juarez N, Lopez-Camelo JS, Nazer J, Orioli IM, Paz JE, Pessoto MA, Pina-Neto JM, Quadrelli R, Rittler M, Rueda S, Saltos M, Sánchez O, Schüler L. Castilla EE, et al. Among authors: giraldo a. Teratology. 1996 Dec;54(6):273-7. doi: 10.1002/(SICI)1096-9926(199612)54:6<273::AID-TERA1>3.0.CO;2-#. Teratology. 1996. PMID: 9098920

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