Salazar-Sanchez L - Search Results

1

High prevalence of FVHR2 polymorphism in Costarician Indians who have no FVL.

Herrmann FH, Salazar-Sanchez L, Jimenez-Arce G, Grimm R, Schröder W. Herrmann FH, et al. Thromb Haemost. 2001 Jun;85(6):1120-1. Thromb Haemost. 2001. PMID: 11434697 No abstract available.

2

Prevalence of eight molecular markers associated with thrombotic diseases in six Amerindian tribes and two African groups of Costa Rica.

Herrmann FH, Salazar-Sánchez L, Schuster G, Jiménez-Arce G, Grimm R, Gomez X, Chavez M, Wulff K, Schröder W. Herrmann FH, et al. Am J Hum Biol. 2004 Jan-Feb;16(1):82-6. doi: 10.1002/ajhb.10229. Am J Hum Biol. 2004. PMID: 14689519

3

The FXIIIVal34Leu, common and risk factors of venous thrombosis in early middle-age Costa Rican patients.

Salazar-Sánchez L, Leon MP, Cartin M, Schuster G, Wulff K, Schröder W, Jiménez-Arce G, Chacon R, Herrmann FH. Salazar-Sánchez L, et al. Cell Biochem Funct. 2007 Nov-Dec;25(6):739-45. doi: 10.1002/cbf.1389. Cell Biochem Funct. 2007. PMID: 17195962

4

Molecular diagnosis of hemophilia A and B. Report of five families from Costa Rica.

Salazar-Sánchez L, Jiménez-Cruz G, Chaverri P, Schröder W, Wulff K, Jiménez-Arce G, Sandoval M, Ramírez P, Herrmann FH. Salazar-Sánchez L, et al. Rev Biol Trop. 2004 Sep;52(3):521-30. doi: 10.15517/rbt.v1i2.15292. Rev Biol Trop. 2004. PMID: 17361545

5

Common polymorphisms and cardiovascular factors in patients with myocardial infarction of Costa Rica.

Salazar-Sánchez L, Chaves L, Cartin M, Schuster G, Wulff K, Schröder W, Herrmann FH. Salazar-Sánchez L, et al. Rev Biol Trop. 2006 Mar;54(1):1-11. doi: 10.15517/rbt.v54i1.13978. Rev Biol Trop. 2006. PMID: 18457169

6

Molecular analysis of FVIII gene in severe HA patients of Costa Rica.

Salazar-Sánchez L, Jiménez-Cruz G, Mendez M, Chaverri P, Alvarado P, Schröder W, Wulff K, Sandoval M, Herrmann FH, Pavlova A, Oldenburg J. Salazar-Sánchez L, et al. Hamostaseologie. 2010 Nov;30 Suppl 1:S150-2. Hamostaseologie. 2010. PMID: 21052611

7

Homozygous Factor X gene mutations Gly380Arg and Tyr163delAT are associated with perinatal intracranial hemorrhage.

Herrmann FH, Navarette M, Salazar-Sanchez L, Carillo JM, Auerswald G, Wulff K. Herrmann FH, et al. J Pediatr. 2005 Jan;146(1):128-30. doi: 10.1016/j.jpeds.2004.08.049. J Pediatr. 2005. PMID: 15644837

8

Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene.

Herrmann FH, Wulff K, Auerswald G, Schulman S, Astermark J, Batorova A, Kreuz W, Pollmann H, Ruiz-Saez A, De Bosch N, Salazar-Sanchez L; Greifswald Factor FVII Deficiency Study Group. Herrmann FH, et al. Haemophilia. 2009 Jan;15(1):267-80. doi: 10.1111/j.1365-2516.2008.01910.x. Epub 2008 Oct 30. Haemophilia. 2009. PMID: 18976247

9

Prevalence and geographic distribution of haemophilia in Costa Rica.

Arroyo J, Salazar-Sánchez L, Jiménez-Cruz G, Chaverri P, Arrieta-Bolaños E, Morera B. Arroyo J, et al. Hamostaseologie. 2010 Nov;30 Suppl 1:S28-31. Hamostaseologie. 2010. PMID: 21042672

10

A novel HLA-A allele, A*74:23, identified in an individual from Costa Rica.

Arrieta-Bolaños E, McWhinnie AJ, Madrigal-Sánchez JJ, Calvo L, Salazar-Sánchez L, Madrigal JA, Marsh SG, Shaw BE. Arrieta-Bolaños E, et al. Among authors: salazar sanchez l. Tissue Antigens. 2014 Dec;84(6):583-4. doi: 10.1111/tan.12470. Epub 2014 Oct 27. Tissue Antigens. 2014. PMID: 25345851

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