Publicaciones

Martínez G, Gómez JA, Bang H, Martínez-Gamboa L, Roggenbuck D, Burmester GR, et al. Carbamylated vimentin represents a relevant autoantigen in Latin American (Cuban) rheumatoid arthritis patients. Rheumatology International. 2016;36: 781-791.

En: http://dx.doi:10.1007/s00296-016-3472-9.

 

Méndez-Rosado LA, Cuétara E, Molina-Gamboa O, Suarez-Mayedo U, Huertas-Perez G, Barrios-Martinez A, Garcia M, Morales E. Avoiding a second amniocentesis to corroborate prenatal diagnosis by using refrigerated samples. J Matern Fetal Neonatal Med. 2016 May 26:1-5.

En: http://dx.doi.org/10.1080/14767058.2016.1188380

 

Contreras-Roura J, Camayd-Viera I, Padrón-Díaz AD, Martínez-Rey L. Diagnóstico bioquímico de la hiperglicinemia no cetósica en Cuba (Carta al Editor). Neurología. 2016

En: http://dx.doi.org/10.1016/j.nrl.2016.05.015

 

Concepción-Alvarez A, Camayd-Viera I, Nuevas-Paz. Validation of an HPLC method for total homocysteine quantification in plasma. Revista del Laboratorio Clínico. 2016; 9(2):40–47.

En: http://dx.doi.org/10.1016/j.labcli.2016.02.003  

 

Acosta T, Morales E, La O A, Martínez L, Marín L, López C, Castillo Y, et al. Markers of oxidative damage and antioxidant defense in MPS IV A and B Cuban patients. Journal of inborn errors of metabolim and screening (Special Supplement with the abstracts). 2016; 4:29-30.

En: https://www.mps2016.com/fileadmin/user_uploads/pdf/Abstractbook_Webversion.pdf

 

Acosta T, Larrinaga L, Campos D, Menendez M,Tamayo V, de Leon N, García A, Lavaut A, Bravo M. Clinical, biochemical and molecular diagnosis of LSD in Cuban in the last decade. Journal of inborn errors of metabolim and screening (Special Supplement with the abstracts). 2016; 4:34.

En: https://www.mps2016.com/fileadmin/user_uploads/pdf/Abstractbook_Webversion.pdf

 

Marcheco-Teruel B, Parra EJ, Fuentes-Smith E, Salas A, Buttenschon HN, et al. Cuba: Exploring the History of Admixture and the Genetic Basis of Pigmentation Using Autosomal and Uniparental Markers. PLoS Genet. 2014;10(7): e1004488.

En: http://dx.doi:10.1371/journal.pgen.1004488.

 

Lavaut K, Rubio T, Esperón A, Reyes L, Collazo T, Acanda AM. Identification of a novel mutation, I403T, in Cuban type Gaucher disease. Blood Cells, Molecules, and Diseases. 2011; 46 (4): 327.

En: http://dx.doi.org/10.1016/j.bcmd.2011.02.002

 

Teruel BM, Rodríguez JJL, McKeigue P, Collazo T, Fuentes E, Valhuerdi A, et al. Interactions between genetic admixture, ethnic identity, APOE genotype and dementia prevalence in an admixed Cuban sample; a cross-sectional population survey and nested case-control study. BMC Medical Genetics. 2011;12:43.

En: http://dx.doi:10.1186/1471-2350-12-43.

 

Campos D, Ledesma Y, Monaga M, Herrera D, Pampín Y. Estudio de las enzimas lisosomales N-acetil-a-D-glucosaminidasa y arilsulfatasa A en adultos cubanos. Acta bioquím. clín. latinoam.  [Internet]. 2010 ;  44( 4 ): 647-652.

En: http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0325-29572010000400005&lng=es.