Facultade de Medicina e Odontoloxía
Facultad
Universidad Nacional de Córdoba
Córdoba, ArgentinaPublicacións en colaboración con investigadores/as de Universidad Nacional de Córdoba (14)
2024
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Mapping oral medicine (stomatology) & oral and maxillofacial pathology international organizations: a scoping review of global data and historical analysis
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
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Oral lesions of systemic lupus erythematosus: A collaborative Latin American study
Lupus, Vol. 33, Núm. 8, pp. 864-873
2013
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Ancestry analysis reveals a predominant Native American component with moderate European admixture in Bolivians
Forensic Science International: Genetics, Vol. 7, Núm. 5, pp. 537-542
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The Genetic Legacy of the Pre-Colonial Period in Contemporary Bolivians
PLoS ONE, Vol. 8, Núm. 3
2012
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Typing short amplicon binary polymorphisms: Supplementary SNP and Indel genetic information in the analysis of highly degraded skeletal remains
Forensic Science International: Genetics, Vol. 6, Núm. 4, pp. 469-476
2011
2010
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Hydrophilic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS/MS) determination of cocaine and its metabolites benzoylecgonine, ecgonine methyl ester, and cocaethylene in hair samples
Analytical and Bioanalytical Chemistry, Vol. 396, Núm. 5, pp. 1703-1712
2009
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A GEP-ISFG collaborative study on the optimization of an X-STR decaplex: Data on 15 Iberian and Latin American populations
International Journal of Legal Medicine, Vol. 123, Núm. 3, pp. 227-234
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Effects of high-dose versus low-dose losartan on clinical outcomes in patients with heart failure (HEAAL study): a randomised, double-blind trial
The Lancet, Vol. 374, Núm. 9704, pp. 1840-1848
2008
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2006 GEP-ISFG collaborative exercise on mtDNA: reflections about interpretation, artefacts, and DNA mixtures
Forensic Science International: Genetics, Vol. 2, Núm. 2, pp. 126-133
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Results of the GEP-ISFG collaborative study on an X-STR Decaplex
Forensic Science International: Genetics Supplement Series, Vol. 1, Núm. 1, pp. 677-679
2007
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Erratum: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America (Journal of Human Genetics 51, (305-313) DOI: 10.1007/s10038-006-0362-0)
Journal of Human Genetics
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Stimulation by ghrelin of p42/p44 mitogen-activated protein kinase through the GHS-R1a receptor: Role of G-proteins and β-arrestins
Journal of Cellular Physiology, Vol. 213, Núm. 1, pp. 187-200
2006
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The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America
Journal of Human Genetics, Vol. 51, Núm. 4, pp. 305-313