Lorena Diaz-Ordoñez

12PUBLICATIONS
25CO-AUTHORS
Medical infection agents (incl. prions)Multicultural, intercultural and cross-cultural studiesAutoimmunityPacific Peoples mothers and babies health and wellbeingGene mapping
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Publications (12)

|Feb 19, 2026
Variable Expressivity in Type 2 Familial Partial Lipodystrophy Related to a Pathogenic LMNA Variant R482: Maternal Transmission to Non-Identical Twins.

Paola Andrea Duque-Cordoba, Lorena Diaz-Ordoñez, Laura Carvajal-Del-Castillo

|Jan 10, 2025
Hearing loss in patients with Morquio A syndrome: A scoping review.

Lorena Diaz-Ordoñez, Paola Andrea Duque-Cordoba, Katherine Silva-Cuero

|Nov 14, 2024
Phenotype-Genotype Correlation in Morquio A Syndrome: Protocol for a Meta-Analysis.

Lorena Diaz-Ordoñez, Paola Andrea Duque-Cordoba, Daniel Andrés Nieva-Posso

|Nov 04, 2024
African-Colombian woman with preeclampsia and high-risk APOL1 genotype: A case report.

Carlos E Duran, Juan David Gutierrez-Medina, Jacobo Triviño Arias

|Feb 26, 2024
Familial LCAT Deficiency and Low HDL-C Levels: In silico Characterization of Two Rare LCAT Missense Mutations.

Sebastian Ciro Acosta, Lorena Díaz-Ordóñez, Juan David Gutierrez-Medina

|Nov 28, 2023
Novel mutation in RPGRIP1L gene causing Joubert syndrome: A case report.

Paola Andrea Duque-Cordoba, Lorena Diaz-Ordoñez, Juan David Gutierrez-Medina

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