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Ocular findings in Colombian patients affected with Fabry disease Manifestaciones oculares de enfermedad de Fabry en pacientes colombianos Ocular findings in Fabry disease

por Rothstein K., Gálvez J.M., Gutiérrez Á.M., Rico L., Criollo E., de-la-Torre A.
Publicado 2019

Biallelic HERC1 mutations in a syndromic form of overgrowth and intellectual disability

por "Ortega?Recalde, O., Beltrán, O.I., Gálvez, J.M., Palma?Montero, A., Restrepo, C.M., Mateus, H.E., Laissue, P."
Publicado 2015

Evidence of an association between 10/10 genotype of DAT1 and endophenotypes of attention deficit/hyperactivity disorder

por Agudelo, J.A., Gálvez, J.M., Fonseca-Mendoza, Dora Janeth, Mateus Arbelaez, Heidi Eliana, Talero-Gutiérrez, Claudia, Velez-Van-Meerbeke, A.
Publicado 2015

Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy

por Calderon-Ospina, C. A., Galvez, J. M., López-Cabra, C., Morales. N., Restrepo, C. M., Rodríguez, J., Aristizábal-Gutiérrez, F. A., Velez-van-Meerbeke, A., Laissue, P., Fonseca-Mendoza, D. J.
Publicado 2020