| Embarazo ectópico abdominal avanzado: reporte de casos y revisión de la literatura MF Escobar-Vidarte, G Caicedo-Herrera, JD Solarte-Erazo, ... Revista Colombiana de Obstetricia y Ginecología 68 (1), 71-82, 2017 | 25 | 2017 |
| Novel ATP7A gene mutation in a patient with Menkes disease G Caicedo-Herrera, E Candelo, J Pinilla, A Vidal, S Cruz, HM Pachajoa The application of clinical genetics, 151-155, 2018 | 19 | 2018 |
| Microcephaly in Colombia before the Zika outbreak: A systematic literature review E Candelo, G Caicedo, MM Feinstein, H Pachajoa Biomedica 38, 127-134, 2018 | 11 | 2018 |
| Microcephaly in Colombia before the Zika outbreak: A systematic literature review E Candelo, G Caicedo, MM Feinstein, H Pachajoa Biomedica 38, 127-134, 2018 | 11 | 2018 |
| Molecular characterization of mucopolysaccharidosis type IVA patients in the Andean region of Colombia H Pachajoa, MA Acosta, CJ Alméciga‐Díaz, Y Ariza, L Diaz‐Ordoñez, ... American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2021 | 9 | 2021 |
| Syndromic progressive neurodegenerative disease of infancy caused by novel variants in HIBCH: report of two cases in Colombia E Candelo, L Cochard, G Caicedo-Herrera, AM Granados, JF Gomez, ... Intractable & Rare Diseases Research 8 (3), 187-193, 2019 | 9 | 2019 |
| Advanced ectopic abdominal pregnancy: Case report and review of the literature MF Escobar-Vidarte, G Caicedo-Herrera, JD Solarte-Erazo, ... Revista Colombiana de Obstetricia y Ginecología 68 (1), 71-82, 2017 | 4 | 2017 |
| First report case with negative genetic study (array CGH, exome sequencing) in patients with vertical transmission of Zika virus infection and associated brain abnormalities E Candelo, G Caicedo, F Rosso, A Ballesteros, J Orrego, L Escobar, ... The Application of Clinical Genetics, 141-150, 2019 | 3 | 2019 |
| Expanding FOXG1 syndrome phenotype E Candelo, G Caicedo, H Pachajoa Neurología (English Edition) 35 (3), 207-211, 2020 | 1 | 2020 |
| Chromosome 17p13. 3 microdeletion syndrome with unaltered PAFAH1B1 gene. E Candelo, G Caicedo, L Mejia, H Pachajoa Neurologia (Barcelona, Spain) 34 (7), 482-484, 2016 | 1 | 2016 |
| Sucecesfull bone marrow transplantation in a case of familial hemophagocytic lymphohistiocytosis type 3 G Caicedo-Herrera, E Candelo, M Olaya, P Pérez, D Medina, H Pachajoa Andes Pediatrica: Revista Chilena de Pediatria 92 (2), 269-273, 2021 | | 2021 |
| Trasplante de médula ósea exitoso en un caso de linfohistiocitosis hemofagocítica familiar tipo 3 G Caicedo-Herrera, E Candelo, M Olaya, P Pérez, D Medina, H Pachajoa Andes pediatrica 92 (2), 269-273, 2021 | | 2021 |
| Ampliando el fenotipo del síndrome FOXG1 E Candelo, G Caicedo, H Pachajoa Neurología 35 (3), 207-211, 2020 | | 2020 |
| Molecular Characterisationof MPS IVA patients in Andean region of Colombia H Pachajoa, E Candelo, G Caicedo, G Porras, D Ramirez, L Diaz EUROPEAN JOURNAL OF HUMAN GENETICS 27, 188-188, 2019 | | 2019 |
| Síndrome de microdeleción 17P13. 3 sin afectación del gen PAFAH1B1 E Candelo, G Caicedo, L Mejia, H Pachajoa Neurología 34 (7), 482-484, 2019 | | 2019 |
| Novel mutation in TSC2 gene in pediatric patient with clinical diagnosis of tuberous sclerosis G Caicedo-Herrera, E Candelo, H Pachajoa Archivos Argentinos de Pediatria 115 (5), e287-e290, 2017 | | 2017 |
| Nueva mutación del gen TSC2 en un paciente pediátrico con diagnóstico clínico de esclerosis tuberosa G Caicedo-Herrera, E Candelo, H Pachajoa Archivos argentinos de pediatría 115 (5), e287-e290, 2017 | | 2017 |
