Showing 61 - 80 results of 98 for search '"Candelo"', query time: 0.13s Refine Results
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    Novel ATP7A gene mutation in a patient with Menkes disease by Caicedo-Herrera G, Candelo E, Pinilla J, Vidal A, Cruz S, Pachajoa HM

    Published 2018-11-01
    “…Gabriela Caicedo-Herrera,1 Estephania Candelo,1 Juan Pinilla,2 Andrés Vidal,2 Santiago Cruz,3 Harry Mauricio Pachajoa1–4 1Health Sciences Faculty, Universidad Icesi, Cali, Colombia; 2Dermatology, Fundación Valle Del Lili, Cali, Colombia; 3Paediatric Neurology, Fundación Valle Del Lili, Cali, Colombia; 4Department of Genetics, Fundación Valle Del Lili, Cali, Colombia Background: Menkes disease is a congenital neurodegenerative disorder caused by ATP7A gene mutations. …”
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    The Oral Health of Patients with DiGeorge Syndrome (22q11) Microdeletion: A Case Report by Candelo E, Estrada-Mesa MA, Jaramillo A, Martinez-Cajas CH, Osorio JC, Pachajoa H

    Published 2021-06-01
    “…Estephania Candelo,1– 3 Maria Alejandra Estrada-Mesa,4 Adriana Jaramillo,4 Carlos Humberto Martinez-Cajas,4 Julio Cesar Osorio,4 Harry Pachajoa1,2 1Congenital Abnormalities and Rare Disease Centre (CIACER), Cali, Colombia; 2Genetics Department, Fundacion Valle del Lili, Cali, Colombia; 3Centro de Investigaciones Clínicas, Fundacion Valle del Lili, Cali, Colombia; 4Institución Universitaria Colegios de Colombia (UNICOC), Cali, ColombiaCorrespondence: Estephania Candelo Email ecandelo@icesi.edu.coBackground: DiGeorge syndrome (DG) is a genetic disorder associated with 22q11 deletion. …”
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