[Cytomegalovirus infection and disease in pediatric solid organ transplantation. Experience in a Chilean multiorganic transplantation center]

Autor: M Paulina, Salazar E, Andrea, Alba G, Angela, Deluchi B, Bessie, Hunter M, Jorge, Godoy L, Mario, Ferrario B, Mario, Uribe M, Erwin, Buckel G

Publikováno v: Revista chilena de infectologia : organo oficial de la Sociedad Chilena de Infectologia. 26(4)

Cytomegalovirus (CMV) infection and disease in transplant (Tx) recipients may severely complicate the patients outcome.To determine the incidence, clinical characteristics and risk factors for CMV infection and disease in liver and kidney transplant

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1f0158c7ceb1ff48159e71c2f4a100f6
https://pubmed.ncbi.nlm.nih.gov/19802397

Estado actual del diagnóstico y presentaciones clínicas de enfermedad celíaca: Estudio multicéntrico

Autor: Magdalena Araya Q, Francisco Alliende G, Eduardo Chávez S., Paulina Canales R, Bessie Hunter M, Teresa Alarcón O

Publikováno v: Revista médica de Chile v.136 n.3 2008
SciELO Chile
CONICYT Chile
instacron:CONICYT

Background: Ample use of serological markers of high sensitivity and specificity led to relevant changes in the epidemiology of celiac disease. The impact of these changes in our country is poorly known. Aim: To assess the diagnostic procedures, clin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e85876420761ff4ecd0f1a39d27cf16
https://doi.org/10.4067/s0034-98872008000300003

Identificación de mutaciones en el gen CFTR en pacientes chilenos con fibrosis quística

Autor: Gabriela Repetto L, Helena Poggi M, Paul Harris D, Héctor Navarro M, Ignacio Sánchez D, Ernesto Guiraldes C, M Angélica Pérez H, M Lina Boza R, Bessie Hunter M, M Elena Wevar C, Marisol Mediavilla R, Arnaldo Foradori C

Publikováno v: Revista médica de Chile, Volume: 129, Issue: 8, Pages: 841-847, Published: AUG 2001
Revista médica de Chile v.129 n.8 2001
SciELO Chile
CONICYT Chile
instacron:CONICYT

Background: Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the CFTR gene, that codes for a chloride channel located in the apical surface of epithelial cells. The main role of this protein is the regulation of chloride

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d88397a99a500a85337334b31b5e991
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872001000800001&lng=en&tlng=en

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