Zobrazeno 1 - 10 of 25 pro vyhledávání: '"Ilse, Contreras"'
1
Akademický článek
HEMOSIDEROSIS PULMONAR IDIOPÁTICA (HPI): PRESENTACIÓN DE UN CASO Y REVISIÓN DE LA LITERATURA
Autor: Ilse Contreras E, Rosa Andrade P
Publikováno v: Neumología Pediátrica, Vol 15, Iss 3, Pp 406-410 (2020)
Se presenta el caso de una lactante de un mes de edad, que se presentó en el Servicio de Urgencia con shock hipovolémico secundario a hemorragia pulmonar. Necesitó medidas de soporte vital, incluyendo drogas vasoactivas y pulsos de metilprednisolo
Externí odkaz: https://doaj.org/article/fe8cd56264a247ee8506b38c1c605cd1
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2
Akademický článek
E D I TO R I A L
Autor: Ilse Contreras
Publikováno v: Neumología Pediátrica, Vol 14, Iss 3 (2019)
N/A
Externí odkaz: https://doaj.org/article/240c3a8926c348dd9e24f114750aa552
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4
[Content validation for the Chilean population of the quality of life assessment instrument in children, adolescents and adults with Cystic Fibrosis: CFQ-R CYSTIC FIBROSIS QUESTIONNAIRE-REVISED version in Spanish, Chile]
Autor: Sandra, Navarro T, María L, Boza C, Yerko, Molina M, Viviana, Lezana S, Joel, Melo T, Leticia, Jakubson S, Jury, Hernández C, Hortensia, Barrientos I, Daniel, Zenteno A, Ilse, Contreras E
Publikováno v: Andes pediatrica : revista Chilena de pediatria. 93(3)
Cystic Fibrosis (CF) is the most frequent chronic hereditary disease in the white race. Although the impact on the quality of life of this disease is significant, there are no validated instruments in the Chilean population to measure it.To carry out
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1544e113129c23ff296c9553b60da31b
https://pubmed.ncbi.nlm.nih.gov/35857002
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6
Congenital Malformations of the Airway
Autor: Luis Enrique Vega-Briceño, Ilse Contreras Estay, Ignacio Sánchez
Publikováno v: Pediatric Respiratory Diseases ISBN: 9783030269609
Airway malformations include a wide range of conditions that generally manifest early in life. These malformations usually present with upper and lower airway obstruction symptoms, which fluctuate in their intensity depending on how serious is the co
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b4edb7be80a7f89f9a436fc18f8af293
https://doi.org/10.1007/978-3-030-26961-6_53
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7
Children with Recurrent Wheezing
Autor: Ilse Contreras Estay, Luis Enrique Vega-Briceño, Ignacio Sánchez
Publikováno v: Pediatric Respiratory Diseases ISBN: 9783030269609
Lower respiratory infections associated with wheezing are common among children under 3 years of age. They represent an important source of morbidity and high health care costs, including high levels of job absenteeism among parents or caregivers. It
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b94dcd846f4c47af8707089215ae5ccf
https://doi.org/10.1007/978-3-030-26961-6_22
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8
Valores espirométricos en niños y adolescentes chilenos sanos
Autor: Ignacio Sánchez, Luis Villarroel, Laura Fierro, N.L. Holmgren, Pablo Bertrand, Ilse Contreras, Solange Caussade
Publikováno v: Revista médica de Chile v.143 n.11 2015
SciELO Chile
CONICYT Chile
instacron:CONICYT
Background: Spirometric flow and volume measurement are essential to evaluate patients with pulmonary disease. In Chile, several reference equations are used. Aim: To measure flow and expiratory volumes in healthy children and adolescents and compare
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebe16aa8eb7dc6c3f933488d53bd4e62
https://doi.org/10.4067/s0034-98872015001100003
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9
Bone mineral density, lung function, vitamin D and body composition in children and adolescents with cystic fibrosis: a multicenter study
Autor: Paulina Bravo M., Sergio Gerardo Weisstaub, Paulina Balboa, Claudia Torrejón, Rodrigo Bozzo, María Lina Boza, Ilse Contreras, Pablo Jorquera, Luis Astorga
Publikováno v: Nutricion hospitalaria. 35(4)
Background: cystic fibrosis (CF) is the most common inherited disease in Caucasian population. Nowadays, long survival has led to the emergence of new complications, such as CF bone disease (CFBD), which is characterized by increased fracture risk. O
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d53da920ea3b7d7b64b343439d599bc7
https://pubmed.ncbi.nlm.nih.gov/30070865
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10
Expandiendo el espectro mutacional en pacientes chilenos con fibrosis quística
Autor: Ilse Contreras E, Marcos Vásquez D, Felipe Vial U, María Lina Boza C, Jaime Lozano C, Daniel Zenteno A, Guillermo Lay-Son R, María Gabriela Repetto L
Publikováno v: Revista chilena de enfermedades respiratorias v.28 n.2 2012
SciELO Chile
CONICYT Chile
instacron:CONICYT
Introducción: La fibrosis quística (FQ) es una enfermedad con herencia autosómica recesiva, que presenta una incidencia de 1 en 8.000 a 9.000 recién nacidos en Chile. A la fecha se han descrito más de 1.800 mutaciones diferentes en el gen CFTR.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae0e3a5b4bd1748a1e0a745d8ba75582
https://doi.org/10.4067/s0717-73482012000200003
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