Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Oscar Contreras-Olea"'
Autor:
Daniela Avila-Smirnow, Audrey Boutron, María de Los Ángeles Beytía-Reyes, Oscar Contreras-Olea, Alfredo Caicedo-Feijoo, Roger Gejman-Enríquez, Raúl Escobar-Henríquez, Jorge Förster-Mujica
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-4 (2018)
Abstract Background The myopathic form of carnitine palmitoyltransferase type II deficiency is an inherited autosomal recessive metabolic myopathy usually starting in childhood. Most reports have been on European and Japanese populations, and no Nati
Externí odkaz:
https://doaj.org/article/58ebe0076def48219906a1b34719a13b
Autor:
Oscar Contreras Olea, Víctor Dinamarca Ortiz, Vinicio Cervilla Oltremani, Cristian García Bruce
Publikováno v:
ARS Medica, Vol 27, Iss 1 (2018)
Externí odkaz:
https://doaj.org/article/27bb074d8af74010ab3f0e07e43ea757
Publikováno v:
ARS Medica, Vol 26, Iss 1 (2018)
SIn resumen
Externí odkaz:
https://doaj.org/article/08d83c02a4b649f994e4a5f67e1e884e
Autor:
Carola Goecke-Hochberger, Cecilia Mellado-Sagredo, Daniela Avila-Smirnow, Rosendo Lobo-Avilés, Hana Karime Rumié-Carmi, Oscar Contreras-Olea
Publikováno v:
Revista médica de Chile v.147 n.3 2019
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Fibrodysplasia ossificans progressiva (FOP) or myositis ossificans, is a genetic disease, with a prevalence of 1 in 2.000.000. It is caused by pathogenic variants in ACVR1 gene and characterized by soft tissue heterotopic ossification, starting in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5fd933bdd0fc320bd825bde887983a6
https://doi.org/10.4067/s0034-98872019000300384
https://doi.org/10.4067/s0034-98872019000300384
Autor:
Oscar Contreras-Olea, Daniela Avila-Smirnow, Jorge Förster-Mujica, Audrey Boutron, Roger Gejman-Enríquez, María de Los Angeles Beytía-Reyes, Alfredo Caicedo-Feijoo, Raúl Escobar-Henríquez
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-4 (2018)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background The myopathic form of carnitine palmitoyltransferase type II deficiency is an inherited autosomal recessive metabolic myopathy usually starting in childhood. Most reports have been on European and Japanese populations, and no Native South
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f48994154b694ef99882bc4fd3f1625
http://link.springer.com/article/10.1186/s13256-018-1702-3
http://link.springer.com/article/10.1186/s13256-018-1702-3
Publikováno v:
Revista médica de Chile v.145 n.6 2017
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
We report a 68 years old woman presenting with pain and swelling in her left elbow. An elbow magnetic resonance with gadolinium evidenced bone marrow infiltration and a bone infarct. Given these findings, a body CT scan was performed which showed mul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::331e2781d286db9a27d91db2e1010577
https://doi.org/10.4067/s0034-98872017000600795
https://doi.org/10.4067/s0034-98872017000600795
Autor:
Carlos, Jaque-Almendras, Raúl G, Escobar, Alfredo, Caicedo-Feijoo, María de Los Angeles, Beytía-Reyes, Sergio, Correa-Pérez, Roger, Gejman-Enríquez, Juan Pablo, Cruz-Quiroga, Oscar, Contreras-Olea, Daniela, Avila-Smirnow
Publikováno v:
Revista chilena de pediatria. 91(1)
Sciatic neuropathy is rare and difficult to diagnose in pediatrics, and its long-term course has not been completely understood.To analyze the clinical presentation and evolution of a group of pediatric patients with sciatic neuropathy.Retrospective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cb90f8449b20c6ef0f4d1fba77b15409
https://pubmed.ncbi.nlm.nih.gov/32730417
https://pubmed.ncbi.nlm.nih.gov/32730417
Autor:
Sergio Correa-Pérez, Oscar Contreras-Olea, María de Los Angeles Beytía-Reyes, Roger Gejman-Enríquez, Juan Pablo Cruz-Quiroga, Raul G. Escobar, Daniela Avila-Smirnow, Alfredo Caicedo-Feijoo, Carlos Jaque-Almendras
Publikováno v:
Revista chilena de pediatría v.91 n.1 2020
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Sciatic neuropathy is rare and difficult to diagnose in pediatrics, and its long-term course has not been completely understood. Objective: To analyze the clinical presentation and evolution of a group of pediatric patients with sciatic neuropathy. P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82dba30dac4299500f1256961591f35d
https://doi.org/10.32641/rchped.v91i1.1355
https://doi.org/10.32641/rchped.v91i1.1355
Autor:
Oscar, Contreras-Olea, Carola, Goecke-Hochberger, Hana Karime, Rumié-Carmi, Rosendo, Lobo-Avilés, Cecilia, Mellado-Sagredo, Daniela, Avila-Smirnow
Publikováno v:
Revista medica de Chile. 147(3)
Fibrodysplasia ossificans progressiva (FOP) or myositis ossificans, is a genetic disease, with a prevalence of 1 in 2.000.000. It is caused by pathogenic variants in ACVR1 gene and characterized by soft tissue heterotopic ossification, starting in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cf887dbb5094654bf74c9edd32c1f105
https://pubmed.ncbi.nlm.nih.gov/31344178
https://pubmed.ncbi.nlm.nih.gov/31344178
Publikováno v:
Revista medica de Chile. 145(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fbab8930e5f210bf860ceb12026be2f2
https://pubmed.ncbi.nlm.nih.gov/29171630
https://pubmed.ncbi.nlm.nih.gov/29171630