Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Roger Gejman-Enríquez"'
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:
Luis Martí-Bonmatí, Roger Gejman-Enríquez, Ulises Guajardo-Hernández, David Rojas-Zalazar, Federico Geisse-Martínez
Publikováno v:
International Journal of Morphology v.39 n.2 2021
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
RESUMEN: La clasificación de los Tumores Primarios del Sistema Nervioso Central (SNC) tiene su origen en la descripción morfológica, cuyo análisis histopatológico ha permitido identificar la línea celular involucrada en estos tumores y obtener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7698ff1fcbe24f82a22fd7e9203f742
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022021000200601
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022021000200601
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
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