Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sebastián, Irarrázaval D"'
Autor:
María Jesús Lira S., Sebastián Irarrázaval D, Luis Irribarra T., Mauricio Campos D., Francisca González L., Pamela Mery I.
Publikováno v:
Revista médica de Chile v.146 n.11 2018
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Background: The high academic burden may hamper the quality of life of medical students. Aim: To evaluate the quality of life (QOL) for medical students attending a Chilean university. Material and Methods: Four hundred eleven medical students aged 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c5a062ef75e9c8128c264eb8c15d40e
https://doi.org/10.4067/s0034-98872018001101294
https://doi.org/10.4067/s0034-98872018001101294
Autor:
Luis, Irribarra T, Pamela, Mery I, María Jesús, Lira S, Mauricio, Campos D, Francisca, González L, Sebastián, Irarrázaval D
Publikováno v:
Revista medica de Chile. 146(11)
The high academic burden may hamper the quality of life of medical students.To evaluate the quality of life (QOL) for medical students attending a Chilean university.Four hundred eleven medical students aged 22 ± 2 years (51% women), studying in San
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0feef8ce723e7c48c9a2e0447f30efbd
https://pubmed.ncbi.nlm.nih.gov/30725043
https://pubmed.ncbi.nlm.nih.gov/30725043
Publikováno v:
Revista médica de Chile v.137 n.6 2009
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Cerebrotendinous xanthomatosis is an inherited autosomal recessive disease caused by a mutation in the gene for the sterol 27-hydroxylase enzyme, which determines the accumulation of plasmatic cholestanol in various tissues. The natural history of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af146b7a5d473f667148b99eb7821863
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872009000600013
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872009000600013
Autor:
Verónica Campos L, Raúl Escobar H, Marta Hernández Ch, Sebastián Irarrázaval D, Tomás Mesa L, María Ester Pizarro G
Publikováno v:
Revista chilena de pediatría v.77 n.1 2006
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Background: Horner syndrome (HS) or oculosympathetic paresis is caused by the interruption of the sympathetic nervous pathway at any point from the brain to the eye. Clinical signs include miosis, upper lid ptosis, anhydrosis of the face, enophtalmus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26389d70b9f3545ca90366a09f28dd9d
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062006000100010
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062006000100010