Zobrazeno 1 - 10
of 119
pro vyhledávání: '"Verdugo Renato"'
Autor:
Matamala, José Manuel, Arias-Carrasco, Raul, Sanchez, Carolina, Uhrig, Markus, Bargsted, Leslie, Matus, Soledad, Maracaja-Coutinho, Vinicius, Abarzua, Sebastian, van Zundert, Brigitte, Verdugo, Renato, Manque, Patricio, Hetz, Claudio
Publikováno v:
In Neurobiology of Aging April 2018 64:123-138
Autor:
Pérez-Sanagustín, Mar, Parra, Denis, Verdugo, Renato, García-Galleguillos, Gonzalo, Nussbaum, Miguel
Publikováno v:
In Computers in Human Behavior July 2016 60:73-85
Autor:
Brito, Alex, Verdugo, Renato, Hertrampf, Eva, Miller, Joshua W, Green, Ralph, Fedosov, Sergey N, Shahab-Ferdows, Setareh, Sanchez, Hugo, Albala, Cecilia, Castillo, Jose L, Matamala, Jose M, Uauy, Ricardo, Allen, Lindsay H *
Publikováno v:
In The American Journal of Clinical Nutrition January 2016 103(1):250-257
Autor:
Cordero, Kristina, Nussbaum, Miguel, Ibaseta, Valentina, Otaíza, María José, Gleisner, Samuel, González, Sebastián, Rodríguez-Montero, Werner, Strasser, Katherine, Verdugo, Renato, Ugarte, Andrés, Chiuminatto, Pablo, Carland, Corinne
Publikováno v:
In Computers & Education March 2015 82:486-496
Akademický článek
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Autor:
Shefner, Jeremy M., Al-Chalabi, Ammar, Baker, Mark R., Cui, Li-Ying, de Carvalho, Mamede, Eisen, Andrew, Grosskreutz, Julian, Hardiman, Orla, Henderson, Robert, Matamala, Jose Manuel, Mitsumoto, Hiroshi, Paulus, Walter, Simon, Neil, Swash, Michael, Talbot, Kevin, Turner, Martin R., Ugawa, Yoshikazu, van den Berg, Leonard H., Verdugo, Renato, Vucic, Steven, Kaji, Ryuji, Burke, David, Kiernan, Matthew C.
Publikováno v:
In Clinical Neurophysiology August 2020 131(8):1975-1978
Autor:
Acosta,Ignacio, Matamala,José Manuel, Jara,Paula, Pino,Francisca, Gallardo,Alejandra, Verdugo,Renato
Publikováno v:
Revista médica de Chile v.147 n.3 2019
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Idiopathic inflammatory myopathies (IIM) are a heterogeneous group of acquired immune-mediated diseases, which typically involve the striated muscle with a variable involvement of the skin and other organs. Clinically, they are characterized by proxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::369ec158dba20813701dc2d4841b2288
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019000300342
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019000300342
Autor:
Acosta, Ignacio, Matamala, José Manuel, Jara, Paula, Pino, Francisca, Gallardo, Alejandra, Verdugo, Renato
Publikováno v:
Revista médica de Chile, Volume: 147, Issue: 3, Pages: 342-355, Published: MAR 2019
Idiopathic inflammatory myopathies (IIM) are a heterogeneous group of acquired immune-mediated diseases, which typically involve the striated muscle with a variable involvement of the skin and other organs. Clinically, they are characterized by proxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______614::369ec158dba20813701dc2d4841b2288
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019000300342&lng=en&tlng=en
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019000300342&lng=en&tlng=en
Publikováno v:
Revista médica de Chile v.146 n.9 2018
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Fabry's disease is an X-linked multisistemic lisosomal storage disorder caused by deficiency or absence in α-Galatosidase A. Symptoms develop early in childhood with small fiber neuropathy, autonomic disorders and skin lesions (angiokeratomas). More
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::89f5ea10d418c790878ec3b149f49084
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872018000901079
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872018000901079
Publikováno v:
Revista médica de Chile, Volume: 146, Issue: 9, Pages: 1079-1084, Published: SEP 2018
Fabry's disease is an X-linked multisistemic lisosomal storage disorder caused by deficiency or absence in α-Galatosidase A. Symptoms develop early in childhood with small fiber neuropathy, autonomic disorders and skin lesions (angiokeratomas). More
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______614::89f5ea10d418c790878ec3b149f49084
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872018000901079&lng=en&tlng=en
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872018000901079&lng=en&tlng=en