Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Luis Muñoz Rodríguez"'
Autor:
José Antonio Franco-Hernández, Luis Muñoz Rodríguez, Pilar Jubera Ortiz de Landázuri, Alejandra García Hernández
Publikováno v:
Brazilian Journal of Anesthesiology, Vol 63, Iss 1, Pp 113-115 (2013)
Content: : Strumpell-Lorrain disease - or familial spastic paraplegia (FSP) - is a rare hereditary neurological disorder, mainly characterized by variable degrees of stiffness and weakening of the muscles, with cognitive impairment, deafness, and ata
Externí odkaz:
https://doaj.org/article/f01db5327b994282b7d77a2659386d2f
Autor:
Luis Muñoz Rodríguez, José Antonio Franco-Hernández, Pilar Jubera Ortiz de Landázuri, Alejandra García Hernández
Publikováno v:
Revista Brasileira de Anestesiologia, Vol 63, Iss 1, Pp 116-118 (2013)
CONTEÚDO: A doença de Strumpell-Lorrain, ou paraparesia espástica familiar (PEF), é uma doença hereditária neurológica rara, caracterizada principalmente por graus variáveis de rigidez e enfraquecimento dos músculos, com comprometimento cogn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::573845304396002a1ef27289fec727f5
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0034-70942013000100010&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0034-70942013000100010&lng=en&tlng=en
Autor:
Alejandra García Hernández, José Antonio Franco-Hernández, Pilar Jubera Ortiz de Landázuri, Luis Muñoz Rodríguez
Publikováno v:
Brazilian Journal of Anesthesiology (Edicion en Espanol). 63(1):113-115
Resumen Contenido: La enfermedad de Strumpell-Lorrain, o paraparesia espastica familiar (PEF), es una enfermedad hereditaria neurologica rara, caracterizada principalmente por grados variables de rigidez y debilitamiento de los musculos, con el compr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd7d89aec9cc19a17fbd2719e7e87cde
Autor:
José Antonio Franco-Hernández, Pilar Jubera Ortiz de Landázuri, Alejandra García Hernández, Luis Muñoz Rodríguez
Publikováno v:
Brazilian Journal of Anesthesiology, Vol 63, Iss 1, Pp 113-115 (2013)
Content: : Strumpell-Lorrain disease - or familial spastic paraplegia (FSP) - is a rare hereditary neurological disorder, mainly characterized by variable degrees of stiffness and weakening of the muscles, with cognitive impairment, deafness, and ata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::387d75db03ef83d121e84bf804d41e81
https://pubmed.ncbi.nlm.nih.gov/24565095
https://pubmed.ncbi.nlm.nih.gov/24565095
Autor:
José Antonio Franco-Hernández, Luis Munoz Rodríguez, Pilar Jubera Ortiz de Landázuri, Alejandra Garcia Hernández
Publikováno v:
Revista Brasileira de Anestesiologia, Vol 63, Iss 1, Pp 116-118 (2013)
CONTEÚDO: A doença de Strumpell-Lorrain, ou paraparesia espástica familiar (PEF), é uma doença hereditária neurológica rara, caracterizada principalmente por graus variáveis de rigidez e enfraquecimento dos músculos, com comprometimento cogn
Externí odkaz:
https://doaj.org/article/95b6569c89a54bfe91679194706b64f2