Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Laura, Díaz Ruiz"'
Autor:
Ana Martínez de Aragón, Sylvia Belda Hofheinz, Enrique Salcedo Lobato, Sara Vila Bedmar, Enrique Medina Benítez, Ana Camacho Salas, Laura Díaz Ruiz
Publikováno v:
Neurology Perspectives. 2:26-33
Introduction Liver transplantation is the only curative treatment for patients with end-stage liver disease. Neurological complications are one of the main causes of morbidity and mortality. Objective To study neurological complications after liver t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67b0a20701aef3399a02828c13e34aed
https://doi.org/10.1016/j.neurop.2021.10.007
https://doi.org/10.1016/j.neurop.2021.10.007
Publikováno v:
J Pediatr Intensive Care
Neurogenic stunned myocardium is described as sudden and reversible cardiac dysfunction induced by an acute neurological event. This phenomenon has not been thoroughly investigated in infants, and is probably underdiagnosed. Here, we report the cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6a1d637c443dfd744cb49e0f6ed470a
https://doi.org/10.1055/s-0039-1693032
https://doi.org/10.1055/s-0039-1693032
Autor:
Ana Barceló Mendiguchía, Elena Bergón Sendín, Pilar Tejada Palacios, Laura Díaz Ruiz, Felisa Vázquez Gómez
Publikováno v:
Archivos Argentinos de Pediatria. 117
Incontinentia pigmenti is a rare neurocutaneous disorder with a frequency of 1 in 40,000 newborn; it is associated with mutations in IKBKG gene in Xq28, inherited as an X-linked dominant trait. Clinical manifestations detected since the newborn perio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e66969b8a2118dabf5d93939971742f5
https://doi.org/10.5546/aap.2019.e252
https://doi.org/10.5546/aap.2019.e252
Autor:
Felisa, Vázquez Gómez, Laura, Díaz Ruiz, Elena, Bergón Sendín, Ana, Barceló Mendiguchía, Pilar, Tejada Palacios
Publikováno v:
Archivos argentinos de pediatria. 117(3)
Incontinentia pigmenti is a rare neurocutaneous disorder with a frequency of 1 in 40,000 newborn; it is associated with mutations in IKBKG gene in Xq28, inherited as an X-linked dominant trait. Clinical manifestations detected since the newborn perio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b785ab5f1b58bc8a85c09fe62fca1af4
https://pubmed.ncbi.nlm.nih.gov/31063312
https://pubmed.ncbi.nlm.nih.gov/31063312