Zobrazeno 1 - 10 of 17 pro vyhledávání: '"Agustin, Calvo"'
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Akademický článek
Nota biobibliográfica + poética + creaciones («El amigo yanki», «Pedraforca» y «Homenajes cardinales» [«Homenaje a Blas de Otero», «Homenaje a Cernuda», «Homenaje a J. V. Foix» y «Homenaje a Pessoa»]) + cuestionario (Victoria Pineda)
Autor: Agustin Calvo Galán
Publikováno v: Tintas : Quaderni di Letterature Iberiche e Iberoamericane, Vol 0, Iss 0, Pp 375-390 (2014)
Nota biobibliográfica + poética + creaciones («El amigo yanki», «Pedraforca» y «Homenajes cardinales» [«Homenaje a Blas de Otero», «Homenaje a Cernuda», «Homenaje a J. V. Foix» y «Homenaje a Pessoa»]) + cuestionario (Victoria Pineda)
Externí odkaz: https://doaj.org/article/ffe57f8524914c11b5adbf99579c2c88
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4
Vitamin B12 Deficiency and West Syndrome: An Uncommon but Preventable Cause of Neurological Disorder. Report on Three Cases, One of Them with Late Onset during Vitamin B12 Treatment
Autor: Filippo Greco, Roberto Caraballo, Agustina Crespo, Raffaele Falsaperla, Federica Sullo, Piero Pavone, Agustin Calvo
Publikováno v: Neuropediatrics. 52(4)
Vitamin B12 is a water-soluble vitamin that plays a fundamental role as an essential cofactor for two enzymes responsible for the production of succinyl-CoA and methionine. Vitamin B12 deficiency can occur in infants and may be related to the breastf
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beacd768fab164cbfeb81033a39879cc
https://pubmed.ncbi.nlm.nih.gov/33657632
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5
Vigabatrin-associated brain abnormalities on MRI and other neurological symptoms in patients with West syndrome
Autor: Gabriela, Reyes Valenzuela, Agustina, Crespo, Juan, Princich, Lorena, Fassulo, Marco, Semprino, Adolfo, Gallo, Carlos, Rugilo, Juan, Pociecha, Agustin, Calvo, Roberto H, Caraballo
Publikováno v: Epilepsy & Behavior. 129:108606
Report a series of children with West syndrome (WS) treated with vigabatrin (VGB) who developed characteristic MRI alterations. In the majority, these adverse events were asymptomatic; however, some of the patients developed movement disorders and ac
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8def271a0e77d4ca3f773e185ed86851
https://doi.org/10.1016/j.yebeh.2022.108606
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8
Rasmussen syndrome: absence seizures may be induced by oxcarbazepine
Autor: Roberto H, Caraballo, Pedro, Cachia, Gabriela Reyes, Valenzuela, Agustin, Calvo
Publikováno v: Epileptic disorders : international epilepsy journal with videotape. 21(1)
A female patient with electroclinical and neuroradiological features compatible with Rasmussen syndrome developed a particular clinical and EEG pattern. As the seizures were refractory to valproate at 750 mg/kg/day, oxcarbazepine (OXC) at 30 mg/kg/da
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0865576d515dfa44ef35324a9c5eb25c
https://pubmed.ncbi.nlm.nih.gov/30767898
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9
Childhood-only epilepsy with generalized tonic-clonic seizures: A well-defined epileptic syndrome
Autor: Ricardo Caballero, Lucas Beltran, Agustin Calvo, Sebastián Silva, Roberto Caraballo
Publikováno v: Epilepsy research. 153
Purpose The aim of this study was to analyze patients whose only manifestation of epilepsy were generalized tonic-clonic seizures (GTCS) during childhood and discuss its validity as separate syndrome of childhood. Methods We included children with at
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab744734a9b68113eda1ca5c2dbdf3d8
https://pubmed.ncbi.nlm.nih.gov/30947078
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