Zobrazeno 1 - 10
of 15
pro vyhledávání: '"María Celeste Buompadre"'
Autor:
María Celeste Buompadre
Publikováno v:
Medicina (Buenos Aires), Vol 79, Iss Suppl 3, Pp 37-41 (2019)
Around 15% of childhood epilepsies are resistant to antiepileptic drugs, 40% of which are caused by malformations of cortical development (MCD). The current classification scheme for MCD is based on the primary developmental steps of cell proliferati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b1276f05e635120168f76f34a95ac55b
https://pubmed.ncbi.nlm.nih.gov/31603842
https://pubmed.ncbi.nlm.nih.gov/31603842
Autor:
María Celeste, Buompadre
Publikováno v:
Medicina. 78
Status epilepticus (SE) is one of the most common neurologic emergencies in pediatrics. It is a condition resulting either from the failure of the mechanisms responsible for seizure termination or from the initiation of mechanisms, which leads to abn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0e7377b457ea91f48c4c861894a08b0c
https://pubmed.ncbi.nlm.nih.gov/30199359
https://pubmed.ncbi.nlm.nih.gov/30199359
Publikováno v:
Journal of Pediatric Neurology. :089-093
X-linked infantile spasms associated with mental retardation have been recognized as a syndrome with an identified gene: ARX. We report a family with eight affected males. Mental retardation was present in all, seven also had epilepsy. In the index c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8867f2fca6619a3f36fd2970a2a1c652
https://doi.org/10.1055/s-0035-1557251
https://doi.org/10.1055/s-0035-1557251
Autor:
Ricardo Cersósimo, Roberto Caraballo, Lorena Ornella, Natalio Fejerman, Juan P. Princich, Pablo Sebastian Fortini, Carolina Vilte, María Celeste Buompadre
Publikováno v:
Epileptic Disorders. 15:417-427
Aim. We retrospectively analysed the electroclinical features, treatment, and outcome in patients with unilateral polymicrogyria (PMG), focussing on epileptic syndrome with or without encephalopathy, with status epilepticus during sleep (ESES) or con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bdc254decc955b7d1eb6cea129e3ccb
https://doi.org/10.1684/epd.2013.0612
https://doi.org/10.1684/epd.2013.0612
Autor:
Mariana Gonzalez, Ricardo Cersósimo, María Francisca Lopez Avaria, Gabriela Reyes, Sebastian Fortini, María Celeste Buompadre, Roberto Caraballo
Publikováno v:
Seizure. 22(7):553-559
Purpose To analyze the electroclinical features, neuroimaging findings, treatment, and outcome of 12 patients with febrile infection-related epilepsy syndrome (FIRES). Methods This is a retrospective study of 12 children with FIRES with a mean time o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bc410bb0dea3dd93f848e5a7b015f1a
Autor:
María Celeste Buompadre
Publikováno v:
Medicina (Buenos Aires), Vol 73, Iss suppl 1, Pp 49-54 (2013)
Las ataxias crónicas cerebelosas autosómicas recesivas constituyen el grupo más amplio de ataxias hereditarias, con presentación principalmente en la edad pediátrica, se caracterizan por degeneración o desarrollo anormal del cerebelo y de la m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::4f238d572a604d22774ab3e336d24f9a
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802013000500008&lng=en&tlng=en
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802013000500008&lng=en&tlng=en
Autor:
Roberto Caraballo, Nidia Escobal, Ariela Agustinho, Araceli Cresta, Santiago Flesler, Sebastian Fortini, Graciela Mestre, Marisa Armeno, María Celeste Buompadre
Publikováno v:
Epilepsy research. 108(10)
The ketogenic diet (KD) has been used as an alternative treatment for patients with refractory status epilepticus (SE).In this retrospective study we assess the efficacy and tolerability of the KD in patients with refractory SE.Between March 1, 2010
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f2a25064f10e2c4a5e13f08ad64ede6
https://pubmed.ncbi.nlm.nih.gov/25454503
https://pubmed.ncbi.nlm.nih.gov/25454503
Publikováno v:
Journal of Child Neurology. 23:121-123
This article describes an 11-year-old girl with a diagnosis of Ebstein's anomaly. Glenn and Fontan surgeries were performed successfully. She had a generalized tonic-clonic seizure after peripheral intravenous infusion under pressure. A computed tomo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76e5cc610d352abb805c7aefc53f2910
https://doi.org/10.1177/0883073807308696
https://doi.org/10.1177/0883073807308696
Autor:
María Celeste, Buompadre
Publikováno v:
Medicina. 73
Autosomal recessive cerebellar ataxias belong to a broader group of disorders known as inherited ataxias. In most cases onset occurs before the age of 20. These neurological disorders are characterized by degeneration or abnormal development of the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::39ad764815b48bae6649cbdc2439daf9
https://pubmed.ncbi.nlm.nih.gov/24072051
https://pubmed.ncbi.nlm.nih.gov/24072051
Autor:
María Celeste, Buompadre
Publikováno v:
Revista de neurologia. 57
Functional impairment of the optic nerve is characterized by visual loss, dyschromatopsia, visual field defects, relative afferent pupillary defect, and swelling or atrophy of the optic nerve.To describe the spectrum of acute optic neuropathies, focu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c427269c0b0bcbbd33e1e9c461595c4c
https://pubmed.ncbi.nlm.nih.gov/23897141
https://pubmed.ncbi.nlm.nih.gov/23897141