Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Carolina Vilte"'
Autor:
Gaston Oscar Camino Willhuber, Mariana Bendersky, Carolina Vilte, Gonzalo Kido, Matias Pereira Duarte, Martin Estefan, Julio Bassani, Matias Petracchi, Marcelo Gruenberg, Carlos Sola
Publikováno v:
Revista de la Facultad de Ciencias Médicas de Córdoba, Vol 78, Iss 3 (2021)
Introduction: Percutaneous cement discoplasty is a minimally invasive procedure to treat low back pain due to advanced degenerative disc disease in elderly patients. Complications of this procedure has been described such as infection, vertebral frac
Externí odkaz:
https://doaj.org/article/c75157b8feab4abfa13f2725ee76f479
Autor:
Roberto Caraballo, Pablo Sebastian Fortini, Ricardo Cersósimo, Belen Ramirez, Carolina Vilte, Noelia Chamorro
Publikováno v:
Journal of Pediatric Epilepsy. :173-180
We present an update of a series of patients with myoclonic status in non-progressive encephalopaties (MSNPE) describing the electroclinical features and outcome. Between February 1, 1990 and June 30, 2011, 41 patients who met diagnostic criteria of
Publikováno v:
Journal of Pediatric Epilepsy. :181-188
Here we present an update of the electroclinical features and evolution of patients with epileptic spasms (ES) in clusters without hypsarrhythmia, with or without focal or generalized paroxysmal discharges on the interictal electroencephalography (EE
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
Autor:
Roberto Caraballo, Santiago Flesler, Sebastian Fortini, Carolina Vilte, María Constanza Pasteris, María Francisca Lopez Avaria
Publikováno v:
Epilepsia. 54:1605-1612
Summary Purpose Myoclonic epilepsy in infancy (MEI) is characterized by brief generalized myoclonic seizures associated with generalized spike-wave paroxysms without other seizure types occurring in the first 3 years of life in developmentally normal
Autor:
Eduardo Monese, Marcelo Bartuluchi, Ricardo Cersósimo, Soledad Monges, Roberto Caraballo, María Gomez, Carolina Vilte, María Celeste Buompadre, Sebastian Fortini, María Constanza Pasteris
Publikováno v:
Seizure. (5):360-367
Purpose The aim of this study is to analyze the electroclinical features, treatment, and evolution of patients with Rasmussen syndrome (RS). Materials and methods We conducted a retrospective, descriptive study in 32 consecutive patients with RS foll