Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ernesto Portuondo"'
Autor:
Barbarrosa, Ernesto Portuondo1 ernestopb@infomed.sld.cu, de la Caridad Pérez Ferrer, Iraida1 ernestopb@infomed.sld.cu, Tovani-Palone, Marcos Roberto2 marcos_palone@hotmail.com
Publikováno v:
Electronic Journal of General Medicine. 2020, Vol. 17 Issue 2, p1-10. 10p.
Autor:
Ernesto Portuondo Barbarrosa, Diana Patricia Durán Casal, Telmah Luz Carrillo Alfonso, Yanae Gonzales Aquino
Publikováno v:
Revista Cubana de Pediatría, Vol 93, Iss 3 (2021)
RESUMEN Introducción: El síndrome de Lowe o síndrome oculocerebrorenal es un trastorno multisistémico. Es una enfermedad rara e infrecuente. Objetivo: Exponer un caso clínico típico, con fracaso renal controlado sin método dialítico y que de
Autor:
Marcos Roberto Tovani-Palone, Iraida de la Caridad Pérez Ferrer, Ernesto Portuondo Barbarrosa
Publikováno v:
Electronic Journal of General Medicine. 17:em190
Introduction: West syndrome (WS) is the most severe, devastating and/or catastrophic epileptic encephalopathy during the lactation period. However, until now, there are few comprehensive clinical studies in this regard in Cuba. Objective: To identify
Publikováno v:
Journal of Pediatric Epilepsy. :059-063
Neurofibromatosis type 1 (NF1) is the most common neurocutaneous disease. The NF1 gene is located on chromosome 17q11.2 and codes for a large tumor suppressor protein, called neurofibromin. The prevalence is around 1 in 3,000 individuals, and it is i
Publikováno v:
Epileptic Disorders. 17:143-149
To present a retrospective study of nine children with Panayiotopoulos syndrome associated with diffuse spikes and waves as the sole EEG manifestation at onset. Charts of children with typical clinical criteria of Panayiotopoulos syndrome, electrocli
Autor:
Luciana Caramuta, Santiago Flesler, María Constanza Pasteris, Ernesto Portuondo, Roberto Caraballo, Sebastian Fortini
Publikováno v:
Seizure. 25:117-125
Purpose To retrospectively analyze the electroclinical characteristics, etiology, treatment, and prognosis of patients with epileptic encephalopathy with status epilepticus during sleep (ESES) with unusual EEG features and to corroborate if this seri
Publikováno v:
Seizure. 23(10):899-902
Purpose We present six patients with epilepsy of infancy with migrating focal seizures (EIMFS) and provide a comprehensive evaluation of potassium bromide therapy. Method Between February 1, 2007 and July 31, 2012, six patients who met the diagnostic
Autor:
Barbarrosa, Ernesto Portuondo1 ernestopb@infomed.sld.cu
Publikováno v:
Revista Cubana de Neurología y Neurocirugía. 2012, Vol. 2 Issue 2, p121-128. 8p.
Autor:
Ernesto Portuondo Barbarrosa
Publikováno v:
Revista Cubana de Pediatría, Vol 88, Iss 4, Pp 428-440
Autor:
Ernesto Portuondo Barbarrosa, Pilar Maria Acuña Guilarte, Estela Morales Peralta, Yanae Gonzales Aquino, Maria Caridad Rigautdi
Publikováno v:
Revista Cubana de Pediatría
RESUMEN Introducción: El síndrome de Proteus es un raro síndrome hamartomoso congenito con manifestaciones neuroectodérmicas, de carácter progresivo y grado de severidad variable. Objetivo: Presentar un caso clínico donde se combinan dismorfias
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::16435f18a1f9bba7153c89c102164d0b
http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S0034-75312019000400011&tlng=es
http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S0034-75312019000400011&tlng=es