Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Jose Roberto Tude Melo"'
Publikováno v:
Archives of Pediatric Neurosurgery, Vol 5, Iss 2, Pp e1882023-e1882023 (2023)
Objective: Interhemispheric arachnoid cysts (IHACs) are a rare congenital malformation arising from the duplication of the arachnoid membrane of the cerebral meninges associated with malformations of the corpus callosum. The scope of this study is to
Externí odkaz:
https://doaj.org/article/9d5648dd6ae743269be92c1dbda7013a
Publikováno v:
Archives of Pediatric Neurosurgery, Vol 3, Iss 3(September-December) (2021)
Introduction: Prognostic models are statistical models that combine two or more items of patient data to predict clinical outcomes. Objective: Identify prognostic models of mortality developed and published in the medical literature for possible ap
Externí odkaz:
https://doaj.org/article/0968c3faef6c4541a992eb29548a39a4
Autor:
Jose Roberto Tude Melo, Felipe Reynan Paiva Vieira Santos, Igor Campos da Silva, José Henrique Silva Barreto
Publikováno v:
Archives of Pediatric Neurosurgery, Vol 3, Iss 2(May-August), Pp e662021-e662021 (2021)
Introduction: the best therapeutic option for the management of craniopharyngioma in younger children remains controversial, ranging from complete surgical resection, partial surgical resection associated with radiotherapy and application of chemothe
Externí odkaz:
https://doaj.org/article/eb05f38528364cf0bd1db882e1b523e0
Autor:
Matheus Fernando Manzolli Ballestero, Alexandre Casagrande Canheu, Alexandre Varella Giannetti, Aline Saré de Melo, Angelo Raimundo da Silva, Artur Henrique Galvão Bruno da Cunha, Carlos Umberto Pereira, Eduardo Jucá, Jose Roberto Tude Melo, Leopoldo Mandic Furtado, Luciano Lopes Furlanetti, Marcelo Volpon Santos, Marcos Devanir Silva da Costa, Patricia Alessandra Dastoli, Paulo Ronaldo Jubé Ribeiro, Ricardo de Amoreira Gepp, Ricardo Santos de Oliveira, Roberto Alexandre Dezena, Sergio Cavalheiro, Simone Mendes Rogerio, Tatiana Protzenko
Publikováno v:
Archives of Pediatric Neurosurgery, Vol 2, Iss 3(September-December), Pp e672020-e672020 (2020)
A scientific journal’s greatest responsibility is to ensure that all contributions accepted for publications are rigorously but fairly reviewed. The Editor-in-Chief and Archives of Pediatric Neurosurgery gratefully acknowledge the qualified and reg
Externí odkaz:
https://doaj.org/article/24a2a714bed647c7b979888e12fc1909
Autor:
Jose Roberto Tude Melo, Pollyana Pacheco, Emília Nunes de Melo, Ângela Vasconcellos, Rosane Klein Passos
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 73, Iss 9, Pp 759-763 (2015)
Objective Hydrocephalus is one of the main complications associated with myelomeningocele (MM). This study aimed to identify clinical and ultrasonographic criteria for using ventriculoperitoneal (VP) shunts in this group of patients.Method A retrospe
Externí odkaz:
https://doaj.org/article/1f19982021844fff87059a38fc74b361
Publikováno v:
Case Reports in Pediatrics, Vol 2013 (2013)
Human tail and multiple spinal dysraphism are unusual congenital malformations. Human tail appeared as a prominent lesion from the lumbosacrococcygeal region, generally without connection between the tail and the neurospinal axis. Spinal dysraphisms
Externí odkaz:
https://doaj.org/article/6eeb026864a44de9a29433087e89e33f
Autor:
Jose Roberto Tude Melo, Emanoel Pires de Lima, Lucas Chaves Lelis, Caio Sander Andrade Portella Junior
Publikováno v:
Pediatric neurosurgery. 49(4)
Background: Resulting from an early fusion of the sagittal suture, scaphocephaly (SC) is the most frequent form of all craniosynostosis and represents 40-60% of all cases. The scope of this study is to describe the first series of Renier's ‘H' tech
Autor:
Caio Nogueira Lessa, Paulo Roberto Tavares Gomes Filho, Jose Roberto Tude Melo, es de Azevedo, Kleber Pimentel Santos, Gilvan da Silva Figueiredo, Vera Lucia Fern
Publikováno v:
Journal of Neurological Disorders.
The myelomeningocele (MMC) is a failure in embryo development during the fourth week of gestation, being the most common form of spinal dysraphism characterized by a protrusion of the meninges, roots and spinal cord by a bony midline defect [1,2]. Th
Publikováno v:
Pediatrics Week; 6/25/2024, p415-415, 1p