Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pedro Neves Fortunato"'
Publikováno v:
Brazilian Neurosurgery, Vol 43, Iss 03, Pp e212-e216 (2024)
Patients who are victims of traumatic injuries in the spine are evaluated by radiological protocols, as recommended by Advanced Trauma Life Support (ATLS), including a computed tomography (CT) scan with the patient in the decubitus position. Spine fr
Externí odkaz:
https://doaj.org/article/0370615b24e04e2e9e0ae02f4a700f38
Autor:
Pedro Neves Fortunato, Danilo Takashi Yoshimatsu Ueno, Mariana Suemi Sukessada, Gabriel Santaterra Barros, João Fernando Cloclet Pio da Silva, Bruna Franchito Freire, Daniela Alves Gulhote, Ana Beatriz Barbosa Piffer, Hilton Mariano da Silva Junior
Publikováno v:
Headache Medicine. 13:280-286
O seio cavernoso é um plexo venoso localizado na base do crânio. Várias patologias, como processos inflamatórios, aneurismáticos ou metastáticos, podem afetar esse plexo. A síndrome do seio cavernoso ocorre quando os nervos estão envolvidos n
Publikováno v:
Thrombosis Research. 213:125-127
Autor:
Daniela Alves Gulhote, Gabriel Santaterra Barros, Mariana Suemi Sukessada, Ana Beatriz Barbosa Piffer, João Fernando Coclet Pio da Silva, Pedro Neves Fortunato, Danilo Takashi Yoshimatsu Ueno, Bruna Franchito Freire, Hilton Mariano da Silva Junior
Publikováno v:
São Paulo Medical Journal.
Context: Intracranial tumor spread is an infrequent and late manifestation of head and neck cancers. We report three cases of painful ophthalmoplegia due to larynx and parotid neoplastic involvement. Data disclosure was authorized by the patients thr
Publikováno v:
São Paulo Medical Journal.
Context: Ramsay Hunt syndrome is a condition caused by the Varicella-Zoster Virus in the geniculate ganglion and leads to peripheral facial nerve palsy and erythematous vesicular rash in the affected area. It is a rare disorder but is the second most
Autor:
Pedro Neves Fortunato, Hilton Mariano da Silva Júnior, Rosana Carandina Maffeis, Caroline Moraes Tapajós Bolzani
Publikováno v:
São Paulo Medical Journal.
Context: Creutzfeldt-Jakob disease (CJD) is a rapidly progressive neurodegenerative disease. Heidenhain’s variant has isolated visual symptoms that persist even without any cognitive decline for a few weeks. Objective: To report a case of the Heide