Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Essam Al Shail"'
Publikováno v:
Case Reports in Neurological Medicine, Vol 2013 (2013)
The ventriculoperitoneal (VP) shunt is a common procedure in pediatric neurosurgery that carries a risk of complications at cranial and abdominal sites. We report on the case of a child with shunt infection and malfunction. The peritoneal catheter wa
Externí odkaz:
https://doaj.org/article/991144bf6cc944fbb6eb43b4d982cd56
Publikováno v:
Case Reports in Oncological Medicine, Vol 2012 (2012)
Turcot syndrome (TS) is a rare hereditary disorder clinically characterized by the occurrence of primary tumors of the colon and the central nervous system (CNS). Here we present the case of an 11-year-old boy with a synchronous clinical presentation
Externí odkaz:
https://doaj.org/article/f06f3f758a7140dd9602dd35987e368d
Publikováno v:
European Journal of Ophthalmology. 32:2604-2614
Publikováno v:
Child's Nervous System. 36:297-304
Craniopharyngiomas are benign tumors of central nervous system which are known to affect both adults and children. Despite their benign origin, the recurrence is still one of the main postoperative challenges. The aim of this study was to investigate
Publikováno v:
Pediatric Neurosurgery. 54:399-404
Pilomyxoid astrocytoma (PMA) is a rare brain tumour generally located in the chiasmatic-hypothalamic region. In comparison to pilocytic astrocytoma, PMA has distinct histopathological features, aggressive clinical behaviour, a high recurrence rate, a
Central nervous system and spinal tuberculosis in children at a tertiary care center in Saudi Arabia
Publikováno v:
Annals of Saudi Medicine, Vol 33, Iss 1, Pp 6-9 (2013)
BACKGROUND AND OBJECTIVES: Tuberculosis (TB) remains a global health problem. There is limited data on pediatric central nervous system tuberculosis (CNSTB) in Saudi Arabia on diagnosis and therapy. DESIGN AND SETTING: Retrospective review of health
Publikováno v:
Case Reports in Oncological Medicine
Case Reports in Oncological Medicine, Vol 2012 (2012)
Case Reports in Oncological Medicine, Vol 2012 (2012)
Turcot syndrome (TS) is a rare hereditary disorder clinically characterized by the occurrence of primary tumors of the colon and the central nervous system (CNS). Here we present the case of an 11-year-old boy with a synchronous clinical presentation
Publikováno v:
Clinical Dysmorphology. 17:165-168
The authors report here a 3-year-old boy with localized absence of calvarial bones (partial acalvaria/hypocalvaria), associated with unique sagittal calcified bone and craniosynostosis. This major skull deformation led to a prominent protrusion of th
Autor:
Don Liu, Essam Al Shail
Publikováno v:
Ophthalmology. 109:393-399
Objective To emphasize the potential complications of a retained orbital wooden foreign body (WFB) and the rationale of a surgical technique. Design Two interventional case reports. Participants Two patients sustained an orbital WFB injury. Both pati