Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Essam Alshail"'
Autor:
Essam AlShail, Ahmed Nasser Alahmari, Anas A. M. Dababo, Maysoon Alsagob, Hindi Al-Hindi, Hala Khalil, Zainab Al Masseri, Razan AlSalamah, Ethar Almohseny, Amjad Alduhaish, Dilek Colak, Namik Kaya
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundPilocytic Astrocytoma (PA) is the most common pediatric brain tumors. PAs are slow-growing tumors with high survival rates. However, a distinct subgroup of tumors defined as pilomyxoid astrocytoma (PMA) presents unique histological characte
Externí odkaz:
https://doaj.org/article/f08c13456b47460f9df6317b98917202
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
Externí odkaz:
https://doaj.org/article/5f6774e39da345ee820cd70ca81934c3
Publikováno v:
Cureus.
Publikováno v:
Neurosciences
Angiocentric glioma is a rare brain tumor commonly found in frontal or temporal lobes. It has a benign course, and surgical resection can be curative. Brainstem location is extremely rare, with only six cases reported so far in the literature. In the
Publikováno v:
Neurosciences
Subependymal giant cell astrocytoma is a benign WHO grade I intraventricular tumor arise in patients with tuberous sclerosis complex. Previous reported described histopathological predictors of more aggressive forms, terms atypical SEGA in infantile
Publikováno v:
Neuro-Oncology. 23:i42-i42
Chordomas are rare tumors believed to be originated from notochordal remnants. Of all intracranial neoplasms, the incidence of cranial chordomas is less than 1%1. The youngest patient with an intracranial chordoma reported in the literature was a new
Publikováno v:
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics and Adolescent Medicine, Vol 8, Iss 3, Pp 154-159 (2021)
International Journal of Pediatrics and Adolescent Medicine, Vol 8, Iss 3, Pp 154-159 (2021)
Background Atypical teratoid rhabdoid tumor is an uncommon aggressive central nervous system tumor. All retrospective series have shown a short mean overall survival rate. Considering the rarity of the disease, few prospective clinical trials address
Publikováno v:
Surgical Neurology International
Background: Moyamoya disease (MMD) is a unique cerebrovascular disorder characterized by progressive stenosis of anterior cerebral circulation. Moyamoya is not an uncommon disease in Saudi Arabia. Although a less common symptom of the disease, the in
Publikováno v:
Human Genetics. 134:1139-1141
Autor:
Asem Salma, Essam Alshail
Publikováno v:
Journal of neurosurgery. 124(6)