Results 61 to 70 of about 10,268 (160)
A Case of Noncommunicating Hydrocephalus Presenting as Isolated Hyposmia
Noncommunicating hydrocephalus causing hyposmia. ABSTRACT Olfactory dysfunction presents in combination with various different symptoms and can be attributed to a range of etiologies, including sinonasal disease, post‐viral infection, post‐traumatic injury, age‐related decline, and less commonly intracranial structural abnormalities and genetic ...
Bartels Walker +3 more
wiley +1 more source
Syringomyelia resulting from arachnoiditis secondary to aneurysmal subarachnoid hemorrhage (SAH) is an extremely rare clinical entity with few cases reported in the literature.
Taylor J Abel +2 more
doaj +1 more source
ABSTRACT Acute‐onset neurological deficits in otherwise healthy individuals warrant a broad differential diagnosis. Neurosarcoidosis presenting as longitudinally extensive transverse myelitis is rare, mimicking demyelinating, infectious, or neoplastic disorders. Early recognition, histopathological confirmation, and timely immunosuppressive therapy are
Areeb Tiwana +2 more
wiley +1 more source
Background: Chiari malformation type I (CM1) with syringomyelia caused by supratentorial lesions is extremely rare, and the mechanism has not been well explained.
Chengjian Lou +4 more
doaj +1 more source
Syringomyelia as a complication of tuberculous meningoencephalitis
Syringomyelia is a rare condition in which a cyst forms within your spinal cord, secondary syringomyelia following Tuberculousis is very rare. In the present paper, we report a case of tuberculous meningoencephalitis in a 30 year-old Morrocan male ...
Maha Ait berri, Abdelhadi Rouimi
doaj +1 more source
Bibliometric Analysis of Charcot Arthropathy (1995–2025): Current Status and Emerging Trends
ABSTRACT Background Charcot Arthropathy (CA) is a destructive joint condition tied to neurotrophic and neuropathic processes. The clinical course is often complicated—high amputation rates and a generally poor prognosis have long made management difficult.
Jian Lin Zhou, Hao Peng, Fei Sun
wiley +1 more source
Ethnic differences in syringomyelia in New Zealand
Objective: To determine the prevalence of syringomyelia in a defined population in New Zealand and measure the prevalence of syringomyelia in the three main ethnic groups (Maori, Pacific people and Caucasians/others) living in this region.
Hope, JKA +5 more
core +1 more source
Dandy–Walker malformation is a rare cause of syringomyelia in adults
Neural tube defects are the most common central nervous system malformation. Dandy–Walker malformation (DWM) is a rare abnormality of the posterior cranial fossa, which is generally diagnosed in the prenatal period or early infancy.The paper describes a ...
G. Yu. Evzikov +3 more
doaj +1 more source
Pediatric spinal ependymomas: Long‐term surgical outcomes in a cohort of 61 cases
Spinal ependymomas are rare in children, with limited long‐term outcome data. In this retrospective study of 61 pediatric patients undergoing surgical resection, gross total resection was achieved in 62.3% and was associated with favorable functional improvement. Recurrence was observed in 31.1% of cases.
Liang Zhang +3 more
wiley +1 more source
Mathematical modelling and analysis of cerebrospinal mechanics: an investigation into the parthogenesis of syringomyelia [PDF]
Syringomyelia is a disease in which fluid-filled cavities, called syrinxes, form in the spinal cord causing progressive loss of sensory and motor functions.
Elliott, Novak Samuel Jon
core

