Results 51 to 60 of about 7,220 (179)

Hypoxia Upregulates RIPK1 via the HIF‐1α–JAK–STAT Pathway Leading to Astrocyte Necroptosis to Promote Cavitation After Spinal Cord Injury

open access: yesCNS Neuroscience &Therapeutics, Volume 32, Issue 5, May 2026.
Abstract This study established a rat spinal cord injury (SCI) model and an in vitro hypoxic astrocyte model, confirming that hypoxia promotes the formation of the cavity of injury (COI) after SCI by activating the HIF‐1α/JAK/STAT pathway, which in turn induces astrocytic necroptosis and ultimately drives the pathological progression of SCI.
Hangchuan Bi   +12 more
wiley   +1 more source

A CASE OF SYRINGOMYELIA [PDF]

open access: yesThe Journal of Nervous and Mental Disease, 1894
n ...
openaire   +2 more sources

Syringomyelia as a complication of tuberculous meningoencephalitis

open access: yesThe Pan African Medical Journal, 2016
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

Miniaturization in Domestic Dogs: Relationships Among Cranial Shape, Head Indexes, and Body Weight

open access: yesVeterinary Radiology &Ultrasound, Volume 67, Issue 3, May 2026.
ABSTRACT Diagnostic interpretation is complicated by normal anatomic variation in canine heads. This retrospective cross‐sectional study examined how miniaturization—proxied by body weight—relates to four cranial shape categories (archetypal, intermediate, round, and extreme round) and three quantitative head measures (cranial index, skull index, and ...
Alyssa M. Froese   +3 more
wiley   +1 more source

Dandy–Walker syndrome associated with syringomyelia in an adult: a case report and literature review

open access: yesJournal of International Medical Research, 2019
Dandy–Walker syndrome associated with syringomyelia is a rare condition, with few reports of adult cases. We describe an adult case of Dandy–Walker syndrome with concomitant syringomyelia.
Nan Zhang   +7 more
doaj   +1 more source

Syringomyelia and spinal arachnoiditis resulting from aneurysmal subarachnoid hemorrhage: Report of two cases and review of the literature

open access: yesJournal of Craniovertebral Junction and Spine, 2014
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

Clinical, Psychosocial, and Care Coordination Concerns in Macrocephaly Capillary Malformation Syndrome: Insights From a Large International Survey

open access: yesPediatric Blood &Cancer, Volume 73, Issue 4, April 2026.
ABSTRACT Macrocephaly capillary malformation syndrome (M‐CM or MCAP) is a rare overgrowth disorder characterized by primary megalencephaly, overgrowth, and a range of additional anomalies. This report presents findings from a survey of 101 caregivers or individuals with M‐CM, collected by the M‐CM Network.
Melanie Bryan   +7 more
wiley   +1 more source

Dandy–Walker malformation is a rare cause of syringomyelia in adults

open access: yesНеврология, нейропсихиатрия, психосоматика, 2017
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

Electro‐clinical features of Mowat–Wilson syndrome: A retrospective study of 31 children in mainland China

open access: yesEpileptic Disorders, Volume 28, Issue 2, Page 344-358, April 2026.
Abstract Objective To summarize the electro‐clinical and genetic characteristics of children with Mowat–Wilson syndrome (MWS). Methods This study is a hospital‐based case series analyzing clinical data from 31 pediatric patients with MWS and epilepsy treated at Peking University First Hospital between June 2020 and December 2024.
Yi Ju, Tao‐yun Ji
wiley   +1 more source

Syringomyelia in Childhood

open access: yesNeurologia medico-chirurgica, 1987
Childhood syringomyelia is rare and its clinical symptoms differ from those in adults. From 1982 to 1985, the authors studied 19 children with syringomyelia with high-resolution computed tomography (Siemens Somatom II) and with magnetic resonance imaging (MRI)(0.15 tesla imager, Toshiba MRT 15A).
ISU, Toyohiko   +6 more
openaire   +3 more sources

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