Results 31 to 40 of about 80,512 (251)

Craniopharyngioma arising from fourth ventricle

open access: yesNepal Journal of Neuroscience, 2020
Craniopharyngiomas usually involve the sellar and suprasellar space. Very few cases of craniopharyngiomas arising in the posterior fossa without extension to the sellar and suprasellar space have been reported in literature. This case describes a patient
Binit Kumar Jha   +3 more
doaj   +1 more source

Risk factors of acquired dysphagia in patients after posterior cranial fossa surgery

open access: yesHuli yanjiu, 2023
ObjectiveTo investigate the status quo and risk factors of acquired dysphagia in patients after posterior cranial fossa surgery,and to provide reference for early intervention of dysphagia and optimization of postoperative rehabilitation.MethodsA total ...
QI Chunxia   +6 more
doaj  

Bilateral Sub-acute Subdural Hematoma of the Posterior Fossa As a Complication of Anti-coagulation Therapy: A Case Report and Literature Review

open access: yesSudan Journal of Medical Sciences, 2022
Background: Subdural hematomas are one of the commonest neurosurgical pathologies faced in practice and it is rarely located in the posterior fossa.
Moayad Ahmed   +3 more
doaj   +1 more source

Organizing the interface—Plasma membrane architecture and receptor dynamics in virus‐cell interactions

open access: yesFEBS Letters, EarlyView.
Plasma membranes contain dynamic nanoscale domains that organize lipids and receptors. Because viruses operate at similar scales, this architecture shapes early infection steps, including attachment, receptor engagement, and entry. Using influenza A virus and HIV‐1 as examples, we highlight how receptor nanoclusters, multivalent glycan interactions ...
Jan Schlegel, Christian Sieben
wiley   +1 more source

“Drowning Brain in a Pool of CSF” — A Rare Complication of Periencephalic Subdural Panhygroma following Removal of a Posterior Fossa Tumor

open access: yesIndian Journal of Neurosurgery, 2017
Posterior fossa tumors are commonly encountered in pediatric age group patients. Most of these tumors present with features of hydrocephalus in the child.
Bikash Ranjan Behera   +4 more
doaj   +1 more source

Understanding Further the Phenotypic Spectrum of Central Nervous System Inflammatory Demyelinating Disorders Using Unsupervised Clustering

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Central nervous system (CNS) inflammatory demyelinating syndromes, including multiple sclerosis (MS), aquaporin‐4 antibody–positive neuromyelitis optica spectrum disorder (AQP4 + NMOSD), and myelin oligodendrocyte glycoprotein (MOG) antibody–associated disease (MOGAD), occasionally overlap.
Bade Gulec   +6 more
wiley   +1 more source

CAR T‐Cell Therapy in Neurology: A Scoping Review of Neuro‐Oncology, Autoimmune Diseases & Neurotoxicity

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Chimeric antigen receptor (CAR) T‐cell therapy has been investigated in neurological diseases, encompassing both central nervous system malignancies and autoimmune disorders, thereby extending its application beyond hematological cancers.
Omar Alqaisi   +5 more
wiley   +1 more source

Posterior fossa tension pneumocephalus

open access: yes, 2000
Posterior fossa tension pneumocephalus (PFTP) is a very rare clinical entity – the few case reports available prove how rare. Five patients with PFTP are presented. All were operated on for posterior fossa lesions.
Suri, A., Mahapatra, A. K., Singh, V. P.
core   +1 more source

Posterior fossa craniotomy: technical report [PDF]

open access: yes, 2000
The use of craniotomy to approach supratentorial lesions is quite well established in the literature. The use of craniotomy for posterior fossa approaches, however, is not well described.
IGOR DE CASTRO   +3 more
core   +1 more source

A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
wiley   +1 more source

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