Results 31 to 40 of about 2,114 (168)

Corpus callosal reference ranges: systematic review of methodology of biometric chart construction and measurements obtained

open access: yesUltrasound in Obstetrics &Gynecology, Volume 62, Issue 2, Page 175-184, August 2023., 2023
ABSTRACT Objective Adequate reference ranges of size of the corpus callosum (CC) are necessary to improve characterization of CC abnormalities and parental counseling. The objective of this study was to evaluate the methodology used in studies developing references charts for CC biometry.
R. Corroenne   +6 more
wiley   +1 more source

Head Injury Exposure in Veterans Presenting to Memory Disorders Clinic: An Observational Study of Clinical Characteristics and Relationship of Event-Related Potentials and Imaging Markers

open access: yesFrontiers in Neurology, 2021
Objective: Traumatic brain injury (TBI) and repetitive head impacts (RHI) related to blasts or contact sports are commonly reported among military service members.
Katherine W. Turk   +13 more
doaj   +1 more source

Regional cerebral blood flow in a patient with restless legs syndrome exhibiting pramipexole-induced hypersexuality. [PDF]

open access: yesPCN Rep
Abstract Background Impulse control disorders (ICDs), including hypersexuality, are associated with adverse effects of dopamine agonists, such as pramipexole, particularly in the treatment of Parkinson's disease and restless legs syndrome (RLS). The underlying mechanisms remain unclear in ICDs in patients with RLS, and no neuroimaging studies have ...
Obata T   +7 more
europepmc   +2 more sources

Novel partial deletions, frameshift and missense mutations of CSF1R in patents with CSF1R‐related leukoencephalopathy

open access: yesEuropean Journal of Neurology, Volume 30, Issue 7, Page 1861-1870, July 2023., 2023
Mutational analysis of CSF1R was performed for 100 consecutive patients with adult‐onset leukoencephalopathy. CSF1R mutations were found in 15 patients, accounting for 15% of the adult‐onset leukoencephalopathy. Seven novel mutations including missense mutations (p.N783D, p.K820N and p.F849I), an in‐frame deletion (p.K883del), frameshift mutation (p ...
Takanobu Ishiguro   +23 more
wiley   +1 more source

Multiloculated Hydrocephalus: Surgical Techniques

open access: yesArchives of Pediatric Neurosurgery, 2021
Objective: Hydrocephalus shunt remains as the most common treatment choice for nonobstructive hydrocephalus, but in some cases multiloculated hydrocephalus (MH) remains a difficult neurosurgical disease despite of the different therapeutic options ...
Ricardo de Amoreira Gepp
doaj   +1 more source

Caval variations in neurologically diseased patients

open access: yesActa Radiologica Short Reports, 2014
Background The import of the cavum variation and its prevalence rate in healthy individuals is still not clear, likewise in neurologically diseased patients.
Rachael A Akinola   +2 more
doaj   +1 more source

Vergae cyst and autism spectrum disorder: a case report [PDF]

open access: yesEur Psychiatry
Introduction The cavum Vergae is a fluid-filled space located posterior to the cavum septum pellucidum, between the bodies of the fornices.
Souidi A, El Maataoui Z, Kisra H.
europepmc   +2 more sources

Chronic daily headache in a patient with Cavum Septum Pellucidum and Cavum Verge [PDF]

open access: yes, 2013
Cavum septum pellucidum (CSP) and cavum Vergae (CV) are unusual variants and usually asymptomatic, but their expansion or inside lesions can produce symptoms by mass effect.
Chen, D-L, Chen, J-J
core   +1 more source

Cavum Septum Pellucidum, da embriologia à clínica: uma revisão da literatura [PDF]

open access: yes, 2018
Introdução: O septo pelúcido (SP) é formado por duas lâminas neurais separadas, que se fundem após o nascimento. Quando não há fusão completa, tem-se a persistência do Cavum embriológico, que pode ser chamado Cavum Septum pellucidum (CSP), Cavum Vergae ...
Jalles Dantas de Lucena   +7 more
core   +1 more source

Movement Disorders Associated with 22q11.2 Microdeletion: A Scoping Review

open access: yesMovement Disorders Clinical Practice, Volume 13, Issue 6, Page 1399-1417, June 2026.
Abstract Background Movement disorders have recently emerged as important neurologic manifestations of the 22q11.2 microdeletion that affects nearly one in every 2000 live births. Objective We aimed to map the existing evidence regarding the spectrum, diagnosis and treatment, and etiopathogenesis of movement disorders associated with 22q11.2 ...
Nikolai Gil D. Reyes   +6 more
wiley   +1 more source

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