Results 151 to 160 of about 56,517 (194)

Cerebellar Dentate Cavernoma Enlargement and Tremor Emergence: Longitudinal Neuroimaging Analysis of Case Report and Literature Review

open access: yes
Movement Disorders Clinical Practice, EarlyView.
Andrew Z. Yang   +15 more
wiley   +1 more source

Malignant Rhabdoid Tumors of Cranial Nerves—A Clinically Distinct Group With Characteristic Neuroradiological, Histopathological, and Molecular Features

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Malignant rhabdoid tumors occasionally develop along cranial nerves, but clinical, histopathological, and molecular features have not been examined in larger series. Procedure We retrospectively interrogated data from the European Rhabdoid Registry, EU‐RHAB, to identify malignant rhabdoid tumors affecting cranial nerves.
Miriam Gruhle   +15 more
wiley   +1 more source

Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter Study

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective To investigate the clinical outcome of fetuses with ventriculomegaly (VM), and to identify risk factors for progression of fetal VM in order to improve prenatal counseling. This was a multicenter, retrospective cohort study, comprising 229 cases with VM.
Anouk Moens   +12 more
wiley   +1 more source

Cranial nerve injury

open access: yesEuropean Journal of Vascular and Endovascular Surgery, 1996
openaire   +2 more sources

Spina bifida as a multifactorial birth defect: Risk factors and genetic underpinnings

open access: yesPediatric Discovery, EarlyView.
Abstract Spina bifida is a birth defect resulting from abnormal embryonic development of the neural tube. Though spina bifida is divided into several subtypes, myelomeningocele—the most severe form of spina bifida often associated with a markedly diminished quality of life—accounts for a significant portion of cases.
Ethan S. Wong   +13 more
wiley   +1 more source

Horner syndrome in a pediatric patient

open access: yesPediatric Investigation, EarlyView.
Horner syndrome (HS) is a rare neurological disorder arising from disruption of the oculosympathetic pathway. paediatric HS is uncommon and may be congenital, however it is imperative that underlying sinister causes are excluded. ABSTRACT Introduction Horner syndrome (HS) is a rare neurological disorder arising from disruption of the oculosympathetic ...
Devansh Tandon   +4 more
wiley   +1 more source

Ocular involvement in newly diagnosed pediatric leukemia: A systematic review and meta‐analysis

open access: yesPediatric Investigation, EarlyView.
The global prevalence of ocular involvement in pediatric leukemia is estimated to be 20.32%, which is more common than previously recognized. Given the high rate of asymptomatic involvement, screening for all newly diagnosed leukemia patients is recommended.
Kristina Nazzicone   +5 more
wiley   +1 more source

Obstruction caused by suprasellar cisterna arachnoid cyst expansion after ventriculoperitoneal shunt in children with hydrocephalus

open access: yesPediatric Investigation, EarlyView.
This article focuses on four cases of hydrocephalus after ventriculoperitoneal (VP) shunt in our center from 2016 to 2021. Imaging follow‐up showed that the secondary suprasellar cisterna arachnoid cyst was enlarged and then formed obstructive hydrocephalus. The clinical symptoms were relieved after a suprasellar cisterna cyst stomy.
Dapeng Li, Wenping Ma, Ming Ge, Di Zhang
wiley   +1 more source

Prevalence of function‐limiting late effects in survivors of head and neck cancer

open access: yesPM&R, EarlyView.
Abstract Background Survivors of head and neck cancer (HNC) are commonly affected by multiple complex and interrelated long‐term and late effects that can adversely affect their function and quality of life. Objective To define the prevalence of neuromuscular, musculoskeletal, visceral, oncologic, and other late effects affecting function and quality ...
Yu Hui Won, Michael D. Stubblefield
wiley   +1 more source

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