22 results match your criteria: "Pediatric Brain Center[Affiliation]"

Immediate postoperative course in the pediatric intensive care unit following epilepsy surgery.

Childs Nerv Syst

December 2024

Department of Pediatric Neurosurgery, The Pediatric Brain Center, affiliated to the Faculty of Medical and Health Sciences, Tel Aviv University, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Purpose: To describe the immediate postoperative PICU course and short-term outcomes of children undergoing various epilepsy surgeries.

Methods: Single-center, retrospective observational study. All patients younger than 20 years of age who had been admitted to the PICU between 2018 and 2022 following epilepsy surgery were eligible for study entry.

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Article Synopsis
  • The study aimed to characterize perinatal intracranial hemorrhage (pICH), focusing on differences between cases diagnosed before and after birth and analyzing their causes and clinical patterns.
  • Conducted over a decade, the research included 110 pICH cases, revealing that intraventricular hemorrhage (IVH) was most prevalent, particularly in prenatally diagnosed cases, while subpial hemorrhage was exclusively identified postnatally.
  • The findings indicated that genetic disorders contributed to nearly a third of pICH cases, highlighting the necessity for next-generation sequencing to better understand genetic factors associated with prenatally diagnosed hemorrhages.
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Pediatric low-grade gliomas.

Childs Nerv Syst

October 2024

Section of Pediatric Neurosurgery, Department of Neurosurgery, Eberhard Karls University, Tübingen, Germany.

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Pediatric low-grade gliomas.

Childs Nerv Syst

October 2024

Section of Pediatric Neurosurgery, Department of Neurosurgery, Eberhard Karls University, Tübingen, Germany.

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Temporal PLGG and epilepsy.

Childs Nerv Syst

October 2024

The Pediatric Brain Center, Gilbert Israeli International Neurofibromatosis Center, Dana Children's Hospital, Tel Aviv Medical Center, Tel Aviv, Israel.

Temporal lobe epilepsy in children is often secondary to various low-grade glial and glioneural tumors and rarely secondary to mesial temporal sclerosis. Despite the benign nature, tumor-associated TLE in children often becomes refractory over time. Abundant literature has shown the significant advantage of tumor resection compared to conservative treatment, in achieving seizure control, as well as the rates of antiseizure medication reduction.

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Beyond words: an investigation of fine motor skills and the verbal communication spectrum in autism.

Front Psychiatry

May 2024

Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA, United States.

Introduction: This study investigated the associations between fine motor skills and expressive verbal abilities in a group of 97 autistic participants (age 8-17, mean=12.41) and 46 typically developing youth (age 8-17, mean=12.48).

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The prepontine block and its relevance for the development and treatment of hydrocephalus.

Childs Nerv Syst

May 2024

Departments of Pediatric Neurosurgery and the Pediatric Brain Center, Dana Children's Hospital, Tel Aviv Medical Center, 6 Weizman Street, Tel Aviv, 64239, Israel.

Objective: Pulsatile CSF flow patterns include flow through the ventricles to the subarachnoid space and cisterns and from the infra- to the supratentorial subarachnoid space. In this study, we demonstrate how an obstruction at the level of the prepontine space may lead to obstructive hydrocephalus with specific radiological characteristics, as well as the implications for treatment options.

Methods: We retrospectively collected data of patients who underwent surgery between February 2010 and December 2022 for hydrocephalus secondary to a suspected prepontine block.

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Epilepsy surgery during infancy: The earlier the better.

Dev Med Child Neurol

September 2024

Department of Pediatric Neurosurgery, The Pediatric Brain Center, Dana Children's Hospital, Tel Aviv Medical Center, Tel Aviv University, Tel Aviv, Israel.

This commentary is on the original article by Wu et al. on pages 1215–1225 of this issue.

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The Pediatric Epilepsy Surgery Interest Group (PESIG) under the auspice of the ISPN Research Committee: Availability of relevant technology and geographical distribution.

Childs Nerv Syst

April 2024

Department of Pediatric Neurosurgery, The Pediatric Brain Center, Dana Children's Hospital, Tel Aviv Medical Center, Tel Aviv University, 6 Weizman Street, Tel Aviv, 64239, Israel.

Purpose: Epilepsy surgery for pediatric drug-resistant epilepsy has been shown to improve seizure control, enhance patient and family QoL, and reduce mortality. However, diagnostic tools and surgical capacity are less accessible worldwide. The International Society Pediatric Neurosurgery (ISPN) has established a Pediatric Epilepsy Surgery Interest Group (PESIG), aiming to enhance global collaboration in research and educational aspects.

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Aim: To identify meaningful outcomes of children and their caregivers attending a paediatric brain centre.

Method: We compiled a long list of outcomes of health and functioning of children with brain-related disorders such as cerebral palsy, spina bifida, (genetic) neurodevelopmental disorders, and acquired brain injury. We incorporated three perspectives: patients, health care professionals, and published outcome sets.

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Article Synopsis
  • - This study compared three surgical methods for correcting sagittal synostosis: frontobiparietal remodeling (FBR), extended strip craniotomy (ESC), and spring-assisted correction (SAC) using 3D imaging techniques.
  • - Researchers analyzed the outcomes of 322 3D images from 218 nonsyndromic patients under six years old, finding no significant differences in cranial growth or shape among the surgical methods post-operation.
  • - The results indicate that all three methods are similarly effective in correcting the condition, highlighting the importance of early diagnosis to facilitate minimally invasive surgery options.
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Common Features Between Stroke Following Varicella in Children and Stroke Following Herpes Zoster in Adults : Varicella-Zoster Virus in Trigeminal Ganglion.

Curr Top Microbiol Immunol

November 2022

Division of Child Neurology and Pediatric Brain Center, Department of Neurology, University of California San Francisco, San Francisco, California, USA.

The cerebral arteries are innervated by afferent fibers from the trigeminal ganglia. Varicella-zoster virus (VZV) frequently resides in the trigeminal ganglion. Reports of arterial ischemic stroke due to VZV cerebral vasculopathy in adults after herpes zoster have been described for decades.

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Expansion of NEUROD2 phenotypes to include developmental delay without seizures.

Am J Med Genet A

April 2021

Pediatric Genomics Discovery Program, Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.

De novo heterozygous variants in the brain-specific transcription factor Neuronal Differentiation Factor 2 (NEUROD2) have been recently associated with early-onset epileptic encephalopathy and developmental delay. Here, we report an adolescent with developmental delay without seizures who was found to have a novel de novo heterozygous NEUROD2 missense variant, p.(Leu163Pro).

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Brain Arteriovenous Malformation Recurrence After Apparent Microsurgical Cure: Increased Risk in Children Who Present With Arteriovenous Malformation Rupture.

Stroke

October 2020

Division of Neurointerventional Radiology, Department of Radiology and Biomedical Imaging (A.C., G.D., M.T.C., E.R.S., D.L.C., M.R.A., C.F.D., V.V.H., R.T.H., S.W.H.), University of California, San Francisco.

Background And Purpose: Do children have an increased risk for brain arteriovenous malformation (AVM) recurrence compared with adults and does this risk vary depending on initial presentation with AVM rupture?

Methods: We retrospectively studied 115 patients initially presenting with brain AVM under age 25 years who underwent complete surgical resection of the AVM as documented by digital subtraction angiography (DSA) and had delayed follow-up DSA to evaluate for AVM recurrence after apparent initial cure.

Results: The mean time from baseline DSA to follow-up DSA was 2.3 years, ranging from 0 to 15 years.

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Background: Rare variants in hundreds of genes have been implicated in developmental delay (DD), intellectual disability (ID) and neurobehavioural phenotypes. encodes a protein important for RNA silencing. Heterozygous truncating variants have been reported in three patients from large cohorts with autism, but no full phenotypic characterisation was described.

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Pediatric Multiple Sclerosis: A Review.

Adv Pediatr

August 2019

Pediatric Neurology and Multiple Sclerosis Clinic, University of California, San Francisco, Pediatric Brain Center, 550 16th Street, 4th Floor Box 0137, San Francisco, CA 94158, USA.

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Occipital Headaches and Neuroimaging in Children.

Curr Pain Headache Rep

July 2018

The University of California, San Francisco (UCSF), Department of Neurology, Pediatric Brain Center, Child & Adolescent Headache Program, Mission Hall, Box 0137, 550 16th Street, 4th Floor, San Francisco, California, 94158, USA.

Purpose Of Review: The goal of this review is to outline the prevalence and significance of occipital headaches in children and how they relate to neuroimaging findings. We seek to evaluate the concern that occipital headaches in children are indicative of secondary headache pathology by reviewing the yield of neuroimaging in pediatric patients with occipital headache location.

Recent Findings: Occipital headaches are a common presentation of primary headache disorders in children, seen in 7-16% of children presenting for evaluation of headache and in up to 20% of children diagnosed with migraine in the emergency department.

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Background: The 2013 International Classification of Headache Disorders-3 was published in a beta version to allow clinicians to confirm the validity of the criteria or suggest improvements based on field studies. The aim of this work was to review the Secondary Headache Disorders and Cranial Neuralgias and Other Headache Disorders sections of ICHD-3 beta data on children and adolescents (age 0-18 years) and to suggest changes, additions, and amendments.

Methods: Several experts in childhood headache across the world applied different aspects of ICHD-3 beta in their normal clinical practice.

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Background: The 2013 International Classification of Headache Disorders-3 (ICHD-3) was published in a beta version to allow the clinicians to confirm the validity of the criteria or to suggest improvements based on field studies. The aim of this work was to review the Primary Headache Disorders Section of ICHD-3 beta data on children and adolescents (age 0-18 years), and to suggest changes, additions, and amendments.

Methods: Several experts in childhood headache across the world applied different aspects of ICHD-3 beta in their normal clinical practice.

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Maternal Infections During Pregnancy and Cerebral Palsy in the Child.

Pediatr Neurol

April 2016

Departments of Neurology and Pediatrics, University of California, San Francisco, UCSF Pediatric Brain Center, San Francisco, California.

Background: Chorioamnionitis is a risk factor for cerebral palsy. The relationship between extra-amniotic infections and cerebral palsy is less well studied. We examined maternal intra-amniotic and extra-amniotic infections and risk of cerebral palsy in the child.

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Emergency mental health admissions for children: a naturalistic study.

Clin Child Psychol Psychiatry

January 2015

National and Specialist Acorn Lodge Inpatient Children's Unit, South London and Maudsley NHS Foundation Trust, London, UK Pediatric BRAIN Center, University of Illinois at Chicago, USA.

Objective: Emergency mental health admissions (EA) for children under 13 years are not routinely offered in the UK, which may be related to preconceptions about their safety, appropriateness and acceptability. Our aim was to evaluate routinely offered EA of children in a national unit over a three-year period.

Method: A retrospective, naturalistic study was conducted, comparing EA with planned admissions (PA) in terms of children's functioning on admission and discharge, clinical characteristics, significant risk-related incidents and parental and children satisfaction.

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Brain functional domains inform therapeutic interventions in attention-deficit/hyperactivity disorder and pediatric bipolar disorder.

Expert Rev Neurother

June 2011

Pediatric BRAIN Center, Institute for Juvenile Research, University of Illinois at Chicago, 1747, West Roosevelt Road, M/C 747, Chicago, IL 60612, USA.

A deeper understanding of how the relationships between impulsivity, reward systems and executive function deficits may be similar or different in attention-deficit/hyperactivity disorder (ADHD) and pediatric bipolar disorder (PBD) is fundamental for better defining phenotypy in these two developmental illnesses, and moving towards improved treatment and intervention. We focus our article on recent neurocognitive and neuroimaging data examining the behavioral and neural aspects of poor behavior regulation, response inhibition and reward systems in ADHD and PBD. In light of recent research evidence, we propose that the common behavioral manifestations of impulsivity in ADHD and PBD may indeed originate from different neural mechanisms mediated by altered reward systems.

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