Ipsilateral constructional apraxia.

Abstract:

:Two boys, aged 7 and 12 years, with nondominant (right) hemispheric acquired vascular lesions and left visual-field disturbances had right spatial constructional disabilities, contralateral to that which would be expected. These unusual disturbances may represent the previously unreported phenomena of ipsilateral neglect or ipsilateral constructional apraxia.

journal_name

J Child Neurol

authors

Lewis DW,Geller T

doi

10.1177/088307389400900109

subject

Has Abstract

pub_date

1994-01-01 00:00:00

pages

41-4

issue

1

eissn

0883-0738

issn

1708-8283

journal_volume

9

pub_type

杂志文章
  • Experimental models of epilepsy in young animals.

    abstract::Seizures occur more frequently early in life. Some of these early seizures may eventually become epilepsy. Others are reactive seizures due to excessive environmental stimuli that, in any other age group, might not have elicited a similar response. To understand the developmental aspects of seizures and epilepsy in hu...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073894009001031

    authors: Kubová H,Moshé SL

    更新日期:1994-10-01 00:00:00

  • Comorbid Medical Conditions in Friedreich Ataxia: Association With Inflammatory Bowel Disease and Growth Hormone Deficiency.

    abstract::Friedreich ataxia is a progressive degenerative disease with neurologic and cardiac involvement. This study characterizes comorbid medical conditions in a large cohort of patients with Friedreich ataxia. Patient diagnoses were collected in a large natural history study of 641 subjects. Prevalence of diagnoses in the c...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1177/0883073816643408

    authors: Shinnick JE,Schadt K,Strawser C,Wilcox N,Perlman SL,Wilmot GR,Gomez CM,Mathews KD,Yoon G,Zesiewicz T,Hoyle C,Subramony SH,Yiu EM,Delatycki MB,Brocht AF,Farmer JM,Lynch DR

    更新日期:2016-08-01 00:00:00

  • Gait assessment in children with duchenne muscular dystrophy during long-distance walking.

    abstract::The aim of this study was to investigate the alteration of the gait pattern in 25 children with Duchenne muscular dystrophy, using body-worn inertial sensors during a long walking distance. Normalized spatiotemporal gait parameters and their variability were extracted from the angular velocity of the shanks; the smoot...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811413581

    authors: Ganea R,Jeannet PY,Paraschiv-Ionescu A,Goemans NM,Piot C,Van den Hauwe M,Aminian K

    更新日期:2012-01-01 00:00:00

  • Trihexyphenidyl improves motor function in children with dystonic cerebral palsy: a retrospective analysis.

    abstract::There are conflicting reports regarding the efficacy of trihexyphenidyl, an anticholinergic drug, for treatment of dystonia in cerebral palsy. The author hypothesized that trihexyphenidyl may be more effective in specific subgroups and performed a retrospective analysis of 31 children (8.2 ± 5.8 years) with dystonia f...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810392582

    authors: Ben-Pazi H

    更新日期:2011-07-01 00:00:00

  • Large Artery Stroke in a Child With Hypoparathyroidism.

    abstract::The association of hypoparathyroidism and ischemic stroke is rare in childhood. We report an interesting case of an 11-year-old girl diagnosed to have hypoparathyroidism and presented with an acute-onset right hemiparesis. Investigations revealed large artery ischemic stroke and uncontrolled hypoparathyroidism. Pediat...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814544366

    authors: Dhawan SR,Jondhale SN,Sahu JK,Vyas S,Singhi PD

    更新日期:2015-07-01 00:00:00

  • Autism Phenotypes in Tuberous Sclerosis Complex: Diagnostic and Treatment Considerations.

    abstract::Tuberous sclerosis complex is a multisystem, chronic genetic condition characterized by systemic growth of benign tumors and often accompanied by epilepsy, autism spectrum disorders, and intellectual disability. Nonetheless, the neurodevelopmental phenotype of these patients is not often detailed. The authors describe...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073815600871

    authors: Gipson TT,Poretti A,Thomas EA,Jenkins KT,Desai S,Johnston MV

    更新日期:2015-12-01 00:00:00

  • Children with central and peripheral neurologic disorders have distinguishable patterns of dysphagia on videofluoroscopic swallow study.

    abstract::To determine whether findings on videofluoroscopic swallow studies reveal different patterns of dysphagia between children with central and peripheral neurologic disorders, a retrospective study of 118 videofluoroscopic swallow studies was completed. There were 3 groups: cerebral palsy with only spastic features (n = ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813501871

    authors: van den Engel-Hoek L,Erasmus CE,van Hulst KC,Arvedson JC,de Groot IJ,de Swart BJ

    更新日期:2014-05-01 00:00:00

  • Paroxysmal tonic upgaze and partial tetrasomy of chromosome 15: a novel genetic association.

    abstract::Paroxysmal tonic upgaze of childhood is an eye movement abnormality characterized by periodic episodes of conjugate upward eye deviation. Although the spectrum of paroxysmal tonic upgaze has broadened considerably, a specific pathophysiology has not been elucidated. We report an infant with paroxysmal tonic upgaze who...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738050200021601

    authors: Joseph K,Avallone J,Difazio M

    更新日期:2005-02-01 00:00:00

  • Migraine and cranial autonomic symptoms in children and adolescents: a clinical study.

    abstract::The frequency of cranial autonomic symptoms in children affected by primary headaches is uncertain. The aim of our study was to estimate the frequency of symptoms in pediatric headaches and correlate it with main migraine characteristics. A questionnaire investigating the presence of cranial autonomic symptoms was adm...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814535494

    authors: Raieli V,Giordano G,Spitaleri C,Consolo F,Buffa D,Santangelo G,Savettieri G,Vanadia F,D'Amelio M

    更新日期:2015-02-01 00:00:00

  • Mumps virus-associated acute encephalopathy: case report and review of the literature.

    abstract::We describe a fatal case of mumps virus-associated acute encephalopathy. In terms of the clinical course and cytokine as well as chemokine profiles, the pathogenesis in our case was different from that of mumps meningoencephalitis but was similar to that of influenza virus-associated acute encephalopathy. ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073812441060

    authors: Watanabe M,Suyama K,Hashimoto K,Sato M,Ohara S,Abe Y,Kawasaki Y,Yamaguchi S,Saijo M,Hosoya M

    更新日期:2013-02-01 00:00:00

  • Familial-Environmental Risk Factors in South African Children With Attention-Deficit Hyperactivity Disorder (ADHD): A Case-Control Study.

    abstract::We investigated familial and environmental risk factors in a cohort of South African children diagnosed with attention-deficit hyperactivity disorder (ADHD). A prospective, hospital-based case control study was conducted comprising 50 children diagnosed with ADHD and 50 matched non-ADHD controls. The adjusted effect o...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814560630

    authors: van Dyk L,Springer P,Kidd M,Steyn N,Solomons R,van Toorn R

    更新日期:2015-09-01 00:00:00

  • A pediatric case of severe pandysautonomia responsive to plasmapheresis.

    abstract::We describe a 13-year-old female with abrupt onset urinary retention progressing rapidly to pandysautonomia with symptoms of postural orthostatic tachycardia syndrome, gastroparesis, anhidrosis, pupillary dysfunction, and abdominal pain. Pandysautonomia has been reported frequently in adults, but is less commonly desc...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073812474099

    authors: Clark MB,Davis T

    更新日期:2013-12-01 00:00:00

  • Pontine Tegmental Cap Dysplasia in an Extremely Preterm Infant and Review of the Literature.

    abstract::Pontine tegmental cap dysplasia is a rare hindbrain malformation syndrome with a hypoplastic pons, a tissue protrusion into the fourth ventricle, and cranial nerve dysfunction. We here report clinical, imaging, and genetic findings of the first extremely low-birth-weight preterm infant with pontine tegmental cap dyspl...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073816680748

    authors: Picker-Minh S,Hartenstein S,Proquitté H,Fröhler S,Raile V,Kraemer N,Apeshiotis S,Leipoldt M,Kalache KD,Morris-Rosendahl D,Boltshauser E,Chen W,Kaindl AM

    更新日期:2017-03-01 00:00:00

  • Organizing logopedic therapy for babies with unilateral and bilateral brain lesion in the prespeech period.

    abstract::The goal of the research was to point out the importance of early prespeech therapy for babies suffering from at-birth-acquired unilateral or bilateral lesion in the prespeech period of development. On the basis of existing studies and experience in the field, a protocol and methodology for the observation of the phon...

    journal_title:Journal of child neurology

    pub_type: 临床试验,杂志文章

    doi:10.1177/0883073807299970

    authors: Gec V

    更新日期:2007-01-01 00:00:00

  • Oral pharmacotherapy of childhood movement disorders.

    abstract::Movement disorders, a common problem in children with neurologic impairment, are receiving increasing clinical attention. The differences in movement disorders between adults and children are striking; presentation is frequently insidious and may be characterized by mild hypotonia. The clinical manifestations of extra...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073803018001S0601

    authors: Edgar TS

    更新日期:2003-09-01 00:00:00

  • Lack of Association Between Polymorphisms in Dopa Decarboxylase and Dopamine Receptor-1 Genes With Childhood Autism in Chinese Han Population.

    abstract::Genetic factors play an important role in childhood autism. This study is to determine the association of single-nucleotide polymorphisms in dopa decarboxylase (DDC) and dopamine receptor-1 (DRD1) genes with childhood autism, in a Chinese Han population. A total of 211 autistic children and 250 age- and gender-matched...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073815601496

    authors: Yu H,Liu J,Yang A,Yang G,Yang W,Lei H,Quan J,Zhang Z

    更新日期:2016-04-01 00:00:00

  • Coexisting muscular dystrophies and epilepsy in children.

    abstract::Muscular dystrophies are composed of a variety of genetic muscle disorders linked to different chromosomes and loci and associated with different gene mutations that lead to progressive muscle atrophy and weakness. Fukuyama congenital muscular dystrophy is frequently associated with partial and generalized epilepsy an...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738060210021601

    authors: Tsao CY,Mendell JR

    更新日期:2006-02-01 00:00:00

  • Respiratory sinus arrhythmia in children with severe cyanotic and pallid breath-holding spells.

    abstract::In this study we investigated centrally mediated parasympathetic regulation of modulated cardiac vagal tone among children with severe cyanotic and pallid breath-holding spells by examining respiratory sinus arrhythmia. Respiratory sinus arrhythmia was evaluated in 41 children; 17 subjects with cyanotic breath-holding...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389801300905

    authors: DiMario FJ Jr,Bauer L,Baxter D

    更新日期:1998-09-01 00:00:00

  • Infantile metabolic encephalopathy due to fumarase deficiency.

    abstract::Fumarase deficiency is a very rare inborn error of metabolism caused by decreased activity of fumarate hydratase enzyme. We describe a fumarase-deficient infant who presented with encephalopathy, metabolic crisis, psychomotor retardation, hypotonia, seizures, and facial dysmorphism. To our knowledge, this is the first...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073812447286

    authors: Saini AG,Singhi P

    更新日期:2013-04-01 00:00:00

  • Pediatric anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: experience of a tertiary care teaching center from north India.

    abstract::Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis is characterized by acute- or subacute-onset encephalopathy with extrapyramidal, psychiatric, and epileptic manifestations. Diagnosis is confirmed by positive antibodies to NMDA receptor in cerebrospinal fluid and serum. Eleven pediatric cases presented over a 2-y...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813494474

    authors: Chakrabarty B,Tripathi M,Gulati S,Yoganathan S,Pandit AK,Sinha A,Rathi BS

    更新日期:2014-11-01 00:00:00

  • Event-related potentials (P300) in primary headache in childhood and adolescence.

    abstract::There is strong evidence for a loss of habituation during cognitive processing in migraine as measured by P300 and contingent negative variation in adults. Event-related potentials evoked by an oddball paradigm have not yet been studied in children and adolescents suffering from different primary headache types. We re...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389801300703

    authors: Evers S,Bauer B,Grotemeyer KH,Kurlemann G,Husstedt IW

    更新日期:1998-07-01 00:00:00

  • Neonatal form of nemaline myopathy, muscle immaturity, and a microvascular injury.

    abstract::An infant with a neonatal form of nemaline myopathy showed ultrastructural features of muscle immaturity. Immaturity was characterized by an abnormal presence of myotubes, as well as cells in clusters within a common basement membrane and a great number of satellite cells adhering to very small muscle fibers. In addit...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389000500209

    authors: Fidziańska A,Goebel HH,Kleine M

    更新日期:1990-04-01 00:00:00

  • Long-term oral baclofen treatment in a child with cerebral palsy: electroencephalographic changes and clinical adverse effects.

    abstract::Baclofen is widely used to control spasticity in children with cerebral palsy. Several publications described clinical adverse effects of baclofen oral treatment, but the effect of baclofen on seizure potentiation is still controversial. We describe a 10-year-old female patient with cerebral palsy, epilepsy, and menta...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809357243

    authors: De Rinaldis M,Losito L,Gennaro L,Trabacca A

    更新日期:2010-10-01 00:00:00

  • The Efficacy of Botulinum Toxin in Pediatric Chronic Migraine: A Literature Review.

    abstract:AIMS:To conduct a review of the literature on the use of botulinum toxin for the treatment of pediatric chronic migraine. METHODS:A review of the literature was performed using EMBASE, PubMed, and Cochrane/Ovid. Using our inclusion and exclusion criteria, we targeted any study, published before April 2020, evaluating ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073820931256

    authors: Marcelo R,Freund B

    更新日期:2020-10-01 00:00:00

  • Pilot study on executive function and adaptive skills in adolescents and young adults with mitochondrial disease.

    abstract::High-functioning adolescents and young adults with mitochondrial disease are now attempting transitions to postsecondary environments. This pilot and case study explores factors that interfere with their successful transition through behavior-rating scales addressing academic skills and behavior. In the Behavior Asses...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073812442589

    authors: Schreiber H

    更新日期:2012-12-01 00:00:00

  • Cerebrospinal fluid neuron-specific enolase following seizures in children: role of etiology.

    abstract::Neuron-specific enolase, a marker for neuronal injury, is elevated following seizures in adults, but relatively few data exist on postictal neuron-specific enolase levels in children. This study measured cerebrospinal fluid (CSF) neuron-specific enolase levels after seizures in 49 consecutive pediatric patients and in...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700404

    authors: Wong M,Ess K,Landt M

    更新日期:2002-04-01 00:00:00

  • Experimental Therapeutic Trial Design for Pediatric Brain Tumors.

    abstract::Pediatric brain tumors are the leading cause of cancer-related death during childhood. Since the first pediatric brain tumor clinical trials, the field has seen improved outcomes in some, but not all tumor types. In the past few decades, a number of promising new therapeutic agents have emerged, yet only a few of thes...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073815604221

    authors: Bornhorst M,Hwang EI

    更新日期:2016-10-01 00:00:00

  • Recurrent acute necrotizing encephalopathy in a Korean child: the first non-Caucasian case.

    abstract::Acute necrotizing encephalopathy is characterized by fever, seizures, acute encephalopathy, and rapid progression to coma. It is usually associated with viral illness and shows characteristic brain magnetic resonance imaging features, including symmetrical involvement of bilateral thalami, brain stem, white matter, an...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811435240

    authors: Lee JH,Lee M,Lee J

    更新日期:2012-10-01 00:00:00

  • Proton magnetic resonance spectroscopy and diffusion-weighted imaging in isolated sulfite oxidase deficiency.

    abstract::Isolated sulfite oxidase deficiency is a rare autosomal recessive disorder of the newborn that can be mistaken for neonatal asphyxia. Diffusion-weighted imaging of the brain demonstrates widespread diffusion restriction, and proton magnetic resonance spectroscopy shows an elevated lactate level, a decrease in the rati...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738060210090601

    authors: Eichler F,Tan WH,Shih VE,Grant PE,Krishnamoorthy K

    更新日期:2006-09-01 00:00:00

  • Pediatric to Adult Transitions of Ketogenic Dietary Therapy for Epilepsy.

    abstract::Ketogenic therapy is now an accepted treatment for pediatric and adult patients with medically refractory epilepsy.1-3 However, young adults treated with a ketogenic diet face unique challenges when transitioning to adult neurology providers.4 The variable acceptance of dietary therapy, paucity of nutritionists and ad...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073820938587

    authors: Seaborg K,Wang X,Olson C,Felton EA

    更新日期:2020-11-01 00:00:00