Auditory brainstem responses of children with developmental language disorders.

Abstract:

:Brainstem auditory evoked potentials (BAEPs) were recorded from 48 children with language disorders (aged four to nine years old, IQs normal to borderline, normal audiometric thresholds and attending special school) and 20 healthy children (four to eight years old, with normal IQs, audiometry and school-level). The language-disabled group showed significantly lower absolute latency values of the BAEPs than controls. There were no significant differences in the central conduction time of the auditory pathway (I-V interval). Therefore, the only significant difference corresponded to a minor value for the first wave (auditory nerve discharge) of the BAEP. A reduction in the control mechanisms of the sensory inputs at the peripheral level, or a disturbance in the inhibitory mechanisms of cortico-subcortical modulation, might explain these findings.

journal_name

Dev Med Child Neurol

authors

Roncagliolo M,Benítez J,Pérez M

doi

10.1111/j.1469-8749.1994.tb11762.x

subject

Has Abstract

pub_date

1994-01-01 00:00:00

pages

26-33

issue

1

eissn

0012-1622

issn

1469-8749

journal_volume

36

pub_type

杂志文章
  • Single-photon emission computed tomography investigations of alternating hemiplegia of childhood.

    abstract::Alterations in regional cerebral blood-flow, as determined by single-photon emission computed tomography (SPECT) using technetium [99mTc] hexamethyl propylenamine oxime, were studied in two children presenting with alternating hemiplegia of childhood. Both experienced hemiplegic episodes several times per month, despi...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1993.tb11647.x

    authors: Siemes H,Cordes M

    更新日期:1993-04-01 00:00:00

  • Learning of grasp control in children with hemiplegic cerebral palsy.

    abstract::This study examined whether children with hemiplegic cerebral palsy (CP) have anticipatory control of fingertip forces during lifts of familiar objects, and what type of practice (blocked or random) best enhances the retention of anticipatory control during lifts of novel objects. Eighteen children with hemiplegic CP ...

    journal_title:Developmental medicine and child neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1017/s0012162203001397

    authors: Duff SV,Gordon AM

    更新日期:2003-11-01 00:00:00

  • Consensus research priorities for cerebral palsy: a Delphi survey of consumers, researchers, and clinicians.

    abstract:AIM:Research funds for cerebral palsy are scarce and competition for them is strong. This study aimed to identify questions for future research that were agreed to be a high priority. METHOD:An expert panel of consumers, researchers, and clinicians was assembled (n=127) and surveyed using a Delphi survey comprising th...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.2009.03358.x

    authors: McIntyre S,Novak I,Cusick A

    更新日期:2010-03-01 00:00:00

  • Motor impairment in very preterm-born children: links with other developmental deficits at 5 years of age.

    abstract:AIM:To elucidate the relation between motor impairment and other developmental deficits in very preterm-born children without disabling cerebral palsy and term-born comparison children at 5 years of (corrected) age. METHOD:In a prospective cohort study, 165 children (81 very preterm-born and 84 term-born)were assessed...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.12295

    authors: Van Hus JW,Potharst ES,Jeukens-Visser M,Kok JH,Van Wassenaer-Leemhuis AG

    更新日期:2014-06-01 00:00:00

  • Cerebral palsy in siblings caused by compound heterozygous mutations in the gene encoding protein C.

    abstract::We report two sisters with extensive bilateral periventricular haemorrhagic infarction (PVHI) causing cerebral palsy (CP). The older sister presented at 20 months with cortical visual blindness, spastic diplegia, and purpura fulminans. The younger sister presented aged 3 days old with apnoeas and multifocal seizures. ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.2010.03618.x

    authors: Fong CY,Mumford AD,Likeman MJ,Jardine PE

    更新日期:2010-05-01 00:00:00

  • Neuromotor development in children. Part 4: new norms from 3 to 18 years.

    abstract:AIM:The aim of this cross-sectional study was to provide normative data for motor proficiency (motor performance and contralateral associated movements [CAMs]) in typically developing children between 3 years and 18 years of age using an updated version of the Zurich Neuromotor Assessment (ZNA-2). METHOD:Six-hundred a...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.13793

    authors: Kakebeeke TH,Knaier E,Chaouch A,Caflisch J,Rousson V,Largo RH,Jenni OG

    更新日期:2018-08-01 00:00:00

  • A systematic review of interventions for children with cerebral palsy: state of the evidence.

    abstract:AIM:The aim of this study was to describe systematically the best available intervention evidence for children with cerebral palsy (CP). METHOD:This study was a systematic review of systematic reviews. The following databases were searched: CINAHL, Cochrane Library, DARE, EMBASE, Google Scholar MEDLINE, OTSeeker, PEDr...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,评审

    doi:10.1111/dmcn.12246

    authors: Novak I,McIntyre S,Morgan C,Campbell L,Dark L,Morton N,Stumbles E,Wilson SA,Goldsmith S

    更新日期:2013-10-01 00:00:00

  • Mild developmental delay due to ring chromosome 19 mosaicism.

    abstract::Children with mild developmental delay without dysmorphic features do not often have identifiable underlying aetiological factors. We report on a 5-year-old girl with mild developmental delay and dysmorphic features which were previously unrecognized. She was found to have supernumerary ring chromosome 19 mosaicism wh...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162299000092

    authors: Vaz I,Larkins SA,Norman A,Green SH

    更新日期:1999-01-01 00:00:00

  • Using non-preferred hand skill to investigate pathological left-handedness in an unselected population.

    abstract::This paper considers whether pathological influences affect hand-preference among children with epilepsy or mental retardation, for whom there is no evidence of gross motor defect. Data on two tasks of manual skill were analysed for a group of over 12,000 children. The predicted association between poor skill with the...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1984.tb04434.x

    authors: Bishop DV

    更新日期:1984-04-01 00:00:00

  • Is routine vitamin E administration justified in very low-birthweight infants?

    abstract::Analysis of nine randomised controlled trials of prophylactic vitamin E supplementation in very low-birthweight infants (less than 1500g) showed no statistically significant reduction in the incidence of acute retinopathy of prematurity. There was a significant reduction (49 per cent) in the incidence of intraventricu...

    journal_title:Developmental medicine and child neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1111/j.1469-8749.1990.tb16963.x

    authors: Law MR,Wijewardene K,Wald NJ

    更新日期:1990-05-01 00:00:00

  • Functional parameter measurements in children with ataxia telangiectasia.

    abstract:AIM:To collect preliminary functional data on ataxia telangiectasia and create a disease specific scale: the Ataxia Telangiectasia Functional Scale (ATFS). METHOD:Retrospective information on patients with ataxia telangiectasia referred to the Assistive Technology Unit was included. Functional mobility scales (the Gro...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.14334

    authors: Shenhod E,Benzeev B,Sarouk I,Heimer G,Nissenkorn A

    更新日期:2020-02-01 00:00:00

  • Autosomal dominant familial spastic paraplegia: description of a large New England family and a study of management.

    abstract::A large New England family with autosomal dominant familial spastic paraplegia (ADFSP) is described. In a pedigree of 173 family members, 71 affected individuals were identified. 16 cases examined by the authors are described with regard to the natural history of ADFSP in this family, and a staging system for followin...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1990.tb08530.x

    authors: Cooley WC,Melkonian G,Moses C,Moeschler JB

    更新日期:1990-12-01 00:00:00

  • Acute bilateral striatal necrosis with rotavirus gastroenteritis and inborn metabolic predisposition.

    abstract::We present a 9-month-old male with acute rotavirus gastroenteritis who developed an acute encephalopathy with focal seizures and developmental regression. Magnetic resonance imaging showed bilateral striatal necrosis and raised glutarylcarnitine levels on tandem mass spectrometry of a (crisis) blood spot, and chromato...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162205000800

    authors: Mordekar S,Jaspan T,Sharrard M,Morton R,Whitehouse WP

    更新日期:2005-06-01 00:00:00

  • Dissociated visual development: electrodiagnostic studies in infants who are 'slow to see'.

    abstract::Four infants were studied who failed to show any visual interest or following responses in the first three months of life. Although no definite ocular abnormalities were found at the time of presentation, both the parents and their medical advisers initially had serious concerns about the infants' visual prognosis. In...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1980.tb03712.x

    authors: Mellor DH,Fielder AR

    更新日期:1980-06-01 00:00:00

  • Magnetic resonance imaging arterial-spin-labelling perfusion alterations in childhood migraine with atypical aura: a case-control study.

    abstract:AIM:Atypical migraine with aura can be challenging to diagnose. Arterial-spin-labelling (ASL) is able to non-invasively quantify brain perfusion. Our aim was to report cerebral blood flow (CBF) alterations using ASL, at the acute phase of atypical migraine with aura in children. METHOD:Paediatric patients were retrosp...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.13123

    authors: Boulouis G,Shotar E,Dangouloff-Ros V,Grévent D,Calmon R,Brunelle F,Naggara O,Kossorotoff M,Boddaert N

    更新日期:2016-09-01 00:00:00

  • Neurofeedback in autism spectrum disorders.

    abstract:AIM:To review current studies on the effectiveness of neurofeedback as a method of treatment of the core symptoms of autism spectrum disorders (ASD). METHOD:Studies were selected based on searches in PubMed, Ovid MEDLINE, EMBASE, ERIC, and CINAHL using combinations of the following keywords: 'Neurofeedback' OR 'EEG Bi...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1469-8749.2011.04043.x

    authors: Holtmann M,Steiner S,Hohmann S,Poustka L,Banaschewski T,Bölte S

    更新日期:2011-11-01 00:00:00

  • Gait analysis by measuring ground reaction forces in children: changes to an adaptive gait pattern between the ages of one and five years.

    abstract::The aim of this study was to look at the maturational profile of gait parameters by measuring ground reaction forces during independent walking in children. Fifty-four normal children aged 1 to 5 years were examined. The children walked with eight force transducers under each sole. Gait velocity and step length increa...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1997.tb07416.x

    authors: Preis S,Klemms A,Müller K

    更新日期:1997-04-01 00:00:00

  • Should the Gross Motor Function Classification System be used for children who do not have cerebral palsy?

    abstract::This literature review addressed four questions. (1) In which populations other than cerebral palsy (CP) has the Gross Motor Function Classification System (GMFCS) been applied? (2) In what types of study, and why was it used? (3) How was it modified to facilitate these applications? (4) What justifications and eviden...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,评审

    doi:10.1111/dmcn.13602

    authors: Towns M,Rosenbaum P,Palisano R,Wright FV

    更新日期:2018-02-01 00:00:00

  • Down's syndrome and the family: follow-up of children first seen in infancy.

    abstract::Twenty-three survivors of a prospective study of infants with Down's syndrome were followed up at eight or nine years of age. All but three lived at home, and those three came home for weekends or school holidays. IQs varied from less than 20 to 80 (mean 48). IQ and adaptive behaviour scores were related to birthweigh...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1984.tb04478.x

    authors: Gath A,Gumley D

    更新日期:1984-08-01 00:00:00

  • Hypothermia as an adjuvant treatment in paediatric refractory or super-refractory status epilepticus.

    abstract::Therapeutic hypothermia is among the adjuvant therapies suggested for refractory or super-refractory status epilepticus (R/SR-SE) in paediatric patients. Experimental evidence of neuroprotective and antiseizure effects provides a strong rationale for using therapeutic hypothermia in patients with status epilepticus. T...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,评审

    doi:10.1111/dmcn.14562

    authors: Legriel S

    更新日期:2020-09-01 00:00:00

  • Atelencephalic microcephaly.

    abstract::A two-month-old child born with marked microcephaly (head circumference 17cm) was found at autopsy to have gliomesodermal tissue replacing the telencephalon (atelencephaly). This finding, together with genital anomalies and hypoplasia of the extremities, suggests arrest at the fifth week of fetal life. The clinical an...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1977.tb07973.x

    authors: Garcia CA,Duncan C

    更新日期:1977-04-01 00:00:00

  • Goldenhar syndrome and autistic behaviour.

    abstract::Two girls with concomitant Goldenhar syndrome (oculo-auriculovertebral spectrum disorder) and autistic disorder are described. One was diagnosed as having Goldenhar syndrome in the first few weeks of life and as having autistic disorder in her fifth year; the other was diagnosed as having Goldenhar syndrome when she w...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1992.tb11405.x

    authors: Landgren M,Gillberg C,Strömland K

    更新日期:1992-11-01 00:00:00

  • The Quality Function Measure: reliability and discriminant validity of a new measure of quality of gross motor movement in ambulatory children with cerebral palsy.

    abstract:AIM:Optimizing movement quality is a common rehabilitation goal for children with cerebral palsy (CP). The new Quality Function Measure (QFM)--a revision of the Gross Motor Performance Measure (GMPM)--evaluates five attributes: Alignment, Co-ordination, Dissociated movement, Stability, and Weight-shift, for the Gross M...

    journal_title:Developmental medicine and child neurology

    pub_type: 临床试验,杂志文章,多中心研究

    doi:10.1111/dmcn.12453

    authors: Wright FV,Rosenbaum P,Fehlings D,Mesterman R,Breuer U,Kim M

    更新日期:2014-08-01 00:00:00

  • Does parent report measure performance? A study of the construct validity of the Functional Mobility Scale.

    abstract:AIM:Parental report is often relied on to measure performance of activities in children with cerebral palsy (CP). This study examined whether the Functional Mobility Scale (FMS) accurately reflects performance of mobility in children with CP. METHOD:Eighteen children with spastic CP (11 males, seven females; mean age ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.2009.03354.x

    authors: Harvey A,Baker R,Morris ME,Hough J,Hughes M,Graham HK

    更新日期:2010-02-01 00:00:00

  • Gross and fine motor development of preterm infants at eight and 12 months of age.

    abstract::Forty-five neurologically normal preterm infants were allocated to one of two groups according to their gestational age at birth (less than 32 weeks; 32 to 36 weeks). Their gross and fine motor development was assessed at eight and 12 months chronological age and eight and 12 months adjusted age. At eight months chron...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1989.tb04044.x

    authors: Piper MC,Byrne PJ,Darrah J,Watt MJ

    更新日期:1989-10-01 00:00:00

  • Early onset calpainopathy with normal non-functional calpain 3 level.

    abstract::Limb girdle muscular dystrophy 2A (LGMD2A), caused by calpain 3 deficiency, is currently diagnosed through the immunodetection of muscle protein by Western blot (WB) analysis . However, WB may provide normal results in patients with LGMD2A. The case of a female (3y 6mo of age) is described. She was found to be affecte...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/S001216220600065X

    authors: Lanzillo R,Aurino S,Fanin M,Aguennoz M,Vitale F,Fiorillo C,Del Giudice E,Nigro V,Santoro L

    更新日期:2006-04-01 00:00:00

  • Neuropsychological functioning in children with early-treated phenylketonuria: impact of white matter abnormalities.

    abstract::Impact of white matter abnormalities (WMAs) on neuropsychological functioning in children with early-treated phenylketonuria (ETPKU) was examined. Children with ETPKU (20 males, 12 females, mean age 11 years 2 months, SD 3 years 6 months) and controls (20 males, 14 females, mean age 10 years 4 months, SD 3 years 1 mon...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162204000386

    authors: Anderson PJ,Wood SJ,Francis DE,Coleman L,Warwick L,Casanelia S,Anderson VA,Boneh A

    更新日期:2004-04-01 00:00:00

  • Exercise interventions improve postural control in children with cerebral palsy: a systematic review.

    abstract:AIM:The aim of this study was to evaluate the efficacy and effectiveness of exercise interventions that may improve postural control in children with cerebral palsy (CP). METHOD:A systematic review was performed using American Academy of Cerebral Palsy and Developmental Medicine (AACPDM) and Preferred Reporting Items ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,评审

    doi:10.1111/dmcn.12660

    authors: Dewar R,Love S,Johnston LM

    更新日期:2015-06-01 00:00:00

  • Management of apnea in infants with trisomy 18.

    abstract::This case series aimed to characterize the clinical features, management, and outcomes of apnea in infants with trisomy 18. Participants in this study were infants with trisomy 18 who were born alive and admitted to the neonatal intensive care unit in Kyushu University Hospital from 2000 to 2018. Retrospective analysi...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.14403

    authors: Taira R,Inoue H,Sawano T,Fujiyoshi J,Ichimiya Y,Torio M,Sanefuji M,Ochiai M,Sakai Y,Ohga S

    更新日期:2020-07-01 00:00:00

  • Dopa-responsive childhood dystonia: a forme fruste with writer's cramp, triggered by exercise.

    abstract::An 11-year-old girl was evaluated for walking difficulties and fatigue at the end of the day in the last 2 years. Handwriting was also difficult with 'cramps' after a short time of writing. Neurological examination was normal most of the time but in the evening and after exercise, an abnormal walking posture and rare ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1997.tb08204.x

    authors: Deonna T,Roulet E,Ghika J,Zesiger P

    更新日期:1997-01-01 00:00:00