Gross and fine motor function and accompanying impairments in cerebral palsy.

abstract：:Status dystonicus is a rare, but life-threatening movement disorder emergency. Urgent assessment is required and management is tailored to patient characteristics and complications. The use of dystonia action plans and early recognition of worsening dystonia may potentially facilitate intervention or prevent progressi...

journal_title：Developmental medicine and child neurology

authors： Allen NM,Lin JP,Lynch T,King MD

更新日期：2014-02-01 00:00:00

abstract：:The importance of the family environment for the development of children with neurodisabilities is undisputed. The objective of this study is to describe how family environment has been measured in research on families of children with neurodisabilities, in order to support researchers and clinicians to select appropr...

journal_title：Developmental medicine and child neurology

authors： Ketelaar M,Bogossian A,Saini M,Visser-Meily A,Lach L

更新日期：2017-03-01 00:00:00

abstract：AIM:To evaluate short-term (1y postoperatively; E1) and long-term (at least 4y postoperatively; E2) changes in hamstring muscle-tendon length (MTL) and lengthening velocity after hamstring lengthening in children with bilateral cerebral palsy (CP). METHOD:Three-dimensional gait analysis was performed in 19 children (1...

journal_title：Developmental medicine and child neurology

authors： Salami F,Brosa J,Van Drongelen S,Klotz MCM,Dreher T,Wolf SI,Thielen M

更新日期：2019-07-01 00:00:00

abstract：:A population-based group of 27 children with total blindness due to retinopathy of prematurity (ROP), born in Sweden from 1980 to 1990, was examined. They constituted all but two of the total of 29 children with total blindness due to ROP known to the national register of visually impaired children when reviewed from ...

journal_title：Developmental medicine and child neurology

authors： Jacobson L,Fernell E,Broberger U,Ek U,Gillberg C

更新日期：1998-03-01 00:00:00

abstract：:Mitofusin 2, a large transmembrane GTPase located in the outer mitochondrial membrane, promotes membrane fusion and is involved in the maintenance of the morphology of axonal mitochondria. Mutations of the gene encoding mitofusin 2 (MFN2) have recently been identified as the cause of approximately one-third of dominan...

journal_title：Developmental medicine and child neurology

authors： Ouvrier R,Grew S

更新日期：2010-04-01 00:00:00

abstract：:Carpal tunnel syndrome is extremely rare in childhood and in almost all previously reported cases it has been secondary to some underlying condition. Three 13- to 14-year-old girls are described with idiopathic carpal tunnel syndrome, confirmed by EMG and relieved by surgical decompression. A noteworthy feature in chi...

journal_title：Developmental medicine and child neurology

authors： Sainio K,Merikanto J,Larsen TA

更新日期：1987-12-01 00:00:00

abstract：AIM:To investigate the diagnostic yield and treatment impact of whole-genome sequencing (WGS) in patients with paediatric neurological disorders. METHOD:From January 2016 to December 2019, paediatric patients who had suspected genetic neurological disorders were assessed using WGS. The phenotypes of eligible patients ...

journal_title：Developmental medicine and child neurology

authors： Lee HF,Chi CS,Tsai CR

更新日期：2020-11-26 00:00:00

abstract：AIM:The aim of this study was to assess whether any memory impairment co-occurring with language impairment is global, affecting both verbal and visual domains, or domain specific. METHOD:Visual and verbal memory, learning, and processing speed were assessed in children aged 6 years to 16 years 11 months (mean 9 y 9 m...

journal_title：Developmental medicine and child neurology

authors： Baird G,Dworzynski K,Slonims V,Simonoff E

更新日期：2010-06-01 00:00:00

abstract：AIM:To review existing guidelines for universal newborn hearing screening (UNHS), identify those that provide comprehensive and clear recommendations on the subject, and provide a brief overview. METHOD:A scoping literature review was performed in PubMed, the Guidelines International Network library, and national guid...

journal_title：Developmental medicine and child neurology

authors： Kamenov K,Chadha S

更新日期：2021-01-01 00:00:00

abstract：:Perinatal hypoxic-ischaemic encephalopathy (HIE) occurs in 1 to 3 per 1000 term births. HIE is not preventable in most cases, and therapies are limited. Hypothermia improves outcomes and is the current standard of care. Yet, clinical trials suggest that 44-53% of infants who receive hypothermia will die or suffer mode...

journal_title：Developmental medicine and child neurology

authors： Wu YW,Gonzalez FF

更新日期：2015-04-01 00:00:00

abstract：:Guanidinoacetate methyltransferase (GAMT) deficiency is a disorder of creatine biosynthesis, characterized by early-onset learning disability and epilepsy in most affected children. Severe expressive language delay is a constant feature even in the mildest clinical phenotypes.We report the clinical, biochemical, imagi...

journal_title：Developmental medicine and child neurology

authors： O'Rourke DJ,Ryan S,Salomons G,Jakobs C,Monavari A,King MD

更新日期：2009-05-01 00:00:00

abstract：AIM:In a prospective, longitudinal study, we investigated the influence of the severity of motor impairment on changes in body characteristics in children with moderate-to-severe cerebral palsy (CP). METHOD:Twenty-six single children and adolescents (15 females, 11 males; mean age 10y 6mo, SD 3y 3mo) with spastic (qua...

journal_title：Developmental medicine and child neurology

authors： Ohata K,Tsuboyama T,Haruta T,Ichihashi N,Nakamura T

更新日期：2009-12-01 00:00:00

abstract：:Monozygotic twin boys with fragile X syndrome underwent thorough genetic, psychiatric, neurological, and language evaluations at 10 years of age. They both demonstrated physical features, speech and language difficulties, social problems, and attentional deficits that characterize the behavioural phenotype of fragile ...

journal_title：Developmental medicine and child neurology

authors： Sheldon L,Turk J

更新日期：2000-11-01 00:00:00

abstract：AIM:To investigate ataxia rating scales in children for reliability and the effect of age and sex. METHOD:Three independent neuropaediatric observers cross-sectionally scored a set of paediatric ataxia rating scales in a group of 52 healthy children (26 males, 26 females) aged 4 to 16 years (mean age 10y 5mo SD 3y 11m...

journal_title：Developmental medicine and child neurology

authors： Brandsma R,Spits AH,Kuiper MJ,Lunsing RJ,Burger H,Kremer HP,Sival DA,Childhood Ataxia and Cerebellar Group.

更新日期：2014-06-01 00:00:00

abstract：:The clinical phenotype in Lesch-Nyhan disease has been analyzed in 19 patients studied in hospital. In each case the diagnosis was made on the basis of inactivity of the enzyme hypoxanthine guanine phosphoribosyltransferase in erythrocyte lysates. All had hyperuricemia, and the presence of 'orange sand' in the diaper ...

journal_title：Developmental medicine and child neurology

authors： Christie R,Bay C,Kaufman IA,Bakay B,Borden M,Nyhan WL

更新日期：1982-06-01 00:00:00

abstract：:The purpose of this study was to report patients with pharmacoresistant West syndrome of unknown cause whose magnetic resonance imaging (MRI) with diffusion weighted imaging (DWI) showed a transient decrease of diffusion in subcortical structures. Of 20 patients investigated over a 2-year period, three males and three...

journal_title：Developmental medicine and child neurology

authors： Desguerre I,Marti I,Valayannopoulos V,Bahi-Buisson N,Dulac O,Plouin P,Delonlay P,Hertz-Pannier L,Boddaert N

更新日期：2008-02-01 00:00:00

abstract：:The authors report the results of two EEG studies on adult patients with phenylketonuria (PKU) who had been treated early. Part I: the authors followed the EEGs of 34 PKU patients from birth to age 21. The frequency of abnormal EEG findings (especially epileptiform activity) steadily increased until age 12, then decre...

journal_title：Developmental medicine and child neurology

authors： Pietz J,Schmidt E,Matthis P,Kobialka B,Kutscha A,de Sonneville L

更新日期：1993-01-01 00:00:00

abstract：:Participation and activity performance (motor and cognitive or behavioural) were examined in 148 children with cerebral palsy (CP; 87 males, 61 females; mean age 9y 8mo, SD 1y 11mo; range 6y 1mo to 13y 7mo), mainstreamed in fully inclusive (n=100) and in self-contained classes (n=48) within general schools in Israel, ...

journal_title：Developmental medicine and child neurology

authors： Schenker R,Coster WJ,Parush S

更新日期：2005-12-01 00:00:00

abstract：AIM:The aim of this study was to compare thermal detection and pain thresholds in children with Down syndrome with those of their siblings. METHOD:Sensory detection and pain thresholds were assessed in children with Down syndrome and their siblings using quantitative testing methods. Parental questionnaires addressing...

journal_title：Developmental medicine and child neurology

authors： Valkenburg AJ,Tibboel D,van Dijk M

更新日期：2015-11-01 00:00:00

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

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

更新日期：1997-01-01 00:00:00

abstract：:Luce's choice theory provided the psychophysical basis for investigating the ability of cerebral-palsied children to detect passive movement of the elbow joint. The method included testing "yes" responses when the forearm was moved, and "false-alarm" responses of "yes" when no arm movement had occurred. The children w...

journal_title：Developmental medicine and child neurology

authors： Jones B

更新日期：1976-02-01 00:00:00

abstract：:According to previous case reports, some congenital abnormalities (CAs) of the brain, such as microcephaly, are a result of intrauterine herpes simplex virus infection. A population-based case-control study was conducted to determine the risk of neural tube defects (NTDs) after maternal herpes labialis infection durin...

journal_title：Developmental medicine and child neurology

authors： Nørgård B,Nørgaard M,Czeizel AE,Puhó E,Sørensen HT

更新日期：2006-08-01 00:00:00

abstract：AIM:To conduct a longitudinal follow-up of the development of global cognitive abilities and adaptive skills in individuals with congenital and childhood forms of myotonic dystrophy type 1 (DM1). METHOD:Fifty-one participants (29 males, 22 females, mean age 19y 5mo, SD 4y 11mo, range 10y 10mo-28y 11mo) were divided in...

journal_title：Developmental medicine and child neurology

authors： Lindeblad G,Kroksmark AK,Ekström AB

更新日期：2019-10-01 00:00:00

abstract：AIM:To determine dimensionality and item-level properties of the Gillette Functional Assessment Questionnaire (FAQ) 22-item skill set using factor and Rasch analyses. METHOD:A retrospective review of parent-reported FAQ 22-item skill set data was conducted of 485 individuals (273 males, 212 females; mean age 9 y 10 mo...

journal_title：Developmental medicine and child neurology

authors： Gorton GE 3rd,Stout JL,Bagley AM,Bevans K,Novacheck TF,Tucker CA

更新日期：2011-03-01 00:00:00

abstract：AIM:To evaluate presence and severity of social impairments in alternating hemiplegia of childhood (AHC) and determine factors that are associated with social impairments. METHOD:This was a retrospective analysis of 34 consecutive patients with AHC (19 females, 15 males; mean age: 9y 7mo, SD 8y 2mo, range 2y 7mo-40y),...

journal_title：Developmental medicine and child neurology

authors： Uchitel J,Abdelnour E,Boggs A,Prange L,Pratt M,Bonner M,Jasien J,Dawson G,Abrahamsen T,Mikati MA

更新日期：2020-07-01 00:00:00

abstract：:We report a longitudinal, prospective, multicentre cohort study designed to measure the outcomes of gastrostomy tube feeding in children with cerebral palsy (CP). Fifty-seven children with CP (28 females, 29 males; median age 4y 4mo, range 5mo to 17y 3mo) were assessed before gastrostomy placement, and at 6 and 12 mon...

journal_title：Developmental medicine and child neurology

authors： Sullivan PB,Juszczak E,Bachlet AM,Lambert B,Vernon-Roberts A,Grant HW,Eltumi M,McLean L,Alder N,Thomas AG

更新日期：2005-02-01 00:00:00

abstract：:Nineteen sightless children and adolescents aged between 11 and 18 years were tested for physical condition and performance. Their residential school provided four adapted physical education lessons a week, lasting for 45 minutes. Their physical condition and performance was found to be comparable with that of normal ...

journal_title：Developmental medicine and child neurology

authors： Lee M,Ward G,Shephard RJ

更新日期：1985-12-01 00:00:00

abstract：:The developmental level and nutritional status of a group of 17 children aged between six and 24 months who were admitted to hospital with severe protein-energy malnutrition were studied from admission to hospital until 36 months after returning home. They were compared with a group of 14 adequately nourished children...

journal_title：Developmental medicine and child neurology

authors： Grantham-McGregor SM,Powell C,Stewart M,Schofield WN

更新日期：1982-06-01 00:00:00

abstract：:Two groups of clinically normal newborns, differing in the number of non-optimal factors in their obstetric history, were compared by measuring heart-rate response to a series of auditory stimuli. There was a significant difference between the groups in the direction of the average heart-rate response. The high risk" ...

journal_title：Developmental medicine and child neurology

authors： Kittner S,Lipsitt LP

更新日期：1976-08-01 00:00:00

abstract：AIM:To identify and critically appraise standardized measures of power mobility skill used with children (18y or younger) with mobility limitations and explore the measures' application for 'exploratory', 'operational', and 'functional' learners. METHOD:Five electronic databases were searched along with hand-searching...

journal_title：Developmental medicine and child neurology

authors： Field DA,Livingstone RW

更新日期：2018-10-01 00:00:00