Qualitative changes in dynamic tripod grip between seven and 14 years of age.

abstract：:Thirteen embryos with various central nervous system (cns) defects were examined macroscopically and by serial sectioning, and were compared with seven control embryos. All had been aborted spontaneously. Examples of anencephaly, anencephaly with spina bifida, spina bifida alone, encephalocele, iniencephaly and cyclop...

journal_title：Developmental medicine and child neurology

authors： Bell JE

更新日期：1979-06-01 00:00:00

abstract：AIM:The aim of the study was to support clinicians in recommending and justifying power mobility for children of different ages and abilities, and with different needs. The study comprised three distinct parts: a literature review; a Delphi consensus; and clinical practice considerations. METHOD:A scoping review of ei...

journal_title：Developmental medicine and child neurology

authors： Livingstone R,Paleg G

更新日期：2014-03-01 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：:This study surveyed 237 schoolchildren in a lead-polluted industrial area in northern Italy to assess the relationship between various biological indicators (lead in blood, hair and teeth, and delta-aminolevulinic dehydratase [ALA-D] activity) and some neuropsychological functions, assessed by a battery of five psycho...

journal_title：Developmental medicine and child neurology

authors： Bergomi M,Borella P,Fantuzzi G,Vivoli G,Sturloni N,Cavazzuti G,Tampieri A,Tartoni PL

更新日期：1989-04-01 00:00:00

abstract：:A behavioural modification package incorporating stimulus control, cueing, and rapid-extinction techniques was applied to a group of 15 children with severe learning disability who had chronic sleep disorders. Improvements in their night-settling and night-waking patterns occurred quickly (within a few days) and, in 1...

journal_title：Developmental medicine and child neurology

authors： Bramble D

更新日期：1997-08-01 00:00:00

abstract：:A care-load study was performed on a homogeneous group of 51 children, adolescents and young adults with spastic tetraplegia, born in Sweden between 1959 and 1978. All were immobile and severely mentally retarded, none could speak and the majority had epilepsy, scoliosis and contractures. 16 were living with their fam...

journal_title：Developmental medicine and child neurology

authors： Edebol-Tysk K

更新日期：1989-12-01 00:00:00

abstract：:According to traditional neurophysiological theory, consciousness requires neocortical functioning, and children born without cerebral hemispheres necessarily remain indefinitely in a developmental vegetative state. Four children between 5 and 17 years old are reported with congenital brain malformations involving tot...

journal_title：Developmental medicine and child neurology

authors： Shewmon DA,Holmes GL,Byrne PA

更新日期：1999-06-01 00:00:00

abstract：:Hand preference and functional hand-dominance of 45 spina bifida patients (aged 13 to 25 years) were assessed by means of self-reports on an ordinal scale and a tapping task. Non-right-handedness was more frequent among patients with accompanying progressive hydrocephalus. Left-hand preference was significantly more f...

journal_title：Developmental medicine and child neurology

authors： Wassing HE,Siebelink BM,Luyendijk W

更新日期：1993-09-01 00:00:00

abstract：:Ohtahara syndrome is a rare cause of epileptic seizures during the neonatal period. This is believed to be the first report of this syndrome with a specific metabolic defect. Defects in respiratory chain function may be more common than previously assumed in patients with this epilepsy syndrome. ...

journal_title：Developmental medicine and child neurology

authors： Williams AN,Gray RG,Poulton K,Ramani P,Whitehouse WP

更新日期：1998-08-01 00:00:00

abstract：AIM:There is a large literature reporting risk factor analyses for poor neurodevelopment in children born very preterm (VPT: ≤32wks) or very low birthweight (VLBW: ≤1250g), which to date has not been formally summarized. The aim of this paper was to identify prognostic factors for cerebral palsy (CP) and motor impairme...

journal_title：Developmental medicine and child neurology

authors： Linsell L,Malouf R,Morris J,Kurinczuk JJ,Marlow N

更新日期：2016-06-01 00:00:00

abstract：:Lesch-Nyhan syndrome (LNS) is a rare disorder of metabolism caused by a defective gene on the X chromosome. It is typically characterized by choreoathetosis, hypertonia, hyperreflexia, and self-mutilation. The present study is a 4-year follow-up investigation of the cognitive status of six subjects with a mean age of ...

journal_title：Developmental medicine and child neurology

authors： Matthews WS,Solan A,Barabas G,Robey K

更新日期：1999-04-01 00:00:00

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

authors： Law MR,Wijewardene K,Wald NJ

更新日期：1990-05-01 00:00:00

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

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

更新日期：2010-02-01 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：:Converging evidence indicates that motor deficits in cerebral palsy (CP) are related not only to problems with execution, but also to impaired motor planning. Current rehabilitation mainly focuses on alleviating compromised motor execution. Motor imagery is a promising method of training the more 'cognitive' aspects o...

journal_title：Developmental medicine and child neurology

authors： Steenbergen B,Crajé C,Nilsen DM,Gordon AM

更新日期：2009-09-01 00:00:00

abstract：:A 14-month-old girl presented after 3 days of fever, floppiness, and diffuse urticarial exanthem. She developed encephalitis and carditis and 1 week later, intractable seizures. Initial CT and MRI showed no changes in the brain parenchyma. On days 14 and 34 after the onset of symptoms, a human herpesvirus-6 (HHV-6) ge...

journal_title：Developmental medicine and child neurology

authors： Rantala H,Mannonen L,Ahtiluoto S,Linnavuori K,Herva R,Vaheri A,Koskiniemi M

更新日期：2000-06-01 00:00:00

abstract：:The objective of this study was to examine the descriptive epidemiology of vision impairment among 6- to 10-year-old children in metropolitan Atlanta, Georgia, USA. Children with vision impairment (n=310; 42% black, 56% white; 57% male, 43% female), defined as a best corrected visual acuity in the better eye of 20/70 ...

journal_title：Developmental medicine and child neurology

authors： Mervis CA,Boyle CA,Yeargin-Allsopp M

更新日期：2002-08-01 00:00:00

abstract：:Background factors of developmental outcome in a group of 386 neonatal 'at-risk' infants and 107 controls were examined in a prospective nine-year follow-up study. Dichotomized outcome variables were computed for each of the assessments; neurodevelopmental, motor, psycholinguistic, cognitive and school progress. In th...

journal_title：Developmental medicine and child neurology

authors： Lindahl E,Michelsson K,Helenius M,Parre M

更新日期：1988-10-01 00:00:00

abstract：AIM:The aim of this study was to conduct a systematic review in order to identify the risk factors for cerebral palsy (CP) in children born at term. The secondary aim was to ascertain if the potential for prevention of these risk factors has been adequately explored. METHOD:A MEDLINE search up to 31 July 2011 was comp...

journal_title：Developmental medicine and child neurology

authors： McIntyre S,Taitz D,Keogh J,Goldsmith S,Badawi N,Blair E

更新日期：2013-06-01 00:00:00

abstract：:Three cases with sensory peripheral neuropathies are reported. Case 1 presented with scoliosis, and cases 2 and 3 presented with abnormal gait. None had trophic limb changes, evidence of weakness, or a tendency to self-mutilation and each had normal motor studies on neurophysiological testing. Sural nerve biopsies sho...

journal_title：Developmental medicine and child neurology

authors： Bye AM,Baker WD,Pollard J,Wise G

更新日期：1990-02-01 00:00:00

abstract：AIM:To explore the views and practices of paediatric occupational therapists and physical therapists in Canada and the USA regarding the implementation of power mobility for children with mobility limitations. METHOD:This descriptive study utilized a web-based survey that included questions pertaining to therapists' d...

journal_title：Developmental medicine and child neurology

authors： Kenyon LK,Jones M,Livingstone R,Breaux B,Tsotsoros J,Williams KM

更新日期：2018-10-01 00:00:00

abstract：:A follow-up study was done of extremely low-birthweight infants (less than or equal to 1000g) born between 1976 and 1979, a period when aggressive intervention was not routine practice. The survival rate was 19 per cent. 44 of the 46 survivors were followed to a mean age of 6 1/2 years. By five years of age 23 of the ...

journal_title：Developmental medicine and child neurology

authors： Lefebvre F,Bard H,Veilleux A,Martel C

更新日期：1988-04-01 00:00:00

abstract：:This research examined family stress and sibling reactions in families of children with 5p- (cri du chat) syndrome aged 1 to 18 years who were living at home. In Study 1, 99 parents reported on themselves and their child with 5p-, as well as on family demographics, social supports, and stress. The best predictor of fa...

journal_title：Developmental medicine and child neurology

authors： Hodapp RM,Wijma CA,Masino LL

更新日期：1997-11-01 00:00:00

abstract：:Available observational tools used in the identification of social communication difficulties and diagnosis of autism spectrum disorder (ASD) rely partly on visual behaviours and therefore may not be valid in children with visual impairment. A pilot observational instrument, the Visual Impairment and Social Communicat...

journal_title：Developmental medicine and child neurology

authors： Absoud M,Parr JR,Salt A,Dale N

更新日期：2011-03-01 00:00:00

abstract：:The aim of the study was to review the psychometric properties and use of goal attainment scaling (GAS) in paediatric rehabilitation research. We performed a critical literature review searching: (1) all studies whose main focus was to assess the psychometric properties of GAS in paediatric rehabilitation; and (2) all...

journal_title：Developmental medicine and child neurology

authors： Steenbeek D,Ketelaar M,Galama K,Gorter JW

更新日期：2007-07-01 00:00:00

abstract：AIM:In female children with drug-resistant seizures and developmental delay from birth, atypical Rett syndrome caused by mutations in the CDKL5 gene should be considered. Several clinical features resemble classic Rett syndrome. Respiratory and sleep abnormalities are frequently present in Rett syndrome, whereas little...

journal_title：Developmental medicine and child neurology

authors： Hagebeuk EE,van den Bossche RA,de Weerd AW

更新日期：2013-05-01 00:00:00

abstract：:A case of multiple mucosal neuromata and a calcitonin-secreting medullary carcinoma of the thyroid is described. Unusual features were the neonatal presentation with large bowel obstruction and severe feeding difficulties associated with giant neuromata of the intestine; severe hypotonia; developmental delay; and the ...

journal_title：Developmental medicine and child neurology

authors： Moyes CD,Alexander FW

更新日期：1977-08-01 00:00:00

abstract：AIM:To describe the clinico-radiological phenotype of children with a CACNA1A mutation and to precisely evaluate their learning ability and cognitive status. METHOD:Children between the ages of 3 and 18 years harboring a pathogenic CACNA1A mutation associated with episodic ataxia, hemiplegic migraine, benign paroxysma...

journal_title：Developmental medicine and child neurology

authors： Humbertclaude V,Riant F,Krams B,Zimmermann V,Nagot N,Annequin D,Echenne B,Tournier-Lasserve E,Roubertie A,Episodic Syndrome Consortium.

更新日期：2020-03-01 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：:Feeding abilities in 20 individuals with Rett syndrome aged 1 1/2 to 33 years were investigated by history and clinical assessment during a meal, followed by videofluoroscopy of feeding. All were shown to have reduced movements of the mid and posterior tongue, with premature spillover of food and liquid from the mouth...

journal_title：Developmental medicine and child neurology

authors： Morton RE,Bonas R,Minford J,Kerr A,Ellis RE

更新日期：1997-05-01 00:00:00