Dépouillements

Intervention - The doctor's Job / Martin C. O. BAX in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.281-282 Titre : Intervention - The doctor's Job Type de document : Texte imprimé et/ou numérique Auteurs : Martin C. O. BAX, Auteur Année de publication : 1985 Article en page(s) : p.281-282 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591 [article] Intervention - The doctor's Job [Texte imprimé et/ou numérique] / Martin C. O. BAX, Auteur . - 1985 . - p.281-282. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.281-282 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591

A critical look at vestibular dysfunction in learning-disabled children / Helene J. POLATAJKO in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.283-292 Titre : A critical look at vestibular dysfunction in learning-disabled children Type de document : Texte imprimé et/ou numérique Auteurs : Helene J. POLATAJKO, Auteur Année de publication : 1985 Article en page(s) : p.283-292 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The purpose of this study was to investigate the vestibular dysfunction hypothesis in learning disabilities. The data indicated that there was no significant difference in vestibular function between normal and learning-disabled children; that there was no significant correlation between vestibular function and academic achievement; and that there was no significant educational relevance in categorizing learning-disabled children according to vestibular dimensions. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591 [article] A critical look at vestibular dysfunction in learning-disabled children [Texte imprimé et/ou numérique] / Helene J. POLATAJKO, Auteur . - 1985 . - p.283-292. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.283-292 Index. décimale : PER Périodiques Résumé : The purpose of this study was to investigate the vestibular dysfunction hypothesis in learning disabilities. The data indicated that there was no significant difference in vestibular function between normal and learning-disabled children; that there was no significant correlation between vestibular function and academic achievement; and that there was no significant educational relevance in categorizing learning-disabled children according to vestibular dimensions. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591

Chromosome abnormalities in infantile autism and other childhood psychoses: a population study of 66 cases / Christopher GILLBERG in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - 293-304 Titre : Chromosome abnormalities in infantile autism and other childhood psychoses: a population study of 66 cases Type de document : Texte imprimé et/ou numérique Auteurs : Christopher GILLBERG, Auteur ; Jan WAHLSTROM, Auteur Année de publication : 1985 Article en page(s) : 293-304 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Sixty-six psychotic children aged between two and 20 years, examined by the same child psychiatrist and diagnosed according to strict criteria as suffering from infantile autism, other psychoses and Asperger's syndrome, were examined with chromosomal cultures in folic-acid deficient medium. 47 per cent of the children showed major or minor chromosomal aberrations. The infantile autistic group comprised a total population of autistic children. The fra(X)(q27) marker was seen in 25 per cent of autistic boys. A subgroup of children with the fra(X)(q27) abnormality, infantile autism, psychomotor epilepsy and brainstem dysfunction was identified. Other chromosome markers and abnormalities occurring in several cases included long Y chromosomes, fra(X)(p22), fra(16)(q23) and fra(6)(q26). The results are discussed and correlated with certain clinical characteristics. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591 [article] Chromosome abnormalities in infantile autism and other childhood psychoses: a population study of 66 cases [Texte imprimé et/ou numérique] / Christopher GILLBERG, Auteur ; Jan WAHLSTROM, Auteur . - 1985 . - 293-304. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - 293-304 Index. décimale : PER Périodiques Résumé : Sixty-six psychotic children aged between two and 20 years, examined by the same child psychiatrist and diagnosed according to strict criteria as suffering from infantile autism, other psychoses and Asperger's syndrome, were examined with chromosomal cultures in folic-acid deficient medium. 47 per cent of the children showed major or minor chromosomal aberrations. The infantile autistic group comprised a total population of autistic children. The fra(X)(q27) marker was seen in 25 per cent of autistic boys. A subgroup of children with the fra(X)(q27) abnormality, infantile autism, psychomotor epilepsy and brainstem dysfunction was identified. Other chromosome markers and abnormalities occurring in several cases included long Y chromosomes, fra(X)(p22), fra(16)(q23) and fra(6)(q26). The results are discussed and correlated with certain clinical characteristics. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591

Chromosome 15 in Prader-Willi syndrome / C. N. FEAR in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.305-311 Titre : Chromosome 15 in Prader-Willi syndrome Type de document : Texte imprimé et/ou numérique Auteurs : C. N. FEAR, Auteur ; Victor DUBOWITZ, Auteur ; David E. MUTTON, Auteur ; John Z. HECKMATT, Auteur ; A. C. BERRY, Auteur Année de publication : 1985 Article en page(s) : p.305-311 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Nineteen children with the clinical features of Prader-Willi syndrome were karyotyped, using both routine Giemsa banding and high-resolution techniques. Chromosome abnormalities involving chromosome 15 were found in 10, entirely normal chromosomes in five and for the remaining four the findings were either equivocal or difficult to interpret. There was no clinical distinction between cases with and without the chromosome anomaly. Examination of three parents and a group of controls showed that the proximal end of the long arm of chromosome 15 may have a considerable degree of normal variation, which can make interpretation difficult. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591 [article] Chromosome 15 in Prader-Willi syndrome [Texte imprimé et/ou numérique] / C. N. FEAR, Auteur ; Victor DUBOWITZ, Auteur ; David E. MUTTON, Auteur ; John Z. HECKMATT, Auteur ; A. C. BERRY, Auteur . - 1985 . - p.305-311. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.305-311 Index. décimale : PER Périodiques Résumé : Nineteen children with the clinical features of Prader-Willi syndrome were karyotyped, using both routine Giemsa banding and high-resolution techniques. Chromosome abnormalities involving chromosome 15 were found in 10, entirely normal chromosomes in five and for the remaining four the findings were either equivocal or difficult to interpret. There was no clinical distinction between cases with and without the chromosome anomaly. Examination of three parents and a group of controls showed that the proximal end of the long arm of chromosome 15 may have a considerable degree of normal variation, which can make interpretation difficult. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591

Neurological manifestations in abused children who have been shaken / Y. FRANK in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - 312-316 Titre : Neurological manifestations in abused children who have been shaken Type de document : Texte imprimé et/ou numérique Auteurs : Y. FRANK, Auteur ; R. ZIMMERMAN, Auteur ; N. M. D. LEEDS, Auteur Année de publication : 1985 Article en page(s) : 312-316 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Four infants with the 'shaken infant syndrome' are described. None had skull fractures and only one had a subdural hematoma. All had extensive retinal and pre-retinal hemorrhages. Follow-up computerized tomography showed severe brain atrophy, multiple hypodense areas and ventricular enlargement. Three of the patients suffered severe, permanent brain damage, with mental retardation, spasticity and blindness. It is suggested that the underlying pathogenesis of this syndrome is acutely increased intrathoracic pressure, transmitted into the head to cause multiple venous infarctions. Retinal and pre-retinal hemorrhages are cardinal features of this syndrome and their presence should raise the suspicion of this form of battering in the absence of the 'classical' signs of battering. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591 [article] Neurological manifestations in abused children who have been shaken [Texte imprimé et/ou numérique] / Y. FRANK, Auteur ; R. ZIMMERMAN, Auteur ; N. M. D. LEEDS, Auteur . - 1985 . - 312-316. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - 312-316 Index. décimale : PER Périodiques Résumé : Four infants with the 'shaken infant syndrome' are described. None had skull fractures and only one had a subdural hematoma. All had extensive retinal and pre-retinal hemorrhages. Follow-up computerized tomography showed severe brain atrophy, multiple hypodense areas and ventricular enlargement. Three of the patients suffered severe, permanent brain damage, with mental retardation, spasticity and blindness. It is suggested that the underlying pathogenesis of this syndrome is acutely increased intrathoracic pressure, transmitted into the head to cause multiple venous infarctions. Retinal and pre-retinal hemorrhages are cardinal features of this syndrome and their presence should raise the suspicion of this form of battering in the absence of the 'classical' signs of battering. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591

Neurological signs in congenital iodine-deficiency disorder (endemic cretinism) / G. Robert DELONG in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.317-324 Titre : Neurological signs in congenital iodine-deficiency disorder (endemic cretinism) Type de document : Texte imprimé et/ou numérique Auteurs : G. Robert DELONG, Auteur ; John B. STANBURY, Auteur ; Rodrigo FIERRO-BENITEZ, Auteur Année de publication : 1985 Article en page(s) : p.317-324 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Neurological examinations were made of 67 children and adults with congenital iodine-deficiency disorder (endemic cretinism) in four rural villages in highland Ecuador. There was a distinct and readily identifiable pattern of neurological deficits. These included, to varying degrees: deaf-mutism or lesser degrees of bilateral hearing-loss or dysarthria; spasticity, particularly involving the proximal lower extremities; mental deficiency of a characteristic type; and rigidity and bradykinesia. Not all of these elements were found in all cases. Less common features were strabismus, kyphoscoliosis and frontal-lobe signs. There were exceptional cases with hypotonia. In contrast, cerebellar function was largely spared, as were functions of emotion and attention, vegetative and autonomic functions, social interaction, and probably memory, except in the most severely involved. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591 [article] Neurological signs in congenital iodine-deficiency disorder (endemic cretinism) [Texte imprimé et/ou numérique] / G. Robert DELONG, Auteur ; John B. STANBURY, Auteur ; Rodrigo FIERRO-BENITEZ, Auteur . - 1985 . - p.317-324. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.317-324 Index. décimale : PER Périodiques Résumé : Neurological examinations were made of 67 children and adults with congenital iodine-deficiency disorder (endemic cretinism) in four rural villages in highland Ecuador. There was a distinct and readily identifiable pattern of neurological deficits. These included, to varying degrees: deaf-mutism or lesser degrees of bilateral hearing-loss or dysarthria; spasticity, particularly involving the proximal lower extremities; mental deficiency of a characteristic type; and rigidity and bradykinesia. Not all of these elements were found in all cases. Less common features were strabismus, kyphoscoliosis and frontal-lobe signs. There were exceptional cases with hypotonia. In contrast, cerebellar function was largely spared, as were functions of emotion and attention, vegetative and autonomic functions, social interaction, and probably memory, except in the most severely involved. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591

Consideration of genetic factors in cerebral palsy / F. Javier MONREAL in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.325-330 Titre : Consideration of genetic factors in cerebral palsy Type de document : Texte imprimé et/ou numérique Auteurs : F. Javier MONREAL, Auteur Année de publication : 1985 Article en page(s) : p.325-330 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Sixty-two patients with cerebral palsy seen consecutively in a pediatric neurology practice were submitted to a prospective protocol which tabulated their neurological findings, birth and developmental histories and an extensive neurodevelopmental pedigree. Their family histories were compared with those of three control groups, consisting of 62 children with headaches, 62 with school/behavior problems and 62 random normal children. The family histories of the cerebral-palsied children revealed an unusual number of relatives with cerebral palsy, mental retardation and seizures. This study suggests that a large proportion of cerebral-palsied individuals may be predisposed to aplasia/hypoplasia of neural tissue. Some affected by presumably static 'brain-damage' may in later years develop indolent degenerative disease. Indirect genetic factors may also play a major predisposing role in cerebral palsy of proven postnatal/perinatal onset. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591 [article] Consideration of genetic factors in cerebral palsy [Texte imprimé et/ou numérique] / F. Javier MONREAL, Auteur . - 1985 . - p.325-330. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.325-330 Index. décimale : PER Périodiques Résumé : Sixty-two patients with cerebral palsy seen consecutively in a pediatric neurology practice were submitted to a prospective protocol which tabulated their neurological findings, birth and developmental histories and an extensive neurodevelopmental pedigree. Their family histories were compared with those of three control groups, consisting of 62 children with headaches, 62 with school/behavior problems and 62 random normal children. The family histories of the cerebral-palsied children revealed an unusual number of relatives with cerebral palsy, mental retardation and seizures. This study suggests that a large proportion of cerebral-palsied individuals may be predisposed to aplasia/hypoplasia of neural tissue. Some affected by presumably static 'brain-damage' may in later years develop indolent degenerative disease. Indirect genetic factors may also play a major predisposing role in cerebral palsy of proven postnatal/perinatal onset. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591

Early detection of brainstem glioma using brainstem auditory evoked potentials / A. Norman GUTHKELCH in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.331-334 Titre : Early detection of brainstem glioma using brainstem auditory evoked potentials Type de document : Texte imprimé et/ou numérique Auteurs : A. Norman GUTHKELCH, Auteur ; John K. VRIES, Auteur ; Robert J. SCLABASSI, Auteur Année de publication : 1985 Article en page(s) : p.331-334 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Brainstem tumor was suspected in an 11-year-old boy presenting with a painless lateral rectus palsy, on the basis of abnormal brainstem auditory evoked potentials (BAEP), despite normal computed tomographic studies, the diagnosis being confirmed by biopsy. The BAEP improved after radiation therapy, but their later deterioration heralded the onset of recurrence two weeks before any adverse clinical symptoms appeared. The value of BAEP studies in the early detection of brainstem lesions and in monitoring their progress, is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591 [article] Early detection of brainstem glioma using brainstem auditory evoked potentials [Texte imprimé et/ou numérique] / A. Norman GUTHKELCH, Auteur ; John K. VRIES, Auteur ; Robert J. SCLABASSI, Auteur . - 1985 . - p.331-334. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.331-334 Index. décimale : PER Périodiques Résumé : Brainstem tumor was suspected in an 11-year-old boy presenting with a painless lateral rectus palsy, on the basis of abnormal brainstem auditory evoked potentials (BAEP), despite normal computed tomographic studies, the diagnosis being confirmed by biopsy. The BAEP improved after radiation therapy, but their later deterioration heralded the onset of recurrence two weeks before any adverse clinical symptoms appeared. The value of BAEP studies in the early detection of brainstem lesions and in monitoring their progress, is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591

Rud syndrome revisited: ichthyosis, mental retardation, epilepsy and hypogonadism / Jane MARXMILLER in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.335-343 Titre : Rud syndrome revisited: ichthyosis, mental retardation, epilepsy and hypogonadism Type de document : Texte imprimé et/ou numérique Auteurs : Jane MARXMILLER, Auteur ; Ingrid TRENKLE, Auteur ; Stephen ASHWAL, Auteur Année de publication : 1985 Article en page(s) : p.335-343 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Rud syndrome is a rare disorder of childhood characterized by ichthyosis, mental retardation, epilepsy and hypogonadism. The authors report a family with this autosomal recessive disorder, review the clinical and dermatopathological findings, and contrast Rud syndrome with the other major neuro-ichthyosiform dermatoses. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591 [article] Rud syndrome revisited: ichthyosis, mental retardation, epilepsy and hypogonadism [Texte imprimé et/ou numérique] / Jane MARXMILLER, Auteur ; Ingrid TRENKLE, Auteur ; Stephen ASHWAL, Auteur . - 1985 . - p.335-343. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.335-343 Index. décimale : PER Périodiques Résumé : Rud syndrome is a rare disorder of childhood characterized by ichthyosis, mental retardation, epilepsy and hypogonadism. The authors report a family with this autosomal recessive disorder, review the clinical and dermatopathological findings, and contrast Rud syndrome with the other major neuro-ichthyosiform dermatoses. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=591

Neuromotor maturation and psychological performance: a developmental study / Peter H. WOLFF in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.344-354 Titre : Neuromotor maturation and psychological performance: a developmental study Type de document : Texte imprimé et/ou numérique Auteurs : Peter H. WOLFF, Auteur ; C. E. GUNNOE, Auteur ; C. COHEN, Auteur Année de publication : 1985 Article en page(s) : p.344-354 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Groups of 50 normal kindergarten and 50 first-grade children were examined three times at six-month intervals on the extended neuromotor examination for children, as well as on measures of reading achievement and language performance. The joint effect of five neuromotor measures accounted for a substantial percentage of variance in reading achievement and language performance 12 months later. As a global measure, neuromotor status therefore may constitute a reliable, independent criterion of developmental age for psychological investigations of young, normal children. The best individual predictors of psychological outcome were mirror movements and speed of timed motor repetitions, while reading achievement and automated naming speed were the dependent measures most closely associated over time with neuromotor status. Such findings suggest that the individual motor signs may also provide indirect clues about the presumed functional relationship between development of motor co-ordination and language competence. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592 [article] Neuromotor maturation and psychological performance: a developmental study [Texte imprimé et/ou numérique] / Peter H. WOLFF, Auteur ; C. E. GUNNOE, Auteur ; C. COHEN, Auteur . - 1985 . - p.344-354. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.344-354 Index. décimale : PER Périodiques Résumé : Groups of 50 normal kindergarten and 50 first-grade children were examined three times at six-month intervals on the extended neuromotor examination for children, as well as on measures of reading achievement and language performance. The joint effect of five neuromotor measures accounted for a substantial percentage of variance in reading achievement and language performance 12 months later. As a global measure, neuromotor status therefore may constitute a reliable, independent criterion of developmental age for psychological investigations of young, normal children. The best individual predictors of psychological outcome were mirror movements and speed of timed motor repetitions, while reading achievement and automated naming speed were the dependent measures most closely associated over time with neuromotor status. Such findings suggest that the individual motor signs may also provide indirect clues about the presumed functional relationship between development of motor co-ordination and language competence. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592

The satellite clinic: a model for the treatment of handicapped children in towns and rural areas / K. O. STEEL in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.355-363 Titre : The satellite clinic: a model for the treatment of handicapped children in towns and rural areas Type de document : Texte imprimé et/ou numérique Auteurs : K. O. STEEL, Auteur ; R. A. SPASOFF, Auteur ; J. O. ALEXANDER, Auteur Année de publication : 1985 Article en page(s) : p.355-363 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A satellite clinic provided treatment for children living in a community 50 miles from an established Crippled Children's Treatment Centre. An evaluation of the service indicated that children attending the Satellite received more frequent treatment, at reduced costs to parents and social agencies. These children showed greater improvement in motor function than a control group, although no corresponding improvement in self-help skills was detected. Parents expressed a high level of satisfaction with the new service. The Satellite Clinic is recommended as a model for children unable to obtain regular treatment at an established centre. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592 [article] The satellite clinic: a model for the treatment of handicapped children in towns and rural areas [Texte imprimé et/ou numérique] / K. O. STEEL, Auteur ; R. A. SPASOFF, Auteur ; J. O. ALEXANDER, Auteur . - 1985 . - p.355-363. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.355-363 Index. décimale : PER Périodiques Résumé : A satellite clinic provided treatment for children living in a community 50 miles from an established Crippled Children's Treatment Centre. An evaluation of the service indicated that children attending the Satellite received more frequent treatment, at reduced costs to parents and social agencies. These children showed greater improvement in motor function than a control group, although no corresponding improvement in self-help skills was detected. Parents expressed a high level of satisfaction with the new service. The Satellite Clinic is recommended as a model for children unable to obtain regular treatment at an established centre. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592

Physical development of hyperactive boys / Rob MCGEE in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.364-368 Titre : Physical development of hyperactive boys Type de document : Texte imprimé et/ou numérique Auteurs : Rob MCGEE, Auteur ; Phil A. SILVA, Auteur ; John BIRKBECK, Auteur Année de publication : 1985 Article en page(s) : p.364-368 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Anthropometric data were collected on groups of seven-year-old Dunedin (New Zealand) boys, identified as hyperactive-only, aggressive-hyperactive, aggressive-only and non-aggressive/non-hyperactive. Measures taken included stature, weight, skeletal maturity, mid-upper arm circumference, triceps and subscapular fatfolds and body-mass index. The hypothesis that hyperactive-only boys would show delayed maturation, as indicated by lower bone-age, was not confirmed. However, these boys had significantly smaller mid-upper arm circumference, triceps fatfold and body-mass index than the other groups. The results suggest that body leanness may discriminate 'pure' hyperactive boys from aggressive-hyperactive boys. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592 [article] Physical development of hyperactive boys [Texte imprimé et/ou numérique] / Rob MCGEE, Auteur ; Phil A. SILVA, Auteur ; John BIRKBECK, Auteur . - 1985 . - p.364-368. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.364-368 Index. décimale : PER Périodiques Résumé : Anthropometric data were collected on groups of seven-year-old Dunedin (New Zealand) boys, identified as hyperactive-only, aggressive-hyperactive, aggressive-only and non-aggressive/non-hyperactive. Measures taken included stature, weight, skeletal maturity, mid-upper arm circumference, triceps and subscapular fatfolds and body-mass index. The hypothesis that hyperactive-only boys would show delayed maturation, as indicated by lower bone-age, was not confirmed. However, these boys had significantly smaller mid-upper arm circumference, triceps fatfold and body-mass index than the other groups. The results suggest that body leanness may discriminate 'pure' hyperactive boys from aggressive-hyperactive boys. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592

Congenital rupture of a neuropathic bladder: report of a case / J. R. BRIGGS in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.369-374 Titre : Congenital rupture of a neuropathic bladder: report of a case Type de document : Texte imprimé et/ou numérique Auteurs : J. R. BRIGGS, Auteur ; I. I. SMITH, Auteur ; Robert A. MINNS, Auteur Année de publication : 1985 Article en page(s) : p.369-374 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A case of intra-uterine rupture of a neurogenic bladder in a female child with spina bifida is reported, together with the unusual histological appearances of detrusor-muscle atrophy at the site of rupture. The literature on ruptured bladder in the neonatal period is reviewed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592 [article] Congenital rupture of a neuropathic bladder: report of a case [Texte imprimé et/ou numérique] / J. R. BRIGGS, Auteur ; I. I. SMITH, Auteur ; Robert A. MINNS, Auteur . - 1985 . - p.369-374. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.369-374 Index. décimale : PER Périodiques Résumé : A case of intra-uterine rupture of a neurogenic bladder in a female child with spina bifida is reported, together with the unusual histological appearances of detrusor-muscle atrophy at the site of rupture. The literature on ruptured bladder in the neonatal period is reviewed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592

Cachexia in a mentally retarded adolescent secondary to mandibular dislocation / Edward M. SONNENBERG in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.374-376 Titre : Cachexia in a mentally retarded adolescent secondary to mandibular dislocation Type de document : Texte imprimé et/ou numérique Auteurs : Edward M. SONNENBERG, Auteur ; Philip ZIRING, Auteur ; Michael L. BARNETT, Auteur ; Kathryn STRASSBURGER, Auteur Année de publication : 1985 Article en page(s) : p.374-376 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A 19-year-old mentally retarded male's cachexia, of five months duration, was attributed to a previously undetected anterior dislocation of the mandible. After reduction of the mandible he improved markedly, with better appetite and rapid weight-gain. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592 [article] Cachexia in a mentally retarded adolescent secondary to mandibular dislocation [Texte imprimé et/ou numérique] / Edward M. SONNENBERG, Auteur ; Philip ZIRING, Auteur ; Michael L. BARNETT, Auteur ; Kathryn STRASSBURGER, Auteur . - 1985 . - p.374-376. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.374-376 Index. décimale : PER Périodiques Résumé : A 19-year-old mentally retarded male's cachexia, of five months duration, was attributed to a previously undetected anterior dislocation of the mandible. After reduction of the mandible he improved markedly, with better appetite and rapid weight-gain. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592

Pyridoxine for neonatal seizures: an unexpected danger / J. S. KROLL in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.377-379 Titre : Pyridoxine for neonatal seizures: an unexpected danger Type de document : Texte imprimé et/ou numérique Auteurs : J. S. KROLL, Auteur Année de publication : 1985 Article en page(s) : p.377-379 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A case of pyridoxine-dependent seizures is reported. Administration of pyridoxine to an infant after a long period of convulsions was followed by acute hypotonia. Other cases have been reported in the literature, in one of which assisted ventilation was required. A possible mechanism for this alarming outcome is discussed, and it is suggested that resuscitation facilities should be quickly available during such trials. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592 [article] Pyridoxine for neonatal seizures: an unexpected danger [Texte imprimé et/ou numérique] / J. S. KROLL, Auteur . - 1985 . - p.377-379. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.377-379 Index. décimale : PER Périodiques Résumé : A case of pyridoxine-dependent seizures is reported. Administration of pyridoxine to an infant after a long period of convulsions was followed by acute hypotonia. Other cases have been reported in the literature, in one of which assisted ventilation was required. A possible mechanism for this alarming outcome is discussed, and it is suggested that resuscitation facilities should be quickly available during such trials. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592

Brainstem glioma presenting as paroxysmal headache / Gerald P. NOVAK in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.379-382 Titre : Brainstem glioma presenting as paroxysmal headache Type de document : Texte imprimé et/ou numérique Auteurs : Gerald P. NOVAK, Auteur ; Solomon L. MOSHE, Auteur Année de publication : 1985 Article en page(s) : p.379-382 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : An unusual case of brainstem glioma is described. The distinctive features were long duration (at least six months) of headaches preceding the appearance of neurological signs, and the intermittent, paroxysmal nature of the symptoms, often precipitated by postural change. The mechanism of headache induced by brain tumor is discussed, and a possible cause for the headaches in this patient is suggested, involving intermittent obstruction of CSF flow. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592 [article] Brainstem glioma presenting as paroxysmal headache [Texte imprimé et/ou numérique] / Gerald P. NOVAK, Auteur ; Solomon L. MOSHE, Auteur . - 1985 . - p.379-382. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.379-382 Index. décimale : PER Périodiques Résumé : An unusual case of brainstem glioma is described. The distinctive features were long duration (at least six months) of headaches preceding the appearance of neurological signs, and the intermittent, paroxysmal nature of the symptoms, often precipitated by postural change. The mechanism of headache induced by brain tumor is discussed, and a possible cause for the headaches in this patient is suggested, involving intermittent obstruction of CSF flow. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592

Recovery from cortical blindness / John FOLEY in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.383-387 Titre : Recovery from cortical blindness Type de document : Texte imprimé et/ou numérique Auteurs : John FOLEY, Auteur ; Neil GORDON, Auteur Année de publication : 1985 Article en page(s) : p.383-387 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592 [article] Recovery from cortical blindness [Texte imprimé et/ou numérique] / John FOLEY, Auteur ; Neil GORDON, Auteur . - 1985 . - p.383-387. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.383-387 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592

Congenital hypothyroidism / Alfred M. BONGIOVANNI in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.387-389 Titre : Congenital hypothyroidism Type de document : Texte imprimé et/ou numérique Auteurs : Alfred M. BONGIOVANNI, Auteur Année de publication : 1985 Article en page(s) : p.387-389 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592 [article] Congenital hypothyroidism [Texte imprimé et/ou numérique] / Alfred M. BONGIOVANNI, Auteur . - 1985 . - p.387-389. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.387-389 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592

Handling stress in the handicapped adolescent / Philip GRAHAM in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.389-391 Titre : Handling stress in the handicapped adolescent Type de document : Texte imprimé et/ou numérique Auteurs : Philip GRAHAM, Auteur Année de publication : 1985 Article en page(s) : p.389-391 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592 [article] Handling stress in the handicapped adolescent [Texte imprimé et/ou numérique] / Philip GRAHAM, Auteur . - 1985 . - p.389-391. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.389-391 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=592

Parental reactions to loss and disappointment: the diagnosis of Down's syndrome / Ann GATH in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.392-400 Titre : Parental reactions to loss and disappointment: the diagnosis of Down's syndrome Type de document : Texte imprimé et/ou numérique Auteurs : Ann GATH, Auteur Année de publication : 1985 Article en page(s) : p.392-400 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=593 [article] Parental reactions to loss and disappointment: the diagnosis of Down's syndrome [Texte imprimé et/ou numérique] / Ann GATH, Auteur . - 1985 . - p.392-400. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.392-400 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=593

Spastic paralytic dislocation of the hip / Jorgen REIMERS in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.401-403 Titre : Spastic paralytic dislocation of the hip Type de document : Texte imprimé et/ou numérique Auteurs : Jorgen REIMERS, Auteur ; Eugene E. BLECK, Auteur Année de publication : 1985 Article en page(s) : p.401-403 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=593 [article] Spastic paralytic dislocation of the hip [Texte imprimé et/ou numérique] / Jorgen REIMERS, Auteur ; Eugene E. BLECK, Auteur . - 1985 . - p.401-403. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.401-403 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=593

CT scans of infants with glutaric aciduria / Jean AICARDI in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.403-404 Titre : CT scans of infants with glutaric aciduria Type de document : Texte imprimé et/ou numérique Auteurs : Jean AICARDI, Auteur ; F. GOUTIERES, Auteur ; J. M. SAUDUBRAY, Auteur ; H. OGIER, Auteur Année de publication : 1985 Article en page(s) : p.403-404 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=593 [article] CT scans of infants with glutaric aciduria [Texte imprimé et/ou numérique] / Jean AICARDI, Auteur ; F. GOUTIERES, Auteur ; J. M. SAUDUBRAY, Auteur ; H. OGIER, Auteur . - 1985 . - p.403-404. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.403-404 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=593

Recording motor defects of children with cerebral palsy / Pamela M. EVANS in Developmental Medicine & Child Neurology, 27-3 (June 1985)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 27-3 (June 1985) . - p.404-406 Titre : Recording motor defects of children with cerebral palsy Type de document : Texte imprimé et/ou numérique Auteurs : Pamela M. EVANS, Auteur ; Eva ALBERMAN, Auteur Année de publication : 1985 Article en page(s) : p.404-406 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=593 [article] Recording motor defects of children with cerebral palsy [Texte imprimé et/ou numérique] / Pamela M. EVANS, Auteur ; Eva ALBERMAN, Auteur . - 1985 . - p.404-406. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.404-406 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=593