Dépouillements

Training in developmental paediatrics / Martin C. O. BAX in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.561-562 Titre : Training in developmental paediatrics Type de document : Texte imprimé et/ou numérique Auteurs : Martin C. O. BAX, Auteur Année de publication : 1979 Article en page(s) : p.561-562 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=499 [article] Training in developmental paediatrics [Texte imprimé et/ou numérique] / Martin C. O. BAX, Auteur . - 1979 . - p.561-562. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.561-562 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=499

Knee flexion deformities and genu recurvatum in cerebral palsy: roentgenographic findings / Joseph J. GUGENHEIM in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.563-570 Titre : Knee flexion deformities and genu recurvatum in cerebral palsy: roentgenographic findings Type de document : Texte imprimé et/ou numérique Auteurs : Joseph J. GUGENHEIM, Auteur ; Robert K. ROSENTHAL, Auteur ; Sheldon R. SIMON, Auteur Année de publication : 1979 Article en page(s) : p.563-570 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Patients with cerebral palsy often have recurvatum or flexion deformities at the knee. To determine whether these are due to a bony or soft-tissue abnormality, four angles were measured on lateral roentgenograms of the knee: the femur-physis angle (angle 1); femur-Blumensaat's line angle (angle 2); tibia-plateau angle (angle 3); and tibia-physis angle (angle 4). These angles were measured for 45 patients with knee flexion deformities and for 31 with genu recurvatum. Values were also obtained from 204 normal lateral knee reoentgenograms. The age range for the whole series was from one to 22 years. Angles 2, 3 and 4 decreased from normal values with increasing age. The angulation of the proximal tibia, as measured by angle 3, is abnormal in patients with flexion deformities. Angles 2 and 3 were abnormal in cerebral-palsied patients with flexion deformities, while patients with genu recurvatum showed no significant bony abnormalities. These results suggest that treatment of flexion and recurvatum should be based on etiology. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=499 [article] Knee flexion deformities and genu recurvatum in cerebral palsy: roentgenographic findings [Texte imprimé et/ou numérique] / Joseph J. GUGENHEIM, Auteur ; Robert K. ROSENTHAL, Auteur ; Sheldon R. SIMON, Auteur . - 1979 . - p.563-570. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.563-570 Index. décimale : PER Périodiques Résumé : Patients with cerebral palsy often have recurvatum or flexion deformities at the knee. To determine whether these are due to a bony or soft-tissue abnormality, four angles were measured on lateral roentgenograms of the knee: the femur-physis angle (angle 1); femur-Blumensaat's line angle (angle 2); tibia-plateau angle (angle 3); and tibia-physis angle (angle 4). These angles were measured for 45 patients with knee flexion deformities and for 31 with genu recurvatum. Values were also obtained from 204 normal lateral knee reoentgenograms. The age range for the whole series was from one to 22 years. Angles 2, 3 and 4 decreased from normal values with increasing age. The angulation of the proximal tibia, as measured by angle 3, is abnormal in patients with flexion deformities. Angles 2 and 3 were abnormal in cerebral-palsied patients with flexion deformities, while patients with genu recurvatum showed no significant bony abnormalities. These results suggest that treatment of flexion and recurvatum should be based on etiology. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=499

Normal development and ear effect for contralateral acoustic reflex in children six to twelve years old / David W. JOHNSON in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.572-581 Titre : Normal development and ear effect for contralateral acoustic reflex in children six to twelve years old Type de document : Texte imprimé et/ou numérique Auteurs : David W. JOHNSON, Auteur ; Robert E. SHERMAN, Auteur Année de publication : 1979 Article en page(s) : p.572-581 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : This study investigated the acoustic reflex, which uses the ventro-medial brain-stem system, to determine laterality superiority with respect to age, sex, dominance for handedness, and their various interactions, 54 normal children and 21 normal adults were evaluated. No major effects for age, sex or handedness for the reflex were found, but the right ear appeared slightly more sensitive to broad-band white noise stimuli than the left, regardless of handedness. An age-handedness effect was also present which suggested that left-handed children mature differently from right-handed children in the acoustic reflex. Data on adults were inconclusive as to whether this maturity effect carried over into adulthood. The findings suggest that there was a laterality effect for the acoustic reflex using the ventro-medial brain-stem, which was thus brain-stem related rather than cortex-level related. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=499 [article] Normal development and ear effect for contralateral acoustic reflex in children six to twelve years old [Texte imprimé et/ou numérique] / David W. JOHNSON, Auteur ; Robert E. SHERMAN, Auteur . - 1979 . - p.572-581. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.572-581 Index. décimale : PER Périodiques Résumé : This study investigated the acoustic reflex, which uses the ventro-medial brain-stem system, to determine laterality superiority with respect to age, sex, dominance for handedness, and their various interactions, 54 normal children and 21 normal adults were evaluated. No major effects for age, sex or handedness for the reflex were found, but the right ear appeared slightly more sensitive to broad-band white noise stimuli than the left, regardless of handedness. An age-handedness effect was also present which suggested that left-handed children mature differently from right-handed children in the acoustic reflex. Data on adults were inconclusive as to whether this maturity effect carried over into adulthood. The findings suggest that there was a laterality effect for the acoustic reflex using the ventro-medial brain-stem, which was thus brain-stem related rather than cortex-level related. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=499

A longitudinal study of very low-birthweight infants. II: Results of controlled trial of intensive care and incidence of handicaps / William H. KITCHEN in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.582-589 Titre : A longitudinal study of very low-birthweight infants. II: Results of controlled trial of intensive care and incidence of handicaps Type de document : Texte imprimé et/ou numérique Auteurs : William H. KITCHEN, Auteur ; Margaret M. RYAN, Auteur ; Anne L. RICKARDS, Auteur ; F. A. BILLSON, Auteur ; E. H. KEIR, Auteur ; A. B. MCDOUGALL, Auteur ; F. D. NAYLOR, Auteur Année de publication : 1979 Article en page(s) : p.582-589 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Between 1966 and 1970, infants with birthweights between 1000 and 1500g entered a randomized controlled trial to determine the short-term and long-term results of neonatal intensive care. Of 158 long-term survivors, five were lost to follow-up, but the multidisciplinary research team prospectively followed 143 children up to the age of eight years. Useful data were available for the other 10 children. Of the long-term survivors 74 had received routine, and 84 had received intensive nursery care. At eight years of age there were no statistically significant differences in the frequencies of a variety of individual abnormalities; fewer of the intensively managed children had cerebral palsy, but sensorineural deafness and ocular abnormalities occurred more frequently. Individual children were graded into four carefully defined groups: (a) profound handicap (4.4 per cent of entire study group); (b) severe handicap (10.1 per cent); (c) significant handicap (37.3 per cent); and (d) trivial or no handicap (41.8 per cent). Inadequate data were available for 6.3 per cent of the children. It was apparent that the improved survival attributed to intensive neonatal care was achieved at the expense of additional severely handicapped children, and this feature is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500 [article] A longitudinal study of very low-birthweight infants. II: Results of controlled trial of intensive care and incidence of handicaps [Texte imprimé et/ou numérique] / William H. KITCHEN, Auteur ; Margaret M. RYAN, Auteur ; Anne L. RICKARDS, Auteur ; F. A. BILLSON, Auteur ; E. H. KEIR, Auteur ; A. B. MCDOUGALL, Auteur ; F. D. NAYLOR, Auteur . - 1979 . - p.582-589. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.582-589 Index. décimale : PER Périodiques Résumé : Between 1966 and 1970, infants with birthweights between 1000 and 1500g entered a randomized controlled trial to determine the short-term and long-term results of neonatal intensive care. Of 158 long-term survivors, five were lost to follow-up, but the multidisciplinary research team prospectively followed 143 children up to the age of eight years. Useful data were available for the other 10 children. Of the long-term survivors 74 had received routine, and 84 had received intensive nursery care. At eight years of age there were no statistically significant differences in the frequencies of a variety of individual abnormalities; fewer of the intensively managed children had cerebral palsy, but sensorineural deafness and ocular abnormalities occurred more frequently. Individual children were graded into four carefully defined groups: (a) profound handicap (4.4 per cent of entire study group); (b) severe handicap (10.1 per cent); (c) significant handicap (37.3 per cent); and (d) trivial or no handicap (41.8 per cent). Inadequate data were available for 6.3 per cent of the children. It was apparent that the improved survival attributed to intensive neonatal care was achieved at the expense of additional severely handicapped children, and this feature is discussed. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500

Neurobehavioral performance of low-birthweight infants at 40 weeks conceptional age: comparison with normal fullterm infants / Diane KURTZBERG in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.590-607 Titre : Neurobehavioral performance of low-birthweight infants at 40 weeks conceptional age: comparison with normal fullterm infants Type de document : Texte imprimé et/ou numérique Auteurs : Diane KURTZBERG, Auteur ; Herbert G. VAUGHAN, Auteur ; Cecelia DAUM, Auteur ; Bruce A. GRELONG, Auteur ; Susan ALBIN, Auteur ; Laurence ROTKIN, Auteur Année de publication : 1979 Article en page(s) : p.590-607 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : This study compares the neurobehavioral status of 118 low-birthweight infants tested at 40 weeks conceptional age with that of 76 normal fullterm infants. A neonatal neurobehavioral examination comprising 21 test and four summary items was used. The most striking differences between the groups were found in visual and auditory orienting, with approximately two-thirds of the low-birthweight infants falling below the range of performance of the fullterm group. Items testing motor performance showed a lower incidence of deviant performance among the low-birthweight infants. Of the 21 test items, 19 could be assigned cut-off scores, below which infants can be considered deviant on the specific items. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500 [article] Neurobehavioral performance of low-birthweight infants at 40 weeks conceptional age: comparison with normal fullterm infants [Texte imprimé et/ou numérique] / Diane KURTZBERG, Auteur ; Herbert G. VAUGHAN, Auteur ; Cecelia DAUM, Auteur ; Bruce A. GRELONG, Auteur ; Susan ALBIN, Auteur ; Laurence ROTKIN, Auteur . - 1979 . - p.590-607. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.590-607 Index. décimale : PER Périodiques Résumé : This study compares the neurobehavioral status of 118 low-birthweight infants tested at 40 weeks conceptional age with that of 76 normal fullterm infants. A neonatal neurobehavioral examination comprising 21 test and four summary items was used. The most striking differences between the groups were found in visual and auditory orienting, with approximately two-thirds of the low-birthweight infants falling below the range of performance of the fullterm group. Items testing motor performance showed a lower incidence of deviant performance among the low-birthweight infants. Of the 21 test items, 19 could be assigned cut-off scores, below which infants can be considered deviant on the specific items. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500

Separation at birth and the mother-child relationship / Julia COLLINGWOOD in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.608-618 Titre : Separation at birth and the mother-child relationship Type de document : Texte imprimé et/ou numérique Auteurs : Julia COLLINGWOOD, Auteur ; Eva ALBERMAN, Auteur Année de publication : 1979 Article en page(s) : p.608-618 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Mother-child relationships were investigated between: (a) 32 mothers and their singleton children with birthweights of 2000g or less who had been separated immediately after birth for a minimum period of 17 days (index families), and (b) 32 control mothers and their singleton children, matched with index cases for type of residence, sex and month of birth, but who had not been separated at birth and whose birthweights were 2700g or greater. From interview, validated by questionnaire and semantic differential scoring, six of the index mothers, but none of the control mothers were assessed as having rejected their children. Comparisons were made between rejected and non-rejected index children. Rejection occurred more commonly in the low-birthweight group if the mother had been a teenager at the birth of her first child or of the study child, especially if she had not planned or wanted the pregnancy. The mothers of rejected children tended to have had poor relations with their own fathers, were unhappy with their life-style, and perceived their children as having difficult or unlikeable personalities. The rejected children were more likely to have had poor health, severe temper tantrums, and to cause their mothers concern over their poor appetite. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500 [article] Separation at birth and the mother-child relationship [Texte imprimé et/ou numérique] / Julia COLLINGWOOD, Auteur ; Eva ALBERMAN, Auteur . - 1979 . - p.608-618. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.608-618 Index. décimale : PER Périodiques Résumé : Mother-child relationships were investigated between: (a) 32 mothers and their singleton children with birthweights of 2000g or less who had been separated immediately after birth for a minimum period of 17 days (index families), and (b) 32 control mothers and their singleton children, matched with index cases for type of residence, sex and month of birth, but who had not been separated at birth and whose birthweights were 2700g or greater. From interview, validated by questionnaire and semantic differential scoring, six of the index mothers, but none of the control mothers were assessed as having rejected their children. Comparisons were made between rejected and non-rejected index children. Rejection occurred more commonly in the low-birthweight group if the mother had been a teenager at the birth of her first child or of the study child, especially if she had not planned or wanted the pregnancy. The mothers of rejected children tended to have had poor relations with their own fathers, were unhappy with their life-style, and perceived their children as having difficult or unlikeable personalities. The rejected children were more likely to have had poor health, severe temper tantrums, and to cause their mothers concern over their poor appetite. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500

Adolescents and young people with spina bifida / I. MCANDREW in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.619-629 Titre : Adolescents and young people with spina bifida Type de document : Texte imprimé et/ou numérique Auteurs : I. MCANDREW, Auteur Année de publication : 1979 Article en page(s) : p.619-629 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : This study investigated how young people with myelomeningocele see their situation, and defines some of their problems. 35 adolescents and young people with this condition were interviewed. The evidence suggests that the over-all problems of these young people are common to many with congenital physical disabilities, but neurogenic bowel and bladder are additional complications not often experienced by others with orthopaedic disabilities. Those with ileal conduits frequently reported both social embarrassment and management difficulties, but bowel incontinence was rarely a dominant problem. The findings indicate that the young person's ability to cope with physical and emotional situations is ultimately not determined by the severity of the disability, but is a product of all the environmental support systems that have been available to him since birth. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500 [article] Adolescents and young people with spina bifida [Texte imprimé et/ou numérique] / I. MCANDREW, Auteur . - 1979 . - p.619-629. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.619-629 Index. décimale : PER Périodiques Résumé : This study investigated how young people with myelomeningocele see their situation, and defines some of their problems. 35 adolescents and young people with this condition were interviewed. The evidence suggests that the over-all problems of these young people are common to many with congenital physical disabilities, but neurogenic bowel and bladder are additional complications not often experienced by others with orthopaedic disabilities. Those with ileal conduits frequently reported both social embarrassment and management difficulties, but bowel incontinence was rarely a dominant problem. The findings indicate that the young person's ability to cope with physical and emotional situations is ultimately not determined by the severity of the disability, but is a product of all the environmental support systems that have been available to him since birth. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500

Long-term outcome in children with temporal lobe seizures. III: Psychiatric aspects in childhood and adult life / Janet LINDSAY in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.630-636 Titre : Long-term outcome in children with temporal lobe seizures. III: Psychiatric aspects in childhood and adult life Type de document : Texte imprimé et/ou numérique Auteurs : Janet LINDSAY, Auteur ; Christopher OUNSTED, Auteur ; Peronelle RICHARDS, Auteur Année de publication : 1979 Article en page(s) : p.630-636 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : One hundred children with temporal lobe epilepsy were followed into adult life. 85 per cent had had psychiatric problems in childhood. The occurrence of overt psychiatric disorder in adult life was low: of those survivors who were not gravely mentally retarded, 70 per cent were regarded as psychiatrically healthy. Overt schizophreniform psychosis has developed in 10 per cent of survivors. Males with continuing epilepsy and left-sided foci were at special risk: 30 per cent of such patients had become psychotic. No patient coded as having a right-sided focus in 1964 had become psychotic by 1977. Though 26 patients had had grossly disordered childhood homes, this factor had no significant relation to adult psychiatric disorder. Antisocial conduct marked the adult life of 12 patients. Their childhood codes showed that male sex, a focus contralateral to the preferred hand, and unremittent epilepsy marked this group. Low intelligence and childhood rages were also prominent. Treated neurotic and depressive illness was quite uncommon. Only five survivors have fallen into this category. Those patients escaping psychiatric ill-health are often notably extraverted and successful. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500 [article] Long-term outcome in children with temporal lobe seizures. III: Psychiatric aspects in childhood and adult life [Texte imprimé et/ou numérique] / Janet LINDSAY, Auteur ; Christopher OUNSTED, Auteur ; Peronelle RICHARDS, Auteur . - 1979 . - p.630-636. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.630-636 Index. décimale : PER Périodiques Résumé : One hundred children with temporal lobe epilepsy were followed into adult life. 85 per cent had had psychiatric problems in childhood. The occurrence of overt psychiatric disorder in adult life was low: of those survivors who were not gravely mentally retarded, 70 per cent were regarded as psychiatrically healthy. Overt schizophreniform psychosis has developed in 10 per cent of survivors. Males with continuing epilepsy and left-sided foci were at special risk: 30 per cent of such patients had become psychotic. No patient coded as having a right-sided focus in 1964 had become psychotic by 1977. Though 26 patients had had grossly disordered childhood homes, this factor had no significant relation to adult psychiatric disorder. Antisocial conduct marked the adult life of 12 patients. Their childhood codes showed that male sex, a focus contralateral to the preferred hand, and unremittent epilepsy marked this group. Low intelligence and childhood rages were also prominent. Treated neurotic and depressive illness was quite uncommon. Only five survivors have fallen into this category. Those patients escaping psychiatric ill-health are often notably extraverted and successful. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500

Aqueductal stenosis in X-linked hydrocephalus: a secondary phenomenon? / P. LANDRIEU in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.637-642 Titre : Aqueductal stenosis in X-linked hydrocephalus: a secondary phenomenon? Type de document : Texte imprimé et/ou numérique Auteurs : P. LANDRIEU, Auteur ; Gilles LYON, Auteur ; J. NINANE, Auteur ; G. FERRIERE, Auteur Année de publication : 1979 Article en page(s) : p.637-642 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Two cases of x-linked hydrocephalus are reported. One underwent postmortem examination: serial sections of the brain stem failed to show stenosis of the aqueduct, the mean and minimal cross-sectional areas of which were normal. However, there were some morphological changes which were compatible with a mechanical compression of the brain stem. It is postulated that in the Bickers and Adams syndrome of x-linked hereditary hydrocephalus the primary defect is a communicating hydrocephalus leading usually, but not always, to aqueductal stenosis. The importance of electrophysiological investigations for the correct diagnosis of the characteristic clasped-thumb deformity is also indicated. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500 [article] Aqueductal stenosis in X-linked hydrocephalus: a secondary phenomenon? [Texte imprimé et/ou numérique] / P. LANDRIEU, Auteur ; Gilles LYON, Auteur ; J. NINANE, Auteur ; G. FERRIERE, Auteur . - 1979 . - p.637-642. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.637-642 Index. décimale : PER Périodiques Résumé : Two cases of x-linked hydrocephalus are reported. One underwent postmortem examination: serial sections of the brain stem failed to show stenosis of the aqueduct, the mean and minimal cross-sectional areas of which were normal. However, there were some morphological changes which were compatible with a mechanical compression of the brain stem. It is postulated that in the Bickers and Adams syndrome of x-linked hereditary hydrocephalus the primary defect is a communicating hydrocephalus leading usually, but not always, to aqueductal stenosis. The importance of electrophysiological investigations for the correct diagnosis of the characteristic clasped-thumb deformity is also indicated. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500

Mixed bacterial and fungal meningitis in a neonate / Richard E. EHLERS in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.643-647 Titre : Mixed bacterial and fungal meningitis in a neonate Type de document : Texte imprimé et/ou numérique Auteurs : Richard E. EHLERS, Auteur ; Paul B. JARRETT, Auteur ; Allen M. KAPLAN, Auteur Année de publication : 1979 Article en page(s) : p.643-647 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Mixed infections of the central nervous system occurring in children without underlying neurological disease may be more frequent than previously suspected. In this case report, a neonate whose cerebrospinal fluid culture at 24 hours showed group B streptococcus only, was found on postmortem examination at six days of age to have disseminated candidiasis with cerebral abscesses. The degree of systemic involvement in this newborn suggested intra-uterine acquired candidiasis. Early diagnosis of polymicrobic infections is difficult, but this case suggests it should be considered in patients not responding to antibiotic therapy. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500 [article] Mixed bacterial and fungal meningitis in a neonate [Texte imprimé et/ou numérique] / Richard E. EHLERS, Auteur ; Paul B. JARRETT, Auteur ; Allen M. KAPLAN, Auteur . - 1979 . - p.643-647. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.643-647 Index. décimale : PER Périodiques Résumé : Mixed infections of the central nervous system occurring in children without underlying neurological disease may be more frequent than previously suspected. In this case report, a neonate whose cerebrospinal fluid culture at 24 hours showed group B streptococcus only, was found on postmortem examination at six days of age to have disseminated candidiasis with cerebral abscesses. The degree of systemic involvement in this newborn suggested intra-uterine acquired candidiasis. Early diagnosis of polymicrobic infections is difficult, but this case suggests it should be considered in patients not responding to antibiotic therapy. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500

Progressive rubella panencephalitis: clinical course and response to 'isoprinosine' / James E. JAN in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.648-652 Titre : Progressive rubella panencephalitis: clinical course and response to 'isoprinosine' Type de document : Texte imprimé et/ou numérique Auteurs : James E. JAN, Auteur ; Aubrey J. TINGLE, Auteur ; G. DONALD, Auteur ; M. KETTYLS, Auteur ; William St. J. BUCKLER, Auteur ; Clarisse L. DOLMAN, Auteur Année de publication : 1979 Article en page(s) : p.648-652 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : This report describes the clinical course of a 16-year-old Canadian-born Chinese boy who has progressive rubella panencephalitis. The progression, the lack of response to 'Isoprenosine', and the additional finding of myopathy are discussed. The clinical and pathological features of this rare, progressive neurological disorder are also summarized. In view of the last major rubella pandemic occuring in the mid-60s, it is likely that during the next few years physicians will diagnose an increased number of patients with this distinct neurological entity. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500 [article] Progressive rubella panencephalitis: clinical course and response to 'isoprinosine' [Texte imprimé et/ou numérique] / James E. JAN, Auteur ; Aubrey J. TINGLE, Auteur ; G. DONALD, Auteur ; M. KETTYLS, Auteur ; William St. J. BUCKLER, Auteur ; Clarisse L. DOLMAN, Auteur . - 1979 . - p.648-652. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.648-652 Index. décimale : PER Périodiques Résumé : This report describes the clinical course of a 16-year-old Canadian-born Chinese boy who has progressive rubella panencephalitis. The progression, the lack of response to 'Isoprenosine', and the additional finding of myopathy are discussed. The clinical and pathological features of this rare, progressive neurological disorder are also summarized. In view of the last major rubella pandemic occuring in the mid-60s, it is likely that during the next few years physicians will diagnose an increased number of patients with this distinct neurological entity. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500

Radiation myelopathy / D. A. HOWELL in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.653-656 Titre : Radiation myelopathy Type de document : Texte imprimé et/ou numérique Auteurs : D. A. HOWELL, Auteur Année de publication : 1979 Article en page(s) : p.653-656 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500 [article] Radiation myelopathy [Texte imprimé et/ou numérique] / D. A. HOWELL, Auteur . - 1979 . - p.653-656. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.653-656 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500

Vestibular dysfunction in autistic children / Ralph G. MAURER in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.656-659 Titre : Vestibular dysfunction in autistic children Type de document : Texte imprimé et/ou numérique Auteurs : Ralph G. MAURER, Auteur ; Antonio R. DAMASIO, Auteur Année de publication : 1979 Article en page(s) : p.656-659 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500 [article] Vestibular dysfunction in autistic children [Texte imprimé et/ou numérique] / Ralph G. MAURER, Auteur ; Antonio R. DAMASIO, Auteur . - 1979 . - p.656-659. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.656-659 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=500

Controversies about Duchenne muscular dystrophy. (2) Bracing for ambulation / David GARDNER-MEDWIN in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.659-662 Titre : Controversies about Duchenne muscular dystrophy. (2) Bracing for ambulation Type de document : Texte imprimé et/ou numérique Auteurs : David GARDNER-MEDWIN, Auteur Année de publication : 1979 Article en page(s) : p.659-662 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=501 [article] Controversies about Duchenne muscular dystrophy. (2) Bracing for ambulation [Texte imprimé et/ou numérique] / David GARDNER-MEDWIN, Auteur . - 1979 . - p.659-662. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.659-662 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=501

Pathogenetic and preventive aspects of non-progressive ataxic syndromes / Gunnar SANNER in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.663-671 Titre : Pathogenetic and preventive aspects of non-progressive ataxic syndromes Type de document : Texte imprimé et/ou numérique Auteurs : Gunnar SANNER, Auteur Année de publication : 1979 Article en page(s) : p.663-671 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The article reviews the collected knowledge concerning the non-progressive syndromes of ataxic cerebral palsy. Three syndromes are described: (1) simple ataxia (signs of dyssynergia); (2) ataxic diplegia (ataxia with added diplegic spasticity); and (3) dysequilibrium syndrome (defective postural control and equilibrium). The probable aetiological factors in each syndrome are discussed. In simple ataxia prenatal factors dominate; a high proportion of cases have an untraceable aetiology. Genetic factors play a large rôle, and birthweight is usually normal. With ataxic diplegia the aetiology is again most commonly prenatal, but the proportion of cases with an untraceable aetiology is low. Fetal deprivation of supply and perinatal factors, either isolated or in combination, are important. Low birthweight is frequently found. Genetic aetiological factors are the rule in the dysequilibrium syndrome. Possible preventive measures are discussed on the basis of the aetiological pattern. It is concluded that the possibilities of prevention are greatest in ataxic diplegia. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=501 [article] Pathogenetic and preventive aspects of non-progressive ataxic syndromes [Texte imprimé et/ou numérique] / Gunnar SANNER, Auteur . - 1979 . - p.663-671. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.663-671 Index. décimale : PER Périodiques Résumé : The article reviews the collected knowledge concerning the non-progressive syndromes of ataxic cerebral palsy. Three syndromes are described: (1) simple ataxia (signs of dyssynergia); (2) ataxic diplegia (ataxia with added diplegic spasticity); and (3) dysequilibrium syndrome (defective postural control and equilibrium). The probable aetiological factors in each syndrome are discussed. In simple ataxia prenatal factors dominate; a high proportion of cases have an untraceable aetiology. Genetic factors play a large rôle, and birthweight is usually normal. With ataxic diplegia the aetiology is again most commonly prenatal, but the proportion of cases with an untraceable aetiology is low. Fetal deprivation of supply and perinatal factors, either isolated or in combination, are important. Low birthweight is frequently found. Genetic aetiological factors are the rule in the dysequilibrium syndrome. Possible preventive measures are discussed on the basis of the aetiological pattern. It is concluded that the possibilities of prevention are greatest in ataxic diplegia. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=501

A social score for kwashiorkor / Tony WATERSON in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.672-675 Titre : A social score for kwashiorkor Type de document : Texte imprimé et/ou numérique Auteurs : Tony WATERSON, Auteur ; Janet GOODALL, Auteur ; J. M. CELEDON, Auteur Année de publication : 1979 Article en page(s) : p.672-675 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=501 [article] A social score for kwashiorkor [Texte imprimé et/ou numérique] / Tony WATERSON, Auteur ; Janet GOODALL, Auteur ; J. M. CELEDON, Auteur . - 1979 . - p.672-675. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.672-675 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=501

Smiling babies / Helen FOLEY in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.675 Titre : Smiling babies Type de document : Texte imprimé et/ou numérique Auteurs : Helen FOLEY, Auteur Année de publication : 1979 Article en page(s) : p.675 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=501 [article] Smiling babies [Texte imprimé et/ou numérique] / Helen FOLEY, Auteur . - 1979 . - p.675. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.675 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=501

Prenatal diagnosis of cystic fibrosis / Ann HARRIS in Developmental Medicine & Child Neurology, 21-5 (October 1979)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 21-5 (October 1979) . - p.675-676 Titre : Prenatal diagnosis of cystic fibrosis Type de document : Texte imprimé et/ou numérique Auteurs : Ann HARRIS, Auteur Année de publication : 1979 Article en page(s) : p.675-676 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=501 [article] Prenatal diagnosis of cystic fibrosis [Texte imprimé et/ou numérique] / Ann HARRIS, Auteur . - 1979 . - p.675-676. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 21-5 (October 1979) . - p.675-676 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=501