Dépouillements

Perinatal Follow-up / Ross G. MITCHELL in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.1-2 Titre : Perinatal Follow-up Type de document : Texte imprimé et/ou numérique Auteurs : Ross G. MITCHELL, Auteur Année de publication : 1980 Article en page(s) : p.1-2 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=503 [article] Perinatal Follow-up [Texte imprimé et/ou numérique] / Ross G. MITCHELL, Auteur . - 1980 . - p.1-2. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.1-2 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=503

Pediatric coma: prognosis and outcome / Robert B. JOHNSTON in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.3-12 Titre : Pediatric coma: prognosis and outcome Type de document : Texte imprimé et/ou numérique Auteurs : Robert B. JOHNSTON, Auteur ; E. David MELLITS, Auteur Année de publication : 1980 Article en page(s) : p.3-12 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A review of 40 previously comatose children identified significant degrees of disability 10 months after the insult. Of all the antecedent factors assessed, duration of coma correlated most highly with outcome, especially in relation to language and intellectual spheres. The literature reveals heterogeneous approaches to the study of sequelae of pediatric coma, and thus disparate results: a more uniform approach is needed to the study of the nature and prognosis of pediatric coma. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504 [article] Pediatric coma: prognosis and outcome [Texte imprimé et/ou numérique] / Robert B. JOHNSTON, Auteur ; E. David MELLITS, Auteur . - 1980 . - p.3-12. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.3-12 Index. décimale : PER Périodiques Résumé : A review of 40 previously comatose children identified significant degrees of disability 10 months after the insult. Of all the antecedent factors assessed, duration of coma correlated most highly with outcome, especially in relation to language and intellectual spheres. The literature reveals heterogeneous approaches to the study of sequelae of pediatric coma, and thus disparate results: a more uniform approach is needed to the study of the nature and prognosis of pediatric coma. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504

An epidemiological study of cerebral palsy in Western Australia, 1956-1975. II: Spastic cerebral palsy and perinatal factors / Alison DALE in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.13-25 Titre : An epidemiological study of cerebral palsy in Western Australia, 1956-1975. II: Spastic cerebral palsy and perinatal factors Type de document : Texte imprimé et/ou numérique Auteurs : Alison DALE, Auteur ; Fiona J. STANLEY, Auteur Année de publication : 1980 Article en page(s) : p.13-25 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : This case:control study demonstrates that although the incidence of spastic cerebral palsy is falling in Western Australia, the contribution made by low-birthweight and small-for-dates infants who have significant neonatal morbidity, and who have been treated in neonatal intensive care units, has increased significantly. This points to factors other than care being important in diminishing the incidence of spastic cerebral palsy. Further falls in incidence may only result from improvements in the management of the very small and very sick neonate, and preventive programmes aimed at preterm births. Obstetric intervention and fetal distress were more frequent in recent cerebral-palsy cases than in the controls. Thus, falling neonatal mortality among low-birthweight infants in Western Australia coincided with an increased incidence of spastic cerebral palsy in these infants, despite an over-all drop in the incidence of cerebral palsy. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504 [article] An epidemiological study of cerebral palsy in Western Australia, 1956-1975. II: Spastic cerebral palsy and perinatal factors [Texte imprimé et/ou numérique] / Alison DALE, Auteur ; Fiona J. STANLEY, Auteur . - 1980 . - p.13-25. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.13-25 Index. décimale : PER Périodiques Résumé : This case:control study demonstrates that although the incidence of spastic cerebral palsy is falling in Western Australia, the contribution made by low-birthweight and small-for-dates infants who have significant neonatal morbidity, and who have been treated in neonatal intensive care units, has increased significantly. This points to factors other than care being important in diminishing the incidence of spastic cerebral palsy. Further falls in incidence may only result from improvements in the management of the very small and very sick neonate, and preventive programmes aimed at preterm births. Obstetric intervention and fetal distress were more frequent in recent cerebral-palsy cases than in the controls. Thus, falling neonatal mortality among low-birthweight infants in Western Australia coincided with an increased incidence of spastic cerebral palsy in these infants, despite an over-all drop in the incidence of cerebral palsy. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504

Low-birthweight children at early school-age: a longitudinal study / C. M. DRILLIEN in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.26-47 Titre : Low-birthweight children at early school-age: a longitudinal study Type de document : Texte imprimé et/ou numérique Auteurs : C. M. DRILLIEN, Auteur ; A. J. M. THOMSON, Auteur ; Kelly BURGOYNE, Auteur Année de publication : 1980 Article en page(s) : p.26-47 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Eighty-seven per cent of a cohort of 299 low-birthweight (LBW) infants (less than or equal to 2000 g) were examined at age 6 years 8 months, together with 111 control children. All the controls and 248 of the LBW children were individually assessed in school. Information about another 13 LBW children was obtained by questionnaire. Problems in primary school were related to social grade, evidence of early intra-uterine insult, sex, postnatal complications and neurological and developmental status in the first year of life. Multiple birth, gestation and intra-uterine growth were not clearly related to problems in school. The incidence of major handicap, as compared with LBW infants born between 1953 and 1955, showed little change when earlier-born infants who had been subjected to severe restriction of fluid and calorie intake were excluded. Ninety-two per cent of LBW children traced were attending normal schools. Those who showed no evidence of early intra-uterine insult and who were neurologically normal in the first year of life were largely indistinguishable from control children reared in similar homes. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504 [article] Low-birthweight children at early school-age: a longitudinal study [Texte imprimé et/ou numérique] / C. M. DRILLIEN, Auteur ; A. J. M. THOMSON, Auteur ; Kelly BURGOYNE, Auteur . - 1980 . - p.26-47. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.26-47 Index. décimale : PER Périodiques Résumé : Eighty-seven per cent of a cohort of 299 low-birthweight (LBW) infants (less than or equal to 2000 g) were examined at age 6 years 8 months, together with 111 control children. All the controls and 248 of the LBW children were individually assessed in school. Information about another 13 LBW children was obtained by questionnaire. Problems in primary school were related to social grade, evidence of early intra-uterine insult, sex, postnatal complications and neurological and developmental status in the first year of life. Multiple birth, gestation and intra-uterine growth were not clearly related to problems in school. The incidence of major handicap, as compared with LBW infants born between 1953 and 1955, showed little change when earlier-born infants who had been subjected to severe restriction of fluid and calorie intake were excluded. Ninety-two per cent of LBW children traced were attending normal schools. Those who showed no evidence of early intra-uterine insult and who were neurologically normal in the first year of life were largely indistinguishable from control children reared in similar homes. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504

Follow-up study of survivors after intra-uterine transfusion / M. Ivonna ELLIS in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.48-54 Titre : Follow-up study of survivors after intra-uterine transfusion Type de document : Texte imprimé et/ou numérique Auteurs : M. Ivonna ELLIS, Auteur Année de publication : 1980 Article en page(s) : p.48-54 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Between 1965 and 1976 a total of 217 infants received intra-uterine transfusions. Perinatal and follow-up data are presented on the 81 survivors, of whom 62 per cent were over five years of age at final follow-up. Assessment included development and general health, audiometric testing and school performance. Abnormalities were found in 29 of the survivors. In 13 cases these were attributed to haemolytic disease, and all had some neurological deficit such as differing degrees of deafness. 10 others had slight abnormalities associated with the procedure of intra-uterine transfusion, while six had abnormalities not associated with either (spastic quadriplegia following infection, congenital heart disease and visual disorders). The remaining 52 children were normal. It is suggested that hyperbilirubinaemia is probably responsible for the neurological deficits. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504 [article] Follow-up study of survivors after intra-uterine transfusion [Texte imprimé et/ou numérique] / M. Ivonna ELLIS, Auteur . - 1980 . - p.48-54. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.48-54 Index. décimale : PER Périodiques Résumé : Between 1965 and 1976 a total of 217 infants received intra-uterine transfusions. Perinatal and follow-up data are presented on the 81 survivors, of whom 62 per cent were over five years of age at final follow-up. Assessment included development and general health, audiometric testing and school performance. Abnormalities were found in 29 of the survivors. In 13 cases these were attributed to haemolytic disease, and all had some neurological deficit such as differing degrees of deafness. 10 others had slight abnormalities associated with the procedure of intra-uterine transfusion, while six had abnormalities not associated with either (spastic quadriplegia following infection, congenital heart disease and visual disorders). The remaining 52 children were normal. It is suggested that hyperbilirubinaemia is probably responsible for the neurological deficits. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504

The use of the Denver Developmental Screening Test in infant welfare clinics / Michael JAFFE in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.55-60 Titre : The use of the Denver Developmental Screening Test in infant welfare clinics Type de document : Texte imprimé et/ou numérique Auteurs : Michael JAFFE, Auteur ; S. T. WINTER, Auteur ; J. HAREL, Auteur ; A. GOLDBERG, Auteur ; M. RUDOLPH-SCHNITZER, Auteur Année de publication : 1980 Article en page(s) : p.55-60 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The results of a single Denver Developmental Screening Test performed at the age of nine months on 823 infants attending maternal and child health centres were compared with the developmental information recorded by public health nurses during their routine well-baby care of these same infants. The single Denver test detected a significantly greater number of infants with developmental delay than did the routine observations, and the nurses tended to under-use the available resources for developmental assessment. Suggestions are made for more effective use of maternal and child health centres in the primary recognition of developmental delay. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504 [article] The use of the Denver Developmental Screening Test in infant welfare clinics [Texte imprimé et/ou numérique] / Michael JAFFE, Auteur ; S. T. WINTER, Auteur ; J. HAREL, Auteur ; A. GOLDBERG, Auteur ; M. RUDOLPH-SCHNITZER, Auteur . - 1980 . - p.55-60. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.55-60 Index. décimale : PER Périodiques Résumé : The results of a single Denver Developmental Screening Test performed at the age of nine months on 823 infants attending maternal and child health centres were compared with the developmental information recorded by public health nurses during their routine well-baby care of these same infants. The single Denver test detected a significantly greater number of infants with developmental delay than did the routine observations, and the nurses tended to under-use the available resources for developmental assessment. Suggestions are made for more effective use of maternal and child health centres in the primary recognition of developmental delay. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504

Food supplementation of pregnant women at risk of malnutrition and their newborns'responsiveness to stimulation / Lea VUORI in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.61-71 Titre : Food supplementation of pregnant women at risk of malnutrition and their newborns'responsiveness to stimulation Type de document : Texte imprimé et/ou numérique Auteurs : Lea VUORI, Auteur ; Lucia DE NAVARRO, Auteur ; Niels CHRISTIANSEN, Auteur ; Jose O. MORA, Auteur ; M. Guillermo HERRERA, Auteur Année de publication : 1980 Article en page(s) : p.61-71 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Pregnant women at risk of malnutrition were enrolled in a health care programme in Colombia, South America, and were randomly assigned to a group receiving supplementary food or to a control group at the beginning of the third trimester of pregnancy. There were no differences between the groups in social or nutritional variables. Supplementary food was found to have an effect on infants' reactions to mild aversive stimulation and their degree of irritability. Infants born to non-supplemented mothers generally responded more irritably to removal of a nipple and to the application of a cold disc to the abdomen. Female infants of non-supplemented mothers also recovered more slowly than the supplemented group from crying in response to both removal of nipple and the cold disc. The findings are believed to show a maturational effect of maternal diet during the last trimester of pregnancy. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504 [article] Food supplementation of pregnant women at risk of malnutrition and their newborns'responsiveness to stimulation [Texte imprimé et/ou numérique] / Lea VUORI, Auteur ; Lucia DE NAVARRO, Auteur ; Niels CHRISTIANSEN, Auteur ; Jose O. MORA, Auteur ; M. Guillermo HERRERA, Auteur . - 1980 . - p.61-71. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.61-71 Index. décimale : PER Périodiques Résumé : Pregnant women at risk of malnutrition were enrolled in a health care programme in Colombia, South America, and were randomly assigned to a group receiving supplementary food or to a control group at the beginning of the third trimester of pregnancy. There were no differences between the groups in social or nutritional variables. Supplementary food was found to have an effect on infants' reactions to mild aversive stimulation and their degree of irritability. Infants born to non-supplemented mothers generally responded more irritably to removal of a nipple and to the application of a cold disc to the abdomen. Female infants of non-supplemented mothers also recovered more slowly than the supplemented group from crying in response to both removal of nipple and the cold disc. The findings are believed to show a maturational effect of maternal diet during the last trimester of pregnancy. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504

Marble brain disease: recessive osteopetrosis, renal tubular acidosis and cerebral calcification in three Saudi Arabian families / Arne OHLSSON in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.72-84 Titre : Marble brain disease: recessive osteopetrosis, renal tubular acidosis and cerebral calcification in three Saudi Arabian families Type de document : Texte imprimé et/ou numérique Auteurs : Arne OHLSSON, Auteur ; Gordon D. STARK, Auteur ; Nadia SAKATI, Auteur Année de publication : 1980 Article en page(s) : p.72-84 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Four children are described from three Saudi Arabian families suffering from osteopetrosis, distal renal tubular acidosis and cerebral calcification associated clinically with mental retardation, stunted growth, abnormal teeth and a similar facial appearance. The syndrome is inherited as an autosomal recessive. The growth retardation is attributed to renal tubular acidosis but no metabolic link is evident between its other major features, and the fundamental defect is unknown. The disorder is radiologically indistinguishable from the classical recessive (malignant) and dominant (benign) forms of osteopetrosis but its other characteristics establish it as a separate disease entity. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504 [article] Marble brain disease: recessive osteopetrosis, renal tubular acidosis and cerebral calcification in three Saudi Arabian families [Texte imprimé et/ou numérique] / Arne OHLSSON, Auteur ; Gordon D. STARK, Auteur ; Nadia SAKATI, Auteur . - 1980 . - p.72-84. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.72-84 Index. décimale : PER Périodiques Résumé : Four children are described from three Saudi Arabian families suffering from osteopetrosis, distal renal tubular acidosis and cerebral calcification associated clinically with mental retardation, stunted growth, abnormal teeth and a similar facial appearance. The syndrome is inherited as an autosomal recessive. The growth retardation is attributed to renal tubular acidosis but no metabolic link is evident between its other major features, and the fundamental defect is unknown. The disorder is radiologically indistinguishable from the classical recessive (malignant) and dominant (benign) forms of osteopetrosis but its other characteristics establish it as a separate disease entity. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504

Developmental dyspraxia in a family with X-linked mental retardation (Renpenning syndrome) / John F. MCLAUGHLIN in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.84-92 Titre : Developmental dyspraxia in a family with X-linked mental retardation (Renpenning syndrome) Type de document : Texte imprimé et/ou numérique Auteurs : John F. MCLAUGHLIN, Auteur ; Elinor KRIEGSMAN, Auteur Année de publication : 1980 Article en page(s) : p.84-92 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : This paper describes the existence of severe developmental speech dyspraxia in a member of a family that is typical of other reports of X-linked mental retardation without physical abnormality (Renpenning syndrome). Other family members have evidence of motor or speech dyspraxia. Other reports of X-linked mental retardation have mentioned "verbal disability", which suggests that developmental dyspraxia may be quite common in these families. Developmental dyspraxia of speech is amenable to specific types of intervention: after two years of such intervention our patient's adaptive skills reflect his normal non-verbal intellectual ability, despite persistent speech deficits. This functional improvement shows how important it is to identify dyspraxia in young children, who may otherwise be labelled mentally retarded. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504 [article] Developmental dyspraxia in a family with X-linked mental retardation (Renpenning syndrome) [Texte imprimé et/ou numérique] / John F. MCLAUGHLIN, Auteur ; Elinor KRIEGSMAN, Auteur . - 1980 . - p.84-92. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.84-92 Index. décimale : PER Périodiques Résumé : This paper describes the existence of severe developmental speech dyspraxia in a member of a family that is typical of other reports of X-linked mental retardation without physical abnormality (Renpenning syndrome). Other family members have evidence of motor or speech dyspraxia. Other reports of X-linked mental retardation have mentioned "verbal disability", which suggests that developmental dyspraxia may be quite common in these families. Developmental dyspraxia of speech is amenable to specific types of intervention: after two years of such intervention our patient's adaptive skills reflect his normal non-verbal intellectual ability, despite persistent speech deficits. This functional improvement shows how important it is to identify dyspraxia in young children, who may otherwise be labelled mentally retarded. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504

Mosaicism for an extra small ring chromosome / Antonino FORABOSCO in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.92-96 Titre : Mosaicism for an extra small ring chromosome Type de document : Texte imprimé et/ou numérique Auteurs : Antonino FORABOSCO, Auteur ; GianPaolo GUARALDI, Auteur ; Anna BARONCINI, Auteur ; Elena FERRARI, Auteur ; Carla BASSI, Auteur Année de publication : 1980 Article en page(s) : p.92-96 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A new case for mosaicism for an extra small ring chromosome is described in a 13-year-old girl with minimal phenotype anomalies and moderate mental retardation. The origin of the extra chromosome could not be determined either cytogenetically or clinically. The present case is compared with six similar cases in the literature. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504 [article] Mosaicism for an extra small ring chromosome [Texte imprimé et/ou numérique] / Antonino FORABOSCO, Auteur ; GianPaolo GUARALDI, Auteur ; Anna BARONCINI, Auteur ; Elena FERRARI, Auteur ; Carla BASSI, Auteur . - 1980 . - p.92-96. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.92-96 Index. décimale : PER Périodiques Résumé : A new case for mosaicism for an extra small ring chromosome is described in a 13-year-old girl with minimal phenotype anomalies and moderate mental retardation. The origin of the extra chromosome could not be determined either cytogenetically or clinically. The present case is compared with six similar cases in the literature. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504

Intractable epilepsy in childhood / Neil GORDON in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.97-100 Titre : Intractable epilepsy in childhood Type de document : Texte imprimé et/ou numérique Auteurs : Neil GORDON, Auteur Année de publication : 1980 Article en page(s) : p.97-100 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504 [article] Intractable epilepsy in childhood [Texte imprimé et/ou numérique] / Neil GORDON, Auteur . - 1980 . - p.97-100. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.97-100 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=504

Benzodiazepine treatment for Lesch-Nyhan syndrome? / Richard M. DASHEIFF in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.101-102 Titre : Benzodiazepine treatment for Lesch-Nyhan syndrome? Type de document : Texte imprimé et/ou numérique Auteurs : Richard M. DASHEIFF, Auteur Année de publication : 1980 Article en page(s) : p.101-102 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=505 [article] Benzodiazepine treatment for Lesch-Nyhan syndrome? [Texte imprimé et/ou numérique] / Richard M. DASHEIFF, Auteur . - 1980 . - p.101-102. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.101-102 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=505

Perinatal asphyxia: factors which predict developmental outcome / Albert P. SCHEINER in Developmental Medicine & Child Neurology, 22-1 (February 1980)

Public ISBD [article]  inDevelopmental Medicine & Child Neurology > 22-1 (February 1980) . - p.102-104 Titre : Perinatal asphyxia: factors which predict developmental outcome Type de document : Texte imprimé et/ou numérique Auteurs : Albert P. SCHEINER, Auteur Année de publication : 1980 Article en page(s) : p.102-104 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=505 [article] Perinatal asphyxia: factors which predict developmental outcome [Texte imprimé et/ou numérique] / Albert P. SCHEINER, Auteur . - 1980 . - p.102-104. Langues : Anglais (eng) in Developmental Medicine & Child Neurology > 22-1 (February 1980) . - p.102-104 Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=505