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Détail de l'auteur
Auteur G. Robert DELONG |
Documents disponibles écrits par cet auteur (6)



Titre : Brain lesions in autism Type de document : Texte imprimé et/ou numérique Auteurs : G. Robert DELONG, Auteur ; Margaret L. BAUMAN, Auteur Année de publication : 1987 Importance : p.229-242 Langues : Anglais (eng) Index. décimale : SCI-D SCI-D - Neurosciences Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=100 Brain lesions in autism [Texte imprimé et/ou numérique] / G. Robert DELONG, Auteur ; Margaret L. BAUMAN, Auteur . - 1987 . - p.229-242.
Langues : Anglais (eng)
Index. décimale : SCI-D SCI-D - Neurosciences Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=100 Exemplaires
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Titre : Dysfunction and hyperfunction of the hippocampus in autism? Type de document : Texte imprimé et/ou numérique Auteurs : G. Robert DELONG, Auteur Année de publication : 2008 Importance : p.103-121 Langues : Anglais (eng) Index. décimale : SCI-F SCI-F - Psychologie Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=675 Dysfunction and hyperfunction of the hippocampus in autism? [Texte imprimé et/ou numérique] / G. Robert DELONG, Auteur . - 2008 . - p.103-121.
Langues : Anglais (eng)
Index. décimale : SCI-F SCI-F - Psychologie Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=675 Exemplaires
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Titre : GABA(A) receptor alpha5 subunit as a candidate gene for autism and bipolar disorder: A proposed endophenotype with parent-of-origin and gain-of-function features,with or without oculocutaneous albinism Type de document : Texte imprimé et/ou numérique Auteurs : G. Robert DELONG, Auteur Année de publication : 2007 Article en page(s) : p.135-147 Langues : Anglais (eng) Mots-clés : Bipolar-disorder GABRA5 Grandmatrilineal Inheritance Special-abilities Index. décimale : PER Périodiques Résumé : Our earlier family history studies of individuals with autism found a high incidence of major affective disorder, especially bipolar disorder, and unusual talents or intellectual abilities among family members. We now describe a subgroup of such families, selected from a large clinical experience, illustrating specific features of major affective disorder, special talents or intellectual ability, and familial patterns of trait transmission, with the additional feature of oculocutaneous albinism in some cases. These observations, suggesting parent-of-origin and gain-of-function effects, considered together with recent genetic findings in the literature, suggest a genetic hypothesis possibly unifying disparate observations found in families of individuals with autism. En ligne : http://dx.doi.org/10.1177/1362361307075705 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=666
in Autism > 11-2 (March 2007) . - p.135-147[article] GABA(A) receptor alpha5 subunit as a candidate gene for autism and bipolar disorder: A proposed endophenotype with parent-of-origin and gain-of-function features,with or without oculocutaneous albinism [Texte imprimé et/ou numérique] / G. Robert DELONG, Auteur . - 2007 . - p.135-147.
Langues : Anglais (eng)
in Autism > 11-2 (March 2007) . - p.135-147
Mots-clés : Bipolar-disorder GABRA5 Grandmatrilineal Inheritance Special-abilities Index. décimale : PER Périodiques Résumé : Our earlier family history studies of individuals with autism found a high incidence of major affective disorder, especially bipolar disorder, and unusual talents or intellectual abilities among family members. We now describe a subgroup of such families, selected from a large clinical experience, illustrating specific features of major affective disorder, special talents or intellectual ability, and familial patterns of trait transmission, with the additional feature of oculocutaneous albinism in some cases. These observations, suggesting parent-of-origin and gain-of-function effects, considered together with recent genetic findings in the literature, suggest a genetic hypothesis possibly unifying disparate observations found in families of individuals with autism. En ligne : http://dx.doi.org/10.1177/1362361307075705 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=666 Neurological signs in congenital iodine-deficiency disorder (endemic cretinism) / G. Robert DELONG in Developmental Medicine & Child Neurology, 27-3 (June 1985)
[article]
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
in Developmental Medicine & Child Neurology > 27-3 (June 1985) . - p.317-324[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
Titre : Psychiatric and Occupational Histories in Families of Children with Autism Type de document : Texte imprimé et/ou numérique Auteurs : G. Robert DELONG, Auteur ; Marie MACDONALD, Auteur ; Vidya KRISHNAMURTHY, Auteur Année de publication : 2011 Importance : p.225-234 Langues : Anglais (eng) Index. décimale : AUT-B AUT-B - L'Autisme - Ouvrages généraux et scientifiques En ligne : http://dx.doi.org/10.5772/18508 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=143 Psychiatric and Occupational Histories in Families of Children with Autism [Texte imprimé et/ou numérique] / G. Robert DELONG, Auteur ; Marie MACDONALD, Auteur ; Vidya KRISHNAMURTHY, Auteur . - 2011 . - p.225-234.
Langues : Anglais (eng)
Index. décimale : AUT-B AUT-B - L'Autisme - Ouvrages généraux et scientifiques En ligne : http://dx.doi.org/10.5772/18508 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=143 Exemplaires
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