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PER : Périodiques |
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Routine analysis of dermatoglyphics and palmar creases in children with developmental disorders / Hannah DAR in Developmental Medicine & Child Neurology, 20-6 (December 1978)
[article]
Titre : Routine analysis of dermatoglyphics and palmar creases in children with developmental disorders Type de document : Texte imprimé et/ou numérique Auteurs : Hannah DAR, Auteur ; D. BOLCHINSKY, Auteur ; Michael JAFFE, Auteur ; S. T. WINTER, Auteur Année de publication : 1978 Article en page(s) : p.735-737 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A dermatoglyphic and palmar crease analysis was carried out in 100 children aged six months to five years with psychomotor retardation (excluding Down's syndrome). When compared with 121 of the parents and a random group of 168 school-children, certain unusual features were found to be twice as common in the retarded children, demonstrating that these features may indicate an 'at risk' infant if found during routine examination of the newborn. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=485
in Developmental Medicine & Child Neurology > 20-6 (December 1978) . - p.735-737[article] Routine analysis of dermatoglyphics and palmar creases in children with developmental disorders [Texte imprimé et/ou numérique] / Hannah DAR, Auteur ; D. BOLCHINSKY, Auteur ; Michael JAFFE, Auteur ; S. T. WINTER, Auteur . - 1978 . - p.735-737.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 20-6 (December 1978) . - p.735-737
Index. décimale : PER Périodiques Résumé : A dermatoglyphic and palmar crease analysis was carried out in 100 children aged six months to five years with psychomotor retardation (excluding Down's syndrome). When compared with 121 of the parents and a random group of 168 school-children, certain unusual features were found to be twice as common in the retarded children, demonstrating that these features may indicate an 'at risk' infant if found during routine examination of the newborn. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=485 Roy Grinker, Unstrange Minds: Remaping the World of Autism / Deborah HILIBRAND in Journal of Autism and Developmental Disorders, 38-1 (January 2008)
[article]
Titre : Roy Grinker, Unstrange Minds: Remaping the World of Autism Type de document : Texte imprimé et/ou numérique Auteurs : Deborah HILIBRAND, Auteur Année de publication : 2008 Article en page(s) : p.202-203 Langues : Anglais (eng) Index. décimale : PER Périodiques En ligne : http://dx.doi.org/10.1007/s10803-007-0483-0 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=317
in Journal of Autism and Developmental Disorders > 38-1 (January 2008) . - p.202-203[article] Roy Grinker, Unstrange Minds: Remaping the World of Autism [Texte imprimé et/ou numérique] / Deborah HILIBRAND, Auteur . - 2008 . - p.202-203.
Langues : Anglais (eng)
in Journal of Autism and Developmental Disorders > 38-1 (January 2008) . - p.202-203
Index. décimale : PER Périodiques En ligne : http://dx.doi.org/10.1007/s10803-007-0483-0 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=317 RPP25 is developmentally regulated in prefrontal cortex and expressed at decreased levels in autism spectrum disorder / Hsien-Sung HUANG in Autism Research, 3-4 (August 2010)
[article]
Titre : RPP25 is developmentally regulated in prefrontal cortex and expressed at decreased levels in autism spectrum disorder Type de document : Texte imprimé et/ou numérique Auteurs : Hsien-Sung HUANG, Auteur ; Iris CHEUNG, Auteur ; Schahram AKBARIAN, Auteur Année de publication : 2010 Article en page(s) : p.153-161 Langues : Anglais (eng) Mots-clés : developmental-neurobiology molecular-genetics GABA Index. décimale : PER Périodiques Résumé : Dysfunction of cerebral cortex in autism is thought to involve alterations in inhibitory neurotransmission. Here, we screened, in prefrontal cortex (PFC) of 15 subjects diagnosed with autism and 15 matched controls the expression of 44 transcripts that are either preferentially expressed in gamma-aminobutyric acidergic interneurons of the mature cortex or important for the development of inhibitory circuitry. Significant alterations in the autism cohort included decreased expression (−45%) of RPP25 (15q24.1), which is located within the autism susceptibility locus, 15q22-26. RPP25, which encodes the 25 kDa subunit of ribonuclease P involved in tRNA and pre-ribosomal RNA processing, was developmentally regulated in cerebral cortex with peak levels of expression during late fetal development (human) or around birth (mouse). In the PFC, RPP25 chromatin showed high levels of histone H3-lysine 4 trimethylation, an epigenetic mark associated with transcriptional regulation. Unexpectedly, and in contrast to peripheral tissues, levels of RPP25 protein remained undetectable in fetal and adult cerebral cortex. Taken together, these findings suggest a potential role for the RPP25 gene transcript in the neurobiology of developmental brain disorders. En ligne : http://dx.doi.org/10.1002/aur.141 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=109
in Autism Research > 3-4 (August 2010) . - p.153-161[article] RPP25 is developmentally regulated in prefrontal cortex and expressed at decreased levels in autism spectrum disorder [Texte imprimé et/ou numérique] / Hsien-Sung HUANG, Auteur ; Iris CHEUNG, Auteur ; Schahram AKBARIAN, Auteur . - 2010 . - p.153-161.
Langues : Anglais (eng)
in Autism Research > 3-4 (August 2010) . - p.153-161
Mots-clés : developmental-neurobiology molecular-genetics GABA Index. décimale : PER Périodiques Résumé : Dysfunction of cerebral cortex in autism is thought to involve alterations in inhibitory neurotransmission. Here, we screened, in prefrontal cortex (PFC) of 15 subjects diagnosed with autism and 15 matched controls the expression of 44 transcripts that are either preferentially expressed in gamma-aminobutyric acidergic interneurons of the mature cortex or important for the development of inhibitory circuitry. Significant alterations in the autism cohort included decreased expression (−45%) of RPP25 (15q24.1), which is located within the autism susceptibility locus, 15q22-26. RPP25, which encodes the 25 kDa subunit of ribonuclease P involved in tRNA and pre-ribosomal RNA processing, was developmentally regulated in cerebral cortex with peak levels of expression during late fetal development (human) or around birth (mouse). In the PFC, RPP25 chromatin showed high levels of histone H3-lysine 4 trimethylation, an epigenetic mark associated with transcriptional regulation. Unexpectedly, and in contrast to peripheral tissues, levels of RPP25 protein remained undetectable in fetal and adult cerebral cortex. Taken together, these findings suggest a potential role for the RPP25 gene transcript in the neurobiology of developmental brain disorders. En ligne : http://dx.doi.org/10.1002/aur.141 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=109 RRO : autopsie d’une controverse / Carole SENECHAL in Bulletin Scientifique de l'arapi (Le), 20 (Décembre 2007)
[article]
Titre : RRO : autopsie d’une controverse Type de document : Texte imprimé et/ou numérique Auteurs : Carole SENECHAL, Auteur ; Serge LARIVEE, Auteur Année de publication : 2007 Article en page(s) : p.32-37 Langues : Français (fre) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=322
in Bulletin Scientifique de l'arapi (Le) > 20 (Décembre 2007) . - p.32-37[article] RRO : autopsie d’une controverse [Texte imprimé et/ou numérique] / Carole SENECHAL, Auteur ; Serge LARIVEE, Auteur . - 2007 . - p.32-37.
Langues : Français (fre)
in Bulletin Scientifique de l'arapi (Le) > 20 (Décembre 2007) . - p.32-37
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=322 rs1007893 and rs2070435 in DIP2A are associated with visual-reaction-behavior phenotype in Chinese Han population with autism spectrum disorder / Yan LI in Research in Autism Spectrum Disorders, 70 (February 2020)
[article]
Titre : rs1007893 and rs2070435 in DIP2A are associated with visual-reaction-behavior phenotype in Chinese Han population with autism spectrum disorder Type de document : Texte imprimé et/ou numérique Auteurs : Yan LI, Auteur ; Shuang QIU, Auteur ; Weijing ZHONG, Auteur ; Jikang SHI, Auteur ; Heran CUI, Auteur ; Yong LI, Auteur ; Yunkai LIU, Auteur ; Yi CHENG, Auteur ; Yawen LIU, Auteur Article en page(s) : p.101475 Langues : Anglais (eng) Mots-clés : Autism spectrum disorder Disco-interacting protein 2 homolog agene Single nucleotide polymorphisms Behavior phenotype Index. décimale : PER Périodiques Résumé : Background The disco-interacting protein 2 homolog A gene (DIP2A) has been reported as a novel candidate gene of Autism spectrum disorder (ASD). Associations between single nucleotide polymorphisms (SNPs) and ASD behavior phenotypes provide an opportunity to timely treat an infant with potential ASD by earlier intervention targeting a specific behavior phenotype. Methods The association of SNPs (rs8130538, rs1007893, rs34736293, rs7279002, rs2070435, rs2255397, rs1107065,rs2248636) of DIP2A with both ASD susceptibility and ASD behaviour phenotypes were investigated in Chinese Han population using a case- control study on the basis of 231 ASD cases and 242 controls. Results The allele frequencies and genotype distributions of the eight SNPs of DIP2A in the cases were not different from those in the controls; the eight DIP2A SNPs were not associated with ASD risk under the five geneticmodels; and haplotypes were not different between the cases and the controls Conclusions We identified that rs1007893 and rs2070435 in DIP2A are associated with "visual reaction" behavior phenotype in Chinese Han population. En ligne : https://doi.org/10.1016/j.rasd.2019.101475 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=414
in Research in Autism Spectrum Disorders > 70 (February 2020) . - p.101475[article] rs1007893 and rs2070435 in DIP2A are associated with visual-reaction-behavior phenotype in Chinese Han population with autism spectrum disorder [Texte imprimé et/ou numérique] / Yan LI, Auteur ; Shuang QIU, Auteur ; Weijing ZHONG, Auteur ; Jikang SHI, Auteur ; Heran CUI, Auteur ; Yong LI, Auteur ; Yunkai LIU, Auteur ; Yi CHENG, Auteur ; Yawen LIU, Auteur . - p.101475.
Langues : Anglais (eng)
in Research in Autism Spectrum Disorders > 70 (February 2020) . - p.101475
Mots-clés : Autism spectrum disorder Disco-interacting protein 2 homolog agene Single nucleotide polymorphisms Behavior phenotype Index. décimale : PER Périodiques Résumé : Background The disco-interacting protein 2 homolog A gene (DIP2A) has been reported as a novel candidate gene of Autism spectrum disorder (ASD). Associations between single nucleotide polymorphisms (SNPs) and ASD behavior phenotypes provide an opportunity to timely treat an infant with potential ASD by earlier intervention targeting a specific behavior phenotype. Methods The association of SNPs (rs8130538, rs1007893, rs34736293, rs7279002, rs2070435, rs2255397, rs1107065,rs2248636) of DIP2A with both ASD susceptibility and ASD behaviour phenotypes were investigated in Chinese Han population using a case- control study on the basis of 231 ASD cases and 242 controls. Results The allele frequencies and genotype distributions of the eight SNPs of DIP2A in the cases were not different from those in the controls; the eight DIP2A SNPs were not associated with ASD risk under the five geneticmodels; and haplotypes were not different between the cases and the controls Conclusions We identified that rs1007893 and rs2070435 in DIP2A are associated with "visual reaction" behavior phenotype in Chinese Han population. En ligne : https://doi.org/10.1016/j.rasd.2019.101475 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=414 Ruben, une petite main indispensable / Vanessa CORNIER in Déclic, 173 (Septembre-Octobre 2016)
PermalinkRUBI parent training as a group intervention for children with autism: A community pilot study / Garet S. EDWARDS in Research in Autism Spectrum Disorders, 66 (October 2019)
PermalinkRubinstein-Taybi syndrome: further evidence of a genetic aetiology / D. GILLIES in Developmental Medicine & Child Neurology, 27-6 (December 1985)
PermalinkRud syndrome revisited: ichthyosis, mental retardation, epilepsy and hypogonadism / Jane MARXMILLER in Developmental Medicine & Child Neurology, 27-3 (June 1985)
PermalinkRudy Simone Forwarded By Liane Holliday Willey, Aspergirls: Empowering Females With Asperger Syndrome / Oren SHTAYERMMAN in Journal of Autism and Developmental Disorders, 44-10 (October 2014)
PermalinkLa rue n'est pas à nous ... in Déclic, 153 (Mai-Juin 2013)
PermalinkRule breaking mediates the developmental association between GABRA2 and adolescent substance abuse / Elisa M. TRUCCO in Journal of Child Psychology and Psychiatry, 55-12 (December 2014)
PermalinkRules versus Prototype Matching: Strategies of Perception of Emotional Facial Expressions in the Autism Spectrum / Melissa D. RUTHERFORD in Journal of Autism and Developmental Disorders, 37-2 (February 2007)
PermalinkRumination and Depression in Adolescence: Investigating Symptom Specificity in a Multiwave Prospective Study / Benjamin L. HANKIN in Journal of Clinical Child & Adolescent Psychology, 37-4 (October-December 2008)
PermalinkRumination and Perceived Impairment Associated With Depressive Symptoms in a Verbal Adolescent–Adult ASD Sample / Katherine GOTHAM in Autism Research, 7-3 (June 2014)
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