Dépouillements

Atypical development of white matter microstructure of the corpus callosum in males with autism: a longitudinal investigation / Brittany G. TRAVERS in Molecular Autism, (March 2015)  

Public ISBD [article]  inMolecular Autism > (March 2015) . - p.1-15 Titre : Atypical development of white matter microstructure of the corpus callosum in males with autism: a longitudinal investigation Type de document : Texte imprimé et/ou numérique Auteurs : Brittany G. TRAVERS, Auteur ; Do P. M. TROMP, Auteur ; Nagesh ADLURU, Auteur ; Nicholas LANGE, Auteur ; Dan DESTICHE, Auteur ; Chad ENNIS, Auteur ; Jared A. NIELSEN, Auteur ; Alyson L. FROEHLICH, Auteur ; Molly B. D. PRIGGE, Auteur ; P. Thomas FLETCHER, Auteur ; Jeffrey S. ANDERSON, Auteur ; Brandon A. ZIELINSKI, Auteur ; Erin D. BIGLER, Auteur ; Janet E. LAINHART, Auteur ; Andrew L. ALEXANDER, Auteur Article en page(s) : p.1-15 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The corpus callosum is the largest white matter structure in the brain, and it is the most consistently reported to be atypical in diffusion tensor imaging studies of autism spectrum disorder. In individuals with typical development, the corpus callosum is known to undergo a protracted development from childhood through young adulthood. However, no study has longitudinally examined the developmental trajectory of corpus callosum in autism past early childhood. En ligne : http://dx.doi.org/10.1186/s13229-015-0001-8 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] Atypical development of white matter microstructure of the corpus callosum in males with autism: a longitudinal investigation [Texte imprimé et/ou numérique] / Brittany G. TRAVERS, Auteur ; Do P. M. TROMP, Auteur ; Nagesh ADLURU, Auteur ; Nicholas LANGE, Auteur ; Dan DESTICHE, Auteur ; Chad ENNIS, Auteur ; Jared A. NIELSEN, Auteur ; Alyson L. FROEHLICH, Auteur ; Molly B. D. PRIGGE, Auteur ; P. Thomas FLETCHER, Auteur ; Jeffrey S. ANDERSON, Auteur ; Brandon A. ZIELINSKI, Auteur ; Erin D. BIGLER, Auteur ; Janet E. LAINHART, Auteur ; Andrew L. ALEXANDER, Auteur . - p.1-15. Langues : Anglais (eng) in Molecular Autism > (March 2015) . - p.1-15 Index. décimale : PER Périodiques Résumé : The corpus callosum is the largest white matter structure in the brain, and it is the most consistently reported to be atypical in diffusion tensor imaging studies of autism spectrum disorder. In individuals with typical development, the corpus callosum is known to undergo a protracted development from childhood through young adulthood. However, no study has longitudinally examined the developmental trajectory of corpus callosum in autism past early childhood. En ligne : http://dx.doi.org/10.1186/s13229-015-0001-8 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277

Reduced isolation-induced pup ultrasonic communication in mouse pups lacking brain serotonin / Valentina MOSIENKO in Molecular Autism, (March 2015)  

Public ISBD [article]  inMolecular Autism > (March 2015) . - p.13 Titre : Reduced isolation-induced pup ultrasonic communication in mouse pups lacking brain serotonin Type de document : Texte imprimé et/ou numérique Auteurs : Valentina MOSIENKO, Auteur ; Daniel BEIS, Auteur ; Natalia ALENINA, Auteur ; Markus WÖHR, Auteur Article en page(s) : p.13 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : BACKGROUND: Serotonin (5-hydroxytryptamine, 5-HT) is a key modulatory neurotransmitter in the mammalian central nervous system (CNS) that plays an important role as a developmental signal. Several lines of evidence associate altered 5-HT signaling with psychopathology in humans, particularly neurodevelopmental disorders such as autism spectrum disorders (ASD). ASD are characterized by persistent social and communication deficits along with stereotyped and repetitive patterns of behavior, with all symptoms emerging early during development. METHODS: Here, we employed a mouse model devoid of brain 5-HT due to the lack of the gene encoding tryptophan hydroxylase 2 (Tph2), the initial and rate-limiting enzyme of 5-HT synthesis in the CNS. Tph2 null mutant (Tph2(-/-)) mice show normal prenatal development; however, they display for yet unknown reasons severe growth retardation during the first postnatal weeks. We investigated, therefore, whether Tph2(-/-) mice display deficits in isolation-induced ultrasonic vocalizations (USV) as pups during early life. Isolation-induced USV are the most commonly studied behavioral measure to assess developmental delays and communication deficits in rodent models for ASD, particularly as they serve an important communicative function in coordinating mother-pup interactions. RESULTS: Tph2(-/-) mouse pups displayed a clear deficit in the emission of isolation-induced USV, as compared to heterozygous and wildtype littermates, exactly during growth retardation onset, including reduced call numbers and deficits in call clustering and temporal organization. CONCLUSIONS: The ultrasonic communication impairment displayed by Tph2(-/-) mouse pups is likely to result in a deficient mother-infant interaction, presumably contributing to their growth retardation phenotype, and represents a prominent feature relevant to ASD. En ligne : http://dx.doi.org/10.1186/s13229-015-0003-6 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] Reduced isolation-induced pup ultrasonic communication in mouse pups lacking brain serotonin [Texte imprimé et/ou numérique] / Valentina MOSIENKO, Auteur ; Daniel BEIS, Auteur ; Natalia ALENINA, Auteur ; Markus WÖHR, Auteur . - p.13. Langues : Anglais (eng) in Molecular Autism > (March 2015) . - p.13 Index. décimale : PER Périodiques Résumé : BACKGROUND: Serotonin (5-hydroxytryptamine, 5-HT) is a key modulatory neurotransmitter in the mammalian central nervous system (CNS) that plays an important role as a developmental signal. Several lines of evidence associate altered 5-HT signaling with psychopathology in humans, particularly neurodevelopmental disorders such as autism spectrum disorders (ASD). ASD are characterized by persistent social and communication deficits along with stereotyped and repetitive patterns of behavior, with all symptoms emerging early during development. METHODS: Here, we employed a mouse model devoid of brain 5-HT due to the lack of the gene encoding tryptophan hydroxylase 2 (Tph2), the initial and rate-limiting enzyme of 5-HT synthesis in the CNS. Tph2 null mutant (Tph2(-/-)) mice show normal prenatal development; however, they display for yet unknown reasons severe growth retardation during the first postnatal weeks. We investigated, therefore, whether Tph2(-/-) mice display deficits in isolation-induced ultrasonic vocalizations (USV) as pups during early life. Isolation-induced USV are the most commonly studied behavioral measure to assess developmental delays and communication deficits in rodent models for ASD, particularly as they serve an important communicative function in coordinating mother-pup interactions. RESULTS: Tph2(-/-) mouse pups displayed a clear deficit in the emission of isolation-induced USV, as compared to heterozygous and wildtype littermates, exactly during growth retardation onset, including reduced call numbers and deficits in call clustering and temporal organization. CONCLUSIONS: The ultrasonic communication impairment displayed by Tph2(-/-) mouse pups is likely to result in a deficient mother-infant interaction, presumably contributing to their growth retardation phenotype, and represents a prominent feature relevant to ASD. En ligne : http://dx.doi.org/10.1186/s13229-015-0003-6 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277

Autistic children at risk of being underestimated: school-based pilot study of a strength-informed assessment / Valérie COURCHESNE in Molecular Autism, (March 2015)  

Public ISBD [article]  inMolecular Autism > (March 2015) . - p.1-10 Titre : Autistic children at risk of being underestimated: school-based pilot study of a strength-informed assessment Type de document : Texte imprimé et/ou numérique Auteurs : Valérie COURCHESNE, Auteur ; Andrée-Anne S. MEILLEUR, Auteur ; Marie-Pier POULIN-LORD, Auteur ; Michelle DAWSON, Auteur ; Isabelle SOULIERES, Auteur Article en page(s) : p.1-10 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : An important minority of school-aged autistic children, often characterized as ‘nonverbal’ or ‘minimally verbal,’ displays little or no spoken language. These children are at risk of being judged ‘low-functioning’ or ‘untestable’ via conventional cognitive testing practices. One neglected avenue for assessing autistic children so situated is to engage current knowledge of autistic cognitive strengths. Our aim was thus to pilot a strength-informed assessment of autistic children whose poor performance on conventional instruments suggests their cognitive potential is very limited. En ligne : http://dx.doi.org/10.1186/s13229-015-0006-3 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] Autistic children at risk of being underestimated: school-based pilot study of a strength-informed assessment [Texte imprimé et/ou numérique] / Valérie COURCHESNE, Auteur ; Andrée-Anne S. MEILLEUR, Auteur ; Marie-Pier POULIN-LORD, Auteur ; Michelle DAWSON, Auteur ; Isabelle SOULIERES, Auteur . - p.1-10. Langues : Anglais (eng) in Molecular Autism > (March 2015) . - p.1-10 Index. décimale : PER Périodiques Résumé : An important minority of school-aged autistic children, often characterized as ‘nonverbal’ or ‘minimally verbal,’ displays little or no spoken language. These children are at risk of being judged ‘low-functioning’ or ‘untestable’ via conventional cognitive testing practices. One neglected avenue for assessing autistic children so situated is to engage current knowledge of autistic cognitive strengths. Our aim was thus to pilot a strength-informed assessment of autistic children whose poor performance on conventional instruments suggests their cognitive potential is very limited. En ligne : http://dx.doi.org/10.1186/s13229-015-0006-3 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277

Neuroendocrine and behavioral response to social rupture and repair in preschoolers with autism spectrum disorders interacting with mother and father / Sharon OSTFELD-ETZION in Molecular Autism, (March 2015)  

Public ISBD [article]  inMolecular Autism > (March 2015) . - p.1-13 Titre : Neuroendocrine and behavioral response to social rupture and repair in preschoolers with autism spectrum disorders interacting with mother and father Type de document : Texte imprimé et/ou numérique Auteurs : Sharon OSTFELD-ETZION, Auteur ; Ofer GOLAN, Auteur ; Yael HIRSCHLER-GUTTENBERG, Auteur ; Orna ZAGOORY-SHARON, Auteur ; Ruth FELDMAN, Auteur Article en page(s) : p.1-13 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Preschoolers with autism spectrum disorder (ASD) exhibit difficulties in handling social stress and utilizing efficient emotion regulation (ER) strategies to manage high arousal. While researchers called to assess ER in ASD, few studies utilized direct observations. We tested children’s behavioral and cortisol response to maternal and paternal unavailability and hypothesized that children with ASD will employ less complex ER strategies and their parents would show increased regulation facilitation effort to accommodate their child’s difficulties. En ligne : http://dx.doi.org/10.1186/s13229-015-0007-2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] Neuroendocrine and behavioral response to social rupture and repair in preschoolers with autism spectrum disorders interacting with mother and father [Texte imprimé et/ou numérique] / Sharon OSTFELD-ETZION, Auteur ; Ofer GOLAN, Auteur ; Yael HIRSCHLER-GUTTENBERG, Auteur ; Orna ZAGOORY-SHARON, Auteur ; Ruth FELDMAN, Auteur . - p.1-13. Langues : Anglais (eng) in Molecular Autism > (March 2015) . - p.1-13 Index. décimale : PER Périodiques Résumé : Preschoolers with autism spectrum disorder (ASD) exhibit difficulties in handling social stress and utilizing efficient emotion regulation (ER) strategies to manage high arousal. While researchers called to assess ER in ASD, few studies utilized direct observations. We tested children’s behavioral and cortisol response to maternal and paternal unavailability and hypothesized that children with ASD will employ less complex ER strategies and their parents would show increased regulation facilitation effort to accommodate their child’s difficulties. En ligne : http://dx.doi.org/10.1186/s13229-015-0007-2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277

Fmrp targets or not: long, highly brain-expressed genes tend to be implicated in autism and brain disorders / Rebecca L. OUWENGA in Molecular Autism, (March 2015)  

Public ISBD [article]  inMolecular Autism > (March 2015) . - p.1-7 Titre : Fmrp targets or not: long, highly brain-expressed genes tend to be implicated in autism and brain disorders Type de document : Texte imprimé et/ou numérique Auteurs : Rebecca L. OUWENGA, Auteur ; Joseph DOUGHERTY, Auteur Article en page(s) : p.1-7 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Many studies have demonstrated a robust statistical overlap between genes whose transcripts are reported as Fragile X Mental Retardation Protein (Fmrp)-binding targets and genes implicated in various psychiatric disorders, including autism. However, it is not clear how to interpret this overlap as the Fmrp protein itself is not considered to be central to all instances of these conditions. En ligne : http://dx.doi.org/10.1186/s13229-015-0008-1 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] Fmrp targets or not: long, highly brain-expressed genes tend to be implicated in autism and brain disorders [Texte imprimé et/ou numérique] / Rebecca L. OUWENGA, Auteur ; Joseph DOUGHERTY, Auteur . - p.1-7. Langues : Anglais (eng) in Molecular Autism > (March 2015) . - p.1-7 Index. décimale : PER Périodiques Résumé : Many studies have demonstrated a robust statistical overlap between genes whose transcripts are reported as Fragile X Mental Retardation Protein (Fmrp)-binding targets and genes implicated in various psychiatric disorders, including autism. However, it is not clear how to interpret this overlap as the Fmrp protein itself is not considered to be central to all instances of these conditions. En ligne : http://dx.doi.org/10.1186/s13229-015-0008-1 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277

A randomized, placebo controlled trial of omega-3 fatty acids in the treatment of young children with autism / Deepali MANKAD in Molecular Autism, (March 2015)  

Public ISBD [article]  inMolecular Autism > (March 2015) . - p.1-11 Titre : A randomized, placebo controlled trial of omega-3 fatty acids in the treatment of young children with autism Type de document : Texte imprimé et/ou numérique Auteurs : Deepali MANKAD, Auteur ; Annie DUPUIS, Auteur ; Sharon SMILE, Auteur ; Wendy ROBERTS, Auteur ; Jessica BRIAN, Auteur ; Toni LUI, Auteur ; Lisa GENORE, Auteur ; Dina ZAGHLOUL, Auteur ; Alana IABONI, Auteur ; Peggy Margaret A. MARCON, Auteur ; Evdokia ANAGNOSTOU, Auteur Article en page(s) : p.1-11 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Autism spectrum disorder (ASD) is a neurodevelopmental disorder affecting more than 1% of children. It is characterized by social communication deficits and repetitive behaviors/restricted interests. In the absence of any medications known to improve core symptom domains, parents often use complementary alternative treatments, including omega-3 fatty acid supplements. En ligne : http://dx.doi.org/10.1186/s13229-015-0010-7 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] A randomized, placebo controlled trial of omega-3 fatty acids in the treatment of young children with autism [Texte imprimé et/ou numérique] / Deepali MANKAD, Auteur ; Annie DUPUIS, Auteur ; Sharon SMILE, Auteur ; Wendy ROBERTS, Auteur ; Jessica BRIAN, Auteur ; Toni LUI, Auteur ; Lisa GENORE, Auteur ; Dina ZAGHLOUL, Auteur ; Alana IABONI, Auteur ; Peggy Margaret A. MARCON, Auteur ; Evdokia ANAGNOSTOU, Auteur . - p.1-11. Langues : Anglais (eng) in Molecular Autism > (March 2015) . - p.1-11 Index. décimale : PER Périodiques Résumé : Autism spectrum disorder (ASD) is a neurodevelopmental disorder affecting more than 1% of children. It is characterized by social communication deficits and repetitive behaviors/restricted interests. In the absence of any medications known to improve core symptom domains, parents often use complementary alternative treatments, including omega-3 fatty acid supplements. En ligne : http://dx.doi.org/10.1186/s13229-015-0010-7 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277

Hypersensitive pupillary light reflex in infants at risk for autism / Pär NYSTRÖM in Molecular Autism, (March 2015)  

Public ISBD [article]  inMolecular Autism > (March 2015) . - p.1-6 Titre : Hypersensitive pupillary light reflex in infants at risk for autism Type de document : Texte imprimé et/ou numérique Auteurs : Pär NYSTRÖM, Auteur ; Gustaf GREDEBACK, Auteur ; Sven BÖLTE, Auteur ; Terje FALCK-YTTER, Auteur Article en page(s) : p.1-6 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Post mortem brain tissue data and animal modeling work indicate cholinergic disruptions in autism. Moreover, the cholinergic system plays a key role in the early neurodevelopmental processes believed to be derailed early in life in individuals with the disorder. Yet, there is no data from human infants supporting a developmentally important role of this neurotransmitter system. Because the pupillary light reflex depends largely on cholinergic synaptic transmission, we assessed this reflex in a sample of infants at risk for autism as well as infants at low (average) risk. En ligne : http://dx.doi.org/10.1186/s13229-015-0011-6 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] Hypersensitive pupillary light reflex in infants at risk for autism [Texte imprimé et/ou numérique] / Pär NYSTRÖM, Auteur ; Gustaf GREDEBACK, Auteur ; Sven BÖLTE, Auteur ; Terje FALCK-YTTER, Auteur . - p.1-6. Langues : Anglais (eng) in Molecular Autism > (March 2015) . - p.1-6 Index. décimale : PER Périodiques Résumé : Post mortem brain tissue data and animal modeling work indicate cholinergic disruptions in autism. Moreover, the cholinergic system plays a key role in the early neurodevelopmental processes believed to be derailed early in life in individuals with the disorder. Yet, there is no data from human infants supporting a developmentally important role of this neurotransmitter system. Because the pupillary light reflex depends largely on cholinergic synaptic transmission, we assessed this reflex in a sample of infants at risk for autism as well as infants at low (average) risk. En ligne : http://dx.doi.org/10.1186/s13229-015-0011-6 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277

The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis / Eriko FUJITA-JIMBO in Molecular Autism, (March 2015)  

Public ISBD [article]  inMolecular Autism > (March 2015) . - p.1-10 Titre : The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis Type de document : Texte imprimé et/ou numérique Auteurs : Eriko FUJITA-JIMBO, Auteur ; Yuko TANABE, Auteur ; Zhiling YU, Auteur ; Karin KOJIMA, Auteur ; Masato MORI, Auteur ; Hong LI, Auteur ; Sadahiko IWAMOTO, Auteur ; Takanori YAMAGATA, Auteur ; Mariko Y. MOMOI, Auteur ; Takashi MOMOI, Auteur Article en page(s) : p.1-10 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Autism spectrum disorder (ASD) has a complex genetic etiology. Some symptoms and mutated genes, including neuroligin (NLGN), neurexin (NRXN), and SH3 and multiple ankyrin repeat domains protein (SHANK), are shared by schizophrenia and ASD. Little is known about the molecular pathogenesis of ASD. One of the possible molecular pathogenesis is an imbalance of excitatory and inhibitory receptors linked with the NLGN-PSD-95-SHANK complex via postsynaptic density protein/Drosophila disc large tumor suppressor/zonula occludens-1 protein (PDZ) binding. In the present study, we focused on GPR85 as a candidate gene for ASD because the C-terminal amino acid sequence of GPR85 [Thr-Cys-Val-Ile (YCVI)] is classified as a type II PDZ-binding motif, and GPR85 is a risk factor for schizophrenia. GPR85 is an orphan receptor that regulates neural and synaptic plasticity and modulates diverse behaviors, including learning and memory. While searching for molecules that associate with GPR85, we found that GPR85 was associated with postsynaptic density protein (PSD)-95 linked with NLGN in the brain. En ligne : http://dx.doi.org/10.1186/s13229-015-0012-5 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis [Texte imprimé et/ou numérique] / Eriko FUJITA-JIMBO, Auteur ; Yuko TANABE, Auteur ; Zhiling YU, Auteur ; Karin KOJIMA, Auteur ; Masato MORI, Auteur ; Hong LI, Auteur ; Sadahiko IWAMOTO, Auteur ; Takanori YAMAGATA, Auteur ; Mariko Y. MOMOI, Auteur ; Takashi MOMOI, Auteur . - p.1-10. Langues : Anglais (eng) in Molecular Autism > (March 2015) . - p.1-10 Index. décimale : PER Périodiques Résumé : Autism spectrum disorder (ASD) has a complex genetic etiology. Some symptoms and mutated genes, including neuroligin (NLGN), neurexin (NRXN), and SH3 and multiple ankyrin repeat domains protein (SHANK), are shared by schizophrenia and ASD. Little is known about the molecular pathogenesis of ASD. One of the possible molecular pathogenesis is an imbalance of excitatory and inhibitory receptors linked with the NLGN-PSD-95-SHANK complex via postsynaptic density protein/Drosophila disc large tumor suppressor/zonula occludens-1 protein (PDZ) binding. In the present study, we focused on GPR85 as a candidate gene for ASD because the C-terminal amino acid sequence of GPR85 [Thr-Cys-Val-Ile (YCVI)] is classified as a type II PDZ-binding motif, and GPR85 is a risk factor for schizophrenia. GPR85 is an orphan receptor that regulates neural and synaptic plasticity and modulates diverse behaviors, including learning and memory. While searching for molecules that associate with GPR85, we found that GPR85 was associated with postsynaptic density protein (PSD)-95 linked with NLGN in the brain. En ligne : http://dx.doi.org/10.1186/s13229-015-0012-5 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277

Effects of autism spectrum disorders on outcome in teenage-onset anorexia nervosa evaluated by the Morgan-Russell outcome assessment schedule: a controlled community-based study / Søren NIELSEN in Molecular Autism, (March 2015)  

Public ISBD [article]  inMolecular Autism > (March 2015) . - p.1-10 Titre : Effects of autism spectrum disorders on outcome in teenage-onset anorexia nervosa evaluated by the Morgan-Russell outcome assessment schedule: a controlled community-based study Type de document : Texte imprimé et/ou numérique Auteurs : Søren NIELSEN, Auteur ; Henrik ANCKARSATER, Auteur ; Carina GILLBERG, Auteur ; Christopher GILLBERG, Auteur ; Maria RASTAM, Auteur ; Elisabeth WENTZ, Auteur Article en page(s) : p.1-10 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : The purpose of the study was to evaluate time trends and effects of co-existing autism spectrum disorders (ASD) on outcome in an ongoing long-term follow-up study of anorexia nervosa (AN). En ligne : http://dx.doi.org/10.1186/s13229-015-0013-4 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] Effects of autism spectrum disorders on outcome in teenage-onset anorexia nervosa evaluated by the Morgan-Russell outcome assessment schedule: a controlled community-based study [Texte imprimé et/ou numérique] / Søren NIELSEN, Auteur ; Henrik ANCKARSATER, Auteur ; Carina GILLBERG, Auteur ; Christopher GILLBERG, Auteur ; Maria RASTAM, Auteur ; Elisabeth WENTZ, Auteur . - p.1-10. Langues : Anglais (eng) in Molecular Autism > (March 2015) . - p.1-10 Index. décimale : PER Périodiques Résumé : The purpose of the study was to evaluate time trends and effects of co-existing autism spectrum disorders (ASD) on outcome in an ongoing long-term follow-up study of anorexia nervosa (AN). En ligne : http://dx.doi.org/10.1186/s13229-015-0013-4 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277

Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder / Anne-Claude TABET in Molecular Autism, (March 2015)  

Public ISBD [article]  inMolecular Autism > (March 2015) . - p.1-14 Titre : Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder Type de document : Texte imprimé et/ou numérique Auteurs : Anne-Claude TABET, Auteur ; Alain VERLOES, Auteur ; Marion PILORGE, Auteur ; Elsa DELABY, Auteur ; Richard DELORME, Auteur ; Gudrun NYGREN, Auteur ; Françoise DEVILLARD, Auteur ; Marion GÉRARD, Auteur ; Sandrine PASSEMARD, Auteur ; Delphine HERON, Auteur ; Jean-Pierre SIFFROI, Auteur ; Aurelia JACQUETTE, Auteur ; Andrée DELAHAYE, Auteur ; Laurence PERRIN, Auteur ; Céline DUPONT, Auteur ; Azzedine ABOURA, Auteur ; Pierre BITOUN, Auteur ; Mary COLEMAN, Auteur ; Marion LEBOYER, Auteur ; Christopher GILLBERG, Auteur ; Brigitte BENZACKEN, Auteur ; Catalina BETANCUR, Auteur Article en page(s) : p.1-14 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Apparently balanced chromosomal rearrangements can be associated with an abnormal phenotype, including intellectual disability and autism spectrum disorder (ASD). Genome-wide microarrays reveal cryptic genomic imbalances, related or not to the breakpoints, in 25% to 50% of patients with an abnormal phenotype carrying a microscopically balanced chromosomal rearrangement. Here we performed microarray analysis of 18 patients with ASD carrying balanced chromosomal abnormalities to identify submicroscopic imbalances implicated in abnormal neurodevelopment. En ligne : http://dx.doi.org/10.1186/s13229-015-0015-2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder [Texte imprimé et/ou numérique] / Anne-Claude TABET, Auteur ; Alain VERLOES, Auteur ; Marion PILORGE, Auteur ; Elsa DELABY, Auteur ; Richard DELORME, Auteur ; Gudrun NYGREN, Auteur ; Françoise DEVILLARD, Auteur ; Marion GÉRARD, Auteur ; Sandrine PASSEMARD, Auteur ; Delphine HERON, Auteur ; Jean-Pierre SIFFROI, Auteur ; Aurelia JACQUETTE, Auteur ; Andrée DELAHAYE, Auteur ; Laurence PERRIN, Auteur ; Céline DUPONT, Auteur ; Azzedine ABOURA, Auteur ; Pierre BITOUN, Auteur ; Mary COLEMAN, Auteur ; Marion LEBOYER, Auteur ; Christopher GILLBERG, Auteur ; Brigitte BENZACKEN, Auteur ; Catalina BETANCUR, Auteur . - p.1-14. Langues : Anglais (eng) in Molecular Autism > (March 2015) . - p.1-14 Index. décimale : PER Périodiques Résumé : Apparently balanced chromosomal rearrangements can be associated with an abnormal phenotype, including intellectual disability and autism spectrum disorder (ASD). Genome-wide microarrays reveal cryptic genomic imbalances, related or not to the breakpoints, in 25% to 50% of patients with an abnormal phenotype carrying a microscopically balanced chromosomal rearrangement. Here we performed microarray analysis of 18 patients with ASD carrying balanced chromosomal abnormalities to identify submicroscopic imbalances implicated in abnormal neurodevelopment. En ligne : http://dx.doi.org/10.1186/s13229-015-0015-2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277

Is it me? Self-recognition bias across sensory modalities and its relationship to autistic traits / Anya CHAKRABORTY in Molecular Autism, (March 2015)  

Public ISBD [article]  inMolecular Autism > (March 2015) . - p.1-8 Titre : Is it me? Self-recognition bias across sensory modalities and its relationship to autistic traits Type de document : Texte imprimé et/ou numérique Auteurs : Anya CHAKRABORTY, Auteur ; Bhismadev CHAKRABARTI, Auteur Article en page(s) : p.1-8 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Atypical self-processing is an emerging theme in autism research, suggested by lower self-reference effect in memory, and atypical neural responses to visual self-representations. Most research on physical self-processing in autism uses visual stimuli. However, the self is a multimodal construct, and therefore, it is essential to test self-recognition in other sensory modalities as well. Self-recognition in the auditory modality remains relatively unexplored and has not been tested in relation to autism and related traits. This study investigates self-recognition in auditory and visual domain in the general population and tests if it is associated with autistic traits. En ligne : http://dx.doi.org/10.1186/s13229-015-0016-1 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277 [article] Is it me? Self-recognition bias across sensory modalities and its relationship to autistic traits [Texte imprimé et/ou numérique] / Anya CHAKRABORTY, Auteur ; Bhismadev CHAKRABARTI, Auteur . - p.1-8. Langues : Anglais (eng) in Molecular Autism > (March 2015) . - p.1-8 Index. décimale : PER Périodiques Résumé : Atypical self-processing is an emerging theme in autism research, suggested by lower self-reference effect in memory, and atypical neural responses to visual self-representations. Most research on physical self-processing in autism uses visual stimuli. However, the self is a multimodal construct, and therefore, it is essential to test self-recognition in other sensory modalities as well. Self-recognition in the auditory modality remains relatively unexplored and has not been tested in relation to autism and related traits. This study investigates self-recognition in auditory and visual domain in the general population and tests if it is associated with autistic traits. En ligne : http://dx.doi.org/10.1186/s13229-015-0016-1 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=277