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The Molecular Forms of Cholinesterase and Acetylcholinesterase in Vertebrates / Jean MASSOULIE in Annual Review of Neuroscience, 5 (1982)
[article]
Titre : The Molecular Forms of Cholinesterase and Acetylcholinesterase in Vertebrates Type de document : Texte imprimé et/ou numérique Auteurs : Jean MASSOULIE, Auteur ; Suzanne BON, Auteur Année de publication : 1982 Article en page(s) : p.57-106 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=351
in Annual Review of Neuroscience > 5 (1982) . - p.57-106[article] The Molecular Forms of Cholinesterase and Acetylcholinesterase in Vertebrates [Texte imprimé et/ou numérique] / Jean MASSOULIE, Auteur ; Suzanne BON, Auteur . - 1982 . - p.57-106.
Langues : Anglais (eng)
in Annual Review of Neuroscience > 5 (1982) . - p.57-106
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=351 The Molecular Genetics of Autism Spectrum Disorders: Genomic Mechanisms, Neuroimmunopathology, and Clinical Implications / Daniel J. GUERRA in Autism Research and Treatment, (March 2011)
[article]
Titre : The Molecular Genetics of Autism Spectrum Disorders: Genomic Mechanisms, Neuroimmunopathology, and Clinical Implications Type de document : Texte imprimé et/ou numérique Auteurs : Daniel J. GUERRA, Auteur Année de publication : 2011 Article en page(s) : 16 p. Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Autism spectrum disorders (ASDs) have become increasingly common in recent years. The discovery of single-nucleotide polymorphisms and accompanying copy number variations within the genome has increased our understanding of the architecture of the disease. These genetic and genomic alterations coupled with epigenetic phenomena have pointed to a neuroimmunopathological mechanism for ASD. Model animal studies, developmental biology, and affective neuroscience laid a foundation for dissecting the neural pathways impacted by these disease-generating mechanisms. The goal of current autism research is directed toward a systems biological approach to find the most basic genetic and environmental causes to this severe developmental disease. It is hoped that future genomic and neuroimmunological research will be directed toward finding the road toward prevention, treatment, and cure of ASD. En ligne : http://dx.doi.org/10.1155/2011/398636 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=131
in Autism Research and Treatment > (March 2011) . - 16 p.[article] The Molecular Genetics of Autism Spectrum Disorders: Genomic Mechanisms, Neuroimmunopathology, and Clinical Implications [Texte imprimé et/ou numérique] / Daniel J. GUERRA, Auteur . - 2011 . - 16 p.
Langues : Anglais (eng)
in Autism Research and Treatment > (March 2011) . - 16 p.
Index. décimale : PER Périodiques Résumé : Autism spectrum disorders (ASDs) have become increasingly common in recent years. The discovery of single-nucleotide polymorphisms and accompanying copy number variations within the genome has increased our understanding of the architecture of the disease. These genetic and genomic alterations coupled with epigenetic phenomena have pointed to a neuroimmunopathological mechanism for ASD. Model animal studies, developmental biology, and affective neuroscience laid a foundation for dissecting the neural pathways impacted by these disease-generating mechanisms. The goal of current autism research is directed toward a systems biological approach to find the most basic genetic and environmental causes to this severe developmental disease. It is hoped that future genomic and neuroimmunological research will be directed toward finding the road toward prevention, treatment, and cure of ASD. En ligne : http://dx.doi.org/10.1155/2011/398636 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=131 The Molecular Neurobiology of the Acetylcholine Receptor / Michael P. MCCARTHY in Annual Review of Neuroscience, 9 (1986)
[article]
Titre : The Molecular Neurobiology of the Acetylcholine Receptor Type de document : Texte imprimé et/ou numérique Auteurs : Michael P. MCCARTHY, Auteur ; Julie P. EARNEST, Auteur ; Ellen F. YOUNG, Auteur ; Seunghyon CHOE, Auteur ; Robert M. STROUD, Auteur Année de publication : 1986 Article en page(s) : p.383-413 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=358
in Annual Review of Neuroscience > 9 (1986) . - p.383-413[article] The Molecular Neurobiology of the Acetylcholine Receptor [Texte imprimé et/ou numérique] / Michael P. MCCARTHY, Auteur ; Julie P. EARNEST, Auteur ; Ellen F. YOUNG, Auteur ; Seunghyon CHOE, Auteur ; Robert M. STROUD, Auteur . - 1986 . - p.383-413.
Langues : Anglais (eng)
in Annual Review of Neuroscience > 9 (1986) . - p.383-413
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=358 The Monash Autism-ADHD genetics and neurodevelopment (MAGNET) project design and methodologies: a dimensional approach to understanding neurobiological and genetic aetiology / R. KNOTT in Molecular Autism, 12 (2021)
[article]
Titre : The Monash Autism-ADHD genetics and neurodevelopment (MAGNET) project design and methodologies: a dimensional approach to understanding neurobiological and genetic aetiology Type de document : Texte imprimé et/ou numérique Auteurs : R. KNOTT, Auteur ; Beth P. JOHNSON, Auteur ; J. TIEGO, Auteur ; O. MELLAHN, Auteur ; A. FINLAY, Auteur ; K. KALLADY, Auteur ; M. KOUSPOS, Auteur ; V. P. MOHANAKUMAR SINDHU, Auteur ; Z. HAWI, Auteur ; A. ARNATKEVICIUTE, Auteur ; T. CHAU, Auteur ; D. MARON, Auteur ; E. C. MERCIECA, Auteur ; K. FURLEY, Auteur ; K. HARRIS, Auteur ; K. WILLIAMS, Auteur ; A. URE, Auteur ; A. FORNITO, Auteur ; K. GRAY, Auteur ; D. COGHILL, Auteur ; A. NICHOLSON, Auteur ; D. PHUNG, Auteur ; E. LOTH, Auteur ; L. MASON, Auteur ; D. MURPHY, Auteur ; Jan K. BUITELAAR, Auteur ; Mark A. BELLGROVE, Auteur Article en page(s) : 55 p. Langues : Anglais (eng) Mots-clés : Adhd Asd Cognition Eye-tracking Genetics HiTOP Neuroimaging RDoC Index. décimale : PER Périodiques Résumé : BACKGROUND: ASD and ADHD are prevalent neurodevelopmental disorders that frequently co-occur and have strong evidence for a degree of shared genetic aetiology. Behavioural and neurocognitive heterogeneity in ASD and ADHD has hampered attempts to map the underlying genetics and neurobiology, predict intervention response, and improve diagnostic accuracy. Moving away from categorical conceptualisations of psychopathology to a dimensional approach is anticipated to facilitate discovery of data-driven clusters and enhance our understanding of the neurobiological and genetic aetiology of these conditions. The Monash Autism-ADHD genetics and neurodevelopment (MAGNET) project is one of the first large-scale, family-based studies to take a truly transdiagnostic approach to ASD and ADHD. Using a comprehensive phenotyping protocol capturing dimensional traits central to ASD and ADHD, the MAGNET project aims to identify data-driven clusters across ADHD-ASD spectra using deep phenotyping of symptoms and behaviours; investigate the degree of familiality for different dimensional ASD-ADHD phenotypes and clusters; and map the neurocognitive, brain imaging, and genetic correlates of these data-driven symptom-based clusters. METHODS: The MAGNET project will recruit 1,200 families with children who are either typically developing, or who display elevated ASD, ADHD, or ASD-ADHD traits, in addition to affected and unaffected biological siblings of probands, and parents. All children will be comprehensively phenotyped for behavioural symptoms, comorbidities, neurocognitive and neuroimaging traits and genetics. CONCLUSION: The MAGNET project will be the first large-scale family study to take a transdiagnostic approach to ASD-ADHD, utilising deep phenotyping across behavioural, neurocognitive, brain imaging and genetic measures. En ligne : http://dx.doi.org/10.1186/s13229-021-00457-3 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=459
in Molecular Autism > 12 (2021) . - 55 p.[article] The Monash Autism-ADHD genetics and neurodevelopment (MAGNET) project design and methodologies: a dimensional approach to understanding neurobiological and genetic aetiology [Texte imprimé et/ou numérique] / R. KNOTT, Auteur ; Beth P. JOHNSON, Auteur ; J. TIEGO, Auteur ; O. MELLAHN, Auteur ; A. FINLAY, Auteur ; K. KALLADY, Auteur ; M. KOUSPOS, Auteur ; V. P. MOHANAKUMAR SINDHU, Auteur ; Z. HAWI, Auteur ; A. ARNATKEVICIUTE, Auteur ; T. CHAU, Auteur ; D. MARON, Auteur ; E. C. MERCIECA, Auteur ; K. FURLEY, Auteur ; K. HARRIS, Auteur ; K. WILLIAMS, Auteur ; A. URE, Auteur ; A. FORNITO, Auteur ; K. GRAY, Auteur ; D. COGHILL, Auteur ; A. NICHOLSON, Auteur ; D. PHUNG, Auteur ; E. LOTH, Auteur ; L. MASON, Auteur ; D. MURPHY, Auteur ; Jan K. BUITELAAR, Auteur ; Mark A. BELLGROVE, Auteur . - 55 p.
Langues : Anglais (eng)
in Molecular Autism > 12 (2021) . - 55 p.
Mots-clés : Adhd Asd Cognition Eye-tracking Genetics HiTOP Neuroimaging RDoC Index. décimale : PER Périodiques Résumé : BACKGROUND: ASD and ADHD are prevalent neurodevelopmental disorders that frequently co-occur and have strong evidence for a degree of shared genetic aetiology. Behavioural and neurocognitive heterogeneity in ASD and ADHD has hampered attempts to map the underlying genetics and neurobiology, predict intervention response, and improve diagnostic accuracy. Moving away from categorical conceptualisations of psychopathology to a dimensional approach is anticipated to facilitate discovery of data-driven clusters and enhance our understanding of the neurobiological and genetic aetiology of these conditions. The Monash Autism-ADHD genetics and neurodevelopment (MAGNET) project is one of the first large-scale, family-based studies to take a truly transdiagnostic approach to ASD and ADHD. Using a comprehensive phenotyping protocol capturing dimensional traits central to ASD and ADHD, the MAGNET project aims to identify data-driven clusters across ADHD-ASD spectra using deep phenotyping of symptoms and behaviours; investigate the degree of familiality for different dimensional ASD-ADHD phenotypes and clusters; and map the neurocognitive, brain imaging, and genetic correlates of these data-driven symptom-based clusters. METHODS: The MAGNET project will recruit 1,200 families with children who are either typically developing, or who display elevated ASD, ADHD, or ASD-ADHD traits, in addition to affected and unaffected biological siblings of probands, and parents. All children will be comprehensively phenotyped for behavioural symptoms, comorbidities, neurocognitive and neuroimaging traits and genetics. CONCLUSION: The MAGNET project will be the first large-scale family study to take a transdiagnostic approach to ASD-ADHD, utilising deep phenotyping across behavioural, neurocognitive, brain imaging and genetic measures. En ligne : http://dx.doi.org/10.1186/s13229-021-00457-3 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=459 The Moro reaction: a scoring system for neonatal narcotic withdrawal / Ira J. CHASNOFF in Developmental Medicine & Child Neurology, 26-4 (August 1984)
[article]
Titre : The Moro reaction: a scoring system for neonatal narcotic withdrawal Type de document : Texte imprimé et/ou numérique Auteurs : Ira J. CHASNOFF, Auteur ; William J. BURNS, Auteur Année de publication : 1984 Article en page(s) : p.484-489 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A Moro Scale was developed to evaluate the immediate and prolonged effects of neonatal addiction in two matched groups of infants, one delivered to women on low-dose methadone maintenance, the other delivered to drug-free mothers. The Moro reaction was elicited five times in succession in each infant and the most complete reaction was scored on a 20-point scale. There were significant differences between the two groups in mean Moro scores at all ages, and in the duration of the Moro reaction. Significant relationships also were found between total Moro scores and certain items on the Brazelton Scale. The Moro Scale score provides a method of following addicted newborns through the process of withdrawal, and of evaluating CNS irritability and possible early cerebral damage. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=580
in Developmental Medicine & Child Neurology > 26-4 (August 1984) . - p.484-489[article] The Moro reaction: a scoring system for neonatal narcotic withdrawal [Texte imprimé et/ou numérique] / Ira J. CHASNOFF, Auteur ; William J. BURNS, Auteur . - 1984 . - p.484-489.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-4 (August 1984) . - p.484-489
Index. décimale : PER Périodiques Résumé : A Moro Scale was developed to evaluate the immediate and prolonged effects of neonatal addiction in two matched groups of infants, one delivered to women on low-dose methadone maintenance, the other delivered to drug-free mothers. The Moro reaction was elicited five times in succession in each infant and the most complete reaction was scored on a 20-point scale. There were significant differences between the two groups in mean Moro scores at all ages, and in the duration of the Moro reaction. Significant relationships also were found between total Moro scores and certain items on the Brazelton Scale. The Moro Scale score provides a method of following addicted newborns through the process of withdrawal, and of evaluating CNS irritability and possible early cerebral damage. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=580 The Mother-Child Relationship Following In Vitro Fertilisation (IVF): Infant Attachment, Responsivity, and Maternal Sensitivity / Frances L. GIBSON in Journal of Child Psychology and Psychiatry, 41-8 (November 2000)
PermalinkThe motivation for special interests in individuals with autism and controls: Development and validation of the special interest motivation scale / Rachel GROVE in Autism Research, 9-6 (June 2016)
PermalinkThe Motivation of Stereotypic and Repetitive Behavior: Examination of Construct Validity of the Motivation Assessment Scale / Annette V. JOOSTEN in Journal of Autism and Developmental Disorders, 38-7 (August 2008)
PermalinkThe motorized wheelchair: new freedom, new responsibility and new problems / Alan L. BREED in Developmental Medicine & Child Neurology, 24-3 (June 1982)
PermalinkThe MTHFR 677CT polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations / Robin P. GOIN-KOCHEL in Autism Research, 2-2 (April 2009)
PermalinkThe multiple molecular facets of fragile X-associated tremor/ataxia syndrome / C. SELLIER in Journal of Neurodevelopmental Disorders, 6-1 (December 2014)
PermalinkThe mutual prospective influence of child and parental post-traumatic stress symptoms in pediatric patients / Markus A. LANDOLT in Journal of Child Psychology and Psychiatry, 53-7 (July 2012)
PermalinkThe Myelodysplasia Hip and Scoliosis / John M. KEGGI in Developmental Medicine & Child Neurology, 34-3 (March 1992)
PermalinkThe N170 event-related potential reflects delayed neural response to faces when visual attention is directed to the eyes in youths with ASD / T. C. PARKER in Autism Research, 14-7 (July 2021)
PermalinkThe NAS EarlyBird Programme: Partnership with Parents in Early Intervention / Jane SHIELDS in Autism, 5-1 (March 2001)
PermalinkThe Nation & Autism Project: aims and objectives / Ian RAGAN in Good Autism Practice - GAP, 16-2 (October 2015)
PermalinkThe National Autism Project (NAP) Legacy Forum 2018: what's happened since the publication of the NAP report in 2017? / Ian RAGAN in Good Autism Practice - GAP, 20-2 (October 2019)
PermalinkThe natural history of the severe form of Hunter's syndrome: a study based on 52 cases / Ian D. YOUNG in Developmental Medicine & Child Neurology, 25-4 (August 1983)
PermalinkThe nature of benefit finding in parents of a child with Asperger syndrome / Christina SAMIOS in Research in Autism Spectrum Disorders, 3-2 (April-june 2009)
PermalinkThe Nature of Covariation Between Autistic Traits and Clumsiness: A Twin Study in a General Population Sample / Sara MORUZZI in Journal of Autism and Developmental Disorders, 41-12 (December 2011)
PermalinkThe Nature of Family Meals: A New Vision of Families of Children with Autism / S. L. CURTISS in Journal of Autism and Developmental Disorders, 49-2 (February 2019)
PermalinkThe nature of friendship in children with autism spectrum disorders: A systematic review / Neysa PETRINA in Research in Autism Spectrum Disorders, 8-2 (February 2014)
PermalinkThe nature of sense making in parenting a child with Asperger syndrome / Christina SAMIOS in Research in Autism Spectrum Disorders, 2-3 (July / September 2008)
PermalinkThe Nature of the Mother's Tie to Her Infant: Maternal Bonding under Conditions of Proximity, Separation, and Potential Loss / Ruth FELDMAN in Journal of Child Psychology and Psychiatry, 40-6 (September 1999)
PermalinkThe nature of trauma memories in acute stress disorder in children and adolescents / Claire H. SALMOND in Journal of Child Psychology and Psychiatry, 52-5 (May 2011)
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