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PER : Périodiques |
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Single-cause Attribution / Christopher OUNSTED in Developmental Medicine & Child Neurology, 30-2 (April 1988)
[article]
Titre : Single-cause Attribution Type de document : Texte imprimé et/ou numérique Auteurs : Christopher OUNSTED, Auteur Année de publication : 1988 Article en page(s) : p.266-267 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=775
in Developmental Medicine & Child Neurology > 30-2 (April 1988) . - p.266-267[article] Single-cause Attribution [Texte imprimé et/ou numérique] / Christopher OUNSTED, Auteur . - 1988 . - p.266-267.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 30-2 (April 1988) . - p.266-267
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=775 Single-cause Attribution / Hanan COSTEFF in Developmental Medicine & Child Neurology, 30-3 (June 1988)
[article]
Titre : Single-cause Attribution Type de document : Texte imprimé et/ou numérique Auteurs : Hanan COSTEFF, Auteur Année de publication : 1988 Article en page(s) : p.410-412 Langues : Anglais (eng) Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=128
in Developmental Medicine & Child Neurology > 30-3 (June 1988) . - p.410-412[article] Single-cause Attribution [Texte imprimé et/ou numérique] / Hanan COSTEFF, Auteur . - 1988 . - p.410-412.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 30-3 (June 1988) . - p.410-412
Index. décimale : PER Périodiques Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=128 Single-locus and Haplotype Associations of GRIN2B Gene with Autism Spectrum Disorders and the Demographic and Clinical Characteristics of Patients in Guilan, Iran / Niloofar FARAJI ; Sajjad REZAEI ; Parvaneh KESHAVARZ in Journal of Autism and Developmental Disorders, 54-2 (February 2024)
[article]
Titre : Single-locus and Haplotype Associations of GRIN2B Gene with Autism Spectrum Disorders and the Demographic and Clinical Characteristics of Patients in Guilan, Iran Type de document : Texte imprimé et/ou numérique Auteurs : Niloofar FARAJI, Auteur ; Sajjad REZAEI, Auteur ; Parvaneh KESHAVARZ, Auteur Article en page(s) : p.607-614 Index. décimale : PER Périodiques Résumé : Autism spectrum disorders (ASDs) are described as generalized developmental disorders, with an average age of onset of 36 months. Genetic and environmental factors may contribute to this multifactorial disorder. The present study aimed to investigate the association of three GRIN2B polymorphisms, including rs1019385, rs1024893, and rs3764028, with ASDs. Based on the results, there was a significant difference regarding the genotype frequency of rs3764028 polymorphism between the control and case (ASD) groups (P?=?0.027). According to the recessive model, this variant was associated with ASDs (P?=?0.23). None of the eight haplotype models with frequencies above 0.5 showed significant differences between the case and control groups in terms of allelic frequency. The present results showed that the rs376028 variant was directly related to the phenotypic symptoms of ASDs. En ligne : https://doi.org/10.1007/s10803-022-05818-2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=520
in Journal of Autism and Developmental Disorders > 54-2 (February 2024) . - p.607-614[article] Single-locus and Haplotype Associations of GRIN2B Gene with Autism Spectrum Disorders and the Demographic and Clinical Characteristics of Patients in Guilan, Iran [Texte imprimé et/ou numérique] / Niloofar FARAJI, Auteur ; Sajjad REZAEI, Auteur ; Parvaneh KESHAVARZ, Auteur . - p.607-614.
in Journal of Autism and Developmental Disorders > 54-2 (February 2024) . - p.607-614
Index. décimale : PER Périodiques Résumé : Autism spectrum disorders (ASDs) are described as generalized developmental disorders, with an average age of onset of 36 months. Genetic and environmental factors may contribute to this multifactorial disorder. The present study aimed to investigate the association of three GRIN2B polymorphisms, including rs1019385, rs1024893, and rs3764028, with ASDs. Based on the results, there was a significant difference regarding the genotype frequency of rs3764028 polymorphism between the control and case (ASD) groups (P?=?0.027). According to the recessive model, this variant was associated with ASDs (P?=?0.23). None of the eight haplotype models with frequencies above 0.5 showed significant differences between the case and control groups in terms of allelic frequency. The present results showed that the rs376028 variant was directly related to the phenotypic symptoms of ASDs. En ligne : https://doi.org/10.1007/s10803-022-05818-2 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=520 Single motor-unit control by normal and cerebral-palsied males / Debra W. ROBERTSON in Developmental Medicine & Child Neurology, 26-3 (June 1984)
[article]
Titre : Single motor-unit control by normal and cerebral-palsied males Type de document : Texte imprimé et/ou numérique Auteurs : Debra W. ROBERTSON, Auteur ; Wynne A. LEE, Auteur ; Michael JACOBS, Auteur Année de publication : 1984 Article en page(s) : p.323-327 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Single motor-unit (SMU) control was compared for three ambulatory cerebral-palsied and three neurologically unimpaired subjects. Both groups were similar in their abilities to produce a discrete whole muscle contraction, to isolate and maintain firing of a single motor unit, and to turn a unit on at a visual signal. Unit inter-spike intervals were very similar for both groups. However, the cerebral-palsied subjects showed a consistent inability to inhibit single motor-unit (or whole muscle) activity if the isolated unit had been firing for some time; normal subjects did not show a similar inability. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=578
in Developmental Medicine & Child Neurology > 26-3 (June 1984) . - p.323-327[article] Single motor-unit control by normal and cerebral-palsied males [Texte imprimé et/ou numérique] / Debra W. ROBERTSON, Auteur ; Wynne A. LEE, Auteur ; Michael JACOBS, Auteur . - 1984 . - p.323-327.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 26-3 (June 1984) . - p.323-327
Index. décimale : PER Périodiques Résumé : Single motor-unit (SMU) control was compared for three ambulatory cerebral-palsied and three neurologically unimpaired subjects. Both groups were similar in their abilities to produce a discrete whole muscle contraction, to isolate and maintain firing of a single motor unit, and to turn a unit on at a visual signal. Unit inter-spike intervals were very similar for both groups. However, the cerebral-palsied subjects showed a consistent inability to inhibit single motor-unit (or whole muscle) activity if the isolated unit had been firing for some time; normal subjects did not show a similar inability. Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=578 Single nucleotide polymorphism heritability and differential patterns of genetic overlap between inattention and four neurocognitive factors in youth / Lauren MICALIZZI in Development and Psychopathology, 33-1 (February 2021)
[article]
Titre : Single nucleotide polymorphism heritability and differential patterns of genetic overlap between inattention and four neurocognitive factors in youth Type de document : Texte imprimé et/ou numérique Auteurs : Lauren MICALIZZI, Auteur ; Leslie A. BRICK, Auteur ; Marisa E. MARRACCINI, Auteur ; Chelsie E. BENCA-BACHMAN, Auteur ; Rohan H. C. PALMER, Auteur ; Valerie S. KNOPIK, Auteur Article en page(s) : p.76-86 Langues : Anglais (eng) Mots-clés : Gcta adolescence genetics heritability inattention neurocognitive functioning Index. décimale : PER Périodiques Résumé : Theoretical models of attention-deficit/hyperactivity disorder implicate neurocognitive dysfunction, yet neurocognitive functioning covers a range of abilities that may not all be linked with inattention. This study (a) investigated the single nucleotide polymorphism (SNP) heritability (h2SNP) of inattention and aspects of neurocognitive efficiency (memory, social cognition, executive function, and complex cognition) based on additive genome-wide effects; (b) examined if there were shared genetic effects among inattention and each aspect of neurocognitive efficiency; and (c) conducted an exploratory genome-wide association study to identify genetic regions associated with inattention. The sample included 3,563 participants of the Philadelphia Neurodevelopmental Cohort, a general population sample aged 8-21 years who completed the Penn Neurocognitive Battery. Data on inattention was obtained with the Kiddie Schedule of Affective Disorders (adapted). Genomic relatedness matrix restricted maximum likelihood was implemented in genome-wide complex trait analysis. Analyses revealed significant h2SNP for inattention (20%, SE = 0.08), social cognition (13%, SE = 0.08), memory (17%, SE = 0.08), executive function (25%, SE = 0.08), and complex cognition (24%, SE = 0.08). There was a positive genetic correlation (0.67, SE = 0.37) and a negative residual covariance (-0.23, SE = 0.06) between inattention and social cognition. No SNPs reached genome-wide significance for inattention. Results suggest specificity in genetic overlap among inattention and different aspects of neurocognitive efficiency. En ligne : http://dx.doi.org/10.1017/s0954579419001573 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=442
in Development and Psychopathology > 33-1 (February 2021) . - p.76-86[article] Single nucleotide polymorphism heritability and differential patterns of genetic overlap between inattention and four neurocognitive factors in youth [Texte imprimé et/ou numérique] / Lauren MICALIZZI, Auteur ; Leslie A. BRICK, Auteur ; Marisa E. MARRACCINI, Auteur ; Chelsie E. BENCA-BACHMAN, Auteur ; Rohan H. C. PALMER, Auteur ; Valerie S. KNOPIK, Auteur . - p.76-86.
Langues : Anglais (eng)
in Development and Psychopathology > 33-1 (February 2021) . - p.76-86
Mots-clés : Gcta adolescence genetics heritability inattention neurocognitive functioning Index. décimale : PER Périodiques Résumé : Theoretical models of attention-deficit/hyperactivity disorder implicate neurocognitive dysfunction, yet neurocognitive functioning covers a range of abilities that may not all be linked with inattention. This study (a) investigated the single nucleotide polymorphism (SNP) heritability (h2SNP) of inattention and aspects of neurocognitive efficiency (memory, social cognition, executive function, and complex cognition) based on additive genome-wide effects; (b) examined if there were shared genetic effects among inattention and each aspect of neurocognitive efficiency; and (c) conducted an exploratory genome-wide association study to identify genetic regions associated with inattention. The sample included 3,563 participants of the Philadelphia Neurodevelopmental Cohort, a general population sample aged 8-21 years who completed the Penn Neurocognitive Battery. Data on inattention was obtained with the Kiddie Schedule of Affective Disorders (adapted). Genomic relatedness matrix restricted maximum likelihood was implemented in genome-wide complex trait analysis. Analyses revealed significant h2SNP for inattention (20%, SE = 0.08), social cognition (13%, SE = 0.08), memory (17%, SE = 0.08), executive function (25%, SE = 0.08), and complex cognition (24%, SE = 0.08). There was a positive genetic correlation (0.67, SE = 0.37) and a negative residual covariance (-0.23, SE = 0.06) between inattention and social cognition. No SNPs reached genome-wide significance for inattention. Results suggest specificity in genetic overlap among inattention and different aspects of neurocognitive efficiency. En ligne : http://dx.doi.org/10.1017/s0954579419001573 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=442 Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome / Jaroslava DURDIAKOVA in Molecular Autism, (March 2014)
PermalinkSingle Nucleotide Polymorphisms Predict Symptom Severity of Autism Spectrum Disorder / Yun JIAO in Journal of Autism and Developmental Disorders, 42-6 (June 2012)
PermalinkSingle-participant structural similarity matrices lead to greater accuracy in classification of participants than function in autism in MRI / M. J. LEMING in Molecular Autism, 12 (2021)
PermalinkSingle-Photon Emission Computed Tomography Of brain Perfusion: Analysis Of 60 Paediatric Cases / Matti IIVANAINEN in Developmental Medicine & Child Neurology, 32-1 (January 1990)
PermalinkA single?session growth mindset intervention for adolescent anxiety and depression: 9?month outcomes of a randomized trial / Jessica SCHLEIDER in Journal of Child Psychology and Psychiatry, 59-2 (February 2018)
PermalinkSitting on the Sidelines: Disparities in Social, Recreational, and Community Participation Among Adolescents with Autism Spectrum Disorder / Alexa C. BUDAVARI in Journal of Autism and Developmental Disorders, 52-8 (August 2022)
PermalinkSitting problems of children with cerebral palsy / George E. FULFORD in Developmental Medicine & Child Neurology, 24-1 (February 1982)
PermalinkLes situation de crise / Jean-Loup DUPOUY in Sésame, 194 (Juillet 2015)
PermalinkLa Situation des élèves TED au Québec / Jo-Ann LAUZON in L'Express, 3 (Printemps 2010)
PermalinkLa situation des personnes autistes en période de pandémie in Link Autisme-Europe, 74 (Avril 2021)
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