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Détail de l'auteur
Auteur Manya T. ANGLEY |
Documents disponibles écrits par cet auteur (7)



Titre : Complementary Medicine Products Used in Autism - Evidence for Efficacy and Safety Type de document : Texte imprimé et/ou numérique Auteurs : Susan SEMPLE, Auteur ; Cassie HEWTON, Auteur ; Fiona PATERSON, Auteur ; Manya T. ANGLEY, Auteur Année de publication : 2011 Importance : p.78-100 Langues : Anglais (eng) Index. décimale : AUT-B AUT-B - L'Autisme - Ouvrages généraux et scientifiques En ligne : http://dx.doi.org/10.5772/32438 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=143 Complementary Medicine Products Used in Autism - Evidence for Efficacy and Safety [Texte imprimé et/ou numérique] / Susan SEMPLE, Auteur ; Cassie HEWTON, Auteur ; Fiona PATERSON, Auteur ; Manya T. ANGLEY, Auteur . - 2011 . - p.78-100.
Langues : Anglais (eng)
Index. décimale : AUT-B AUT-B - L'Autisme - Ouvrages généraux et scientifiques En ligne : http://dx.doi.org/10.5772/32438 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=143 Exemplaires
Code-barres Cote Support Localisation Section Disponibilité aucun exemplaire
Titre : Complementary Medicine Products Used in Autism - Evidence for Rationale Type de document : Texte imprimé et/ou numérique Auteurs : Susan SEMPLE, Auteur ; Cassie HEWTON, Auteur ; Fiona PATERSON, Auteur ; Manya T. ANGLEY, Auteur Année de publication : 2011 Importance : p.47-76 Langues : Anglais (eng) Index. décimale : AUT-B AUT-B - L'Autisme - Ouvrages généraux et scientifiques En ligne : http://dx.doi.org/10.5772/17357 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=143 Complementary Medicine Products Used in Autism - Evidence for Rationale [Texte imprimé et/ou numérique] / Susan SEMPLE, Auteur ; Cassie HEWTON, Auteur ; Fiona PATERSON, Auteur ; Manya T. ANGLEY, Auteur . - 2011 . - p.47-76.
Langues : Anglais (eng)
Index. décimale : AUT-B AUT-B - L'Autisme - Ouvrages généraux et scientifiques En ligne : http://dx.doi.org/10.5772/17357 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=143 Exemplaires
Code-barres Cote Support Localisation Section Disponibilité aucun exemplaire Increased abundance of Sutterella spp. and Ruminococcus torques in feces of children with autism spectrum disorder / Lv WANG in Molecular Autism, (November 2013)
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Titre : Increased abundance of Sutterella spp. and Ruminococcus torques in feces of children with autism spectrum disorder Type de document : Texte imprimé et/ou numérique Auteurs : Lv WANG, Auteur ; Claus CHRISTOPHERSEN, Auteur ; Michael SORICH, Auteur ; Jacobus GERBER, Auteur ; Manya T. ANGLEY, Auteur ; Michael CONLON, Auteur Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : A recent report indicated that numbers of Sutterella spp. are elevated in gastrointestinal biopsies taken from children with autism spectrum disorder (ASD). We have recently reported changes in the numbers of some bacteria within the stool of ASD children, and now examine whether numbers of Sutterella spp. and some other mucosa-associated bacteria linked with gastrointestinal disease (Ruminococcus gnavus and Ruminococcus torques) are also altered in the stool of these children.FINDINGS:We show that numbers of Sutterella spp. are elevated in feces of ASD children relative to controls, and that numbers of R. torques are higher in the children with ASD with a reported functional gastrointestinal disorder than those without such a disorder. We show further evidence of changes in the gut microbiota of children with ASD and confirm that the abundance of Sutterella spp. is altered in stool. En ligne : http://dx.doi.org/10.1186/2040-2392-4-42 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=227
in Molecular Autism > (November 2013)[article] Increased abundance of Sutterella spp. and Ruminococcus torques in feces of children with autism spectrum disorder [Texte imprimé et/ou numérique] / Lv WANG, Auteur ; Claus CHRISTOPHERSEN, Auteur ; Michael SORICH, Auteur ; Jacobus GERBER, Auteur ; Manya T. ANGLEY, Auteur ; Michael CONLON, Auteur.
Langues : Anglais (eng)
in Molecular Autism > (November 2013)
Index. décimale : PER Périodiques Résumé : A recent report indicated that numbers of Sutterella spp. are elevated in gastrointestinal biopsies taken from children with autism spectrum disorder (ASD). We have recently reported changes in the numbers of some bacteria within the stool of ASD children, and now examine whether numbers of Sutterella spp. and some other mucosa-associated bacteria linked with gastrointestinal disease (Ruminococcus gnavus and Ruminococcus torques) are also altered in the stool of these children.FINDINGS:We show that numbers of Sutterella spp. are elevated in feces of ASD children relative to controls, and that numbers of R. torques are higher in the children with ASD with a reported functional gastrointestinal disorder than those without such a disorder. We show further evidence of changes in the gut microbiota of children with ASD and confirm that the abundance of Sutterella spp. is altered in stool. En ligne : http://dx.doi.org/10.1186/2040-2392-4-42 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=227 Is there a role for routinely screening children with autism spectrum disorder for creatine deficiency syndrome? / Lv WANG in Autism Research, 3-5 (October 2010)
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Titre : Is there a role for routinely screening children with autism spectrum disorder for creatine deficiency syndrome? Type de document : Texte imprimé et/ou numérique Auteurs : Lv WANG, Auteur ; Manya T. ANGLEY, Auteur ; Michael J. SORICH, Auteur ; Robyn L. YOUNG, Auteur ; Ross A. MCKINNON, Auteur ; Jacobus P. GERBER, Auteur Année de publication : 2010 Article en page(s) : p.268-272 Langues : Anglais (eng) Mots-clés : autism spectrum disorder (ASD) creatine deficiency syndrome (CDS) creatine (CR) guanidinoacetate (GAA) liquid chromatography tandem mass spectrometry (LC-MS/MS) diagnostic biomarkers Index. décimale : PER Périodiques Résumé : Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder that presents in the first three years of life. Currently, diagnosis of ASD is based on its behavioural manifestations, as laboratory diagnostic tests do not exist. Creatine deficiency syndrome (CDS) is one form of inborn error of metabolism where affected individuals have similar clinical features to individuals with ASD. Abnormal urinary creatine (CR) and guanidinoacetate (GAA) levels have been reported as biomarkers of CDS. We hypothesized that screening for abnormal levels of urinary CR and GAA in children with ASD may assist in identifying a subgroup of ASD individuals who can be managed with dietary interventions. Morning urine samples were collected from children with and without autism and analyzed for CR and GAA levels. Results showed there was no statistically significant difference in urinary CR:creatinine and GAA:creatinine between the children with ASD and sibling or unrelated controls. In conclusion, routine screening for abnormal urinary CR and GAA could be considered in ASD diagnostic protocols; however, individuals positive for CDS are likely to be rare in an ASD cohort. En ligne : http://dx.doi.org/10.1002/aur.145 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=115
in Autism Research > 3-5 (October 2010) . - p.268-272[article] Is there a role for routinely screening children with autism spectrum disorder for creatine deficiency syndrome? [Texte imprimé et/ou numérique] / Lv WANG, Auteur ; Manya T. ANGLEY, Auteur ; Michael J. SORICH, Auteur ; Robyn L. YOUNG, Auteur ; Ross A. MCKINNON, Auteur ; Jacobus P. GERBER, Auteur . - 2010 . - p.268-272.
Langues : Anglais (eng)
in Autism Research > 3-5 (October 2010) . - p.268-272
Mots-clés : autism spectrum disorder (ASD) creatine deficiency syndrome (CDS) creatine (CR) guanidinoacetate (GAA) liquid chromatography tandem mass spectrometry (LC-MS/MS) diagnostic biomarkers Index. décimale : PER Périodiques Résumé : Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder that presents in the first three years of life. Currently, diagnosis of ASD is based on its behavioural manifestations, as laboratory diagnostic tests do not exist. Creatine deficiency syndrome (CDS) is one form of inborn error of metabolism where affected individuals have similar clinical features to individuals with ASD. Abnormal urinary creatine (CR) and guanidinoacetate (GAA) levels have been reported as biomarkers of CDS. We hypothesized that screening for abnormal levels of urinary CR and GAA in children with ASD may assist in identifying a subgroup of ASD individuals who can be managed with dietary interventions. Morning urine samples were collected from children with and without autism and analyzed for CR and GAA levels. Results showed there was no statistically significant difference in urinary CR:creatinine and GAA:creatinine between the children with ASD and sibling or unrelated controls. In conclusion, routine screening for abnormal urinary CR and GAA could be considered in ASD diagnostic protocols; however, individuals positive for CDS are likely to be rare in an ASD cohort. En ligne : http://dx.doi.org/10.1002/aur.145 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=115 Lack of Evidence for Genomic Instability in Autistic Children as Measured by the Cytokinesis-Block Micronucleus Cytome Assay / Penelope A. E. MAIN in Autism Research, 8-1 (February 2015)
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Titre : Lack of Evidence for Genomic Instability in Autistic Children as Measured by the Cytokinesis-Block Micronucleus Cytome Assay Type de document : Texte imprimé et/ou numérique Auteurs : Penelope A. E. MAIN, Auteur ; Philip THOMAS, Auteur ; Manya T. ANGLEY, Auteur ; Robyn L. YOUNG, Auteur ; Adrian ESTERMAN, Auteur ; Catherine E. KING, Auteur ; Michael F. FENECH, Auteur Article en page(s) : p.94-104 Langues : Anglais (eng) Mots-clés : autism genomic instability DNA damage B vitamins behaviour riboflavin Index. décimale : PER Périodiques Résumé : Autism spectrum disorders are a set of neurodevelopmental disorders that are highly hereditable. Increased genomic instability has been observed in other heritable paediatric neurobiological disorders; therefore, the aim of our study was to test the hypothesis that DNA damage is increased in children with autism and that B vitamin status may explain variations in genome integrity between autistic and normal children. We compared 35 children with autism, 27 of their siblings without autism and 25 age- and gender-matched community controls for genomic stability using the cytokinesis-block micronucleus cytome (CBMN-cyt) assay, B vitamins and homocysteine, as well as autism-related behaviours. It was found that there were no differences in CBMN-cyt biomarkers between the three groups. Vitamin B2 was significantly raised in children with autism and their siblings compared with controls (P?=?0.027 and P?=?0.016 respectively) but there was no difference in other B vitamins or homocysteine. In conclusion, although replication using a larger cohort is needed, it appears unlikely that genomic instability is a feature of the aetiology of autism. We cannot rule out in utero effects or other types of DNA damage not measured by the CBMN-cyt assay. En ligne : http://dx.doi.org/10.1002/aur.1428 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=256
in Autism Research > 8-1 (February 2015) . - p.94-104[article] Lack of Evidence for Genomic Instability in Autistic Children as Measured by the Cytokinesis-Block Micronucleus Cytome Assay [Texte imprimé et/ou numérique] / Penelope A. E. MAIN, Auteur ; Philip THOMAS, Auteur ; Manya T. ANGLEY, Auteur ; Robyn L. YOUNG, Auteur ; Adrian ESTERMAN, Auteur ; Catherine E. KING, Auteur ; Michael F. FENECH, Auteur . - p.94-104.
Langues : Anglais (eng)
in Autism Research > 8-1 (February 2015) . - p.94-104
Mots-clés : autism genomic instability DNA damage B vitamins behaviour riboflavin Index. décimale : PER Périodiques Résumé : Autism spectrum disorders are a set of neurodevelopmental disorders that are highly hereditable. Increased genomic instability has been observed in other heritable paediatric neurobiological disorders; therefore, the aim of our study was to test the hypothesis that DNA damage is increased in children with autism and that B vitamin status may explain variations in genome integrity between autistic and normal children. We compared 35 children with autism, 27 of their siblings without autism and 25 age- and gender-matched community controls for genomic stability using the cytokinesis-block micronucleus cytome (CBMN-cyt) assay, B vitamins and homocysteine, as well as autism-related behaviours. It was found that there were no differences in CBMN-cyt biomarkers between the three groups. Vitamin B2 was significantly raised in children with autism and their siblings compared with controls (P?=?0.027 and P?=?0.016 respectively) but there was no difference in other B vitamins or homocysteine. In conclusion, although replication using a larger cohort is needed, it appears unlikely that genomic instability is a feature of the aetiology of autism. We cannot rule out in utero effects or other types of DNA damage not measured by the CBMN-cyt assay. En ligne : http://dx.doi.org/10.1002/aur.1428 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=256 Sensory Processing Subtypes in Autism: Association with Adaptive Behavior / Alison E. LANE in Journal of Autism and Developmental Disorders, 40-1 (January 2010)
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PermalinkThe Relationship Between Sensory Processing Patterns and Behavioural Responsiveness in Autistic Disorder: A Pilot Study / Amy E. Z. BAKER in Journal of Autism and Developmental Disorders, 38-5 (May 2008)
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