المؤلفون: Raun Melmed, Caroline Bliss Larsen

Resource Type: eBook.

Categories: JUVENILE FICTION / Social Themes / Depression & Mental Illness, JUVENILE FICTION / Social Themes / Adolescence & Coming of Age, JUVENILE FICTION / Social Themes / Bullying

المؤلفون: Raun Melmed, Wendela Whitcomb Marsh

Resource Type: eBook.

Categories: FAMILY & RELATIONSHIPS / Autism Spectrum Disorders, FAMILY & RELATIONSHIPS / Children with Special Needs, PSYCHOLOGY / Psychopathology / Autism Spectrum Disorders

المؤلفون: Raun Melmed, Caroline Bliss Larsen

Resource Type: eBook.

Categories: JUVENILE FICTION / Social Themes / Friendship, JUVENILE FICTION / Monsters

المؤلفون: Daniel Openden, Alexander J. Stein, Janet Kirwan, Sharman Ober-Reynolds, Amanda Malligo, Raun Melmed, Elena L. Pollard, Nicole L. Matthews, Christopher J. Smith

المصدر: Journal of Applied School Psychology. 31:115-140

مصطلحات موضوعية: education, General education, medicine.disease, Education, Psychological evaluation, Screening questionnaire, Psychiatry and Mental health, Autism spectrum disorder, Internal consistency, Developmental and Educational Psychology, Asperger's disorder, medicine, Social responsiveness, Autism, Psychology, Applied Psychology, Clinical psychology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9055ee3e5c3301ced748b8636551ab3f
https://doi.org/10.1080/15377903.2014.995391

المؤلفون: Raun Melmed, Annette Sexton

Resource Type: eBook.

Categories: JUVENILE FICTION / Computers & Digital Media, JUVENILE FICTION / Technology / General, JUVENILE FICTION / Social Themes / Self-Esteem & Self-Reliance

المؤلفون: Raun Melmed, Maria Wheeler

Resource Type: eBook.

الموضوعات: Parents of autistic children--United States, Autistic children--Family relationships--United States

Categories: FAMILY & RELATIONSHIPS / Autism Spectrum Disorders

المؤلفون: Paolo Curatolo, Margot Redman, Matthew J. Huentelman, Tracy L. Pawlowski, Sharman Ober-Reynolds, Roberto Sacco, Barbara Manzi, Federica Lombardi, Judith Marsillach, Raun Melmed, Antonio M. Persico, Sarah Brautigam, Christopher J. Smith, Jordi Camps, David Craig, Laura Gaita, Carla Lintas, Laura Altieri

المصدر: Psychiatry Research. 180:105-113

مصطلحات موضوعية: Pervasive developmental disorders, Enzymologic, Male, Autistic disorder, Diazoxonase, Immune, Organophosphate, Paraoxonase, Adolescent, Adult, Aryldialkylphosphatase, Carboxylic Ester Hydrolases, Child, Child Development Disorders, Pervasive, Child, Preschool, Enzyme-Linked Immunosorbent Assay, European Continental Ancestry Group, Family, Female, Gene Expression Regulation, Enzymologic, Genetic Testing, Genotype, Humans, Italy, Middle Aged, Polymorphism, Single Nucleotide, Statistics, Nonparametric, Young Adult, Psychiatry and Mental Health, Biological Psychiatry, Arylesterase, Child Development Disorders, Pervasive, Preschool, Gene Expression Regulation, Polymorphism, Single Nucleotide, Statistics, Nonparametric, Genetics, biology, PON1, Settore MED/39 - Neuropsichiatria Infantile, Psychiatry and Mental health, medicine.medical_specialty, Single-nucleotide polymorphism, White People, Internal medicine, medicine, First-degree relatives, business.industry, medicine.disease, Developmental disorder, Endocrinology, biology.protein, Autism, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fced0c1f538be6ffdab9b1919873092
https://doi.org/10.1016/j.psychres.2010.04.010

المؤلفون: Tiziana Pascucci, Riccardo Alessandrelli, Valerio Napolioni, Stefano Puglisi-Allegra, Roberto Sacco, Patricia Lewin, Paolo Curatolo, C. Lenti, Carmela Bravaccio, Karl L. Reichelt, Raun Melmed, Barbara Manzi, Cindy Schneider, Roberto Militerni, Federica Lombardi, Antonio M. Persico, Monica Saccani, Francis Rousseau

المساهمون: Napolioni, V, Lombardi, F, Sacco, R, Curatolo, P, Manzi, B, Alessandrelli, R, Militerni, R, Bravaccio, Carmela, Lenti, C, Saccani, M, Schneider, C, Melmed, R, Pascucci, T, Puglisi Allegra, S, Reichelt, Kl, Rousseau, F, Lewin, P, Persico, A. M.

المصدر: European Journal of Human Genetics. 19:353-359

مصطلحات موضوعية: Adult, Male, Serotonin, Candidate gene, Adolescent, Endophenotypes, Quantitative Trait Loci, autism, integrin-beta 3, quantitative trait locus, SLC6A4, serotonin, serotonin transporter, Autistic Disorder, Child, Preschool, Female, Haplotypes, Humans, Infant, Integrin beta3, Introns, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Regression Analysis, Serotonin Plasma Membrane Transport Proteins, Young Adult, Genetic Predisposition to Disease, Locus (genetics), Quantitative trait locus, Biology, Polymorphism, Single Nucleotide, Article, integrin-βb 3, slc6a4, Genetics, medicine, Pervasive developmental disorder, Genetics (clinical), Child, Preschool, Haplotype, medicine.disease, Settore MED/39 - Neuropsichiatria Infantile, Developmental disorder, Autism spectrum disorder, Autism

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::897e0f6f4ba071efdb22d2599b7bfa70
https://doi.org/10.1038/ejhg.2010.180

المؤلفون: Roberto Sacco, Roberto Militerni, Alessandro Frolli, Carmela Bravaccio, Antonella Gritti, Maurizio Elia, Paolo Curatolo, Barbara Manzi, Simona Trillo, Carlo Lenti, Monica Saccani, Cindy Schneider, Raun Melmed, Karl Ludvig Reichelt, Antonio M. Persico, PASCUCCI, Tiziana, PUGLISI ALLEGRA, Stefano

المساهمون: Sacco, Roberto, Roberto, Militerni, Alessandro, Frolli, Carmela, Bravaccio, Antonella, Gritti, Maurizio, Elia, Paolo, Curatolo, Barbara, Manzi, Simona, Trillo, Carlo, Lenti, Monica, Saccani, Cindy, Schneider, Raun, Melmed, Karl Ludvig Reichelt, Pascucci, Tiziana, PUGLISI ALLEGRA, Stefano, Persico, Antonio M.

مصطلحات موضوعية: autistic disorder, cranial circumference, immune system, macrocephaly, macrosomy, microcephaly

Relation: info:eu-repo/semantics/altIdentifier/pmid/17644070; info:eu-repo/semantics/altIdentifier/wos/WOS:000250528300014; volume:62; issue:9; firstpage:1038; lastpage:1047; numberofpages:10; journal:BIOLOGICAL PSYCHIATRY; http://hdl.handle.net/11573/239456; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-35148885109; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000250528300014&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a; http://www.sciencedirect.com/science/article/pii/S; http://www.scopus.com/inward/record.url?eid=2-s2.0-35148885109&partnerID=65&md5=885142c14b7c1322544f48de7440ce5e

الاتاحة: http://hdl.handle.net/11573/239456
https://doi.org/10.1016/j.biopsych.2007.04.039
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000250528300014&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a
http://www.sciencedirect.com/science/article/pii/S
http://www.scopus.com/inward/record.url?eid=2-s2.0-35148885109&partnerID=65&md5=885142c14b7c1322544f48de7440ce5e

المؤلفون: Monica Conciatori, Christopher J. Stodgell, Susan L. Hyman, Melanie O'Bara, Roberto Militerni, Carmela Bravaccio, Simona Trillo, Francesco Montecchi, Cindy Schneider, Raun Melmed, Maurizio Elia, Lori Crawford, Sarah J. Spence, Lucianna Muscarella, Vito Guarnieri, Leonardo D'Agruma, Alessandro Quattrone, Leopoldo Zelante, Daniel Rabinowitz, Karl Ludvig Reichelt, Patricia M. Rodier, Antonio M. Persico, PASCUCCI, Tiziana, PUGLISI ALLEGRA, Stefano

المساهمون: Monica, Conciatori, Christopher J., Stodgell, Susan L., Hyman, Melanie, O'Bara, Roberto, Militerni, Carmela, Bravaccio, Simona, Trillo, Francesco, Montecchi, Cindy, Schneider, Raun, Melmed, Maurizio, Elia, Lori, Crawford, Sarah J., Spence, Lucianna, Muscarella, Vito, Guarnieri, Leonardo, D'Agruma, Alessandro, Quattrone, Leopoldo, Zelante, Daniel, Rabinowitz, Pascucci, Tiziana, PUGLISI ALLEGRA, Stefano, Karl Ludvig, Reichelt, Patricia M., Rodier, Antonio M., Persico

مصطلحات موضوعية: autistic disorder, cranial circumference, homeobox, macrocephaly, megalencephaly, pervasive developmental disorders

Relation: info:eu-repo/semantics/altIdentifier/pmid/14960295; info:eu-repo/semantics/altIdentifier/wos/WOS:000188964700012; volume:55; issue:4; firstpage:413; lastpage:419; numberofpages:7; journal:BIOLOGICAL PSYCHIATRY; http://hdl.handle.net/11573/235205; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-10744221938; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000188964700012&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a; http://www.sciencedirect.com/science/article/pii/S; http://www.scopus.com/inward/record.url?eid=2-s2.0-10744221938&partnerID=65&md5=1a378235434072d0a65cd0c5c58b4305

الاتاحة: http://hdl.handle.net/11573/235205
https://doi.org/10.1016/j.biopsych.2003.10.005
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000188964700012&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a
http://www.sciencedirect.com/science/article/pii/S
http://www.scopus.com/inward/record.url?eid=2-s2.0-10744221938&partnerID=65&md5=1a378235434072d0a65cd0c5c58b4305

المؤلفون: Raun Melmed

Resource Type: eBook.

الموضوعات: Autism in children--Treatment, Autistic children--Rehabilitation

Categories: FAMILY & RELATIONSHIPS / Children with Special Needs

المؤلفون: Antonio M. Persico, Roberto Militerni, Carmela Bravaccio, Cindy Schneider, Raun Melmed, Simona Trillo, Francesco Montecchi, Mark Palermo, Karl Ludvig Reichelt, Monica Conciatori, Flavio Keller, PASCUCCI, Tiziana, PUGLISI ALLEGRA, Stefano

المساهمون: Antonio M., Persico, Roberto, Militerni, Carmela, Bravaccio, Cindy, Schneider, Raun, Melmed, Simona, Trillo, Francesco, Montecchi, Mark, Palermo, Pascucci, Tiziana, PUGLISI ALLEGRA, Stefano, Karl Ludvig, Reichelt, Monica, Conciatori, Flavio, Keller

مصطلحات موضوعية: autism, macrocephaly, plasminogen, protease, serotonin, serpin family, urokinase

Relation: info:eu-repo/semantics/altIdentifier/pmid/11525425; info:eu-repo/semantics/altIdentifier/wos/WOS:000170303000008; volume:11; issue:2; firstpage:99; lastpage:103; numberofpages:5; journal:PSYCHIATRIC GENETICS; http://hdl.handle.net/11573/255084; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0034942039; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000170303000008&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a; http://journals.lww.com/psychgenetics/pages/articl; http://www.scopus.com/inward/record.url?eid=2-s2.0-0034942039&partnerID=65&md5=538d3e4cf658e63b9b47241c441792c7

الاتاحة: http://hdl.handle.net/11573/255084
https://doi.org/10.1097/00041444-200106000-00008
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000170303000008&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a
http://journals.lww.com/psychgenetics/pages/articl
http://www.scopus.com/inward/record.url?eid=2-s2.0-0034942039&partnerID=65&md5=538d3e4cf658e63b9b47241c441792c7

المؤلفون: Valerio Napolioni, Jason J. Corneveaux, David Craig, Christopher J. Smith, Antonio M. Persico, Matthew J. Huentelman, Janet Kirwan, Raun Melmed, Traci Pawlowski, Benjamin Ober-Reynolds, Szabolcs Szelinger, Sharman Ober-Reynolds

المصدر: Journal of Neuroinflammation

مصطلحات موضوعية: Male, Immunology, Quantitative Trait Loci, behavioral disciplines and activities, Cellular and Molecular Neuroscience, mental disorders, medicine, Humans, Biomarkers, Case-Control Studies, Child, Child Development Disorders, Pervasive, Preschool, Cytokines, Gene Expression Profiling, Siblings, Child Development Disorders, Pervasive, Child, Preschool, Sibling, Genetics, Intelligence quotient, Genetic heterogeneity, General Neuroscience, Research, Regressive autism, medicine.disease, Vineland Adaptive Behavior Scale, Neurology, Autism spectrum disorder, Endophenotype, Autism, Psychology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2931522614600231f1d5e2fe98c34f67
http://hdl.handle.net/11570/3121757

المؤلفون: René Hen, Josh J. Jones, Mark D. Alter, R. Curtis Bay, Keri E. Ramsey, Sharman Ober-Reynolds, J. Blake Turner, Janet Kirwan, Dietrich A. Stephan, David Craig, Raun Melmed, Rutwik Kharkar, Theresa A. Grebe

المصدر: PLoS ONE
PLoS ONE, Vol 6, Iss 2, p e16715 (2011)

مصطلحات موضوعية: Male, Microarray, Microarrays, Molecular biology, lcsh:Medicine, Gene Expression, Validation Studies as Topic, Developmental and Pediatric Neurology, Bioinformatics, Pediatrics, Risk Factors, Gene expression, Molecular Cell Biology, Transcriptional regulation, Heritability of autism, lcsh:Science, Child, Genetics, Regulation of gene expression, Multidisciplinary, Genomics, Middle Aged, Child, Preschool, Medicine, Female, Epigenetics, Algorithms, Research Article, Adult, Biology, Medical sciences, Paternal Age, Molecular Genetics, Young Adult, mental disorders, medicine, Humans, Autistic Disorder, Blood Cells, Genetic regulation, Microarray analysis techniques, Gene Expression Profiling, lcsh:R, Computational Biology, medicine.disease, Microarray Analysis, Gene expression profiling, Gene Expression Regulation, Case-Control Studies, FOS: Biological sciences, Autism--Etiology, Autism, lcsh:Q, Genome Expression Analysis, DNA microarrays--Data processing

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21f785e61459e83874853ac765f59339

المؤلفون: Carmela Bravaccio, Riccardo Alessandrelli, Roberto Sacco, Vito Guarnieri, Barbara Manzi, Cindy Schneider, Leonardo D'Agruma, Monica Saccani, Paolo Curatolo, Antonio M. Persico, Grazia Giana, Roberto Militerni, Raun Melmed, Lucia Anna Muscarella, C. Lenti

المصدر: Molecular Autism, Vol 1, Iss 1, p 9 (2010)
Molecular Autism

مصطلحات موضوعية: Genetics, Candidate gene, education.field_of_study, Research, Population, Single-nucleotide polymorphism, Biology, medicine.disease, Molecular Biology, Developmental Neuroscience, Developmental Biology, Psychiatry and Mental Health, lcsh:RC346-429, Settore MED/39 - Neuropsichiatria Infantile, Denaturing high performance liquid chromatography, Psychiatry and Mental health, Autism spectrum disorder, medicine, Autism, Allele, education, lcsh:Neurology. Diseases of the nervous system, Genetic association

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30e051af23134e8ff4412dfa2f844cb7
http://hdl.handle.net/2108/19072

المؤلفون: Antonio M. Persico, Krassimira A. Garbett, Karoly Mirnics, Raun Melmed, Barbara Manzi, Carmela Bravaccio, Maurizio Elia, Paolo Curatolo, Karl L. Reichelt, Roberto Sacco, Cindy Schneider, Tiziana Pascucci, Roberto Militerni, Stefano Puglisi-Allegra, Carla Lintas

المساهمون: Lintas, C, Sacco, R, Garbett, K, Mirnics, K, Militerni, R, Bravaccio, Carmela, Curatolo, P, Manzi, B, Schneider, C, Melmed, R, Elia, M, Pascucci, T, PUGLISI ALLEGRA, S, Reichelt, Kl, Persico, A. M.

المصدر: Molecular psychiatry. 14(7)

مصطلحات موضوعية: Male, Autism, Gene Expression, Genome-wide association study, Neocortex, tgf-β, Protein kinase C-β, PRKCB1, Gene Frequency, protein kinase c-beta, Gene expression, pervasive developmental disorders, Temporal cortex, TGF-β, Adolescent, Adult, Autistic Disorder, Chi-Square Distribution, Child, Preschool, Family Health, Female, Genome-Wide Association Study, Genotype, Humans, Polymorphism, Single Nucleotide, Protein Kinase C, Protein Kinase C beta, Young Adult, Genetic Predisposition to Disease, Molecular Biology, Psychiatry and Mental Health, Cellular and Molecular Neuroscience, autism, prkcb1, protein kinase c beta, protein kinase c-β, temporal cortex, tgf beta, tgf-beta, Regulation of gene expression, Genetics, Child, Preschool, Gene isoform, Biology, Polymorphism, Single Nucleotide, medicine, Gene, Alternative splicing, medicine.disease, Molecular biology

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::919c97c550dccb1cd0ca405805c9f94c
https://pubmed.ncbi.nlm.nih.gov/18317465

المؤلفون: Maurizio Elia, Roberto Sacco, Monica Saccani, Alessandro Frolli, Antonio M. Persico, Cindy Schneider, Carmela Bravaccio, Karl L. Reichelt, Antonella Gritti, Paolo Curatolo, Roberto Militerni, Tiziana Pascucci, C. Lenti, Stefano Puglisi-Allegra, Raun Melmed, Barbara Manzi, Simona Trillo

المساهمون: Sacco, R, Militerni, R, Frolli, A, Bravaccio, Carmela, Gritti, A, Elia, M, Curatolo, P, Manzi, B, Trillo, S, Lenti, C, Saccani, M, Schneider, C, Melmed, R, Reichelt, Kl, Pascucci, T, PUGLISI ALLEGRA, S, Persico, Am

المصدر: Biological psychiatry. 62(9)

مصطلحات موضوعية: Male, Pediatrics, medicine.medical_specialty, Microcephaly, Serotonin, Adolescent, Cephalometry, Intelligence, macrocephaly, Autism Diagnostic Observation Schedule, Developmental psychology, Craniofacial Abnormalities, Child Development, Reference Values, autistic disorder, cranial circumference, immune system, macrosomy, microcephaly, medicine, Humans, Autistic disorder, Age Factors, Analysis of Variance, Autistic Disorder, Body Weight, Child, Child, Preschool, Female, Head, Physical Examination, Regression Analysis, Biological Psychiatry, Preschool, Intelligence quotient, Macrocephaly, medicine.disease, Circumference, Developmental disorder, Endophenotype, Autism, medicine.symptom, Psychology

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31a592475affff14686112699bc4383c
https://pubmed.ncbi.nlm.nih.gov/17644070

المؤلفون: Raun Melmed, Leonardo D'Agruma, Vito Guarnieri, Lucia Anna Muscarella, Maria Lucia Mascia, Simona Trillo, Roberto Sacco, Maurizio Elia, Emanuela Rucci, Antonio M. Persico, Cindy Schneider, Maria Rosaria Piemontese, Carmela Bravaccio, Roberto Militerni

المساهمون: Muscarella, La, Guarnieri, V, Sacco, R, Militerni, R, Bravaccio, Carmela, Trillo, S, Schneider, C, Melmed, R, Elia, M, Mascia, Ml, Rucci, E, Piemontese, Mr, D'Agruma, L, Persico, Am

المصدر: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (3)

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Adolescent, Autism, Neurological disorder, Biology, Polymorphism, Single Nucleotide, Cellular and Molecular Neuroscience, Child Development, Internal medicine, Fragile-X syndrome, medicine, Homeobox, Macrocephaly, Humans, Megalencephaly, Allele, Polymorphism, Autistic Disorder, Preschool, Child, Genetics (clinical), Homeodomain Proteins, Case-control study, Single Nucleotide, Middle Aged, medicine.disease, Developmental disorder, Fragile X syndrome, Case-Control Studies, Child, Preschool, Female, Fragile X Syndrome, Head, Transcription Factors, Psychiatry and Mental Health, Psychiatry and Mental health, Endocrinology, medicine.symptom

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5e7fb7984f014f57472726021910ae1
https://pubmed.ncbi.nlm.nih.gov/17171652

المؤلفون: James S. Sutcliffe, Pat Levitt, Cindy Schneider, Antonio M. Persico, Carmela Bravaccio, Simona Trillo, Daniel B. Campbell, Roberto Militerni, Maurizio Elia, Philip J. Ebert, Raun Melmed, Roberto Sacco

مصطلحات موضوعية: Male, Candidate gene, Transcription, Genetic, Linkage Disequilibrium, Genotype, Receptors, Association, Autism spectrum disorder, Hepatocyte growth factor, Hepatocyte growth factor receptor, Alleles, Autistic Disorder, Base Sequence, Case-Control Studies, Chromosome Mapping, Chromosomes, Human, Pair 7, DNA, Female, Genetic Predisposition to Disease, Humans, Polymorphism, Single Nucleotide, Promoter Regions, Genetic, Proto-Oncogene Proteins, Proto-Oncogene Proteins c-met, Growth Factor, Transcription Factors, Transcription, Genetic Variation, Multidisciplinary, Heritability of autism, Promoter Regions, Genetic, Genetics, Biological Sciences, Chromosomes, Human, Pair 7, Biology, Polymorphism, Single Nucleotide, Models, Biological, Receptors, Growth Factor, Genetic predisposition, medicine, Allele, Genetic association, medicine.disease, Commentary, Autism, Measles-Mumps-Rubella Vaccine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::811e942b4d746c676b7a931e7484a3e9
http://hdl.handle.net/11570/3121928

المؤلفون: Fabio Macciardi, Roberto Militerni, Carmela Bravaccio, Xudong Liu, Leonardo D'Agruma, Karl L. Reichelt, Roberto Sacco, I. Ricci, Simona Trillo, Cindy Schneider, Jeanette J. A. Holden, Tiziana Pascucci, Maurizio Elia, Raun Melmed, Marcello D'Amelio, Lucia Anna Muscarella, Vito Guarnieri, Antonio M. Persico, Stefano Puglisi-Allegra

المساهمون: D'Amelio, M, Ricci, I, Sacco, R, Liu, X, D'Agruma, L, Muscarella, La, Guarnieri, V, Militerni, R, Bravaccio, C, Elia, M, Schneider, C, Melmed, R, Trillo, S, Pascucci, T, Puglisi-Allegra, S, Reichelt, Kl, Macciardi, F, Holden, Jj, Persico, Am.

المصدر: Molecular psychiatry. 10(11)

مصطلحات موضوعية: Proband, Male, Linkage disequilibrium, Insecticides, APOE, Autistic disorder, Chlorpyrifos, Diazinon, Organophosphates, Reelin, Aryldialkylphosphatase, Autistic Disorder, Base Sequence, Case-Control Studies, Child, DNA, DNA Mutational Analysis, Environment, Female, Genetic Variation, Humans, Italy, Linkage Disequilibrium, Models, Biological, Peptides, Polymorphism, Single Nucleotide, Serotonin, United States, Molecular Biology, Psychiatry and Mental Health, Cellular and Molecular Neuroscience, Models, Biological, Polymorphism, Single Nucleotide, diazinon, chlorpyrifos, Gene–environment interaction, Genetics, biology, autistic disorder, organophosphates, PON1, Psychiatry and Mental health, Single-nucleotide polymorphism, medicine, Paraoxonase, medicine.disease, Developmental disorder, Reelin Protein, biology.protein, Autism

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdc8e4c71817d5ac8361b5f8ca51ff4e
https://pubmed.ncbi.nlm.nih.gov/16027737