Lista de obras - Antonio M Persico - Dominio Público Uruguay

2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

artículo científico publicado en 2011

A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease

artículo científico publicado en 2004

A genetic variant that disrupts MET transcription is associated with autism

artículo científico publicado en 2006

A human dopamine transporter cDNA predicts reduced glycosylation, displays a novel repetitive element and provides racially-dimorphic TaqI RFLPs

artículo científico publicado en 1992

A prospective assessment of opiate addiction treatment protocols for inpatients with HIV-related syndromes

artículo científico publicado en 1991

Activity of L-carnitine and L-acetylcarnitine on cholinoceptive neocortical neurons of the rat in vivo

artículo científico publicado en 1991

Advancing the science of developmental neurotoxicity (DNT): testing for better safety evaluation

artículo científico publicado en 2012

Age- and gender-specific epistasis between ADA and TNF-α influences human life-expectancy.

artículo científico publicado en 2011

Age-dependent decrease and alternative splicing of methionine synthase mRNA in human cerebral cortex and an accelerated decrease in autism

artículo científico publicado en 2013

Alterations of neocortical neuronal responses to acetylcholine and GABA in rats born to alcohol-dependent mothers

artículo científico publicado en 1994

Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.

artículo científico publicado en 2008

Altered neocortical cell density and layer thickness in serotonin transporter knockout mice: a quantitation study.

artículo científico publicado en 2006

Anti-brain antibodies are associated with more severe cognitive and behavioral profiles in Italian children with Autism Spectrum Disorder.

artículo científico publicado en 2014

Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism

artículo científico publicado en 2004

Association of autism with polyomavirus infection in postmortem brains

artículo científico publicado en 2010

Autism genetics.

artículo científico

Autism: where genetics meets the immune system

artículo científico publicado en 2012

Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist

artículo científico publicado en 2009

BDNF and NT-3 applied in the whisker pad reverse cortical changes after peripheral deafferentation in neonatal rats

artículo científico publicado en 1998

Barrel pattern formation requires serotonin uptake by thalamocortical afferents, and not vesicular monoamine release.

artículo científico publicado en 2001

Behavioral assessment of high-dose amphetamine withdrawal: importance of training and testing conditions

artículo científico publicado en 1994

Benzodiazepines consumption and risk of dependence in institutionalized geriatric patients

artículo científico publicado en 1991

Biomarkers in autism spectrum disorder: the old and the new.

artículo científico

Blood serotonin levels in autism spectrum disorder: a systematic review and meta-analysis.

artículo científico

Brain transcription factor expression: effects of acute and chronic amphetamine and injection stress

artículo científico publicado en 1993

Brain transcription factor gene expression, neurotransmitter levels, and novelty response behaviors: alterations during rat amphetamine withdrawal and following chronic injection stress

artículo científico publicado en 1995

Candidate gene study of HOXB1 in autism spectrum disorder

artículo científico publicado el 25 de mayo de 2010

Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1.

artículo científico publicado en 2007

Clinical evidence of decreased olfaction in Bardet-Biedl syndrome caused by a deletion in theBBS4Gene

article

Clinical reports on recent abuse of an antitussive

scientific article published on 01 June 1990

Clinical, morphological, and biochemical correlates of head circumference in autism.

artículo científico publicado en 2007

Cluster analysis of autistic patients based on principal pathogenetic components

artículo científico publicado en 2012

Consensus paper: pathological role of the cerebellum in autism

artículo científico publicado en 2012

Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects.

artículo científico publicado en 2011

Copy number variation in 19 Italian multiplex families with autism spectrum disorder: Importance of synaptic and neurite elongation genes.

artículo científico

Current excitement with D2 dopamine receptor gene alleles in substance abuse

artículo científico publicado en 1992

D2 dopamine receptor gene TaqI A1 and B1 restriction fragment length polymorphisms: enhanced frequencies in psychostimulant-preferring polysubstance abusers

artículo científico publicado en 1996

Deafferentation-induced apoptosis of neurons in thalamic somatosensory nuclei of the newborn rat: critical period and rescue from cell death by peripherally applied neurotrophins

artículo científico publicado en 2000

Decreased serum arylesterase activity in autism spectrum disorders

artículo científico publicado en 2010

Differential regulation of adenosine A1 and A2A receptors in serotonin transporter and monoamine oxidase A-deficient mice

scientific article published on 01 December 2000

Disruption of cerebral cortex MET signaling in autism spectrum disorder.

artículo científico publicado en 2007

Dopamine D2 receptor RFLPs, haplotypes and their association with substance use in black and Caucasian research volunteers

artículo científico publicado en 1993

Dopamine D2 receptor gene Taq I 'A' locus map including 'A4' variant: relevance for alcoholism and drug abuse

artículo científico publicado en 1993

Dopamine D2 receptor gene polymorphisms and vulnerability to substance abuse in African Americans

artículo científico publicado en 1996

Dopamine transporter gene polymorphisms are not associated with polysubstance abuse

artículo científico publicado en 1993

Dopaminergic gene expression during amphetamine withdrawal

artículo científico publicado en 1993

Dual effects of lephetamine on spontaneous and evoked neuronal firing in the somatosensory cortex of the rat.

artículo científico publicado en 1989

Endocannabinoid Signaling in Autism

artículo científico publicado en 2015

Enhanced APOE2 transmission rates in families with autistic probands

artículo científico publicado en 2004

Exclusion of close linkage between the synaptic vesicular monoamine transporter locus and schizophrenia spectrum disorders.

artículo científico publicado en 1995

Exclusion of close linkage of the dopamine transporter gene with schizophrenia spectrum disorders

artículo científico publicado en 1995

FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family

artículo científico publicado en 2020

Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes.

artículo científico publicado en 2010

Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder

artículo científico publicado en 2008

Genetic vulnerability to drug abuse. The D2 dopamine receptor Taq I B1 restriction fragment length polymorphism appears more frequently in polysubstance abusers

artículo científico publicado en 1992

Genome-wide expression studies in autism spectrum disorder, Rett syndrome, and Down syndrome

artículo científico publicado en 2010

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

artículo científico publicado en 2009

Genotypic association between dopamine transporter gene polymorphisms and schizophrenia

artículo científico publicado en 1997

HOXA1 gene variants influence head growth rates in humans

artículo científico publicado en 2007

Headache and comorbidity in children and adolescents

artículo científico publicado en 2013

Huntingtin gene CAG repeat size affects autism risk: Family-based and case-control association study

artículo científico publicado en 2020

Identification and validation of biomarkers for autism spectrum disorders

artículo científico publicado en 2015

Immune transcriptome alterations in the temporal cortex of subjects with autism.

artículo científico publicado en 2008

Implants for sustained drug release over the somatosensory cortex of the newborn rat: a comparison of materials and surgical procedures

artículo científico publicado en 1997

Increased hippocampal DNA oxidation in serotonin transporter deficient mice

artículo científico publicado en 2002

Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression

artículo científico publicado en 2009

Lack of association between dopamine transporter gene polymorphisms and delusional disorder

artículo científico publicado en 1998

Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples

artículo científico publicado en 2000

Lack of infection with XMRV or other MLV-related viruses in blood, post-mortem brains and paternal gametes of autistic individuals

artículo científico publicado en 2011

Medial prefrontal cortical injections of c-fos antisense oligonucleotides transiently lower c-Fos protein and mimic amphetamine withdrawal behaviours

artículo científico publicado en 1998

Methodological factors influencing measurement and processing of plasma reelin in humans

artículo científico publicado en 2003

Migraine genetics: current findings and future lines of research

artículo científico publicado en 2014

Mitochondrial dysfunction in autism spectrum disorders: cause or effect?

scientific article published on 09 May 2010

Multiple receptors mediate the trophic effects of serotonin on ventroposterior thalamic neurons in vitro

artículo científico publicado en 2006

Neocortical RELN promoter methylation increases significantly after puberty

artículo científico publicado en 2010

Neurotransmitter transporter family cDNAs in a rat midbrain library: 'orphan transporters' suggest sizable structural variations

artículo científico publicado el 1 de diciembre de 1992

No association between the 4g/5G polymorphism of the plasminogen activator inhibitor-1 gene promoter and autistic disorder

artículo científico publicado en 2001

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.

artículo científico publicado en 2005

Parkinsonian patients report blunted subjective effects of methylphenidate

artículo científico publicado en 1998

Persistent decrease in heart rate after smoking cessation: a 1-year follow-up study

artículo científico publicado el 1 de enero de 1992

Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review

artículo científico publicado en 2019

Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder ⬇️

artículo científico publicado el 14 de marzo de 2013

Polymorphic GGC repeat differentially regulates human reelin gene expression levels

artículo científico publicado en 2006

Predictors of smoking cessation in a sample of Italian smokers

artículo científico publicado en 1992

Preliminary Transcriptome Analysis in Lymphoblasts from Cluster Headache and Bipolar Disorder Patients Implicates Dysregulation of Circadian and Serotonergic Genes.

artículo científico publicado en 2015

Principal pathogenetic components and biological endophenotypes in autism spectrum disorders

artículo científico publicado en 2010

Pro-opiomelanocortin (POMC) gene excluded as a cause of panic disorder in a large family

artículo científico publicado en 1987

Reduced programmed cell death in brains of serotonin transporter knockout mice

artículo científico publicado en 2003

Serotonergic regulation of somatosensory cortical development: lessons from genetic mouse models.

artículo científico publicado en 2003

Serotonin depletion and barrel cortex development: impact of growth impairment vs. serotonin effects on thalamocortical endings

scientific article published on 01 February 2000

Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children

artículo científico publicado en 2002

Stratified medicine for mental disorders

artículo científico publicado en 2013

Stratifying the autistic phenotype using electrophysiological indices of social perception

artículo científico publicado en 2022

Subjective tinnitus, temporomandibular joint dysfunction, and serotonin modulation of neural plasticity: causal or casual triad?

artículo científico publicado en 2003

The EU-AIMS Longitudinal European Autism Project (LEAP): clinical characterisation

artículo científico publicado en 2017

The EU-AIMS Longitudinal European Autism Project (LEAP): design and methodologies to identify and validate stratification biomarkers for autism spectrum disorders

artículo científico publicado en 2017

The GLO1 C332 (Ala111) allele confers autism vulnerability: family-based genetic association and functional correlates.

artículo científico publicado en 2014

The mitochondrial aspartate/glutamate carrier AGC1 and calcium homeostasis: physiological links and abnormalities in autism

scientific article published on 21 June 2011

The neurobiological context of autism.

artículo científico publicado en 2003

Transcription factors: potential roles in drug-induced neuroplasticity

artículo científico publicado en 1996

Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband

artículo científico publicado en 2007

Unmet needs in paediatric psychopharmacology: Present scenario and future perspectives

artículo científico

Urinary p-cresol in autism spectrum disorder.

artículo científico publicado en 2012

Urinary p-cresol is elevated in small children with severe autism spectrum disorder

artículo científico publicado en 2011

Urinary p-cresol is elevated in young French children with autism spectrum disorder: a replication study

artículo científico publicado en 2014

Using genetic findings in autism for the development of new pharmaceutical compounds.

artículo científico publicado en 2013

Zipeprol is a newly abused antitussive with an opioid spectrum and hallucinogenic effects

artículo científico publicado en 1991

cDNA cloning of an orphan opiate receptor gene family member and its splice variant

artículo científico

Lista de obras de Antonio M Persico

2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease

A genetic variant that disrupts MET transcription is associated with autism

A human dopamine transporter cDNA predicts reduced glycosylation, displays a novel repetitive element and provides racially-dimorphic TaqI RFLPs

A prospective assessment of opiate addiction treatment protocols for inpatients with HIV-related syndromes

Activity of L-carnitine and L-acetylcarnitine on cholinoceptive neocortical neurons of the rat in vivo

Advancing the science of developmental neurotoxicity (DNT): testing for better safety evaluation

Age- and gender-specific epistasis between ADA and TNF-α influences human life-expectancy.

Age-dependent decrease and alternative splicing of methionine synthase mRNA in human cerebral cortex and an accelerated decrease in autism

Alterations of neocortical neuronal responses to acetylcholine and GABA in rats born to alcohol-dependent mothers

Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.

Altered neocortical cell density and layer thickness in serotonin transporter knockout mice: a quantitation study.

Anti-brain antibodies are associated with more severe cognitive and behavioral profiles in Italian children with Autism Spectrum Disorder.

Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism

Association of autism with polyomavirus infection in postmortem brains

Autism genetics.

Autism: where genetics meets the immune system

Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist

BDNF and NT-3 applied in the whisker pad reverse cortical changes after peripheral deafferentation in neonatal rats

Barrel pattern formation requires serotonin uptake by thalamocortical afferents, and not vesicular monoamine release.

Behavioral assessment of high-dose amphetamine withdrawal: importance of training and testing conditions

Benzodiazepines consumption and risk of dependence in institutionalized geriatric patients

Biomarkers in autism spectrum disorder: the old and the new.

Blood serotonin levels in autism spectrum disorder: a systematic review and meta-analysis.

Brain transcription factor expression: effects of acute and chronic amphetamine and injection stress

Brain transcription factor gene expression, neurotransmitter levels, and novelty response behaviors: alterations during rat amphetamine withdrawal and following chronic injection stress

Candidate gene study of HOXB1 in autism spectrum disorder

Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1.

Clinical evidence of decreased olfaction in Bardet-Biedl syndrome caused by a deletion in theBBS4Gene

Clinical reports on recent abuse of an antitussive

Clinical, morphological, and biochemical correlates of head circumference in autism.

Cluster analysis of autistic patients based on principal pathogenetic components

Consensus paper: pathological role of the cerebellum in autism

Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects.

Copy number variation in 19 Italian multiplex families with autism spectrum disorder: Importance of synaptic and neurite elongation genes.

Current excitement with D2 dopamine receptor gene alleles in substance abuse

D2 dopamine receptor gene TaqI A1 and B1 restriction fragment length polymorphisms: enhanced frequencies in psychostimulant-preferring polysubstance abusers

Deafferentation-induced apoptosis of neurons in thalamic somatosensory nuclei of the newborn rat: critical period and rescue from cell death by peripherally applied neurotrophins

Decreased serum arylesterase activity in autism spectrum disorders

Differential regulation of adenosine A1 and A2A receptors in serotonin transporter and monoamine oxidase A-deficient mice

Disruption of cerebral cortex MET signaling in autism spectrum disorder.

Dopamine D2 receptor RFLPs, haplotypes and their association with substance use in black and Caucasian research volunteers

Dopamine D2 receptor gene Taq I 'A' locus map including 'A4' variant: relevance for alcoholism and drug abuse

Dopamine D2 receptor gene polymorphisms and vulnerability to substance abuse in African Americans

Dopamine transporter gene polymorphisms are not associated with polysubstance abuse

Dopaminergic gene expression during amphetamine withdrawal

Dual effects of lephetamine on spontaneous and evoked neuronal firing in the somatosensory cortex of the rat.

Endocannabinoid Signaling in Autism

Enhanced APOE2 transmission rates in families with autistic probands

Exclusion of close linkage between the synaptic vesicular monoamine transporter locus and schizophrenia spectrum disorders.

Exclusion of close linkage of the dopamine transporter gene with schizophrenia spectrum disorders

FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family

Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes.

Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder

Genetic vulnerability to drug abuse. The D2 dopamine receptor Taq I B1 restriction fragment length polymorphism appears more frequently in polysubstance abusers

Genome-wide expression studies in autism spectrum disorder, Rett syndrome, and Down syndrome

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

Genotypic association between dopamine transporter gene polymorphisms and schizophrenia

HOXA1 gene variants influence head growth rates in humans

Headache and comorbidity in children and adolescents

Huntingtin gene CAG repeat size affects autism risk: Family-based and case-control association study

Identification and validation of biomarkers for autism spectrum disorders

Immune transcriptome alterations in the temporal cortex of subjects with autism.

Implants for sustained drug release over the somatosensory cortex of the newborn rat: a comparison of materials and surgical procedures

Increased hippocampal DNA oxidation in serotonin transporter deficient mice

Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression

Lack of association between dopamine transporter gene polymorphisms and delusional disorder

Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples

Lack of infection with XMRV or other MLV-related viruses in blood, post-mortem brains and paternal gametes of autistic individuals

Medial prefrontal cortical injections of c-fos antisense oligonucleotides transiently lower c-Fos protein and mimic amphetamine withdrawal behaviours

Methodological factors influencing measurement and processing of plasma reelin in humans

Migraine genetics: current findings and future lines of research

Mitochondrial dysfunction in autism spectrum disorders: cause or effect?

Multiple receptors mediate the trophic effects of serotonin on ventroposterior thalamic neurons in vitro

Neocortical RELN promoter methylation increases significantly after puberty

Neurotransmitter transporter family cDNAs in a rat midbrain library: 'orphan transporters' suggest sizable structural variations

No association between the 4g/5G polymorphism of the plasminogen activator inhibitor-1 gene promoter and autistic disorder

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.

Parkinsonian patients report blunted subjective effects of methylphenidate