0000000000549167

AUTHOR

Miranda A

showing 9 related works from this author

Postfazione al volume Migrazioni Diritto e Società

2018

The post-faction re-consider the chapters of the book in a critical manner, explaining the point of view of the author of the post-faction.

Migrazioni diritti umaniSettore IUS/02 - Diritto Privato Comparato
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Lo “stingimento” delle regole giuridiche tra diritti e limiti nell’era dei flussi migratori e della crisi delle nazioni

2018

Questo articolo, supponendo che i moderni flussi migratori e l'enorme circolazione di persone e regole comportino comunque uno "scolorimento" di principi e pratiche aliene sulla tela dell'ordinamento giuridico ospitante, vuole indagare i "limiti" oltre i quali l'ordinamento (e la sua tradizione socio-culturale, o il suo "spirito nazionale") finisce per rispondere a protezione della sua integrità e all'interno dei quali lo stesso sistema ospitante accolga lo "scolorimento" o la contaminazione. Confronteremo alcuni aspetti di alcuni sistemi per valutarne la risposta allo stingimento di norme "aliene" sul sistema indigeno e per valutarne il grado di coerenza sistematica e di "tenuta" dello ste…

Legal Systems Comparative Law Traditional LawSettore IUS/02 - Diritto Privato ComparatoSettore IUS/21 - Diritto Pubblico Comparato
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The Bleeding of Legal Rules Between Rights and Limits, in the Age of Migration Flows and the Crisis of the Nations

2018

This paper assumes that the modern migratory flows, together with the enormous circulation of people and rules, still involve the ‘bleeding’ of alien principles and practices on the canvas of the host legal system. Accordingly the paper investigates the ‘limits’ beyond which the order ends up responding to the protection of its integrity and within which the same hosting system welcomes and transpires the ‘discoloration’ or contamination, evaluating the responses to the bleeding of ‘alien’ rules and assessing the degree of systematic coherence and ‘holding’. The paper looks at what happens in the legal system of the hosting society, namely to the ‘reaction’ to an ‘imposition’ or to the graf…

RightSocietySettore IUS/02 - Diritto Privato ComparatoComparative Law
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La Tutela del Consumatore. Itinerari Normativi tra Legislazione e Prassi

2004

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Searching for mediation’s common standards at the cross road of different legal cultures

2014

Mediation European Union Law ADRSettore IUS/02 - Diritto Privato Comparato
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La Tutela Privatistica dei Beni Ambientali e Culturali tra Prescrizione e Cooperazione. Modello inglese e prospettive italiane

2004

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Diritto e Tradizione. Circolazione, decodificazione e persistenza delle norme giuridiche

2004

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No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder.

2008

Contains fulltext : 71091.pdf (Publisher’s version ) (Closed access) Several independent studies have reported association between serotonin transporter gene (SLC6A4) polymorphisms and attention deficit hyperactivity disorder (ADHD). Five studies found evidence for association between the long-allele of a 44-bp insertion/deletion polymorphism (5-HTTLPR) and ADHD. Another two studies corroborated this finding while a further six studies did not find such an association. For a second polymorphism within the gene, a variable number tandem repeat (VNTR) within intron 2, one study demonstrated that the 12/12 genotype was significantly less frequent in ADHD cases compared to controls, while a sec…

Genetics and epigenetic pathways of disease [NCMLS 6]MedizinNeuroinformatics [DCN 3]0302 clinical medicinePolymorphism (computer science)GenotypePerception and Action [DCN 1]Childhealth care economics and organizationsSerotonin transporterGenetics (clinical)GeneticsSerotonin Plasma Membrane Transport Proteins0303 health sciencesDepression030305 genetics & heredityTransmission disequilibrium testhumanitiesVariable number tandem repeatPsychiatry and Mental healthChild Preschool/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingFunctional Neurogenomics [DCN 2]medicine.medical_specialtyAdolescenteducationBiologybehavioral disciplines and activitiesMental health [NCEBP 9]Genomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular NeuroscienceSDG 3 - Good Health and Well-beingCognitive neurosciences [UMCN 3.2]Internal medicinemental disordersmedicineAttention deficit hyperactivity disorderHumansGenetic Predisposition to Diseaseddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersAssociation (psychology)Gene030304 developmental biologyFamily HealthPolymorphism Geneticbusiness.industryMood Disordersmedicine.diseaseMoodEndocrinologyMood disordersGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with Hyperactivitybiology.proteinbusiness030217 neurology & neurosurgery
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The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes.

2006

Contains fulltext : 35205.pdf (Publisher’s version ) (Closed access) Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder, starting in early childhood and persisting into adulthood in the majority of cases. Family and twin studies have demonstrated the importance of genetic factors and candidate gene association studies have identified several loci that exert small but significant effects on ADHD. To provide further clarification of reported associations and identify novel associated genes, we examined 1,038 single-nucleotide polymorphisms (SNPs) spanning 51 candidate genes involved in the regulation of neurotransmitter pathways, particularly dopamine, nor…

Candidate geneGenetics and epigenetic pathways of disease [NCMLS 6]MedizinReceptors NicotinicTryptophan HydroxylaseNeuroinformatics [DCN 3]0302 clinical medicinePerception and Action [DCN 1]Determinants in Health and Disease [EBP 1]ChildOncogene ProteinsGenetics0303 health sciencesbiologyDNA POOLING ANALYSISPedigree3. Good healthserotoninPsychiatry and Mental healthConduct disorderChild Preschool/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingMonoamine oxidase AdopaminePsychologyFunctional Neurogenomics [DCN 2]Genetic MarkersAdolescentSynaptosomal-Associated Protein 25Single-nucleotide polymorphismassociation studyPolymorphism Single NucleotideMental health [NCEBP 9]Genetic determinismGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular NeuroscienceMONOAMINE-OXIDASE-ACognitive neurosciences [UMCN 3.2]SDG 3 - Good Health and Well-beingmental disordersmedicineHumansAttention deficit hyperactivity disorderADHDGenetic Predisposition to Disease5-HT1B RECEPTOR GENEddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und JugendaltersMonoamine OxidaseMolecular Biology030304 developmental biologyGenetic associationDopamine Plasma Membrane Transport ProteinsSEROTONIN TRANSPORTER GENEDOPAMINE-BETA-HYDROXYLASESiblingsReceptors Dopamine D4candidate genemedicine.diseaseTwin studyPREFERENTIAL TRANSMISSIONHaplotypesCATECHOL-O-METHYLTRANSFERASEAttention Deficit Disorder with HyperactivityCONDUCT DISORDERbiology.proteinnoradrenalineDEFICIT/HYPERACTIVITY DISORDERNO EVIDENCE030217 neurology & neurosurgerylinkage disequilibriumMolecular Psychiatry
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