Lista de obras - Filippo Arrigoni - Dominio Público Uruguay

A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype.

artículo científico publicado en 2015

A diffusion tensor magnetic resonance imaging study of paediatric patients with severe non-traumatic brain injury.

artículo científico publicado en 2016

A framework for the automatic detection and characterization of brain malformations: Validation on the corpus callosum.

artículo científico publicado en 2016

A novel mutation in STXBP1 gene in a child with epileptic encephalopathy and an atypical electroclinical pattern

artículo científico publicado en 2013

A robust deconvolution method to disentangle multiple water pools in diffusion MRI

artículo científico publicado en 2018

Aberrant supracallosal longitudinal bundle: MR features, pathogenesis and associated clinical phenotype

artículo científico publicado en 2015

Altered Recruitment of the Attention Network Is Associated with Disability and Cognitive Impairment in Pediatric Patients with Acquired Brain Injury

artículo científico publicado en 2015

Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert Syndrome.

artículo científico publicado en 2017

Automatic localization of cerebral cortical malformations using fractal analysis.

artículo científico publicado en 2016

Bedside assessment of residual functional activation in minimally conscious state using NIRS and general linear models.

artículo científico publicado en 2013

Brain malformations and mutations in α- and β-tubulin genes: a review of the literature and description of two new cases.

artículo científico publicado en 2014

Cerebroretinal microangiopathy with calcifications and cysts associated with CTC1 and NDP mutations.

artículo científico publicado en 2012

Characterizing White Matter Tract Organization in Polymicrogyria and Lissencephaly: A Multifiber Diffusion MRI Modeling and Tractography Study

artículo científico publicado en 2020

Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus Callosum.

artículo científico publicado en 2016

Cognitive rehabilitation in a child with Joubert Syndrome: Developmental trends and adaptive changes in a single case report

artículo científico publicado en 2015

Constructing fMRI connectivity networks: a whole brain functional parcellation method for node definition.

artículo científico publicado en 2014

Cortico-Cerebellar Connectivity in Autism Spectrum Disorder: What Do We Know So Far?

artículo científico publicado en 2016

Coupling of fMRI and NIRS measurements in the study of negative BOLD response to intermittent photic stimulation.

artículo científico publicado en 2013

Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI.

artículo científico publicado en 2012

Detection of corpus callosum malformations in pediatric population using the discriminative direction in multiple kernel learning

artículo científico publicado en 2014

Diffusion tensor imaging of early changes in corpus callosum after acute cerebral hemisphere lesions in newborns.

artículo científico publicado en 2010

Early Formative Stage of Human Focal Cortical Gyration Anomalies: Fetal MRI ⬇️

artículo científico publicado el 1 de febrero de 2012

Early cerebral lesions in cytomegalovirus infection: prenatal MR imaging

artículo científico publicado en 2010

Early prenatal magnetic resonance imaging of glutaric aciduria type 1: case report.

artículo científico publicado en 2010

Erratum to: Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

artículo científico publicado en 2017

Feasibility Randomized Trial for an Intensive Memory-Focused Training Program for School-Aged Children with Acquired Brain Injury

artículo científico publicado en 2020

Fetal MRI features related to the Chiari malformations.

artículo científico publicado en 2011

Greater brain response to emotional expressions of their own children in mothers of preterm infants: an fMRI study

artículo científico publicado en 2017

Investigation of negative BOLD responses in human brain through NIRS technique. A visual stimulation study.

artículo científico publicado en 2015

Investigation of the electrophysiological correlates of negative BOLD response during intermittent photic stimulation: An EEG-fMRI study

artículo científico publicado en 2016

Is fetal magnetic resonance imaging indicated when ultrasound isolated mild ventriculomegaly is present in pregnancies with no risk factors? ⬇️

artículo científico publicado el 14 de mayo de 2012

Learning to live without the cerebellum.

artículo científico publicado en 2015

Multiparametric quantitative MRI assessment of thigh muscles in limb-girdle muscular dystrophy 2A and 2B

artículo científico publicado en 2018

Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis

artículo científico publicado en 2013

Mutations in α- and β-tubulin encoding genes: implications in brain malformations

artículo científico

Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms

artículo científico publicado en 2017

Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agents

artículo científico publicado en 2013

Prenatal MR Imaging Detection of Deep Medullary Vein Involvement in Fetal Brain Damage ⬇️

artículo científico publicado el 14 de octubre de 2010

Sleep/Wake Modulation of Polysomnographic Patterns has Prognostic Value in Pediatric Unresponsive Wakefulness Syndrome.

artículo científico publicado en 2016

The spectrum of brainstem malformations associated to mutations of the tubulin genes family: MRI and DTI analysis

artículo científico publicado en 2018

Tubulin genes and malformations of cortical development

artículo científico publicado en 2018

Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

artículo científico publicado en 2017

When one is Enough: Impaired Multisensory Integration in Cerebellar Agenesis.

artículo científico publicado en 2016

Whole-Brain DTI Assessment of White Matter Damage in Children with Bilateral Cerebral Palsy: Evidence of Involvement beyond the Primary Target of the Anoxic Insult

artículo científico publicado en 2016

Lista de obras de Filippo Arrigoni

A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype.

A diffusion tensor magnetic resonance imaging study of paediatric patients with severe non-traumatic brain injury.

A framework for the automatic detection and characterization of brain malformations: Validation on the corpus callosum.

A novel mutation in STXBP1 gene in a child with epileptic encephalopathy and an atypical electroclinical pattern

A robust deconvolution method to disentangle multiple water pools in diffusion MRI

Aberrant supracallosal longitudinal bundle: MR features, pathogenesis and associated clinical phenotype

Altered Recruitment of the Attention Network Is Associated with Disability and Cognitive Impairment in Pediatric Patients with Acquired Brain Injury

Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert Syndrome.

Automatic localization of cerebral cortical malformations using fractal analysis.

Bedside assessment of residual functional activation in minimally conscious state using NIRS and general linear models.

Brain malformations and mutations in α- and β-tubulin genes: a review of the literature and description of two new cases.

Cerebroretinal microangiopathy with calcifications and cysts associated with CTC1 and NDP mutations.

Characterizing White Matter Tract Organization in Polymicrogyria and Lissencephaly: A Multifiber Diffusion MRI Modeling and Tractography Study

Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus Callosum.

Cognitive rehabilitation in a child with Joubert Syndrome: Developmental trends and adaptive changes in a single case report

Constructing fMRI connectivity networks: a whole brain functional parcellation method for node definition.

Cortico-Cerebellar Connectivity in Autism Spectrum Disorder: What Do We Know So Far?

Coupling of fMRI and NIRS measurements in the study of negative BOLD response to intermittent photic stimulation.

Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI.

Detection of corpus callosum malformations in pediatric population using the discriminative direction in multiple kernel learning

Diffusion tensor imaging of early changes in corpus callosum after acute cerebral hemisphere lesions in newborns.

Early Formative Stage of Human Focal Cortical Gyration Anomalies: Fetal MRI ⬇️

Early cerebral lesions in cytomegalovirus infection: prenatal MR imaging

Early prenatal magnetic resonance imaging of glutaric aciduria type 1: case report.

Erratum to: Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

Feasibility Randomized Trial for an Intensive Memory-Focused Training Program for School-Aged Children with Acquired Brain Injury

Fetal MRI features related to the Chiari malformations.

Greater brain response to emotional expressions of their own children in mothers of preterm infants: an fMRI study

Investigation of negative BOLD responses in human brain through NIRS technique. A visual stimulation study.

Investigation of the electrophysiological correlates of negative BOLD response during intermittent photic stimulation: An EEG-fMRI study

Is fetal magnetic resonance imaging indicated when ultrasound isolated mild ventriculomegaly is present in pregnancies with no risk factors? ⬇️

Learning to live without the cerebellum.

Multiparametric quantitative MRI assessment of thigh muscles in limb-girdle muscular dystrophy 2A and 2B

Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis

Mutations in α- and β-tubulin encoding genes: implications in brain malformations

Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms

Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agents

Prenatal MR Imaging Detection of Deep Medullary Vein Involvement in Fetal Brain Damage ⬇️

Sleep/Wake Modulation of Polysomnographic Patterns has Prognostic Value in Pediatric Unresponsive Wakefulness Syndrome.

The spectrum of brainstem malformations associated to mutations of the tubulin genes family: MRI and DTI analysis

Tubulin genes and malformations of cortical development

Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation

When one is Enough: Impaired Multisensory Integration in Cerebellar Agenesis.

Whole-Brain DTI Assessment of White Matter Damage in Children with Bilateral Cerebral Palsy: Evidence of Involvement beyond the Primary Target of the Anoxic Insult