Lista de obras -

A registration method for improving quantitative assessment in probabilistic diffusion tractography

artículo científico publicado en 2019

Acute Dyskinetic Reaction in a Healthy Toddler Following Methylphenidate Ingestion ⬇️

artículo científico publicado el 16 de mayo de 2013

Association between regulator of G protein signaling 9-2 and body weight

artículo científico publicado en 2011

Autoimmune Movement Disorders in Children

artículo científico publicado en 2017

Benign hereditary chorea related to NKX2-1 with ataxia and dystonia

artículo científico publicado en 2015

Clinical Reasoning: A 16-year-old girl with fixed unilateral grimace

Clinical neurogenetics: dystonia from phenotype to genotype

artículo científico publicado en 2013

De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

artículo científico publicado en 2017

Deep brain stimulation for monogenic dystonia

artículo científico publicado en 2017

Defining Hand Stereotypies in Rett Syndrome: A Movement Disorders Perspective

artículo científico publicado en 2017

Education in medical billing benefits both neurology trainees and academic departments

artículo científico publicado en 2014

Functional neurological symptom disorders in a pediatric emergency room: diagnostic accuracy, features, and outcome

artículo científico publicado en 2014

Increased insula-putamen connectivity in X-linked dystonia-parkinsonism

artículo científico publicado en 2017

Increased pediatric functional neurological symptom disorders after the Boston marathon bombings: a case series

artículo científico publicado en 2014

Inherited and Acquired Choreas

artículo científico publicado en 2018

Juvenile Huntington disease exacerbated by methylphenidate: case report.

artículo científico publicado en 2008

Localization of Basal Ganglia and Thalamic Damage in Dyskinetic Cerebral Palsy

artículo científico publicado en 2015

Management of Infantile Spasms During the COVID-19 Pandemic

artículo científico publicado en 2020

Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

artículo científico publicado en 2020

PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature

artículo científico publicado en 2017

Progressive multifocal leukoencephalopathy in pediatric patients: case report and literature review

artículo científico publicado en 2014

Prolonged direct catheter thrombolysis of cerebral venous sinus thrombosis in children: a case series.

artículo científico publicado en 2011

RGS9-2 negatively modulates L-3,4-dihydroxyphenylalanine-induced dyskinesia in experimental Parkinson's disease.

artículo científico publicado en 2007

Regional, cellular, and subcellular localization of RGS10 in rodent brain

scientific journal article

Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region

artículo científico publicado en 2019

Striatal dysfunction in X-linked dystonia-parkinsonism is associated with disease progression.

artículo científico publicado en 2017

Subtle Imaging Findings Aid the Diagnosis of Adolescent Hereditary Spastic Paraplegia and Ataxia

artículo científico publicado en 2018

Thalamic Volume Is Reduced in Cervical and Laryngeal Dystonias

artículo científico publicado en 2016

Treatment of ADCY5-Associated Dystonia, Chorea, and Hyperkinetic Disorders With Deep Brain Stimulation: A Multicenter Case Series

artículo científico publicado en 2016

Lista de obras de

A registration method for improving quantitative assessment in probabilistic diffusion tractography

Acute Dyskinetic Reaction in a Healthy Toddler Following Methylphenidate Ingestion ⬇️

Association between regulator of G protein signaling 9-2 and body weight

Autoimmune Movement Disorders in Children

Benign hereditary chorea related to NKX2-1 with ataxia and dystonia

Clinical Reasoning: A 16-year-old girl with fixed unilateral grimace

Clinical neurogenetics: dystonia from phenotype to genotype

De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

Deep brain stimulation for monogenic dystonia

Defining Hand Stereotypies in Rett Syndrome: A Movement Disorders Perspective

Education in medical billing benefits both neurology trainees and academic departments

Functional neurological symptom disorders in a pediatric emergency room: diagnostic accuracy, features, and outcome

Increased insula-putamen connectivity in X-linked dystonia-parkinsonism

Increased pediatric functional neurological symptom disorders after the Boston marathon bombings: a case series

Inherited and Acquired Choreas

Juvenile Huntington disease exacerbated by methylphenidate: case report.

Localization of Basal Ganglia and Thalamic Damage in Dyskinetic Cerebral Palsy

Management of Infantile Spasms During the COVID-19 Pandemic

Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature

Progressive multifocal leukoencephalopathy in pediatric patients: case report and literature review

Prolonged direct catheter thrombolysis of cerebral venous sinus thrombosis in children: a case series.

RGS9-2 negatively modulates L-3,4-dihydroxyphenylalanine-induced dyskinesia in experimental Parkinson's disease.

Regional, cellular, and subcellular localization of RGS10 in rodent brain

Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region

Striatal dysfunction in X-linked dystonia-parkinsonism is associated with disease progression.

Subtle Imaging Findings Aid the Diagnosis of Adolescent Hereditary Spastic Paraplegia and Ataxia

Thalamic Volume Is Reduced in Cervical and Laryngeal Dystonias

Treatment of ADCY5-Associated Dystonia, Chorea, and Hyperkinetic Disorders With Deep Brain Stimulation: A Multicenter Case Series