Lista de obras -

A Practical Primer on Prion Pathology

artículo científico publicado en 2018

A Review: Treatment of Alzheimer’s Disease Discovered in Repurposed Agents ⬇️

artículo científico publicado el 9 de enero de 2013

A case report of genetic prion disease with two different PRNP variants

artículo científico publicado en 2020

A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease

scientific article published on 19 June 2020

A young-onset frontal dementia with dramatic calcifications due to a novel CSF1R mutation

artículo científico publicado en 2016

Aerophagia as the initial presenting symptom of a depressed patient

artículo científico publicado en 2006

Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint

scientific article published on 01 January 2020

Autoimmune-mediated cognitive impairment: a case report

artículo científico publicado en 2014

Caregiver burden in atypical dementias: comparing frontotemporal dementia, Creutzfeldt-Jakob disease, and Alzheimer's disease.

artículo científico publicado en 2015

Characteristics of established and proposed sporadic Creutzfeldt-Jakob disease variants

artículo científico publicado en 2009

Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species

artículo científico publicado en 2019

Clinical Laboratory Tests Used To Aid in Diagnosis of Human Prion Disease

scientific article published on 24 September 2019

Clinical Use of Improved Diagnostic Testing for Detection of Prion Disease

artículo científico publicado en 2021

Clinical and imaging characteristics of late onset mitochondrial membrane protein-associated neurodegeneration (MPAN)

artículo científico publicado en 2016

Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration

artículo científico publicado en 2020

Clozapine for treatment-resistant agitation in dementia

artículo científico publicado en 2007

Co-occurrence of chronic traumatic encephalopathy and prion disease

Comprehensive and Methodical: Diagnostic and Management Approaches to Rapidly Progressive Dementia

artículo científico publicado en 2017

Correction to: In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP Mutation

artículo científico publicado en 2019

D178N, 129Val and N171S, 129Val Genotype in a Family with Creutzfeldt-Jakob Disease ⬇️

artículo científico publicado el 12 de noviembre de 2010

Diagnosis of Prion Diseases by RT-QuIC Results in Improved Surveillance

artículo científico publicado en 2020

Diagnostic and prognostic value of human prion detection in cerebrospinal fluid

artículo científico publicado en 2017

Discovering new treatments for Alzheimer's disease by repurposing approved medications

artículo científico publicado en 2013

Distinct prion-like strains of amyloid beta implicated in phenotypic diversity of Alzheimer's disease

artículo científico publicado en 2016

Does the presentation of Creutzfeldt-Jakob disease vary by age or presumed etiology? A meta-analysis of the past 10 years

scientific article published on January 2007

Early detection of periodic sharp wave complexes on EEG by independent component analysis in patients with Creutzfeldt-Jakob disease

artículo científico publicado en 2008

Early preclinical detection of prions in the skin of prion-infected animals

artículo científico publicado en 2019

Estimating severity of illness and disability in Frontotemporal Dementia: Preliminary analysis of the Dementia Disability Rating (DDR).

artículo científico publicado en 2011

Evaluation of a New Criterion for Detecting Prion Disease With Diffusion Magnetic Resonance Imaging

artículo científico publicado en 2020

Fatal familial insomnia and sporadic fatal insomnia

artículo científico publicado en 2018

Feasibility of Remote Assessment of Human Prion Diseases for Research and Surveillance

artículo científico publicado en 2019

Fluorodeoxyglucose Positron Emission Tomography (FDG-PET) Correlation of Histopathology and MRI in Prion Disease

artículo científico publicado en 2017

From Neurodegeneration to Brain Health: An Integrated Approach.

artículo científico

Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases

artículo científico publicado en 2020

Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases

artículo científico publicado en 2016

Human Prion Disease Surveillance in Washington State, 2006-2017

artículo científico publicado en 2020

Human prion diseases

scientific article published on 01 June 2019

Iatrogenic Creutzfeldt-Jakob disease from commercial cadaveric human growth hormone.

artículo científico publicado en 2013

Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study

artículo científico publicado en 2018

Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study

scientific article published on 16 September 2020

Impaired transmissibility of atypical prions from genetic CJD

In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP Mutation

scientific article published on 05 January 2019

Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration

artículo científico publicado en 2020

Initial diagnoses of patients ultimately diagnosed with prion disease

artículo científico publicado en 2014

Mania as a possible prodrome to dementia

artículo científico publicado en 2007

Many challenges of conducting clinical trials in CJD.

artículo científico publicado en 2016

Neuropsychiatric symptoms in MCI subtypes: the importance of executive dysfunction.

artículo científico publicado en 2010

Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type

artículo científico publicado en 2017

PMCA-replicated PrPD in urine of vCJD patients maintains infectivity and strain characteristics of brain PrPD: Transmission study

article

Patient With voltage-gated potassium-channel (VGKC) limbic encephalitis found to have Creutzfeldt-Jakob disease (CJD) at autopsy

artículo científico publicado en 2013

Predictors of depression and anxiety in patients with intracranial neoplasms

scientific article published on January 2008

Prion disease incidence in the United States: 2003-2015

scientific article published on 22 November 2019

Prion diseases: targets and treatments of symptoms and disease progression. Editorial

artículo científico publicado en 2009

Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt-Jakob disease

artículo científico publicado en 2020

Prion seeding activity and infectivity in skin samples from patients with sporadic Creutzfeldt-Jakob disease.

artículo científico publicado en 2017

Psychiatric and neuropsychiatric adverse events associated with deep brain stimulation: A meta-analysis of ten years' experience.

artículo científico publicado en 2007

Psychotropic medications and the treatment of human prion diseases

artículo científico publicado en 2009

Publisher Correction: Early preclinical detection of prions in the skin of prion-infected animals

artículo científico publicado en 2019

Racial and Ethnic Differences in Individuals with Sporadic Creutzfeldt-Jakob Disease in the United States of America ⬇️

artículo científico publicado el 18 de junio de 2012

Rapidly Progressive Alzheimer's Disease in Two Distinct Autopsy Cohorts.

artículo científico publicado en 2018

Rapidly progressive Alzheimer's disease features distinct structures of amyloid-β.

artículo científico publicado en 2015

Rapidly progressive dementias and the treatment of human prion diseases ⬇️

artículo científico publicado el 23 de noviembre de 2010

Rapidly progressive young-onset dementias: neuropsychiatric aspects

artículo científico

Scientific and ethical issues related to deep brain stimulation for disorders of mood, behavior, and thought

artículo científico publicado en 2009

Severe hyponatremia and seizures secondary to psychogenic polydipsia in a case of frontotemporal dementia

artículo científico publicado en 2014

Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions

scientific article published on 31 October 2019

Should we be teaching philosophy to psychiatrists-in-training?

scientific article published on 01 May 2007

Sporadic Creutzfeldt-Jakob disease: changes not only in the brain?

artículo científico publicado en 2012

Streamlined alpha-synuclein RT-QuIC assay for various biospecimens in Parkinson's disease and dementia with Lewy bodies

artículo científico publicado en 2021

Subclavian steal syndrome presenting as a reversible dementia

artículo científico publicado en 2015

Subtype diagnosis of sporadic Creutzfeldt-Jakob disease with diffusion MRI

scientific article published on 03 December 2020

Symptomatic treatment, care, and support of CJD patients

artículo científico publicado en 2018

The Complexity of Deep Brain Stimulation and Suicidality in Patients with Treatment Resistant Depression

The association of neuropsychiatric symptoms in MCI with incident dementia and Alzheimer disease.

artículo científico publicado en 2013

Therapeutic strategies for prion disease: a practical perspective

scientific article published on 30 November 2018

Trace and transference: therapy in a post-structuralist era.

artículo científico publicado en 2008

Unusual Case of Sporadic Creutzfeldt-Jakob Disease Subtype VV1.

artículo científico publicado en 2015

Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium

scientific article published on 01 January 2020

Variably protease-sensitive prionopathy

artículo científico publicado en 2018

Visual art therapy in sporadic Creutzfeldt-Jakob disease: a case study

artículo científico publicado en 2016

Lista de obras de

A Practical Primer on Prion Pathology

A Review: Treatment of Alzheimer’s Disease Discovered in Repurposed Agents ⬇️

A case report of genetic prion disease with two different PRNP variants

A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease

A young-onset frontal dementia with dramatic calcifications due to a novel CSF1R mutation

Aerophagia as the initial presenting symptom of a depressed patient

Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint

Autoimmune-mediated cognitive impairment: a case report

Caregiver burden in atypical dementias: comparing frontotemporal dementia, Creutzfeldt-Jakob disease, and Alzheimer's disease.

Characteristics of established and proposed sporadic Creutzfeldt-Jakob disease variants

Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species

Clinical Laboratory Tests Used To Aid in Diagnosis of Human Prion Disease

Clinical Use of Improved Diagnostic Testing for Detection of Prion Disease

Clinical and imaging characteristics of late onset mitochondrial membrane protein-associated neurodegeneration (MPAN)

Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration

Clozapine for treatment-resistant agitation in dementia

Co-occurrence of chronic traumatic encephalopathy and prion disease

Comprehensive and Methodical: Diagnostic and Management Approaches to Rapidly Progressive Dementia

Correction to: In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP Mutation

D178N, 129Val and N171S, 129Val Genotype in a Family with Creutzfeldt-Jakob Disease ⬇️

Diagnosis of Prion Diseases by RT-QuIC Results in Improved Surveillance

Diagnostic and prognostic value of human prion detection in cerebrospinal fluid

Discovering new treatments for Alzheimer's disease by repurposing approved medications

Distinct prion-like strains of amyloid beta implicated in phenotypic diversity of Alzheimer's disease

Does the presentation of Creutzfeldt-Jakob disease vary by age or presumed etiology? A meta-analysis of the past 10 years

Early detection of periodic sharp wave complexes on EEG by independent component analysis in patients with Creutzfeldt-Jakob disease

Early preclinical detection of prions in the skin of prion-infected animals

Estimating severity of illness and disability in Frontotemporal Dementia: Preliminary analysis of the Dementia Disability Rating (DDR).

Evaluation of a New Criterion for Detecting Prion Disease With Diffusion Magnetic Resonance Imaging

Fatal familial insomnia and sporadic fatal insomnia

Feasibility of Remote Assessment of Human Prion Diseases for Research and Surveillance

Fluorodeoxyglucose Positron Emission Tomography (FDG-PET) Correlation of Histopathology and MRI in Prion Disease

From Neurodegeneration to Brain Health: An Integrated Approach.

Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases

Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases

Human Prion Disease Surveillance in Washington State, 2006-2017

Human prion diseases

Iatrogenic Creutzfeldt-Jakob disease from commercial cadaveric human growth hormone.

Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study

Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study

Impaired transmissibility of atypical prions from genetic CJD

In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP Mutation

Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration

Initial diagnoses of patients ultimately diagnosed with prion disease

Mania as a possible prodrome to dementia

Many challenges of conducting clinical trials in CJD.

Neuropsychiatric symptoms in MCI subtypes: the importance of executive dysfunction.

Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type

PMCA-replicated PrPD in urine of vCJD patients maintains infectivity and strain characteristics of brain PrPD: Transmission study

Patient With voltage-gated potassium-channel (VGKC) limbic encephalitis found to have Creutzfeldt-Jakob disease (CJD) at autopsy

Predictors of depression and anxiety in patients with intracranial neoplasms

Prion disease incidence in the United States: 2003-2015

Prion diseases: targets and treatments of symptoms and disease progression. Editorial

Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt-Jakob disease

Prion seeding activity and infectivity in skin samples from patients with sporadic Creutzfeldt-Jakob disease.

Psychiatric and neuropsychiatric adverse events associated with deep brain stimulation: A meta-analysis of ten years' experience.

Psychotropic medications and the treatment of human prion diseases

Publisher Correction: Early preclinical detection of prions in the skin of prion-infected animals

Racial and Ethnic Differences in Individuals with Sporadic Creutzfeldt-Jakob Disease in the United States of America ⬇️

Rapidly Progressive Alzheimer's Disease in Two Distinct Autopsy Cohorts.

Rapidly progressive Alzheimer's disease features distinct structures of amyloid-β.

Rapidly progressive dementias and the treatment of human prion diseases ⬇️

Rapidly progressive young-onset dementias: neuropsychiatric aspects

Scientific and ethical issues related to deep brain stimulation for disorders of mood, behavior, and thought

Severe hyponatremia and seizures secondary to psychogenic polydipsia in a case of frontotemporal dementia

Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions

Should we be teaching philosophy to psychiatrists-in-training?

Sporadic Creutzfeldt-Jakob disease: changes not only in the brain?

Streamlined alpha-synuclein RT-QuIC assay for various biospecimens in Parkinson's disease and dementia with Lewy bodies

Subclavian steal syndrome presenting as a reversible dementia

Subtype diagnosis of sporadic Creutzfeldt-Jakob disease with diffusion MRI

Symptomatic treatment, care, and support of CJD patients

The Complexity of Deep Brain Stimulation and Suicidality in Patients with Treatment Resistant Depression

The association of neuropsychiatric symptoms in MCI with incident dementia and Alzheimer disease.

Therapeutic strategies for prion disease: a practical perspective

Trace and transference: therapy in a post-structuralist era.

Unusual Case of Sporadic Creutzfeldt-Jakob Disease Subtype VV1.

Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium

Variably protease-sensitive prionopathy