Lista de obras - Thomas Gasser - Dominio Público Uruguay

123I-iodobenzamide-SPECT predicts dopaminergic responsiveness in patients with de novo parkinsonism

artículo científico publicado el 1 de marzo de 1992

123IBZM Binding predicts dopaminergic responsiveness in patients with parkinsonism and previous dopaminomimetic therapy ⬇️

artículo científico publicado el 1 de noviembre de 1997

123I‐IBZM binding compared with long‐term clinical follow up in patients with de novo parkinsonism ⬇️

artículo científico publicado el 1 de enero de 1998

A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

article by Sven J. van der Lee et al published 27 May 2019 in Acta Neuropathologica

A patient-based model of RNA mis-splicing uncovers treatment targets in Parkinson's disease

scientific article published on 01 September 2020

A susceptibility locus for Parkinson's disease maps to chromosome 2p13 ⬇️

artículo científico publicado el 1 de marzo de 1998

Abolishing the 1-year rule: How much evidence will be enough?

artículo científico publicado en 2016

Advances in the genetics of movement disorders: implications for molecular diagnosis ⬇️

artículo científico publicado el 1 de junio de 1997

Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients

scholarly article by Daniela Berg et al published 2005 in Movement Disorders

Association of Body Mass Index and Parkinson Disease

artículo científico publicado en 2024

Autosomal-dominant Parkinson's disease linked to 2p13 is not caused by mutations in transforming growth factor alpha (TGF alpha) ⬇️

artículo científico publicado el 1 de enero de 2001

Botulinum toxin A in orthopaedic surgery ⬇️

artículo científico publicado el 21 de septiembre de 1991

CADASIL: clinical aspects and diagnosis ⬇️

artículo científico publicado el 14 de agosto de 1998

CADASIL: skin biopsy allows diagnosis in early stages ⬇️

artículo científico publicado el 1 de junio de 1997

Candidate gene studies in focal dystonia ⬇️

artículo científico publicado el 28 de octubre de 2003

Changing the research criteria for the diagnosis of Parkinson's disease: obstacles and opportunities

artículo científico publicado en 2013

Cholinergic Pathway SNPs and Postural Control in 477 Older Adults

Cognitive impairment in Glucocerebrosidase (GBA)-associated PD: Not primarily associated with cerebrospinal fluid Abeta and Tau profiles

artículo científico publicado en 2017

Data protection in biomaterial banks for Parkinson's disease research: the model of GEPARD (Gene Bank Parkinson's Disease Germany).

artículo científico publicado en 2007

Folinic acid therapy fails to improve early Parkinson's disease: a two week placebo controlled clinical trial

artículo científico publicado el 1 de enero de 1992

Genetic basis of Parkinson's disease: inheritance, penetrance, and expression ⬇️

artículo científico publicado el 1 de enero de 2011

Genetic complexity and Parkinson's disease ⬇️

artículo científico publicado el 18 de julio de 1997

Genetics of Parkinson's disease

artículo científico publicado en 2005

Genetics of parkinson's disease ⬇️

artículo científico publicado el 1 de septiembre de 1998

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

artículo científico publicado en 2021

Idiopathic, myoclonic and Dopa-responsive dystonia ⬇️

artículo científico publicado el 1 de agosto de 1997

Inherited myoclonus-dystonia syndrome

artículo científico publicado el 1 de enero de 1998

Lack of association between the interleukin-1 alpha (-889) polymorphism and early-onset Parkinson's disease

artículo científico publicado en 2004

Lack of association of interleukin-10 promoter region polymorphisms with Alzheimer's disease ⬇️

artículo científico publicado el 15 de mayo de 2003

Linking the phenotype of SNCA Triplication with PET-MRI imaging pattern and alpha-synuclein CSF seeding

artículo científico publicado en 2022

MDS clinical diagnostic criteria for Parkinson's disease

artículo científico publicado en 2015

MDS research criteria for prodromal Parkinson's disease

artículo científico publicado en 2015

Minocycline 1-year therapy in multiple-system-atrophy: effect on clinical symptoms and [(11)C] (R)-PK11195 PET (MEMSA-trial).

artículo científico publicado en 2010

Movement disorder society criteria for clinically established early Parkinson's disease

scholarly article by Daniela Berg et al published 25 August 2018 in Movement Disorders

NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL ⬇️

artículo científico publicado el 13 de noviembre de 2001

Paroxysmal choreoathetosis - a disorder related to Huntington's disease? ⬇️

artículo científico publicado el 1 de junio de 1997

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

artículo científico publicado en 2008

Phenotypic expression of the DYT1 mutation: A family with writer's cramp of juvenile onset ⬇️

artículo científico publicado el 1 de julio de 1998

Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registry

artículo científico publicado en 2010

Prevention of interferon-stimulated gene expression using microRNA-designed hairpins

artículo científico publicado en 2008

Rapid emergence of temporal and pulvinar lesions in MELAS mimicking Creutzfeldt-Jakob disease ⬇️

artículo científico publicado el 30 de agosto de 2011

Red flags for multiple system atrophy

artículo científico publicado en 2008

SNCA variants are associated with increased risk for multiple system atrophy

artículo científico publicado en 2009

Serum Inflammatory Profile for the Discrimination of Clinical Subtypes in Parkinson's Disease

scholarly article by Rezzak Yilmaz et al published 2018 in Frontiers in Neurology

The D2 receptor Nco I allele: Absence of allelic association with migraine with aura ⬇️

artículo científico publicado el 1 de septiembre de 1998

The autosomal dominant dystonias

artículo científico publicado el 1 de octubre de 1992

The natural history of multiple system atrophy: a prospective European cohort study

artículo científico publicado en 2013

The new definition and diagnostic criteria of Parkinson's disease

artículo científico publicado en 2016

The ubiquitin pathway in Parkinson's disease ⬇️

artículo científico publicado el 1 de octubre de 1998

UCHL-1 gene in multiple system atrophy: a haplotype tagging approach

artículo científico publicado en 2005

Lista de obras de Thomas Gasser

123I-iodobenzamide-SPECT predicts dopaminergic responsiveness in patients with de novo parkinsonism

123IBZM Binding predicts dopaminergic responsiveness in patients with parkinsonism and previous dopaminomimetic therapy ⬇️

123I‐IBZM binding compared with long‐term clinical follow up in patients with de novo parkinsonism ⬇️

A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

A patient-based model of RNA mis-splicing uncovers treatment targets in Parkinson's disease

A susceptibility locus for Parkinson's disease maps to chromosome 2p13 ⬇️

Abolishing the 1-year rule: How much evidence will be enough?

Advances in the genetics of movement disorders: implications for molecular diagnosis ⬇️

Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients

Association of Body Mass Index and Parkinson Disease

Autosomal-dominant Parkinson's disease linked to 2p13 is not caused by mutations in transforming growth factor alpha (TGF alpha) ⬇️

Botulinum toxin A in orthopaedic surgery ⬇️

CADASIL: clinical aspects and diagnosis ⬇️

CADASIL: skin biopsy allows diagnosis in early stages ⬇️

Candidate gene studies in focal dystonia ⬇️

Changing the research criteria for the diagnosis of Parkinson's disease: obstacles and opportunities

Cholinergic Pathway SNPs and Postural Control in 477 Older Adults

Cognitive impairment in Glucocerebrosidase (GBA)-associated PD: Not primarily associated with cerebrospinal fluid Abeta and Tau profiles

Data protection in biomaterial banks for Parkinson's disease research: the model of GEPARD (Gene Bank Parkinson's Disease Germany).

Folinic acid therapy fails to improve early Parkinson's disease: a two week placebo controlled clinical trial

Genetic basis of Parkinson's disease: inheritance, penetrance, and expression ⬇️

Genetic complexity and Parkinson's disease ⬇️

Genetics of Parkinson's disease

Genetics of parkinson's disease ⬇️

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

Idiopathic, myoclonic and Dopa-responsive dystonia ⬇️

Inherited myoclonus-dystonia syndrome

Lack of association between the interleukin-1 alpha (-889) polymorphism and early-onset Parkinson's disease

Lack of association of interleukin-10 promoter region polymorphisms with Alzheimer's disease ⬇️

Linking the phenotype of SNCA Triplication with PET-MRI imaging pattern and alpha-synuclein CSF seeding

MDS clinical diagnostic criteria for Parkinson's disease

MDS research criteria for prodromal Parkinson's disease

Minocycline 1-year therapy in multiple-system-atrophy: effect on clinical symptoms and [(11)C] (R)-PK11195 PET (MEMSA-trial).

Movement disorder society criteria for clinically established early Parkinson's disease

NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL ⬇️

Paroxysmal choreoathetosis - a disorder related to Huntington's disease? ⬇️

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

Phenotypic expression of the DYT1 mutation: A family with writer's cramp of juvenile onset ⬇️

Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registry

Prevention of interferon-stimulated gene expression using microRNA-designed hairpins

Rapid emergence of temporal and pulvinar lesions in MELAS mimicking Creutzfeldt-Jakob disease ⬇️

Red flags for multiple system atrophy

SNCA variants are associated with increased risk for multiple system atrophy

Serum Inflammatory Profile for the Discrimination of Clinical Subtypes in Parkinson's Disease

The D2 receptor Nco I allele: Absence of allelic association with migraine with aura ⬇️

The autosomal dominant dystonias

The natural history of multiple system atrophy: a prospective European cohort study

The new definition and diagnostic criteria of Parkinson's disease

The ubiquitin pathway in Parkinson's disease ⬇️

UCHL-1 gene in multiple system atrophy: a haplotype tagging approach