Filtros de búsqueda

Lista de obras de Thomas Gasser

"Jerky" dystonia in children: spectrum of phenotypes and genetic testing

artículo científico publicado en 2009

A large genome scan for rare CNVs in amyotrophic lateral sclerosis

artículo científico publicado en 2010

A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease

artículo científico publicado en 2009

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

artículo científico publicado en 2012

A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies

artículo científico publicado en 2013

A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder

artículo científico publicado en 2007

A novel mutation in LRSAM1 causes axonal Charcot-Marie-Tooth disease with dominant inheritance

artículo científico publicado en 2014

A novelLRRK2 mutation in an Austrian cohort of patients with Parkinson's disease

scholarly article by Dietrich Haubenberger et al published 2007 in Movement Disorders

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

artículo científico publicado en 2012

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

artículo científico publicado en 2013

A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample

artículo científico publicado en 2005

A single-nucleotide polymorphism of the osteopontin gene may contribute to a susceptibility to Lewy body disease

artículo científico publicado en 2009

A unique case of coincidence of early onset Parkinson's disease and multiple sclerosis

artículo científico publicado en 2007

ATP13A2 variants in early-onset Parkinson's disease patients and controls

artículo científico publicado en 2009

Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation

artículo científico publicado en 2011

Acupuncture-related modulation of pain-associated brain networks during electrical pain stimulation: a functional magnetic resonance imaging study

artículo científico publicado en 2014

Acute parkinsonism with corresponding lesions in the basal ganglia after heroin abuse

artículo científico publicado en 2007

Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance

artículo científico publicado en 2016

Alpha-synuclein gene variants may predict neurostimulation outcome

artículo científico publicado en 2016

Alpha2-macroglobulin, lipoprotein receptor-related protein and lipoprotein receptor-associated protein and the genetic risk for developing Alzheimer's disease

artículo científico publicado en 2006

An interleukin-6 promoter variant is not associated with an increased risk for Alzheimer's disease

artículo científico publicado en 2004

Analysis of Intrathecal Interleukin-6 As a Potential Predictive Factor for Vasospasm in Subarachnoid Hemorrhage

article

Analysis of differential DNA damage in the mitochondrial genome employing a semi-long run real-time PCR approach

artículo científico publicado en 2009

Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk

artículo científico publicado en 2013

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis

artículo científico

Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease

article

Association of clusterin gene polymorphisms with late-onset Alzheimer's disease

artículo científico publicado en 2011

Ataxia with ophthalmoplegia or sensory neuropathy is frequently caused by POLG mutations

artículo científico publicado en 2009

Broad clinical phenotype in Parkinsonism associated with a base pair deletion in RAB39B and additional POLG variant

artículo científico publicado en 2016

CHCHD2 and Parkinson's disease.

artículo científico publicado en 2015

Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia

artículo científico publicado en 2016

Changes in matrix metalloprotease activity and progranulin levels may contribute to the pathophysiological function of mutant leucine-rich repeat kinase 2.

artículo científico publicado en 2014

Characterization of peripheral hematopoietic stem cells and monocytes in Parkinson's disease

artículo científico publicado en 2013

Clinical and brain imaging characteristics in leucine-rich repeat kinase 2-associated PD and asymptomatic mutation carriers

artículo científico publicado en 2011

Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation

artículo científico publicado en 2008

Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia

artículo científico publicado en 2007

Clinical variability in ataxia-telangiectasia

artículo científico publicado en 2015

Clozapine serum concentrations in dopamimetic psychosis in Parkinson's disease and related disorders

artículo científico publicado en 2014

Combined flow cytometric analysis of surface and intracellular antigens reveals surface molecule markers of human neuropoiesis

artículo científico publicado en 2013

Common variants of LRRK2 are not associated with sporadic Parkinson's disease

scholarly article by Saskia Biskup et al published December 2005 in Annals of Neurology

Comparable autoantibody serum levels against amyloid- and inflammation-associated proteins in Parkinson's disease patients and controls

artículo científico publicado en 2014

Complex relationship between Parkin mutations and Parkinson disease

artículo científico publicado en 2002

Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families

article

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

artículo científico publicado en 2006

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

artículo científico publicado en 2012

Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease

artículo científico publicado en 2012

Cortical PIB binding in Lewy body disease is associated with Alzheimer-like characteristics

artículo científico publicado en 2008

Creatine supplementation lowers brain glutamate levels in Huntington's disease

artículo científico publicado en 2005

DJ-1 and prevention of oxidative stress in Parkinson's disease and other age-related disorders

scientific article published on 14 August 2009

Deep-brain-stimulation does not impair deglutition in Parkinson's disease

artículo científico publicado en 2012

Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

artículo científico publicado en 2016

Delta-like 1 participates in the specification of ventral midbrain progenitor derived dopaminergic neurons

artículo científico publicado en 2007

Derivation and expansion using only small molecules of human neural progenitors for neurodegenerative disease modeling

artículo científico publicado en 2013

Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study

artículo científico publicado en 2015

Diagnostic value of proton magnetic resonance spectroscopy in the noninvasive grading of solid gliomas: comparison of maximum and mean choline values

artículo científico publicado en 2009

Diurnal Variation of Hypothalamic Function and Chronic Subthalamic Nucleus Stimulation in Parkinson's Disease ⬇️

artículo científico publicado el 22 de noviembre de 2012

Dual-Task Performance in GBA Parkinson's Disease

artículo científico publicado en 2017

E2F3 amplification and overexpression is associated with invasive tumor growth and rapid tumor cell proliferation in urinary bladder cancer

artículo científico publicado en 2004

EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts

artículo científico publicado en 2014

Enlarged hyperechogenic substantia nigra as a risk marker for Parkinson's disease

artículo científico publicado en 2012

Enlarged hyperechogenic substantia nigra is related to motor performance and olfaction in the elderly

artículo científico publicado en 2010

Enlarged substantia nigra hyperechogenicity and risk for Parkinson disease: a 37-month 3-center study of 1847 older persons

artículo científico publicado en 2011

Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome

artículo científico publicado en 2005

Establishing the role of rare coding variants in known Parkinson's disease risk loci

artículo científico publicado en 2017

Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study

artículo científico publicado en 2016

Excellent response to apomorphine in Parkinsonism with optic atrophy unresponsive to oral antiparkinsonian medication

artículo científico publicado en 2006

Excessive daytime sleepiness in multiple system atrophy (SLEEMSA study).

artículo científico publicado en 2011

Familial carpal tunnel syndrome: further evidence for a genetic contribution

article

Favourable outcome after biopsy and decompression of a holocord intramedullary spinal cord astrocytoma in a newborn.

artículo científico publicado en 2002

Feasibility of Polestar N20, an ultra-low-field intraoperative magnetic resonance imaging system in resection control of pituitary macroadenomas: lessons learned from the first 40 cases

artículo científico publicado en 2008

Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus

artículo científico publicado en 2013

From genome-wide association studies to next-generation sequencing: lessons from the past and planning for the future

artículo científico publicado en 2014

Fruit flies, bile acids, and Parkinson disease: a mitochondrial connection?

artículo científico publicado en 2015

Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias

artículo científico publicado en 2017

Functional magnetic resonance imaging in anesthetized patients: a relevant step toward real-time intraoperative functional neuroimaging

artículo científico publicado en 2005

Fusion of the cerebellar hemispheres ventral to the brainstem: a rare hindbrain-related malformation.

artículo científico publicado en 2004

GBA-associated PD. Neurodegeneration, altered membrane metabolism, and lack of energy failure

artículo científico publicado en 2012

GBA-associated Parkinson's disease: reduced survival and more rapid progression in a prospective longitudinal study

artículo científico publicado en 2014

GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak

artículo científico publicado en 2008

Generation of iPSCs carrying a common LRRK2 risk allele for in vitro modeling of idiopathic Parkinson's disease.

artículo científico publicado en 2018

Generation of induced pluripotent stem cells derived from a 77-year-old healthy woman as control for age related diseases

artículo científico publicado en 2016

Genes associated with Parkinson syndrome

artículo científico publicado en 2008

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

artículo científico publicado el 1 de enero de 2011

Genetic comorbidities in Parkinson's disease

artículo científico publicado en 2013

Genetic correction of a LRRK2 mutation in human iPSCs links parkinsonian neurodegeneration to ERK-dependent changes in gene expression

artículo científico publicado en 2013

Genetic factors influencing age at onset in LRRK2-linked Parkinson disease

artículo científico publicado en 2008

Genetic testing in neurological diseases

artículo científico

Genetic variability in the SNCA gene influences α-synuclein levels in the blood and brain

article

Genome-Scale Networks Link Neurodegenerative Disease Genes to α-Synuclein through Specific Molecular Pathways

artículo científico publicado en 2017

Genome-Wide Association Analysis of the Sense of Smell in U.S. Older Adults: Identification of Novel Risk Loci in African-Americans and European-Americans.

artículo científico publicado en 2016

Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

artículo científico publicado en 2017

Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?

artículo científico publicado en 2013

Genomic and proteomic biomarkers for Parkinson disease

artículo científico publicado en 2009

Genomic deletion size at the epsilon-sarcoglycan locus determines the clinical phenotype

artículo científico publicado en 2007

Genomic investigation of alpha-synuclein multiplication and parkinsonism

artículo científico publicado en 2008

GreenLight laser vs diode laser vaporization of the prostate: 3-year results of a prospective nonrandomized study

artículo científico publicado en 2014

HER-2 and TOP2A coamplification in urinary bladder cancer

artículo científico publicado en 2003

High doses of pergolide improve clinical global impression in advanced Parkinson's disease:- a preliminary open label study

artículo científico publicado en 2005

High-throughput tissue microarray analysis of 11q13 gene amplification (CCND1, FGF3, FGF4, EMS1) in urinary bladder cancer

article

High-throughput tissue microarray analysis ofCMYC amplificationin urinary bladder cancer

article

Higher frequency of regulatory T cells in the elderly and increased suppressive activity in neurodegeneration

artículo científico publicado en 2007

How much phenotypic variation can be attributed to parkin genotype?

artículo científico publicado en 2003

Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis

artículo científico publicado en 2009

Identifying PD-causing genes and genetic susceptibility factors: current approaches and future prospects

artículo científico publicado en 2010

Implementation of the Ultra Low Field Intraoperative MRI PoleStar N20 During Resection Control of Pituitary Adenomas ⬇️

artículo científico publicado el 1 de enero de 2011

Improved detection of microbial ureteral stent colonisation by sonication

artículo científico publicado en 2010

In vivo markers of Parkinson's disease and dementia with Lewy bodies: current value of the 5G4 α-synuclein antibody

artículo científico publicado en 2014

In-vivo evidence that high mobility group box 1 exerts deleterious effects in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model and Parkinson's disease which can be attenuated by glycyrrhizin

artículo científico publicado en 2016

Increase of BDNF serum concentration in lithium treated patients with early Alzheimer's disease

artículo científico publicado en 2009

Increased serum insulin-like growth factor 1 in early idiopathic Parkinson's disease

artículo científico publicado en 2010

Inflammatory profile in LRRK2-associated prodromal and clinical PD

artículo científico publicado en 2016

Influence of iMRI-guidance on the extent of resection and survival of patients with glioblastoma multiforme

artículo científico publicado en 2010

Influence of lithium treatment on GDNF serum and CSF concentrations in patients with early Alzheimer's disease

artículo científico publicado en 2011

Instable cervical spine injury in a toddler: technical note

artículo científico publicado en 2010

Insulin-Like Growth Factor 1 (IGF-1) in Parkinson's Disease: Potential as Trait-, Progression- and Prediction Marker and Confounding Factors

artículo científico publicado en 2016

Integrative pathway-based approach for genome-wide association studies: identification of new pathways for rheumatoid arthritis and type 1 diabetes

artículo científico publicado en 2013

Interrogating Parkinson's disease LRRK2 kinase pathway activity by assessing Rab10 phosphorylation in human neutrophils

artículo científico publicado en 2017

Intrafamilial variability in fragile X-associated tremor/ataxia syndrome

artículo científico publicado en 2006

Intramedullary spinal cord cavernous malformations: clinical features and risk of hemorrhage ⬇️

artículo científico publicado el 1 de abril de 2003

Intraoperative MRI and functional mapping.

artículo científico publicado en 2011

Intraoperative MRI guidance and extent of resection in glioma surgery: a randomised, controlled trial

artículo científico publicado el 23 de agosto de 2011

Intraoperative functional MRI: implementation and preliminary experience

artículo científico publicado en 2005

Intraoperative magnetic resonance imaging in the surgical treatment of cerebral metastases

artículo científico publicado en 2010

Intraoperative microelectrode recording for the delineation of subthalamic nucleus topography in Parkinson's disease

artículo científico publicado en 2011

Intraoperative neurophysiological monitoring in an open low-field magnetic resonance imaging system: clinical experience and technical considerations

artículo científico publicado en 2008

Involuntary eyelid closure after STN-DBS: evidence for different pathophysiological entities

artículo científico publicado en 2010

Is the MC1R variant p.R160W associated with Parkinson's?

artículo científico publicado en 2015

Kick and rush: paradoxical kinesia in Parkinson disease

artículo científico publicado en 2008

Kick and rush: paradoxical kinesia in Parkinson disease

artículo científico publicado en 2009

LINGO1 is not associated with Parkinson's disease in German patients

artículo científico publicado en 2010

LRRK2 (Leucine-Rich Repeat Kinase 2) Gene on PARK8 Locus in Families with Parkinsonism

article

LRRK2 functions as a scaffolding kinase of ASK1-mediated neuronal cell death.

artículo científico publicado en 2017

LRRK2: Understanding the role of common and rare variants in Parkinson's disease

artículo científico publicado en 2012

Large-scale assessment of polyglutamine repeat expansions in Parkinson disease

artículo científico publicado en 2015

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

artículo científico publicado en 2014

Large-scale replication and heterogeneity in Parkinson disease genetic loci

artículo científico publicado en 2012

Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson's disease

artículo científico publicado en 2007

Leucine-rich repeat kinase 2 functionally interacts with microtubules and kinase-dependently modulates cell migration

artículo científico publicado en 2013

Leucine-rich repeat kinase 2 induces alpha-synuclein expression via the extracellular signal-regulated kinase pathway

artículo científico publicado en 2010

Lipid-mediated glial cell line-derived neurotrophic factor gene transfer to cultured porcine ventral mesencephalic tissue

artículo científico publicado en 2002

Lithium trial in Alzheimer's disease: a randomized, single-blind, placebo-controlled, multicenter 10-week study.

artículo científico

Long-term follow-up of subthalamic nucleus stimulation in glucocerebrosidase-associated Parkinson's disease

artículo científico publicado en 2012

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

scientific journal article

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

artículo científico publicado en 2005

Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease

artículo científico publicado en 2015

Low field intraoperative MRI-guided surgery of gliomas: a single center experience

artículo científico publicado en 2009

Mendelian forms of Parkinson's disease

artículo científico publicado en 2009

Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease

artículo científico publicado en 2007

Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson's disease

artículo científico publicado en 2017

Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants

artículo científico publicado en 2014

Microbial colonization and ureteral stent-associated storage lower urinary tract symptoms: the forgotten piece of the puzzle? ⬇️

artículo científico publicado el 4 de marzo de 2012

Milestones in PD genetics

artículo científico publicado en 2011

Molecular pathogenesis of Parkinson disease: insights from genetic studies

artículo científico publicado en 2009

Morphometric characterisation of pterygium associated with corneal stromal scarring using high-resolution anterior segment optical coherence tomography

artículo científico publicado en 2016

Multiple regions of alpha-synuclein are associated with Parkinson's disease

artículo científico publicado en 2005

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

artículo científico publicado en 2004

Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease

artículo científico publicado en 2005

Myoclonus-dystonia due to genomic deletions in the epsilon-sarcoglycan gene

artículo científico publicado en 2005

Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype

artículo científico publicado en 2002

Needs and Requirements of Modern Biobanks on the Example of Dystonia Syndromes

artículo científico publicado en 2017

NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases

artículo científico publicado en 2017

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

artículo científico publicado en 2015

Neurodegenerative CSF markers in genetic and sporadic PD: Classification and prediction in a longitudinal study

artículo científico publicado en 2015

Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria

artículo científico publicado en 2009

New aspects of genetic contributions to Parkinson's disease

artículo científico publicado en 2004

New family with paroxysmal exercise-induced dystonia and epilepsy

artículo científico publicado en 2007

No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease

scientific article published on 06 February 2013

No differences of butyrylcholinesterase protein activity and allele frequency in Lewy body diseases

artículo científico publicado en 2009

No evidence of association of FLJ10986 and ITPR2 with ALS in a large German cohort

artículo científico publicado en 2009

Nutrition and the risk for Parkinson's disease: review of the literature

artículo científico publicado en 2008

Olfactory dysfunction: common in later life and early warning of neurodegenerative disease

artículo científico publicado en 2013

Osteopontin is elevated in Parkinson's disease and its absence leads to reduced neurodegeneration in the MPTP model

artículo científico publicado en 2006

Overview of the genetics of parkinsonism

artículo científico publicado en 2003

PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease

artículo científico publicado en 2009

PARK11 is not linked with Parkinson's disease in European families

article

PARK6-linked parkinsonism occurs in several European families

artículo científico publicado en 2002

PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation

artículo científico publicado en 2005

Pallidal deep brain stimulation relieves camptocormia in primary dystonia ⬇️

artículo científico publicado el 13 de marzo de 2013

Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repair

artículo científico publicado en 2009

Parkinson disease GWAS: the question of lumping or splitting is back again

artículo científico publicado en 2015

Parkinson patient fibroblasts show increased alpha-synuclein expression

artículo científico publicado en 2008

Parkinson's disease in GTP cyclohydrolase 1 mutation carriers

artículo científico publicado en 2014

Parkinson's disease: From human genetics to clinical trials

artículo científico publicado en 2015

Parkinson's disease: is it all in the genes?

artículo científico publicado en 2013

Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson's disease

artículo científico publicado en 2010

Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants

artículo científico publicado en 2015

Plasma ceramide and glucosylceramide metabolism is altered in sporadic Parkinson's disease and associated with cognitive impairment: a pilot study

artículo científico publicado en 2013

Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease

artículo científico publicado en 2003

Polygenic risk of Parkinson disease is correlated with disease age at onset

artículo científico publicado en 2015

Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor

scientific journal article

Predictive value of transcranial sonography in the diagnosis of Parkinson's disease

artículo científico publicado en 2006

Priorities in Parkinson's disease research

artículo científico publicado en 2011

Prognostic relevance of MAGE-A4 tumor antigen expression in transitional cell carcinoma of the urinary bladder: a tissue microarray study

artículo científico publicado en 2002

Proteasomal inhibition reduces parkin mRNA in PC12 and SH-SY5Y cells

artículo científico publicado en 2008

Psychiatric disorders, myoclonus dystonia and SGCE: an international study

artículo científico publicado en 2015

Radicular and nonradicular back pain in Parkinson's disease: a controlled study

artículo científico publicado en 2007

Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort

artículo científico publicado en 2016

Re: Validation of the 2015 Prostate Cancer Grade Groups for Predicting Long-term Oncologic Outcomes in a Shared Equal-access Health System

artículo científico publicado en 2017

Recommendations of the Global Multiple System Atrophy Research Roadmap Meeting.

artículo científico publicado en 2017

Reduction of susceptibility-induced signal losses in multi-gradient-echo images: application to improved visualization of the subthalamic nucleus

artículo científico publicado en 2009

Reply

Rivastigmine for the treatment of dementia in patients with progressive supranuclear palsy: Clinical observations as a basis for power calculations and safety analysis

artículo científico publicado en 2010

Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey

artículo científico publicado en 2017

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

artículo científico publicado en 2011

SNCA: major genetic modifier of age at onset of Parkinson's disease

artículo científico publicado en 2013

SNPs in Aβ clearance proteins: Lower CSF Aβ1-42 levels and earlier onset of dementia in PD.

artículo científico publicado en 2017

Self estimated quality of life in monogenetic Parkinson's disease

artículo científico publicado en 2010

Serum and cerebrospinal fluid levels of transthyretin in Lewy body disorders with and without dementia

artículo científico publicado en 2012

Severe muscular fasciculations as an uncommon side-effect due to microdefect of an extension wire in deep brain stimulation

artículo científico publicado en 2009

Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease gene

artículo científico publicado en 2009

Sonographic abnormalities of brainstem structures in restless legs syndrome

artículo científico publicado en 2007

Spontaneous cerebellar hemorrhage--experience with 57 surgically treated patients and review of the literature

artículo científico publicado en 2010

State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis

artículo científico publicado en 2003

Stereotactic biopsy in gliomas guided by 3-tesla 1H-chemical-shift imaging of choline

artículo científico publicado en 2008

Surgical treatment of cerebral abscess with the use of a mobile ultralow-field MRI.

artículo científico publicado en 2008

The 80-W KTP GreenLight laser vaporization of the prostate versus transurethral resection of the prostate (TURP): adjusted analysis of 5-year results of a prospective non-randomized bi-center study

artículo científico publicado en 2015

The Birth of the Modern Era of Parkinson's Disease Genetics

scientific article published on January 2017

The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort

artículo científico publicado en 2015

The Luxembourg Parkinson's Study: A Comprehensive Approach for Stratification and Early Diagnosis

scholarly article by Geraldine Hipp et al published 2018 in Frontiers in Aging Neuroscience

The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval

artículo científico publicado en 2003

The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism

artículo científico publicado en 2013

The effect of increased maximum power output on perioperative and early postoperative outcome in photoselective vaporization of the prostate ⬇️

artículo científico publicado el 31 de diciembre de 2012

The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted

artículo científico publicado en 2003

The etiopathogenesis of Parkinson disease and suggestions for future research. Part I.

artículo científico publicado en 2007

The etiopathogenesis of Parkinson disease and suggestions for future research. Part II.

artículo científico publicado en 2007

The human sideroflexin 5 (SFXN5) gene: sequence, expression analysis and exclusion as a candidate for PARK3.

artículo científico publicado en 2002

The role of inflammation in sporadic and familial Parkinson's disease

artículo científico publicado en 2013

The specificity and sensitivity of transcranial ultrasound in the differential diagnosis of Parkinson's disease: a prospective blinded study

artículo científico publicado en 2008

The transcription factor PITX3 is associated with sporadic Parkinson's disease

artículo científico publicado en 2009

The variable phenotype of FXTAS: a common cause of "idiopathic" disorders

artículo científico publicado en 2005

Toxic effects of lipid-mediated gene transfer in ventral mesencephalic explant cultures

artículo científico publicado en 2006

Transcranial ultrasound in different monogenetic subtypes of Parkinson's disease

artículo científico publicado en 2007

Transcriptional regulation of the α-synuclein gene in human brain tissue

artículo científico publicado en 2015

Treatment of dementia in parkinsonian syndromes with cholinesterase inhibitors

artículo científico publicado en 2007

Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.

artículo científico publicado en 2005

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.

artículo científico publicado en 2018

UCHL1 is a Parkinson's disease susceptibility gene

artículo científico publicado en 2004

Unmet Needs in Dystonia: Genetics and Molecular Biology-How Many Dystonias?

artículo científico publicado en 2016

Update on the genetics of Parkinson's disease

artículo científico publicado en 2007

Urological Diseases in Men and their Prevention

artículo científico publicado en 2016

Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities

artículo científico publicado en 2012

Usefulness of intraoperative ultra low-field magnetic resonance imaging in glioma surgery

artículo científico publicado en 2008

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

artículo científico publicado en 2012

Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease

artículo científico publicado en 2013

Variation in PARK10 is not associated with risk and age at onset of Parkinson's disease in large clinical cohorts

artículo científico publicado en 2015

Visual evoked potentials for intraoperative neurophysiologic monitoring using total intravenous anesthesia

artículo científico publicado en 2003

[11C]PIB binding in Parkinson's disease dementia

artículo científico publicado en 2007

iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasis

artículo científico publicado en 2014

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda