Early-onset Parkinson's disease in a Chinese population: 99mTc-TRODAT-1 SPECT, Parkin gene analysis and clinical study.

No abstract is available for this paper.

• Publication year

  2005

• Venue

  Parkinsonism & Related Disorders

• Publication date

  2005-05-01

• Fields of study

  Medicine, Psychology

• Identifiers
  DOI 10.1016/J.PARKRELDIS.2004.12.004PMID 15823482
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early‐onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients

  2004cited by this paper
• PINK1 (PARK6) associated Parkinson disease in Ireland

  2004cited by this paper
• The role of pathogenic DJ‐1 mutations in Parkinson's disease

  2003cited by this paper
• Long-term follow up of bilateral deep brain stimulation of the subthalamic nucleus in patients with advanced Parkinson disease.

  2003cited by this paper
• A linkage study of candidate loci in familial Parkinson's Disease

  2003cited by this paper
• Evaluation of 50 probands with early-onset Parkinson’s disease for Parkin mutations

  2002cited by this paper
• Evaluation of early-stage Parkinson's disease with 99mTc-TRODAT-1 imaging.

  2001cited by this paper
• The optimal imaging time for [99Tcm]TRODAT-1/SPET in normal subjects and patients with Parkinson's disease

  2001cited by this paper
• An apparently sporadic case with parkin gene mutation in a Korean woman.

  2001cited by this paper
• Prevalence of homozygous deletions of the parkin gene in a cohort of patients with sporadic and familial Parkinson's disease

  2001cited by this paper
• MinireviewParkin and the Molecular Pathways of Parkinson ’ s Disease led to phenomenal progression in the characterization of Lewy pathology

  2001cited by this paper
• Differential diagnosis of Parkinson's disease and vascular parkinsonism by (99m)Tc-TRODAT-1.

  2001cited by this paper
• [123I] beta-CIT binding and SPET compared with clinical diagnosis in parkinsonism.

  2000cited by this paper
• Parkin Suppresses Unfolded Protein Stress-induced Cell Death through Its E3 Ubiquitin-protein Ligase Activity*

  2000cited by this paper
• Polymorphisms of the Parkin Gene in Sporadic Parkinson’s Disease among Chinese in Taiwan

  2000cited by this paper
• Binding of [99mTc]TRODAT-1 to dopamine transporters in patients with Parkinson's disease and in healthy volunteers.

  2000cited by this paper
• Association between early-onset Parkinson's disease and mutations in the parkin gene.

  2000cited by this paper
• A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.

  1999cited by this paper
• Polymorphism in the parkin gene in sporadic Parkinson's disease

  1999cited by this paper
• Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin gene.

  1999cited by this paper
• The ubiquitin pathway in Parkinson's disease

  1998cited by this paper
• Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

  1998cited by this paper
• Tau is a candidate gene for chromosome 17 frontotemporal dementia

  1998cited by this paper
• Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the Parkin gene in affected individuals

  1998influential reference
• Young‐onset Parkinson's disease revisited—clinical features, natural history, and mortality

  1998cited by this paper
• Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease.

  1998cited by this paper
• Mutation in the tau gene in familial multiple system tauopathy with presenile dementia.

  1998cited by this paper
• Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease.

  1998cited by this paper
• Early onset parkinsonism with diurnal fluctuation maps to a locus for juvenile parkinsonism

  1998cited by this paper
• AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease

  1998cited by this paper
• Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.

  1997cited by this paper
• Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease

  1997cited by this paper
• Pharmacological effects of dopaminergic drugs on in vivo binding of [99mTc]TRODAT-1 to the central dopamine transporters in rats

  1997cited by this paper
• Relationship between clinical features of Parkinson's disease and presynaptic dopamine transporter binding assessed with [123I]IPT and single-photon emission tomography

  1997cited by this paper
• [123I] beta-CIT/SPECT imaging demonstrates bilateral loss of dopamine transporters in hemi-Parkinson's disease.

  1996cited by this paper
• [sup 123 I] beta-CIT/SPECT imaging demonstrates bilateral loss of dopamine transporters in hemi-Parkinson's disease

  1996cited by this paper
• Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism

  1996cited by this paper
• Positron emission tomographic imaging of the dopamine transporter with 11C‐WIN 35,428 reveals marked declines in mild Parkinson's disease

  1993cited by this paper
• Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases.

  1992cited by this paper
• What features improve the accuracy of clinical diagnosis in Parkinson's disease

  1992cited by this paper
• A post-mortem study on striatal dopamine receptors in Parkinson's disease.

  1991cited by this paper

• PRKN-Gene-Related Parkinsonism: An Experience from a Tertiary Centre and Literature Review of Asian Cohort

  2025cites this paper
• Enhanced IRE1α Phosphorylation/Oligomerization-Triggered XBP1 Splicing Contributes to Parkin-Mediated Prevention of SH-SY5Y Cell Death under Nitrosative Stress

  2023influential citation
• Pain in monogenic Parkinson’s disease: a comprehensive review

  2023cites this paper
• 99m-Tc TRODAT Single-Photon Emission Computerized Tomography Scan Image Compression using Singular Value Decomposition

  2023cites this paper
• Acetylation, Phosphorylation, Ubiquitination (Oh My!): Following Post-Translational Modifications on the Ubiquitin Road

  2022cites this paper
• Aspek genetik dan manifestasi klinis varian young onset Parkinson disease

  2020cites this paper
• Dopaminergic Degeneration and Small Vessel Disease in Patients with Normal Pressure Hydrocephalus Who Underwent Shunt Surgery

  2020cites this paper
• A phase 2, open-label, multi-center study to evaluate the efficacy and safety of 99mTc-TRODAT-1 SPECT to detect Parkinson’s disease

  2019cites this paper
• Chapter 2 Dopamine and Early Onset Parkinson ’ s Disease

  2018cites this paper
• SPECT Molecular Imaging in Familial Parkinson's Disease.

  2018cites this paper
• Dopamine and Early Onset Parkinson’s Disease Dopamine and Early Onset Parkinson ’ s Disease

  2018cites this paper
• Dopamine and Early Onset Parkinson’s Disease

  2018cites this paper
• 99mTc-TRODAT-1 SPECT Imaging in Early and Late Onset Parkinson’s Disease

  2017influential citation
• Twenty years since the discovery of the parkin gene

  2017cites this paper
• A comprehensive computational study on pathogenic mis-sense mutations spanning the RING2 and REP domains of Parkin protein.

  2017cites this paper
• Nonmotor Signs in Genetic Forms of Parkinson's Disease.

  2017cites this paper
• Neuroprotection of Granulocyte Colony-Stimulating Factor for Early Stage Parkinson's Disease

  2017cites this paper
• The Effects of Variants in the Parkin, PINK1, and DJ-1 Genes along with Evidence for their Pathogenicity.

  2017cites this paper
• Methamphetamine Neurotoxicity and the Ubiquitin-Proteasome System

  2016cites this paper
• The effects of variants in the PARK2 (parkin), PINK1, and PARK7 (DJ-1) genes along with evidence for their pathogenicity.

  2016cites this paper
• Genetic mutations in early‐onset Parkinson's disease Mexican patients: Molecular testing implications

  2014cites this paper
• Genetic Insights into Sporadic Parkinson's Disease Pathogenesis

  2013cites this paper
• Structure and function of Parkin E3 ubiquitin ligase reveals aspects of RING and HECT ligases

  2013cites this paper
• High frequency of Parkin exon rearrangements in Mexican‐mestizo patients with early‐onset Parkinson's disease

  2012cites this paper
• Enhanced low‐frequency oscillatory activity of the subthalamic nucleus in a patient with dystonia

  2012cites this paper
• Intraoperative x‐ray to measure distance between DBS leads: A reliability study

  2012cites this paper
• Short latency afferent inhibition in Parkinson's disease patients with dementia

  2012cites this paper
• Parkinson’s disease in China

  2011cites this paper
• Genetic Etiology of Parkinson Disease Associated with Mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 Genes: A Mutation Update

  2010cites this paper
• Protein aggregation as a paradigm of aging.

  2009cites this paper
• Genetic analysis of Parkin in early onset Parkinson's disease (PD): Novel intron 9 g > a single nucleotide polymorphism and risk of Taiwanese PD

  2009cites this paper
• In vivo imaging of synaptic function in the central nervous system: I. Movement disorders and dementia.

  2009cites this paper
• Biochemical alteration in cerebrospinal fluid precedes behavioral deficits in Parkinsonian rats induced by 6-hydroxydopamine.

  2009cites this paper
• Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India

  2009cites this paper
• Identification of a Novel Zn2+-binding Domain in the Autosomal Recessive Juvenile Parkinson-related E3 Ligase Parkin*

  2009cites this paper
• A Multitracer Dopaminergic PET Study of Young-Onset Parkinsonian Patients With and Without Parkin Gene Mutations

  2009cites this paper
• Aus dem Institut für Humangenetik der Universität Tübingen Ärztlicher Direktor: Professor Dr. O. Rieß Abteilung für Medizinische Genetik Abteilungsleiter: Professor Dr. O. Rieß Mutationsanalyse und Haplotypenvergleich in CDCrel-1 und GPR37 bei Patienten mit Morbus Parkinson

  2009cites this paper
• Team of Excellence Research Program I. General Information

  2009cites this paper
• Molecular imaging in hereditary forms of parkinsonism

  2007cites this paper
• Investigating the Dopaminergic Synapse In Vivo. I. Molecular Imaging Studies in Humans

  2007cites this paper
• Applications of Clinical Dopamine Imaging.

  2007cites this paper
• A Drosophila Model of Mutant Human Parkin-Induced Toxicity Demonstrates Selective Loss of Dopaminergic Neurons and Dependence on Cellular Dopamine

  2007cites this paper
• Parkin Disrupts the α-Synuclein/Dopamine Transporter Interaction: Consequences Toward Dopamine-induced Toxicity

  2007cites this paper
• Neuroimagem do transportador de dopamina na doença de Parkinson: primeiro estudo com [99mTc]-TRODAT-1 e SPECT no Brasil

  2006cites this paper
• [Neuroimaging of the dopamine transporter in Parkinsons disease: first study using [99mTc]-TRODAT-1 and SPECT in Brazil].

  2006cites this paper
• Applications of clinical dopamine imaging.

  2006cites this paper
• Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan.

  2006cites this paper
• Biochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin-protein ligase with monoubiquitylation capacity.

  2006cites this paper
• Laser literature watch.

  2005cites this paper