نتایج جستجو برای: parkinson

تعداد نتایج: 68985  

2015
Alina Abulaiti Koji Kamagata Yumiko Motoi Masaaki Hori Nobutaka Hattori Shigeki Aoki

Diffusion tensor tractography was used to evaluate whether diffusion metrics in the nigrostriatal pathway could diagnose Parkinson disease. Diffusion tensor imaging was performed on 30 patients with Parkinson disease and 32 healthy controls by using a 3.0 Tesla magnetic resonance imaging system. Diffusion tensor tractography was used for both groups to visualize the nigrostriatal and corticospi...

2016
Christian Dölle Irene Flønes Gonzalo S Nido Hrvoje Miletic Nelson Osuagwu Stine Kristoffersen Peer K Lilleng Jan Petter Larsen Ole-Bjørn Tysnes Kristoffer Haugarvoll Laurence A Bindoff Charalampos Tzoulis

Increased somatic mitochondrial DNA (mtDNA) mutagenesis causes premature aging in mice, and mtDNA damage accumulates in the human brain with aging and neurodegenerative disorders such as Parkinson disease (PD). Here, we study the complete spectrum of mtDNA changes, including deletions, copy-number variation and point mutations, in single neurons from the dopaminergic substantia nigra and other ...

Journal: :IJHISI 2016
Saloni Rajender K. Sharma Anil K. Gupta

Parkinson disease is a neurological disorder. In this disease control over body muscles get disturbed. In almost 90% of the cases, people suffering from Parkinson disease (PD) have speech disorders. The goal of the paper is to differentiate healthy and PD affected persons using voice analysis. There are no well-developed lab techniques available for Parkinson detection. Parkinson detection usin...

Journal: :Neurorehabilitation and neural repair 2009
Minna Hong Joel S Perlmutter Gammon M Earhart

BACKGROUND Parkinson disease frequently causes difficulty turning that can lead to falls, loss of independence, and diminished quality of life. Turning in tight spaces, which may be particularly impaired in Parkinson disease, is an essential part of our daily lives, yet a comprehensive analysis of in-place turning has not been published. OBJECTIVE This study was conducted to determine whether...

2009
Christian Kier Günter Seidel Norbert Brüggemann Johann Hagenah Christine Klein Til Aach Alfred Mertins

Eine frühe Diagnose der Parkinsonkrankheit ist enorm wichtig, da klinische Symptome erst sichtbar werden, wenn schon ein Großteil der betroffenen Nervenzellen unwiderruflich geschädigt ist. Neuere Arbeiten deuten darauf hin, daß mit der transkraniellen Sonografie (TCS) ein Werkzeug verfügbar ist, das die Manifestation einer genetischen Form der Parkinson-Krankheit bereits zu einem sehr frühen Z...

Journal: :Archives of neurology 2004
Ekaterina Rogaeva Janel Johnson Anthony E Lang Cindy Gulick Katrina Gwinn-Hardy Toshitaka Kawarai Christine Sato Angharad Morgan John Werner Robert Nussbaum Agnes Petit Michael S Okun Aideen McInerney Ronald Mandel Justus L Groen Hubert H Fernandez Ron Postuma Kelly D Foote Shabnam Salehi-Rad Yan Liang Sharon Reimsnider Anurag Tandon John Hardy Peter St George-Hyslop Andrew B Singleton

BACKGROUND Mutations in the PTEN-induced kinase (PINK1) gene located within the PARK6 locus on chromosome 1p35-p36 have recently been identified in patients with recessive early-onset Parkinson disease. OBJECTIVE To assess the prevalence of PINK1 mutations within a series of early- and late-onset Parkinson disease patients living in North America. DESIGN All coding exons of the PINK1 gene w...

2012
Xiangmin Lin Travis J. Cook Cyrus P. Zabetian James B. Leverenz Elaine R. Peskind Shu-Ching Hu Kevin C. Cain Catherine Pan John Scott Edgar David R. Goodlett Brad A. Racette Harvey Checkoway Thomas J. Montine Min Shi Jing Zhang

DJ-1 is a multifunctional protein that plays an important role in oxidative stress, cell death, and synucleinopathies, including Parkinson disease. Previous studies have demonstrated that total DJ-1 levels decrease in the cerebrospinal fluid, but do not change significantly in human plasma from patients with Parkinson disease when compared with controls. In this study, we measured total DJ-1 an...

2012
Christine Klein

Recent findings Mutations in VPS35 were identified as a novel cause of autosomal dominant Parkinson disease using exome sequencing. Next generation sequencing (NGS) was also used to identify PRRT2 mutations as a cause of paroxysmal kinesigenic dyskinesia (DYT10). Using a different technique, that is linkage analysis, mutations in EIF4G1 were implicated as a cause of Parkinson disease and mutati...

Journal: :caspian journal of neurological sciences 0
babak bakhshayesh neurosciences research center, neurology department, pouursina hospital, school of medicine, guilan university of medical sciences, rasht, iran shaghayegh sayyar department of sport sciences, university of guilan, rasht, iran; [email protected] hasan daneshmandi professor, department of sport sciences, university of guilan, rasht, iran

background: parkinson's disease as a progressive disorder of the nervous system leads to the disability of postural control system. objectives: in the present study the effects of pilates exercises on functional balance in patients with parkinson's was investigated. materials and methods: this control trial included 30 patients with idiopathic parkinson's disease who were selecte...

Ali Sarbazi Golezari, Arvin Babayan, Ayda Faraji, Gilda Khandan, Hashem Haghdoost Yazdi, Nafiseh Rastgoo, Tahereh Dargahi,

Introduction: Parkinson’s disease (PD) is the second most neurodegenerative disorder which is characterized by a progressive loss of dopaminergic neurons in the substantia nigra pars compacta. Clinical symptoms do not appear until approximately 70% of dopaminergic neurons and 80% of the striatal dopaminergic terminals have been lost. Thus, detecting nonclinical factors such as detecting b...

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