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A novel nonsense mutation in the TYMP gene causing MNGIE with multiple intracranial hemorrhages on brain MRI.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Assessment of TREM2 rs75932628 association with Parkinson's disease and multiple system atrophy in a Chinese population.
- Published in:
- 2015
- By:
- Publication type:
- journal article
An exploratory study of serum creatinine levels in patients with amyotrophic lateral sclerosis.
- Published in:
- Neurological Sciences, 2014, v. 35, n. 10, p. 1591, doi. 10.1007/s10072-014-1807-4
- By:
- Publication type:
- Article
Altered intrinsic brain activity in patients with paroxysmal kinesigenic dyskinesia by <i>PRRT2</i> mutation: mutation.
- Published in:
- Neurological Sciences, 2013, v. 34, n. 11, p. 1925, doi. 10.1007/s10072-013-1408-7
- By:
- Publication type:
- Article
Deep brain stimulation of the globus pallidus internal improves symptoms of chorea-acanthocytosis.
- Published in:
- Neurological Sciences, 2012, v. 33, n. 2, p. 269, doi. 10.1007/s10072-011-0741-y
- By:
- Publication type:
- Article
White matter microstructure damage in tremor-dominant Parkinson's disease patients.
- Published in:
- Neuroradiology, 2017, v. 59, n. 7, p. 691, doi. 10.1007/s00234-017-1846-7
- By:
- Publication type:
- Article
Decreased Resting-State Interhemispheric Functional Connectivity in Parkinson’s Disease.
- Published in:
- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/692684
- By:
- Publication type:
- Article
Unique characteristics of the genetics epidemiology of amyotrophic lateral sclerosis in China.
- Published in:
- SCIENCE CHINA Life Sciences, 2019, v. 62, n. 4, p. 517, doi. 10.1007/s11427-018-9453-x
- By:
- Publication type:
- Article
The trajectory of disturbed resting-state cerebral function in Parkinson's disease at different Hoehn and Yahr stages.
- Published in:
- Human Brain Mapping, 2015, v. 36, n. 8, p. 3104, doi. 10.1002/hbm.22831
- By:
- Publication type:
- Article
Single-cell RNA sequencing reveals B cell–related molecular biomarkers for Alzheimer's disease.
- Published in:
- Experimental & Molecular Medicine EMM, 2021, v. 53, n. 12, p. 1888, doi. 10.1038/s12276-021-00714-8
- By:
- Publication type:
- Article
Camptocormia in patients with multiple system atrophy at different disease durations: frequency and related factors.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Determining the Effect of the <italic>HNMT</italic>, <italic>STK39</italic>, and <italic>NMD3</italic> Polymorphisms on the Incidence of Parkinson’s Disease, Amyotrophic Lateral Sclerosis, and Multiple System Atrophy in Chinese Populations.
- Published in:
- Journal of Molecular Neuroscience, 2018, v. 64, n. 4, p. 574, doi. 10.1007/s12031-018-1048-8
- By:
- Publication type:
- Article
Factors influencing cognitive function in patients with Huntington's disease from China: A cross‐sectional clinical study.
- Published in:
- Brain & Behavior, 2023, v. 13, n. 11, p. 1, doi. 10.1002/brb3.3258
- By:
- Publication type:
- Article
Nonmotor symptoms in primary adult-onset cervical dystonia and blepharospasm.
- Published in:
- Brain & Behavior, 2017, v. 7, n. 2, p. n/a, doi. 10.1002/brb3.592
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- Publication type:
- Article
Analysis of SOD1 mutations in a Chinese population with amyotrophic lateral sclerosis: a case-control study and literature review.
- Published in:
- Scientific Reports, 2017, p. 44606, doi. 10.1038/srep44606
- By:
- Publication type:
- Article
The Global Cognition, Frontal Lobe Dysfunction and Behavior Changes in Chinese Patients with Multiple System Atrophy.
- Published in:
- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0139773
- By:
- Publication type:
- Article
Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson’s Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.
- Published in:
- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0133776
- By:
- Publication type:
- Article
Different Human Copper-Zinc Superoxide Dismutase Mutants, SOD1<sup>G93A</sup> and SOD1<sup>H46R</sup>, Exert Distinct Harmful Effects on Gross Phenotype in Mice.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0033409
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- Publication type:
- Article
Assessment of a multiple biomarker panel for diagnosis of amyotrophic lateral sclerosis.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Impact of sleep-related breathing disorder on motor and non-motor symptoms in multiple system atrophy.
- Published in:
- Sleep & Breathing, 2018, v. 22, n. 4, p. 981, doi. 10.1007/s11325-018-1632-8
- By:
- Publication type:
- Article
Gray Matter Atrophy in Behavioral Variant Frontotemporal Dementia: A Meta-Analysis of Voxel-Based Morphometry Studies.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2012, v. 33, n. 2/3, p. 141, doi. 10.1159/000338176
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- Publication type:
- Article
Systemic overexpression of SQSTM1/p62 accelerates disease onset in a SOD1<sup>H46R</sup>-expressing ALS mouse model.
- Published in:
- Molecular Brain, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13041-018-0373-8
- By:
- Publication type:
- Article
Genetic factors for survival in amyotrophic lateral sclerosis: an integrated approach combining a systematic review, pairwise and network meta-analysis.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Enrichment of rare variants of BIN1 but not APOE genes in Chinese patients with Parkinson's disease.
- Published in:
- Journal of Internal Medicine, 2022, v. 291, n. 5, p. 698, doi. 10.1111/joim.13444
- By:
- Publication type:
- Article
Cortical thinning in drug-naive Parkinson's disease patients with depression.
- Published in:
- Journal of Neurology, 2016, v. 263, n. 10, p. 2114, doi. 10.1007/s00415-016-8241-x
- By:
- Publication type:
- Article
Functional connectome assessed using graph theory in drug-naive Parkinson's disease.
- Published in:
- Journal of Neurology, 2015, v. 262, n. 6, p. 1557, doi. 10.1007/s00415-015-7750-3
- By:
- Publication type:
- Article
Frontal lobe function and behavioral changes in amyotrophic lateral sclerosis: a study from Southwest China.
- Published in:
- Journal of Neurology, 2014, v. 261, n. 12, p. 2393, doi. 10.1007/s00415-014-7508-3
- By:
- Publication type:
- Article
Diffusion tensor imaging in blepharospasm and blepharospasm-oromandibular dystonia.
- Published in:
- Journal of Neurology, 2014, v. 261, n. 7, p. 1413, doi. 10.1007/s00415-014-7359-y
- By:
- Publication type:
- Article
Uric acid is associated with the prevalence but not disease progression of multiple system atrophy in Chinese population.
- Published in:
- Journal of Neurology, 2013, v. 260, n. 10, p. 2511, doi. 10.1007/s00415-013-7006-z
- By:
- Publication type:
- Article
Impact of Frontal Lobe Function and Behavioral Changes on Health-Related Quality of Life in Patients with Parkinson's Disease: A Cross-Sectional Study from Southwest China.
- Published in:
- European Neurology, 2015, v. 74, n. 3/4, p. 147, doi. 10.1159/000439084
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- Publication type:
- Article
Association Analysis of Single-Nucleotide Polymorphisms of USP24 and USP40 with Parkinson's Disease in the Han Chinese Population.
- Published in:
- European Neurology, 2012, v. 68, n. 3, p. 181, doi. 10.1159/000339641
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- Publication type:
- Article
GLIS1 rs797906: An Increased Risk Factor for Late-Onset Parkinson's Disease in the Han Chinese Population.
- Published in:
- European Neurology, 2012, v. 68, n. 2, p. 89, doi. 10.1159/000337955
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- Publication type:
- Article
Screening for Cognitive Impairments in Primary Blepharospasm.
- Published in:
- PLoS ONE, 2016, v. 11, n. 8, p. 1, doi. 10.1371/journal.pone.0160867
- By:
- Publication type:
- Article
Association Analysis of WNT3 , HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson's Disease and Multiple System Atrophy.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.765833
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- Publication type:
- Article
Genome-wide genetic links between amyotrophic lateral sclerosis and autoimmune diseases.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Life and disease status of patients with Parkinson's disease during and after zero-COVID in China: an online survey.
- Published in:
- Translational Neurodegeneration, 2024, v. 13, n. 1, p. 1, doi. 10.1186/s40035-024-00399-9
- By:
- Publication type:
- Article
Multivariable clinical-genetic model for predicting dyskinesia in early-onset Parkinson's disease.
- Published in:
- 2021
- By:
- Publication type:
- Letter
C9ORF72 repeat expansions in Chinese patients with Parkinson's disease and multiple system atrophy.
- Published in:
- Journal of Neural Transmission, 2016, v. 123, n. 11, p. 1341, doi. 10.1007/s00702-016-1598-2
- By:
- Publication type:
- Article
Genetic Analysis of ZNF Protein Family Members for Early-Onset Parkinson's Disease in Chinese Population.
- Published in:
- Molecular Neurobiology, 2021, v. 58, n. 7, p. 3435, doi. 10.1007/s12035-021-02354-5
- By:
- Publication type:
- Article
Genetic Analysis of Prosaposin, the Lysosomal Storage Disorder Gene in Parkinson's Disease.
- Published in:
- Molecular Neurobiology, 2021, v. 58, n. 4, p. 1583, doi. 10.1007/s12035-020-02218-4
- By:
- Publication type:
- Article
<italic>TMEM230</italic> Mutations Are Rare in Han Chinese Patients with Autosomal Dominant Parkinson’s Disease.
- Published in:
- Molecular Neurobiology, 2018, v. 55, n. 4, p. 2851, doi. 10.1007/s12035-017-0542-2
- By:
- Publication type:
- Article
Mutation Screening of the CHCHD10 Gene in Chinese Patients with Amyotrophic Lateral Sclerosis.
- Published in:
- Molecular Neurobiology, 2017, v. 54, n. 5, p. 3189, doi. 10.1007/s12035-016-9888-0
- By:
- Publication type:
- Article
Desferrioxamine treatment of aceruloplasminemia: Long-term follow-up.
- Published in:
- Movement Disorders, 2011, v. 26, n. 11, p. 2142, doi. 10.1002/mds.23797
- By:
- Publication type:
- Article
GCH1 mutation and clinical study of Chinese patients with dopa-responsive dystonia.
- Published in:
- Movement Disorders, 2010, v. 25, n. 4, p. 447, doi. 10.1002/mds.22976
- By:
- Publication type:
- Article
A novel mutation of the ε-sarcoglycan gene in a Chinese family with myoclonus-dystonia syndrome.
- Published in:
- Movement Disorders, 2008, v. 23, n. 10, p. 1472, doi. 10.1002/mds.22008
- By:
- Publication type:
- Article
High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.
- Published in:
- Movement Disorders, 2008, v. 23, n. 6, p. 916, doi. 10.1002/mds.21980
- By:
- Publication type:
- Article
Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.
- Published in:
- Movement Disorders, 2008, v. 23, n. 6, p. 917, doi. 10.1002/mds.21942
- By:
- Publication type:
- Article
Novel mutation in the ceruloplasmin gene causing a cognitive and movement disorder with diabetes mellitus.
- Published in:
- Movement Disorders, 2006, v. 21, n. 12, p. 2217, doi. 10.1002/mds.21121
- By:
- Publication type:
- Article
New advance for disease modification therapy in Parkinson's disease.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2022, v. 22, n. 3, p. 147, doi. 10.3969/j.issn.1672-6731.2022.03.005
- By:
- Publication type:
- Article
Associated factors for quality of life in patients with progressive supranuclear palsy.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2021, v. 21, n. 5, p. 411, doi. 10.3969/j.issn.1672-6731.2021.05.014
- By:
- Publication type:
- Article