المؤلفون: Chen Y; Department of Neurology, West China Hospital, Sichuan University, 37# Guoxuexiang, Chengdu, Sichuan, China., Cao B; Department of Neurology, West China Hospital, Sichuan University, 37# Guoxuexiang, Chengdu, Sichuan, China., Ou R; Department of Neurology, West China Hospital, Sichuan University, 37# Guoxuexiang, Chengdu, Sichuan, China., Wei Q; Department of Neurology, West China Hospital, Sichuan University, 37# Guoxuexiang, Chengdu, Sichuan, China., Chen X; Department of Neurology, West China Hospital, Sichuan University, 37# Guoxuexiang, Chengdu, Sichuan, China., Zhao B; Department of Neurology, West China Hospital, Sichuan University, 37# Guoxuexiang, Chengdu, Sichuan, China., Wu Y; Department of Neurology, West China Hospital, Sichuan University, 37# Guoxuexiang, Chengdu, Sichuan, China., Song W; Department of Neurology, West China Hospital, Sichuan University, 37# Guoxuexiang, Chengdu, Sichuan, China., Shang HF; Department of Neurology, West China Hospital, Sichuan University, 37# Guoxuexiang, Chengdu, Sichuan, China. hfshang2002@126.com.

المصدر: Journal of molecular neuroscience : MN [J Mol Neurosci] 2018 Apr; Vol. 64 (4), pp. 574-580. Date of Electronic Publication: 2018 Mar 21.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Humana Press Country of Publication: United States NLM ID: 9002991 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1559-1166 (Electronic) Linking ISSN: 08958696 NLM ISO Abbreviation: J Mol Neurosci Subsets: MEDLINE

مواضيع طبية MeSH: Polymorphism, Single Nucleotide*, Amyotrophic Lateral Sclerosis/*genetics , Histamine N-Methyltransferase/*genetics , Multiple System Atrophy/*genetics , Parkinson Disease/*genetics , Protein Serine-Threonine Kinases/*genetics , RNA-Binding Proteins/*genetics, Aged ; China ; Female ; Humans ; Male ; Middle Aged

المؤلفون: Hu T; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China; Department of Neurology, Chengdu Aerospace Hospital, Chengdu, Sichuan, China., Chen Y; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Ou R; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Wei Q; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Cao B; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Zhao B; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Wu Y; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Song W; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Chen X; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Shang HF; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China. Electronic address: hfshang2002@126.com.

المصدر: Journal of the neurological sciences [J Neurol Sci] 2017 Jun 15; Vol. 377, pp. 65-71. Date of Electronic Publication: 2017 Mar 21.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 0375403 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-5883 (Electronic) Linking ISSN: 0022510X NLM ISO Abbreviation: J Neurol Sci Subsets: MEDLINE

مواضيع طبية MeSH: Amyotrophic Lateral Sclerosis/*genetics , Membrane Proteins/*genetics , Multiple System Atrophy/*genetics , Nerve Tissue Proteins/*genetics , Parkinson Disease/*genetics , Polymorphism, Single Nucleotide/*genetics , Vesicular Monoamine Transport Proteins/*genetics, Adult ; Aged ; DNA Mutational Analysis ; Female ; Gene Frequency ; Genetic Association Studies ; Genetic Predisposition to Disease/genetics ; Genotype ; Humans ; Male ; Middle Aged

المؤلفون: Xu Y; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Cao B; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Chen Y; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Ou R; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Wei Q; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Yang J; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Zhao B; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Song W; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Shang HF; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China. Electronic address: hfshang2002@163.com.

المصدر: Journal of the neurological sciences [J Neurol Sci] 2016 Jun 15; Vol. 365, pp. 96-100. Date of Electronic Publication: 2016 Apr 08.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 0375403 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-5883 (Electronic) Linking ISSN: 0022510X NLM ISO Abbreviation: J Neurol Sci Subsets: MEDLINE

مواضيع طبية MeSH: Amyotrophic Lateral Sclerosis/*genetics , Essential Tremor/*genetics , Genetic Predisposition to Disease/*genetics , Glutamate Plasma Membrane Transport Proteins/*genetics , Multiple System Atrophy/*genetics , Parkinson Disease/*genetics , Polymorphism, Single Nucleotide/*genetics, Adult ; Aged ; China ; Cohort Studies ; Excitatory Amino Acid Transporter 2 ; Female ; Gene Frequency ; Genome-Wide Association Study ; Genotype ; Humans ; Male ; Middle Aged ; Severity of Illness Index

المؤلفون: Chen Y; Department of Neurology, West China Hospital, Sichuan University, 610041, Chengdu, Sichuan, People's Republic of China., Yuan X; Department of Neurology, West China Hospital, Sichuan University, 610041, Chengdu, Sichuan, People's Republic of China., Cao B; Department of Neurology, West China Hospital, Sichuan University, 610041, Chengdu, Sichuan, People's Republic of China., Wei Q; Department of Neurology, West China Hospital, Sichuan University, 610041, Chengdu, Sichuan, People's Republic of China., Ou R; Department of Neurology, West China Hospital, Sichuan University, 610041, Chengdu, Sichuan, People's Republic of China., Yang J; Department of Neurology, West China Hospital, Sichuan University, 610041, Chengdu, Sichuan, People's Republic of China., Chen X; Department of Neurology, West China Hospital, Sichuan University, 610041, Chengdu, Sichuan, People's Republic of China., Zhao B; Department of Neurology, West China Hospital, Sichuan University, 610041, Chengdu, Sichuan, People's Republic of China., Song W; Department of Neurology, West China Hospital, Sichuan University, 610041, Chengdu, Sichuan, People's Republic of China., Wu Y; Department of Neurology, West China Hospital, Sichuan University, 610041, Chengdu, Sichuan, People's Republic of China., Shang H; Department of Neurology, West China Hospital, Sichuan University, 610041, Chengdu, Sichuan, People's Republic of China. hfshang2002@126.com.

المصدر: Journal of neural transmission (Vienna, Austria : 1996) [J Neural Transm (Vienna)] 2015 Nov; Vol. 122 (11), pp. 1547-52. Date of Electronic Publication: 2015 Jul 30.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer-Verlag Country of Publication: Austria NLM ID: 9702341 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1435-1463 (Electronic) Linking ISSN: 03009564 NLM ISO Abbreviation: J Neural Transm (Vienna) Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease* , Polymorphism, Single Nucleotide*, Lysosomal Membrane Proteins/*genetics , Parkinson Disease/*genetics , Receptors, Scavenger/*genetics , Syntaxin 1/*genetics, Age Factors ; Asian People/genetics ; Case-Control Studies ; China/epidemiology ; Cohort Studies ; Female ; Genetic Association Studies ; Humans ; Male ; Middle Aged ; Models, Genetic ; Parkinson Disease/epidemiology ; Sex Factors

المؤلفون: Chen Y; Department of Neurology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China., Chen X; Department of Neurology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China., Guo X; Department of Neurology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China., Song W; Department of Neurology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China., Cao B; Department of Neurology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China., Wei Q; Department of Neurology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China., Ou R; Department of Neurology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China., Zhao B; Department of Neurology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China., Shang HF; Department of Neurology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China. hfshang@yahoo.com.

المصدر: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2015 Oct; Vol. 36 (10), pp. 1903-6. Date of Electronic Publication: 2015 Jun 10.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1590-3478 (Electronic) Linking ISSN: 15901874 NLM ISO Abbreviation: Neurol Sci Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease/*genetics , Membrane Glycoproteins/*genetics , Multiple System Atrophy/*genetics , Parkinson Disease/*genetics , Polymorphism, Single Nucleotide/*genetics , Receptors, Immunologic/*genetics, Adult ; Aged ; Asian People/genetics ; Female ; Genetic Association Studies ; Genotype ; Humans ; Male ; Middle Aged

المؤلفون: Chen X; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Chen Y; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Wei Q; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Guo X; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Cao B; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Ou R; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Zhao B; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Shang HF; Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, China. Electronic address: hfshang2002@163.com.

المصدر: Journal of the neurological sciences [J Neurol Sci] 2015 Aug 15; Vol. 355 (1-2), pp. 193-5. Date of Electronic Publication: 2015 May 16.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 0375403 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-5883 (Electronic) Linking ISSN: 0022510X NLM ISO Abbreviation: J Neurol Sci Subsets: MEDLINE

مواضيع طبية MeSH: Amyotrophic Lateral Sclerosis/*genetics , Genetic Predisposition to Disease/*genetics , Membrane Glycoproteins/*genetics , Polymorphism, Single Nucleotide/*genetics , Receptors, Immunologic/*genetics, Adult ; Aged ; Asian People/genetics ; Female ; Genetic Association Studies ; Genotype ; Humans ; Male ; Middle Aged

المؤلفون: Chen X; Department of Neurology and State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, SiChuan University, Chengdu, Sichuan, 610041, China., Huang R, Chen Y, Zheng Z, Chen K, Song W, Zhao B, Yang Y, Yuan L, Shang H

المصدر: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2014 Jul; Vol. 35 (7), pp. 1089-95. Date of Electronic Publication: 2014 Feb 04.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer-Verlag Italia Country of Publication: Italy NLM ID: 100959175 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1590-3478 (Electronic) Linking ISSN: 15901874 NLM ISO Abbreviation: Neurol Sci Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease*, Amyotrophic Lateral Sclerosis/*genetics , Epithelial Sodium Channels/*genetics , Guanine Nucleotide Exchange Factors/*genetics , Nerve Tissue Proteins/*genetics , Polymorphism, Single Nucleotide/*genetics , Superoxide Dismutase/*genetics, Adolescent ; Adult ; Aged ; Aged, 80 and over ; Amyotrophic Lateral Sclerosis/ethnology ; Asian People/genetics ; C9orf72 Protein ; Female ; Gene Frequency ; Genetic Association Studies ; Genotype ; Humans ; Male ; Middle Aged ; Proteins/genetics ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Superoxide Dismutase-1 ; T-Lymphoma Invasion and Metastasis-inducing Protein 1 ; Young Adult

المؤلفون: Chen Y; Department of Neurology, West China Hospital, Sichuan University, 610041 Chengdu, Sichuan, China., Song W, Yang J, Chen K, Huang R, Zhao B, Cao B, Burgunder J, Shang HF

المصدر: Parkinsonism & related disorders [Parkinsonism Relat Disord] 2013 Nov; Vol. 19 (11), pp. 1043-5. Date of Electronic Publication: 2013 Jun 29.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Science Country of Publication: England NLM ID: 9513583 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-5126 (Electronic) Linking ISSN: 13538020 NLM ISO Abbreviation: Parkinsonism Relat Disord Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Association Studies*/methods, Brain-Derived Neurotrophic Factor/*genetics , Methionine/*genetics , Polymorphism, Single Nucleotide/*genetics , Torticollis/*congenital , Valine/*genetics, Adult ; China/epidemiology ; Dystonia/congenital ; Female ; Humans ; Male ; Middle Aged ; Torticollis/diagnosis ; Torticollis/epidemiology ; Torticollis/genetics ; Young Adult

SCR Disease Name: Cervical Dystonia, Primary

المؤلفون: Chen Y; Department of Neurology and State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, SiChuan University, Chengdu, Sichuan, China., Zheng ZZ, Huang R, Chen K, Song W, Zhao B, Chen X, Yang Y, Yuan L, Shang HF

المصدر: Neurobiology of aging [Neurobiol Aging] 2013 Jul; Vol. 34 (7), pp. 1922.e1-5. Date of Electronic Publication: 2013 Feb 19.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 8100437 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1558-1497 (Electronic) Linking ISSN: 01974580 NLM ISO Abbreviation: Neurobiol Aging Subsets: MEDLINE

مواضيع طبية MeSH: Amyotrophic Lateral Sclerosis/*genetics , Asian People/*genetics , Mutation/*genetics , Polymorphism, Single Nucleotide/*genetics , Profilins/*genetics, Adult ; Amino Acid Sequence ; Amyotrophic Lateral Sclerosis/diagnosis ; Amyotrophic Lateral Sclerosis/ethnology ; Asian People/ethnology ; Female ; Humans ; Male ; Middle Aged ; Molecular Sequence Data

المؤلفون: Chen YP; Department of Neurology, West China Hospital, SiChuan University, Chengdu Sichuan, China., Song W, Huang R, Chen K, Zhao B, Li J, Yang Y, Shang HF

المصدر: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia [J Clin Neurosci] 2013 Jun; Vol. 20 (6), pp. 880-3. Date of Electronic Publication: 2013 Apr 23.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Churchill Livingstone Country of Publication: Scotland NLM ID: 9433352 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2653 (Electronic) Linking ISSN: 09675868 NLM ISO Abbreviation: J Clin Neurosci Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease*, Diacylglycerol Kinase/*genetics , Intracellular Signaling Peptides and Proteins/*genetics , Parkinson Disease/*genetics , Polymorphism, Single Nucleotide/*genetics , Protein Serine-Threonine Kinases/*genetics, Asian People/genetics ; China/epidemiology ; Female ; Gene Frequency ; Genetic Association Studies ; Genotype ; Humans ; Male ; Parkinson Disease/ethnology ; Retrospective Studies