Lorne Zinman Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre University of Toronto Biography Publications Institution JoVE Articles Lorne Zinman has not added a biography. If you are Lorne Zinman and would like to personalize this page please email our Author Liaison for assistance. Publications Genome-wide Analyses Identify KIF5A As a Novel ALS Gene Neuron. Mar, 2018 | Pubmed ID: 29566793 Clinical Reasoning: A 42-year-old Man with Unilateral Leg Weakness Neurology. Mar, 2018 | Pubmed ID: 29555890 Downregulation of Exosomal MiR-204-5p and MiR-632 As a Biomarker for FTD: a GENFI Study Journal of Neurology, Neurosurgery, and Psychiatry. Feb, 2018 | Pubmed ID: 29434051 Motor Unit Number Index and Neurophysiological Index As Candidate Biomarkers of Presymptomatic Motor Neuron Loss in Amyotrophic Lateral Sclerosis Muscle & Nerve. Jan, 2018 | Pubmed ID: 29381812 Unaffected Mosaiccase: RNA Foci, Dipeptide Proteins, but Upregulated C9orf72 Expression Neurology. Jan, 2018 | Pubmed ID: 29282338 Loss of CHCHD10-CHCHD2 Complexes Required for Respiration Underlies the Pathogenicity of a CHCHD10 Mutation in ALS Human Molecular Genetics. Jan, 2018 | Pubmed ID: 29121267 Clinical and Neuropathological Features of ALS/FTD with TIA1 Mutations Acta Neuropathologica Communications. Dec, 2017 | Pubmed ID: 29216908 Neuroleptics As Therapeutic Compounds Stabilizing Neuromuscular Transmission in Amyotrophic Lateral Sclerosis JCI Insight. Nov, 2017 | Pubmed ID: 29202456 Dysregulation of Chromatin Remodelling Complexes in Amyotrophic Lateral Sclerosis Human Molecular Genetics. Nov, 2017 | Pubmed ID: 28973294 TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics Neuron. Aug, 2017 | Pubmed ID: 28817800 Motor Phenotype in Neurodegenerative Disorders: Gait and Balance Platform Study Design Protocol for the Ontario Neurodegenerative Research Initiative (ONDRI) Journal of Alzheimer's Disease : JAD. 2017 | Pubmed ID: 28671116 DNA Methylation Age-acceleration is Associated with Disease Duration and Age at Onset in C9orf72 Patients Acta Neuropathologica. Aug, 2017 | Pubmed ID: 28439722 Speech Movement Measures As Markers of Bulbar Disease in Amyotrophic Lateral Sclerosis Journal of Speech, Language, and Hearing Research : JSLHR. Oct, 2016 | Pubmed ID: 27679842 Physician-assisted Death: A Canada-wide Survey of ALS Health Care Providers Neurology. Sep, 2016 | Pubmed ID: 27178703 Genetic and Epigenetic Study of ALS-discordant Identical Twins with Double Mutations in SOD1 and ARHGEF28 Journal of Neurology, Neurosurgery, and Psychiatry. 11, 2016 | Pubmed ID: 27154192 Predicting Speech Intelligibility Decline in Amyotrophic Lateral Sclerosis Based on the Deterioration of Individual Speech Subsystems PloS One. 2016 | Pubmed ID: 27148967 C9orf72 Isoforms in Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration Brain Research. 09, 2016 | Pubmed ID: 27134035 Profiling Speech and Pausing in Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD) PloS One. 2016 | Pubmed ID: 26789001 MTHFSD and DDX58 Are Novel RNA-binding Proteins Abnormally Regulated in Amyotrophic Lateral Sclerosis Brain : a Journal of Neurology. Jan, 2016 | Pubmed ID: 26525917 Isoform-specific Antibodies Reveal Distinct Subcellular Localizations of C9orf72 in Amyotrophic Lateral Sclerosis Annals of Neurology. Oct, 2015 | Pubmed ID: 26174152 Jump from Pre-mutation to Pathologic Expansion in C9orf72 American Journal of Human Genetics. Jun, 2015 | Pubmed ID: 26004200 Mutation Analysis of CHCHD10 in Different Neurodegenerative Diseases Brain : a Journal of Neurology. Sep, 2015 | Pubmed ID: 25833818 Low Molecular Weight Species of TDP-43 Generated by Abnormal Splicing Form Inclusions in Amyotrophic Lateral Sclerosis and Result in Motor Neuron Death Acta Neuropathologica. Jul, 2015 | Pubmed ID: 25788357 The C9orf72 Repeat Expansion Itself is Methylated in ALS and FTLD Patients Acta Neuropathologica. May, 2015 | Pubmed ID: 25716178 Electrical Impedance Myography in the Evaluation of the Tongue Musculature in Amyotrophic Lateral Sclerosis Muscle & Nerve. Oct, 2015 | Pubmed ID: 25580728 Mutation Analysis of Patients with Neurodegenerative Disorders Using NeuroX Array Neurobiology of Aging. Jan, 2015 | Pubmed ID: 25174650 Identical Twins with the C9orf72 Repeat Expansion Are Discordant for ALS Neurology. Oct, 2014 | Pubmed ID: 25209579 Economic Burden of Amyotrophic Lateral Sclerosis: a Canadian Study of Out-of-pocket Expenses Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Sep, 2014 | Pubmed ID: 25025935 Hypermethylation of the CpG-island Near the C9orf72 G₄C₂-repeat Expansion in FTLD Patients Human Molecular Genetics. Nov, 2014 | Pubmed ID: 24908669 Venous Thromboembolism in Amyotrophic Lateral Sclerosis: a Prospective Study Neurology. May, 2014 | Pubmed ID: 24727309 Mutations in the Matrin 3 Gene Cause Familial Amyotrophic Lateral Sclerosis Nature Neuroscience. May, 2014 | Pubmed ID: 24686783 Speech in ALS: Longitudinal Changes in Lips and Jaw Movements and Vowel Acoustics Journal of Medical Speech-language Pathology. Mar, 2013 | Pubmed ID: 27453680 Bulbar and Speech Motor Assessment in ALS: Challenges and Future Directions Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. Jul, 2013 | Pubmed ID: 23898888 Hypermethylation of the CpG Island Near the G4C2 Repeat in ALS with a C9orf72 Expansion American Journal of Human Genetics. Jun, 2013 | Pubmed ID: 23731538 Mortality Associated with Periodic Limb Movements During Sleep in Amyotrophic Lateral Sclerosis Patients Einstein (Sao Paulo, Brazil). Oct-Dec, 2012 | Pubmed ID: 23386081 Enhancing Clinical Trials in Neurodegenerative Disorders: Lessons from Amyotrophic Lateral Sclerosis Current Opinion in Neurology. Dec, 2012 | Pubmed ID: 23160423 C9orf72 在 4 调查神经退行性疾病。 Archives of Neurology. Sep, 2012 | Pubmed ID: 22964832 Tongue Movements and Their Acoustic Consequences in Amyotrophic Lateral Sclerosis Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP). 2012 | Pubmed ID: 22555651 Hexanucleotide 重复 C9ORF72 扩张是染色体的原因 9 P 21 链接 ALS 直升机。 Neuron. Oct, 2011 | Pubmed ID: 21944779 椎旁肌病新型陶片样紧凑聚合的细丝。 Muscle & Nerve. Jul, 2011 | Pubmed ID: 21660984 FUS 突变与肌萎缩侧索硬化病理异质性: 关联与疾病严重程度和突变的两种不同模式。 Acta Neuropathologica. Jul, 2011 | Pubmed ID: 21604077 新兴的目标和肌萎缩侧索硬化的治疗方法。 Lancet Neurology. May, 2011 | Pubmed ID: 21511200 RNA 靶标的 TDP 43 由紫外线剪辑标识被撤销在 ALS。 Molecular and Cellular Neurosciences. Jul, 2011 | Pubmed ID: 21421050 不同的生化签名的特点是感光异构体表达在外伤性神经损伤和运动神经元病。 Journal of Neurochemistry. Aug, 2010 | Pubmed ID: 20533992 利鲁唑治疗肌萎缩侧索硬化结合锂的安全性和有效性: 随机、 双盲、 安慰剂对照试验。 Lancet Neurology. May, 2010 | Pubmed ID: 20363190 加拿大 ALS 患者无创通气: 我们有共识吗? The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. Jan, 2010 | Pubmed ID: 20169767 肌萎缩侧索硬化是广泛的 SOD1 折叠在特有的家族形式非淀粉样蛋白疾病。 Acta Neuropathologica. Mar, 2010 | Pubmed ID: 20111867 运动学分析在球部 ALS 疾病进展。 Journal of Communication Disorders. Jan-Feb, 2010 | Pubmed ID: 19683250 重症肌无力患者接种流感疫苗的安全: 一项基于人口的研究。 Muscle & Nerve. Dec, 2009 | Pubmed ID: 19902540 缺乏证据的单体/misfolded 超氧化物歧化酶-1 中零星肌萎缩侧索硬化。 Annals of Neurology. Jul, 2009 | Pubmed ID: 19670443 ALS 患者安全的药物他汀类药物是吗? Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases. Aug, 2008 | Pubmed ID: 18608105 IVIG 治疗重症肌无力: 有效性、 限制和新型的治疗策略。 Annals of the New York Academy of Sciences. 2008 | Pubmed ID: 18567877 代理与重症肌无力患者的治疗结果措施。 Muscle & Nerve. Feb, 2008 | Pubmed ID: 17918748 手摇和 IFT74 在萎缩侧索硬化症的遗传学研究。 Neurobiology of Aging. Aug, 2008 | Pubmed ID: 17383054 TDP 43 不是主要的泛素化目标内的肌萎缩侧索硬化的病理夹杂物的证据。 Journal of Neuropathology and Experimental Neurology. Dec, 2007 | Pubmed ID: 18090923 四、 免疫球蛋白在重症肌无力患者: 随机对照试验。 Neurology. Mar, 2007 | Pubmed ID: 17353471 重症肌无力患者的重复性面部神经刺激的敏感性。 Muscle & Nerve. May, 2006 | Pubmed ID: 16421884 冷却评估糖尿病感官性多发性神经病的检测阈值: 案例四和梅多克文书的比较。 Diabetes Care. Jul, 2004 | Pubmed ID: 15220245 低强度激光疗法治疗糖尿病感觉性多发性神经病的痛苦症状: 对照的试验。 Diabetes Care. Apr, 2004 | Pubmed ID: 15047649 有针对性的下一代测序和生物信息学管道评价宪政疾病的遗传决定因素 Allison A. Dilliott1,2, Sali M.K. Farhan3, Mahdi Ghani4, Christine Sato4, Eric Liang5, Ming Zhang4, Adam D. McIntyre1, Henian Cao1, Lemuel Racacho6,7, John F. Robinson1, Michael J. Strong1,8, Mario Masellis9,10, Dennis E. Bulman6,7, Ekaterina Rogaeva4, Anthony Lang10,11, Carmela Tartaglia4,10, Elizabeth Finger12,13, Lorne Zinman9, John Turnbull14, Morris Freedman10,15, Rick Swartz9, Sandra E. Black9,16, Robert A. Hegele1,2 1Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, 2Department of Biochemistry, Schulich School of Medicine and Dentistry, Western University, 3Analytic and Translational Genetics Unit, Center for Genomic Medicine, Harvard Medical School, Massachusetts General Hospital, Stanley Centre for Psychiatric Research, Broad Institute of MIT and Harvard, 4Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 5School of Medicine, Faculty of Health Sciences, Queen's University, 6Faculty of Medicine, Department of Biochemistry, Microbiology and Immunology, University of Ottawa, 7CHEO Research Institute, Faculty of Medicine, University of Ottawa, 8Department of Clinical Neurological Sciences, Western University, 9Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, 10Division of Neurology, Department of Medicine, University of Toronto, 11Morton and Gloria Shulman Movement Disorders Centre, Toronto Western Hospital, 12Department of Clinical Neurological Sciences, Schulich School of Medicine and Dentistry, Western University, 13Parkwood Institute, St. Joseph's Health Care, 14Department of Medicine, Division of Neurology, McMaster University, 15Division of Neurology, Department of Medicine, Baycrest Health Sciences, 16Canadian Partnership for Stroke Recovery Sunnybrook Site, Sunnybrook Health Science Centre, University of Toronto JoVE 57266 Genetik 延髓功能障碍肌萎缩性脊髓侧索硬化症(ALS)的综合评估议定书 Yana Yunusova1,2, Jordan R. Green3, Jun Wang3, Gary Pattee4, Lorne Zinman2,5 1Department of Speech-Language Pathology, University of Toronto, 2ALS/ MN Clinic, Sunnybrook Health Science Centre, 3Department of Special Education and Communication Disorders, University of Nebraska-Lincoln, 4Department of Neurology, Munroe-Meyer Institute, University of Nebraska Medical Center, 5Department of Neurology, University of Toronto JoVE 2422 Medizin
有针对性的下一代测序和生物信息学管道评价宪政疾病的遗传决定因素 Allison A. Dilliott1,2, Sali M.K. Farhan3, Mahdi Ghani4, Christine Sato4, Eric Liang5, Ming Zhang4, Adam D. McIntyre1, Henian Cao1, Lemuel Racacho6,7, John F. Robinson1, Michael J. Strong1,8, Mario Masellis9,10, Dennis E. Bulman6,7, Ekaterina Rogaeva4, Anthony Lang10,11, Carmela Tartaglia4,10, Elizabeth Finger12,13, Lorne Zinman9, John Turnbull14, Morris Freedman10,15, Rick Swartz9, Sandra E. Black9,16, Robert A. Hegele1,2 1Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, 2Department of Biochemistry, Schulich School of Medicine and Dentistry, Western University, 3Analytic and Translational Genetics Unit, Center for Genomic Medicine, Harvard Medical School, Massachusetts General Hospital, Stanley Centre for Psychiatric Research, Broad Institute of MIT and Harvard, 4Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, 5School of Medicine, Faculty of Health Sciences, Queen's University, 6Faculty of Medicine, Department of Biochemistry, Microbiology and Immunology, University of Ottawa, 7CHEO Research Institute, Faculty of Medicine, University of Ottawa, 8Department of Clinical Neurological Sciences, Western University, 9Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, 10Division of Neurology, Department of Medicine, University of Toronto, 11Morton and Gloria Shulman Movement Disorders Centre, Toronto Western Hospital, 12Department of Clinical Neurological Sciences, Schulich School of Medicine and Dentistry, Western University, 13Parkwood Institute, St. Joseph's Health Care, 14Department of Medicine, Division of Neurology, McMaster University, 15Division of Neurology, Department of Medicine, Baycrest Health Sciences, 16Canadian Partnership for Stroke Recovery Sunnybrook Site, Sunnybrook Health Science Centre, University of Toronto JoVE 57266 Genetik
延髓功能障碍肌萎缩性脊髓侧索硬化症(ALS)的综合评估议定书 Yana Yunusova1,2, Jordan R. Green3, Jun Wang3, Gary Pattee4, Lorne Zinman2,5 1Department of Speech-Language Pathology, University of Toronto, 2ALS/ MN Clinic, Sunnybrook Health Science Centre, 3Department of Special Education and Communication Disorders, University of Nebraska-Lincoln, 4Department of Neurology, Munroe-Meyer Institute, University of Nebraska Medical Center, 5Department of Neurology, University of Toronto JoVE 2422 Medizin