Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Przeglądasz jako GOŚĆ

Wyszukujesz frazę ""PARKINSONIAN disorders"" wg kryterium: Temat


Starter badań:

Tytuł :
Exercise Management Using a Mobile App in Patients With Parkinsonism: Prospective, Open-Label, Single-Arm Pilot Study.
Autorzy :
Kim A; Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Yun SJ; Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Sung KS; Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Kim Y; Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Jo JY; Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Cho H; College of Medicine, Kyung Hee University, Seoul, Republic of Korea.
Park K; School of Information Convergence, Kwangwoon University, Seoul, Republic of Korea.
Oh BM; Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Republic of Korea.; Institute on Aging, Seoul National University, Seoul, Republic of Korea.; National Traffic Injury Rehabilitation Hospital, Yangpyeong, Republic of Korea.
Seo HG; Department of Rehabilitation Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Pokaż więcej
Źródło :
JMIR mHealth and uHealth [JMIR Mhealth Uhealth] 2021 Aug 31; Vol. 9 (8), pp. e27662. Date of Electronic Publication: 2021 Aug 31.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
COVID-19*
Mobile Applications*
Parkinsonian Disorders*
Aged ; Exercise ; Female ; Humans ; Male ; Pandemics ; Pilot Projects ; Prospective Studies ; Quality of Life ; SARS-CoV-2
Czasopismo naukowe
Tytuł :
Comparison of perfusion 18F-FP-CIT PET and 99mTc-ECD SPECT in parkinsonian disorders.
Autorzy :
Chun K; Department of Nuclear Medicine, Yeungnam University Hospital, Daegu, Korea.
Kong E
Cho I
Pokaż więcej
Źródło :
Medicine [Medicine (Baltimore)] 2021 Aug 27; Vol. 100 (34), pp. e27019.
Typ publikacji :
Journal Article
MeSH Terms :
Brain/*diagnostic imaging
Parkinsonian Disorders/*diagnostic imaging
Parkinsonian Disorders/*pathology
Positron Emission Tomography Computed Tomography/*methods
Tomography, Emission-Computed, Single-Photon/*methods
Aged ; Brain/pathology ; Cysteine/analogs & derivatives ; Dopamine Plasma Membrane Transport Proteins/metabolism ; Female ; Fluorine Radioisotopes ; Humans ; Male ; Middle Aged ; Organotechnetium Compounds ; Parkinsonian Disorders/diagnosis ; Radiopharmaceuticals ; Retrospective Studies ; Tropanes
Czasopismo naukowe
Tytuł :
Development of parkinsonism after long-standing cervical dystonia - A cohort.
Autorzy :
Balint B; UCL Queen Square Institute of Neurology Department of Clinical and Movement Neurosciences, Queen Square, London WC1N 3BG, United Kingdom; Department of Neurology, University Hospital Heidelberg, Germany. Electronic address: .
Mulroy E; UCL Queen Square Institute of Neurology Department of Clinical and Movement Neurosciences, Queen Square, London WC1N 3BG, United Kingdom.
Gövert F; Department of Neurology, Christian-Albrechts-University, Kiel, Germany.
Latorre A; UCL Queen Square Institute of Neurology Department of Clinical and Movement Neurosciences, Queen Square, London WC1N 3BG, United Kingdom; Department of Human Neurosciences, Sapienza University of Rome, Italy.
Di Lazarro G; Department of Systems Medicine, University of Rome Tor Vergata, Italy; Institute of Neurology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Erro R; Center for Neurodegenerative Diseases, Department of Medicine, Surgery and Dentistry 'Scuola Medica Salernitana,', University of Salerno, Baronissi (Salerno), Italy.
Batla A; UCL Queen Square Institute of Neurology Department of Clinical and Movement Neurosciences, Queen Square, London WC1N 3BG, United Kingdom.
Holton JL; Queen Square Brain Bank for Neurological Disorders, UCL Institute of Neurology, London, United Kingdom.
Miki Y; Queen Square Brain Bank for Neurological Disorders, UCL Institute of Neurology, London, United Kingdom.
Warner TT; Queen Square Brain Bank for Neurological Disorders, UCL Institute of Neurology, London, United Kingdom.
Bhatia KP; UCL Queen Square Institute of Neurology Department of Clinical and Movement Neurosciences, Queen Square, London WC1N 3BG, United Kingdom. Electronic address: .
Pokaż więcej
Źródło :
Journal of the neurological sciences [J Neurol Sci] 2021 Aug 15; Vol. 427, pp. 117477. Date of Electronic Publication: 2021 May 04.
Typ publikacji :
Journal Article
MeSH Terms :
Multiple System Atrophy*
Parkinson Disease*
Parkinsonian Disorders*/complications
Parkinsonian Disorders*/epidemiology
Supranuclear Palsy, Progressive*
Torticollis*/complications
Torticollis*/epidemiology
Aged ; Aged, 80 and over ; Female ; Humans ; Middle Aged
Czasopismo naukowe
Tytuł :
Early suspicion of progressive supranuclear palsy using dopamine transporter imaging: an illustrative case presenting with levodopa-responsive parkinsonism.
Autorzy :
Ju H; Department of Neurology, Soonchunhyang University Seoul Hospital, Soonchunhyang University School of Medicine, 59 Daesagwan-ro, Yongsan-gu, Seoul, 04401, Republic of Korea.
Lee EJ; Department of Neurology, Soonchunhyang University Seoul Hospital, Soonchunhyang University School of Medicine, 59 Daesagwan-ro, Yongsan-gu, Seoul, 04401, Republic of Korea.
Lee M; Department of Neurology, Soonchunhyang University Seoul Hospital, Soonchunhyang University School of Medicine, 59 Daesagwan-ro, Yongsan-gu, Seoul, 04401, Republic of Korea.
Kwon KY; Department of Neurology, Soonchunhyang University Seoul Hospital, Soonchunhyang University School of Medicine, 59 Daesagwan-ro, Yongsan-gu, Seoul, 04401, Republic of Korea. .
Pokaż więcej
Źródło :
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2021 Aug; Vol. 42 (8), pp. 3435-3437. Date of Electronic Publication: 2021 Apr 16.
Typ publikacji :
Letter
MeSH Terms :
Parkinson Disease*
Parkinsonian Disorders*/diagnostic imaging
Parkinsonian Disorders*/drug therapy
Supranuclear Palsy, Progressive*/diagnostic imaging
Supranuclear Palsy, Progressive*/drug therapy
Dopamine Plasma Membrane Transport Proteins ; Humans ; Levodopa/therapeutic use
Opinia redakcyjna
Tytuł :
Diagnostic performance of loss of nigral hyperintensity on susceptibility-weighted imaging in parkinsonism: an updated meta-analysis.
Autorzy :
Kim PH; Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Olympic-ro 33, Seoul, 05505, Republic of Korea.
Lee DH; Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Olympic-ro 33, Seoul, 05505, Republic of Korea.
Suh CH; Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Olympic-ro 33, Seoul, 05505, Republic of Korea. .
Kim M; Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Olympic-ro 33, Seoul, 05505, Republic of Korea.
Shim WH; Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Olympic-ro 33, Seoul, 05505, Republic of Korea.
Kim SJ; Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Olympic-ro 33, Seoul, 05505, Republic of Korea.
Pokaż więcej
Źródło :
European radiology [Eur Radiol] 2021 Aug; Vol. 31 (8), pp. 6342-6352. Date of Electronic Publication: 2021 Jan 15.
Typ publikacji :
Journal Article; Meta-Analysis
MeSH Terms :
Parkinson Disease*/diagnostic imaging
Parkinsonian Disorders*/diagnostic imaging
Humans ; Magnetic Resonance Imaging ; Sensitivity and Specificity ; Substantia Nigra/diagnostic imaging
Czasopismo naukowe
Tytuł :
Teaching NeuroImages: Parkinsonism Presenting With Watershed Pattern Lesions.
Autorzy :
Dong Y; From the Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China. .
Cheng X; From the Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China.
Dong Q; From the Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China. .
Pokaż więcej
Źródło :
Neurology [Neurology] 2021 Jul 13; Vol. 97 (2), pp. e222-e223. Date of Electronic Publication: 2021 Apr 26.
Typ publikacji :
Journal Article
MeSH Terms :
Brain/*diagnostic imaging
Brain/*pathology
Leukoencephalopathies/*diagnostic imaging
Leukoencephalopathies/*pathology
Parkinsonian Disorders/*diagnostic imaging
Parkinsonian Disorders/*pathology
Diffusion Magnetic Resonance Imaging ; Humans ; Leukoencephalopathies/complications ; Male ; Middle Aged ; Neurology/education ; Parkinsonian Disorders/complications
SCR Disease Name :
Hereditary Diffuse Leukoencephalopathy with Spheroids
Czasopismo naukowe
Tytuł :
Early Onset Degenerative Parkinsonism - Consider SPG7 Mutation.
Autorzy :
Bhattacharjee S; Department of Neurology, Plymouth Hospital NHS Trust, Plymouth, United Kingdom.
Noushad M; Department of Neurology, Plymouth Hospital NHS Trust, Plymouth, United Kingdom.
Sadler M; Department of Neurology, Plymouth Hospital NHS Trust, Plymouth, United Kingdom.
Pokaż więcej
Źródło :
Neurology India [Neurol India] 2021 Jul-Aug; Vol. 69 (4), pp. 1051-1052.
Typ publikacji :
Case Reports
MeSH Terms :
Paraparesis, Spastic*
Parkinsonian Disorders*/diagnostic imaging
Parkinsonian Disorders*/genetics
Spastic Paraplegia, Hereditary*/diagnostic imaging
Spastic Paraplegia, Hereditary*/genetics
ATPases Associated with Diverse Cellular Activities/genetics ; Adult ; Humans ; Magnetic Resonance Imaging ; Male ; Metalloendopeptidases/genetics ; Mutation
Raport
Tytuł :
Reduction of falls in a rat model of PD falls by the M1 PAM TAK-071.
Autorzy :
Kucinski A; Department of Psychology, University of Michigan, 530 Church Street, Ann Arbor, MI, 48103, USA.
Sarter M; Department of Psychology, University of Michigan, 530 Church Street, Ann Arbor, MI, 48103, USA. .
Pokaż więcej
Źródło :
Psychopharmacology [Psychopharmacology (Berl)] 2021 Jul; Vol. 238 (7), pp. 1953-1964. Date of Electronic Publication: 2021 Mar 18.
Typ publikacji :
Journal Article
MeSH Terms :
Accidental Falls/*prevention & control
Muscarinic Agonists/*therapeutic use
Oxidopamine/*toxicity
Parkinsonian Disorders/*chemically induced
Parkinsonian Disorders/*drug therapy
Receptor, Muscarinic M1/*agonists
Administration, Oral ; Allosteric Regulation/drug effects ; Allosteric Regulation/physiology ; Animals ; Basal Forebrain/drug effects ; Basal Forebrain/metabolism ; Cholinergic Neurons/drug effects ; Cholinergic Neurons/metabolism ; Corpus Striatum/drug effects ; Corpus Striatum/metabolism ; Dopamine/metabolism ; Female ; Muscarinic Agonists/pharmacology ; Parkinsonian Disorders/metabolism ; Rats ; Rats, Sprague-Dawley ; Receptor, Muscarinic M1/metabolism
Czasopismo naukowe
Tytuł :
Coexisting Lewy body disease and clinical parkinsonism in amyotrophic lateral sclerosis.
Autorzy :
Forrest SL; Faculty of Medicine, Health and Human Sciences, School of Biomedical Sciences, Dementia Research Centre, Macquarie University, Sydney, NSW, Australia.; Faculty of Medicine and Health, Discipline of Pathology and Charles Perkins Centre, University of Sydney, Sydney, NSW, Australia.
Kim JH; Faculty of Medicine and Health, Discipline of Pathology and Charles Perkins Centre, University of Sydney, Sydney, NSW, Australia.
De Sousa C; Faculty of Medicine and Health, Discipline of Pathology and Charles Perkins Centre, University of Sydney, Sydney, NSW, Australia.
Cheong R; Faculty of Medicine and Health, Discipline of Pathology and Charles Perkins Centre, University of Sydney, Sydney, NSW, Australia.
Crockford DR; Faculty of Medicine and Health, Discipline of Pathology and Charles Perkins Centre, University of Sydney, Sydney, NSW, Australia.
Sheedy D; Faculty of Medicine and Health, Discipline of Pathology and Charles Perkins Centre, University of Sydney, Sydney, NSW, Australia.
Stevens J; Faculty of Medicine and Health, Discipline of Pathology and Charles Perkins Centre, University of Sydney, Sydney, NSW, Australia.
McCrossin T; Faculty of Medicine and Health, Discipline of Pathology and Charles Perkins Centre, University of Sydney, Sydney, NSW, Australia.
Tan RH; Faculty of Medicine and Health, Brain and Mind Centre, University of Sydney, Sydney, NSW, Australia.
McCann H; Neuroscience Research Australia, Randwick, NSW, Australia.
Shepherd CE; Neuroscience Research Australia, Randwick, NSW, Australia.
Rowe DB; Department of Clinical Medicine, Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, NSW, Australia.; Department of Biomedical Science, Faculty of Medicine, Health and Human Sciences, Centre for MND Research, Macquarie University, Sydney, NSW, Australia.
Kiernan MC; Faculty of Medicine and Health, Brain and Mind Centre, University of Sydney, Sydney, NSW, Australia.
Halliday GM; Faculty of Medicine and Health, Brain and Mind Centre, University of Sydney, Sydney, NSW, Australia.; Neuroscience Research Australia, Randwick, NSW, Australia.
Kril JJ; Faculty of Medicine, Health and Human Sciences, School of Biomedical Sciences, Dementia Research Centre, Macquarie University, Sydney, NSW, Australia.; Faculty of Medicine and Health, Discipline of Pathology and Charles Perkins Centre, University of Sydney, Sydney, NSW, Australia.
Pokaż więcej
Źródło :
European journal of neurology [Eur J Neurol] 2021 Jul; Vol. 28 (7), pp. 2192-2199. Date of Electronic Publication: 2021 Apr 16.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Amyotrophic Lateral Sclerosis*/complications
Amyotrophic Lateral Sclerosis*/epidemiology
Amyotrophic Lateral Sclerosis*/genetics
Lewy Body Disease*/complications
Lewy Body Disease*/epidemiology
Lewy Body Disease*/genetics
Parkinsonian Disorders*/complications
Parkinsonian Disorders*/epidemiology
Parkinsonian Disorders*/genetics
DNA-Binding Proteins/genetics ; Humans ; Inclusion Bodies
Czasopismo naukowe
Tytuł :
When does postural instability appear in monogenic parkinsonisms? An individual-patient meta-analysis.
Autorzy :
Marsili L; Department of Neurology, Gardner Family Center for Parkinson's Disease and Movement Disorders, University 6 of Cincinnati, Cincinnati, OH, USA.
Vizcarra JA; Department of Neurology, Gardner Family Center for Parkinson's Disease and Movement Disorders, University 6 of Cincinnati, Cincinnati, OH, USA.; Department of Neurology, Emory University, Atlanta, GA, USA.
Sturchio A; Department of Neurology, Gardner Family Center for Parkinson's Disease and Movement Disorders, University 6 of Cincinnati, Cincinnati, OH, USA.
Dwivedi AK; Division of Biostatistics and Epidemiology, Department of Molecular and Translational Medicine, Texas Tech University Health Sciences Center, El Paso, TX, USA.
Keeling EG; Department of Neurology, Gardner Family Center for Parkinson's Disease and Movement Disorders, University 6 of Cincinnati, Cincinnati, OH, USA.
Patel D; Department of Neurology, Gardner Family Center for Parkinson's Disease and Movement Disorders, University 6 of Cincinnati, Cincinnati, OH, USA.
Mishra M; Department of Neurology, Gardner Family Center for Parkinson's Disease and Movement Disorders, University 6 of Cincinnati, Cincinnati, OH, USA.; St. George's University School of Medicine, St. George, Grenada.
Farooqi A; Department of Neurology, Gardner Family Center for Parkinson's Disease and Movement Disorders, University 6 of Cincinnati, Cincinnati, OH, USA.
Merola A; Wexner Medical Center Department of Neurology, Ohio State University, Columbus, Ohio, USA.
Fasano A; Division of Neurology, Edmond J. Safra Program in Parkinson's Disease and Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, UHN, University of Toronto, Toronto, ON, Canada.; Krembil Brain Institute, Toronto, ON, Canada.; CenteR for Advancing Neurotechnological Innovation To Application (CRANIA), Toronto, ON, Canada.
Mata IF; Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.
Kauffman MA; Consultorio Y Laboratorio de Neurogenética, Centro Universitario de Neurología José María Ramos Mejía, Buenos Aires, Argentina.
Espay AJ; Department of Neurology, Gardner Family Center for Parkinson's Disease and Movement Disorders, University 6 of Cincinnati, Cincinnati, OH, USA. .
Pokaż więcej
Źródło :
Journal of neurology [J Neurol] 2021 Sep; Vol. 268 (9), pp. 3203-3211. Date of Electronic Publication: 2020 May 20.
Typ publikacji :
Journal Article; Meta-Analysis; Review; Systematic Review
MeSH Terms :
Parkinson Disease*/genetics
Parkinsonian Disorders*
Cohort Studies ; Female ; Genotype ; Humans ; Retrospective Studies
Czasopismo naukowe
Tytuł :
A novel Q93H missense mutation in DCTN1 caused distal hereditary motor neuropathy type 7B and Perry syndrome from a Chinese family.
Autorzy :
Zhang J; Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, China.
Wang H; Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, China.
Liu W; School of Mathematics and Statistics, Shandong University, Shandong, China.
Wang J; Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, China.
Zhang J; Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, China.
Chang X; Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, China.
Huang S; Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, China.
Pang X; Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, China.
Guo J; Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, China.
Wang Q; Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, China.
Zhang W; Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, China. .
Pokaż więcej
Źródło :
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2021 Sep; Vol. 42 (9), pp. 3695-3705. Date of Electronic Publication: 2021 Jan 14.
Typ publikacji :
Journal Article
MeSH Terms :
Mutation, Missense*/genetics
Parkinsonian Disorders*
China ; Depression ; Dynactin Complex/genetics ; Humans ; Hypoventilation ; Mutation
SCR Disease Name :
Perry Syndrome
Czasopismo naukowe
Tytuł :
Cognitive and behavioral profile of progressive supranuclear palsy and its phenotypes.
Autorzy :
Horta-Barba A; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Mas Casanovas, 90-08041, Barcelona, Spain.; Universitat Autònoma de Barcelona (U.A.B.), Barcelona, Spain.; Institut d'Investigacions Biomèdiques- Sant Pau (IIB-Sant Pau), Barcelona, Spain.; Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain.; Faculty of Health Sciences, Universitat Oberta de Catalunya (UOC), Barcelona, Spain.
Pagonabarraga J; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Mas Casanovas, 90-08041, Barcelona, Spain. .; Universitat Autònoma de Barcelona (U.A.B.), Barcelona, Spain. .; Institut d'Investigacions Biomèdiques- Sant Pau (IIB-Sant Pau), Barcelona, Spain. .; Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain. .
Martínez-Horta S; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Mas Casanovas, 90-08041, Barcelona, Spain.; Universitat Autònoma de Barcelona (U.A.B.), Barcelona, Spain.; Institut d'Investigacions Biomèdiques- Sant Pau (IIB-Sant Pau), Barcelona, Spain.; Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain.
Busteed L; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Mas Casanovas, 90-08041, Barcelona, Spain.
Pascual-Sedano B; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Mas Casanovas, 90-08041, Barcelona, Spain.; Universitat Autònoma de Barcelona (U.A.B.), Barcelona, Spain.; Institut d'Investigacions Biomèdiques- Sant Pau (IIB-Sant Pau), Barcelona, Spain.; Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain.; Faculty of Health Sciences, Universitat Oberta de Catalunya (UOC), Barcelona, Spain.
Illán-Gala I; Institut d'Investigacions Biomèdiques- Sant Pau (IIB-Sant Pau), Barcelona, Spain.; Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain.; Memory Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Marin-Lahoz J; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Mas Casanovas, 90-08041, Barcelona, Spain.; Universitat Autònoma de Barcelona (U.A.B.), Barcelona, Spain.; Institut d'Investigacions Biomèdiques- Sant Pau (IIB-Sant Pau), Barcelona, Spain.
Aracil-Bolaños I; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Mas Casanovas, 90-08041, Barcelona, Spain.; Universitat Autònoma de Barcelona (U.A.B.), Barcelona, Spain.; Institut d'Investigacions Biomèdiques- Sant Pau (IIB-Sant Pau), Barcelona, Spain.; Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain.
Pérez-Pérez J; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Mas Casanovas, 90-08041, Barcelona, Spain.; Universitat Autònoma de Barcelona (U.A.B.), Barcelona, Spain.; Institut d'Investigacions Biomèdiques- Sant Pau (IIB-Sant Pau), Barcelona, Spain.; Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain.
Sampedro F; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Mas Casanovas, 90-08041, Barcelona, Spain.; Institut d'Investigacions Biomèdiques- Sant Pau (IIB-Sant Pau), Barcelona, Spain.; Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain.
Bejr-Kasem H; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Mas Casanovas, 90-08041, Barcelona, Spain.; Universitat Autònoma de Barcelona (U.A.B.), Barcelona, Spain.; Institut d'Investigacions Biomèdiques- Sant Pau (IIB-Sant Pau), Barcelona, Spain.; Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain.; Faculty of Health Sciences, Universitat Oberta de Catalunya (UOC), Barcelona, Spain.
Kulisevsky J; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Mas Casanovas, 90-08041, Barcelona, Spain. .; Universitat Autònoma de Barcelona (U.A.B.), Barcelona, Spain. .; Institut d'Investigacions Biomèdiques- Sant Pau (IIB-Sant Pau), Barcelona, Spain. .; Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain. .; Faculty of Health Sciences, Universitat Oberta de Catalunya (UOC), Barcelona, Spain. .
Pokaż więcej
Źródło :
Journal of neurology [J Neurol] 2021 Sep; Vol. 268 (9), pp. 3400-3408. Date of Electronic Publication: 2021 Mar 11.
Typ publikacji :
Journal Article
MeSH Terms :
Parkinsonian Disorders*
Supranuclear Palsy, Progressive*
Cognition ; Humans ; Neuropsychological Tests ; Phenotype
Czasopismo naukowe
Tytuł :
Discrimination of idiopathic Parkinson's disease and vascular parkinsonism based on gait time series and the levodopa effect.
Autorzy :
Fernandes C; Algoritmi Center, University of Minho, Portugal. Electronic address: .
Ferreira F; Center of Mathematics, University of Minho, Portugal.
Lopes RL; INESC TEC, Porto, Portugal.
Bicho E; Algoritmi Center, University of Minho, Portugal. Electronic address: .
Erlhagen W; Center of Mathematics, University of Minho, Portugal. Electronic address: .
Sousa N; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Portugal; ICVS-3Bs PT Government Associate Laboratory, Portugal. Electronic address: .
Gago MF; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Portugal; ICVS-3Bs PT Government Associate Laboratory, Portugal; Neurology Department, Hospital da Senhora da Oliveira, Guimarães, EPE, Portugal.
Pokaż więcej
Źródło :
Journal of biomechanics [J Biomech] 2021 Aug 26; Vol. 125, pp. 110214. Date of Electronic Publication: 2021 May 11.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Parkinson Disease*/drug therapy
Parkinsonian Disorders*/drug therapy
Antiparkinson Agents ; Gait ; Humans ; Levodopa/therapeutic use
Czasopismo naukowe
Tytuł :
Rare Gain-of-Function KCND3 Variant Associated with Cerebellar Ataxia, Parkinsonism, Cognitive Dysfunction, and Brain Iron Accumulation.
Autorzy :
Hsiao CT; Department of Neurology, Taipei Veterans General Hospital, Taipei 11217, Taiwan.; Department of Physiology, College of Medicine, National Taiwan University, Taipei 10051, Taiwan.; Department of Neurology, School of Medicine, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan.; Brain Research Center, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan.
Tropea TF; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Fu SJ; Department of Physiology, College of Medicine, National Taiwan University, Taipei 10051, Taiwan.; Institute of Anatomy and Cell Biology, College of Medicine, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan.
Bardakjian TM; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Gonzalez-Alegre P; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Soong BW; Department of Neurology, School of Medicine, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan.; Brain Research Center, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan.; Department of Neurology, Shuang Ho Hospital and Taipei Neuroscience Institute, Taipei Medical University, Taipei 11031, Taiwan.
Tang CY; Department of Physiology, College of Medicine, National Taiwan University, Taipei 10051, Taiwan.
Jeng CJ; Brain Research Center, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan.; Institute of Anatomy and Cell Biology, College of Medicine, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan.
Pokaż więcej
Źródło :
International journal of molecular sciences [Int J Mol Sci] 2021 Jul 31; Vol. 22 (15). Date of Electronic Publication: 2021 Jul 31.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Gain of Function Mutation*
Cognitive Dysfunction/*genetics
Iron/*metabolism
Parkinsonian Disorders/*genetics
Shal Potassium Channels/*genetics
Spinocerebellar Ataxias/*genetics
Action Potentials ; Aged ; Brain/metabolism ; Cognitive Dysfunction/pathology ; HEK293 Cells ; Humans ; Male ; Parkinsonian Disorders/pathology ; Protein Domains ; Shal Potassium Channels/chemistry ; Shal Potassium Channels/metabolism ; Spinocerebellar Ataxias/pathology
Czasopismo naukowe
Tytuł :
Hydrogen sulfide attenuates induction and prevents progress of the 6-hydroxydopamine-induced Parkinsonism in rat through activation of ATP-sensitive potassium channels and suppression of ER stress.
Autorzy :
Minaei A; Cellular and Molecular Research Center, Research Institute for Prevention of Non-Communicable Disease, Qazvin University of Medical Sciences, Qazvin, Iran.
Sarookhani MR; Cellular and Molecular Research Center, Research Institute for Prevention of Non-Communicable Disease, Qazvin University of Medical Sciences, Qazvin, Iran.
Haghdoost-Yazdi H; Cellular and Molecular Research Center, Research Institute for Prevention of Non-Communicable Disease, Qazvin University of Medical Sciences, Qazvin, Iran. Electronic address: .
Rajaei F; Cellular and Molecular Research Center, Research Institute for Prevention of Non-Communicable Disease, Qazvin University of Medical Sciences, Qazvin, Iran.
Pokaż więcej
Źródło :
Toxicology and applied pharmacology [Toxicol Appl Pharmacol] 2021 Jul 15; Vol. 423, pp. 115558. Date of Electronic Publication: 2021 May 04.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Disease Progression*
Endoplasmic Reticulum Stress/*drug effects
Hydrogen Sulfide/*therapeutic use
KATP Channels/*metabolism
Oxidopamine/*toxicity
Parkinsonian Disorders/*metabolism
Animals ; Endoplasmic Reticulum Stress/physiology ; Gasotransmitters/pharmacology ; Gasotransmitters/therapeutic use ; Hydrogen Sulfide/pharmacology ; Male ; Parkinsonian Disorders/chemically induced ; Rats ; Rats, Wistar
Czasopismo naukowe
Tytuł :
Catatonia as the Initial Manifestation of Dementia with Lewy Bodies.
Autorzy :
Saito Y; Department of Psychiatry, Yamagata University School of Medicine, Iidanishi, Yamagata, Japan.; Department of Psychiatry, Okitama Public General Hospital, Nishiotsuka, Yamagata, Japan.
Noto K; Department of Psychiatry, Yamagata University School of Medicine, Iidanishi, Yamagata, Japan.
Kobayashi R; Department of Psychiatry, Yamagata University School of Medicine, Iidanishi, Yamagata, Japan.
Suzuki A; Department of Psychiatry, Yamagata University School of Medicine, Iidanishi, Yamagata, Japan.
Morioka D; Department of Psychiatry, Yamagata University School of Medicine, Iidanishi, Yamagata, Japan.
Hayashi H; Department of Psychiatry, Yamagata University School of Medicine, Iidanishi, Yamagata, Japan.
Otani K; Department of Psychiatry, Yamagata University School of Medicine, Iidanishi, Yamagata, Japan.
Pokaż więcej
Źródło :
The American journal of case reports [Am J Case Rep] 2021 Jul 07; Vol. 22, pp. e932018. Date of Electronic Publication: 2021 Jul 07.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Catatonia*/diagnosis
Catatonia*/drug therapy
Catatonia*/etiology
Cognitive Dysfunction*
Lewy Body Disease*/complications
Lewy Body Disease*/diagnosis
Lewy Body Disease*/drug therapy
Parkinsonian Disorders*
Aged, 80 and over ; Female ; Humans ; Lewy Bodies
Czasopismo naukowe
Tytuł :
Genotype-Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic Review.
Autorzy :
Wittke C; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Petkovic S; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Dobricic V; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Schaake S; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Respondek G; Department of Neurology, Technische Universität München, Munich, Germany.; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Weissbach A; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Madoev H; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Trinh J; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Vollstedt EJ; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Kuhnke N; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Lohmann K; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Dulovic Mahlow M; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Marras C; Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.
König IR; Institute of Medical Biometry and Statistics, University of Luebeck, Luebeck, Germany.
Stamelou M; Parkinson's Disease and Movement Disorders Department, HYGEIA Hospital, Athens, Greece.; School of Medicine, European University of Cyprus, Nicosia, Cyprus.; Neurology Clinic, Philipps-University, Marburg, Germany.
Bonifati V; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
Lill CM; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Kasten M; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.; Department of Psychiatry and Psychotherapy, University of Luebeck, Luebeck, Germany.
Huppertz HJ; Swiss Epilepsy Center, Klinik Lengg AG, Zurich, Switzerland.
Höglinger G; German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.; Department of Neurology, Hannover Medical School, Hannover, Germany.
Klein C; Institute of Neurogenetics, University of Luebeck, Luebeck, Germany.
Pokaż więcej
Corporate Authors :
MDS‐endorsed PSP Study Group
Źródło :
Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2021 Jul; Vol. 36 (7), pp. 1499-1510. Date of Electronic Publication: 2021 Mar 19.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Systematic Review
MeSH Terms :
Parkinson Disease*
Parkinsonian Disorders*/genetics
Genotype ; Humans ; Levodopa ; Phenotype
Czasopismo naukowe
Tytuł :
Parkinsonism as a Sequela of SARS-CoV-2 Infection: Pure Hypoxic Injury or Additional COVID-19-Related Response?
Autorzy :
Fearon C; Edmond J. Safra Program in Parkinson's Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital - University Health Network (UHN), Division of Neurology, University of Toronto, Toronto, Ontario, Canada.
Mikulis DJ; Division of Neuroradiology, Joint Department of Medical Imaging, Toronto Western Hospital, University Health Network, Toronto, Ontario, Canada.
Lang AE; Edmond J. Safra Program in Parkinson's Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital - University Health Network (UHN), Division of Neurology, University of Toronto, Toronto, Ontario, Canada.
Pokaż więcej
Źródło :
Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2021 Jul; Vol. 36 (7), pp. 1483-1484. Date of Electronic Publication: 2021 May 27.
Typ publikacji :
Letter
MeSH Terms :
COVID-19*
Parkinsonian Disorders*/etiology
Disease Progression ; Humans ; SARS-CoV-2
Opinia redakcyjna
Tytuł :
Emerging concepts on bradykinesia in non-parkinsonian conditions.
Autorzy :
Paparella G; IRCCS Neuromed, Pozzilli, Italy.
Fasano A; Edmond J. Safra Program in Parkinson's Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, University Health Network, Toronto, Ontario, Canada.; Division of Neurology, University of Toronto, Toronto, Ontario, Canada.; Krembil Brain Institute, Toronto, Ontario, Canada.
Hallett M; Human Motor Control Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.
Berardelli A; IRCCS Neuromed, Pozzilli, Italy.; Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.
Bologna M; IRCCS Neuromed, Pozzilli, Italy.; Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.
Pokaż więcej
Źródło :
European journal of neurology [Eur J Neurol] 2021 Jul; Vol. 28 (7), pp. 2403-2422. Date of Electronic Publication: 2021 May 18.
Typ publikacji :
Journal Article; Research Support, N.I.H., Intramural; Review
MeSH Terms :
Dystonia*
Essential Tremor*
Parkinson Disease*/complications
Parkinsonian Disorders*
Humans ; Hypokinesia/etiology
Czasopismo naukowe
Tytuł :
X-Linked Parkinsonism: Phenotypic and Genetic Heterogeneity.
Autorzy :
Di Lazzaro G; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.; Department of Systems Medicine, Tor Vergata University of Rome, Rome, Italy.
Magrinelli F; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.; Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Estevez-Fraga C; Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Valente EM; Department of Molecular Medicine, University of Pavia, Pavia, Italy.; IRCCS Mondino Foundation, Pavia, Italy.
Pisani A; IRCCS Mondino Foundation, Pavia, Italy.; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Bhatia KP
Pokaż więcej
Źródło :
Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2021 Jul; Vol. 36 (7), pp. 1511-1525. Date of Electronic Publication: 2021 May 07.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Dystonic Disorders*
Genetic Diseases, X-Linked*/genetics
Parkinson Disease*
Parkinsonian Disorders*/genetics
Carrier Proteins/genetics ; Child ; Genetic Heterogeneity ; Humans ; Male
Czasopismo naukowe

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies