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Wyświetlanie 1-13 z 13
Tytuł :
Hippocampal α-synuclein pathology correlates with memory impairment in multiple system atrophy.
Autorzy :
Miki Y; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.; Department of Neuropathology, Institute of Brain Science, Hirosaki University Graduate School of Medicine, Hirosaki 036-8562, Japan.
Foti SC; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.
Hansen D; Reta Lila Weston Institute of Neurological Studies, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.
Strand KM; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.
Asi YT; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.
Tsushima E; Department of Comprehensive Rehabilitation Science, Hirosaki University Graduate School of Health Sciences, Hirosaki 036-8564, Japan.
Jaunmuktane Z; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.
Lees AJ; Reta Lila Weston Institute of Neurological Studies, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.
Warner TT; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.; Reta Lila Weston Institute of Neurological Studies, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.
Quinn N; UCL Queen Square Institute of Neurology, London WC1N 3BG, UK.
Ling H; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.; Reta Lila Weston Institute of Neurological Studies, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.
Holton JL; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London WC1N 1PJ, UK.
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Źródło :
Brain : a journal of neurology [Brain] 2020 Jun 01; Vol. 143 (6), pp. 1798-1810.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
Czasopismo naukowe
Tytuł :
Improving diagnostic accuracy of multiple system atrophy: a clinicopathological study.
Autorzy :
Miki Y; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London, UK.; Department of Neuropathology, Institute of Brain Science, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Foti SC; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London, UK.
Asi YT; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London, UK.
Tsushima E; Department of Comprehensive Rehabilitation Science, Hirosaki University Graduate School of Health Sciences, Hirosaki, Japan.
Quinn N; UCL Queen Square Institute of Neurology, London, UK.
Ling H; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London, UK.; Reta Lila Weston Institute of Neurological Studies, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London, UK.
Holton JL; Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology, 1 Wakefield Street, London, UK.
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Źródło :
Brain : a journal of neurology [Brain] 2019 Sep 01; Vol. 142 (9), pp. 2813-2827.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Multiple System Atrophy/*pathology
Multiple System Atrophy/*physiopathology
Adult ; Aged ; Aged, 80 and over ; Diagnosis, Differential ; Female ; Humans ; Lewy Body Disease/diagnosis ; Lewy Body Disease/pathology ; Lewy Body Disease/physiopathology ; Male ; Middle Aged ; Multiple System Atrophy/diagnosis ; Retrospective Studies ; Supranuclear Palsy, Progressive/diagnosis ; Supranuclear Palsy, Progressive/pathology ; Supranuclear Palsy, Progressive/physiopathology ; Tissue Banks/standards
Czasopismo naukowe
Tytuł :
TDP-43 extracted from frontotemporal lobar degeneration subject brains displays distinct aggregate assemblies and neurotoxic effects reflecting disease progression rates.
Autorzy :
Laferrière F; Institute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Maniecka Z; Institute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Pérez-Berlanga M; Institute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Hruska-Plochan M; Institute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Gilhespy L; Institute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Hock EM; Institute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Wagner U; Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
Afroz T; Institute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Boersema PJ; Institute of Biochemistry, Department of Biology, ETH Zurich (ETHZ), Zurich, Switzerland.
Barmettler G; Center for Microscopy and Image Analysis, University of Zurich, Zurich, Switzerland.
Foti SC; Queen Square Brain Bank for Neurological diseases, Department of Movement Disorders, UCL Institute of Neurology, London, UK.; Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK.
Asi YT; Queen Square Brain Bank for Neurological diseases, Department of Movement Disorders, UCL Institute of Neurology, London, UK.; Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK.
Isaacs AM; Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK.; UK Dementia Research Institute at UCL, UCL Institute of Neurology, London, UK.
Al-Amoudi A; Center for Cellular Imaging and NanoAnalytics (C-CINA), Biozentrum, University of Basel, Basel, Switzerland.
Lewis A; Center for Cellular Imaging and NanoAnalytics (C-CINA), Biozentrum, University of Basel, Basel, Switzerland.
Stahlberg H; Center for Cellular Imaging and NanoAnalytics (C-CINA), Biozentrum, University of Basel, Basel, Switzerland.
Ravits J; Department of Neuroscience, University of California, San Diego, La Jolla, CA, USA.
De Giorgi F; INSERM U1084, Laboratoire des Neurosciences Expérimentales et Cliniques, Université de Poitiers, Poitiers, France.; Université de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France.; CNRS, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France.
Ichas F; INSERM U1084, Laboratoire des Neurosciences Expérimentales et Cliniques, Université de Poitiers, Poitiers, France.; Université de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France.; CNRS, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France.
Bezard E; Université de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France.; CNRS, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France.
Picotti P; Center for Microscopy and Image Analysis, University of Zurich, Zurich, Switzerland.
Lashley T; Queen Square Brain Bank for Neurological diseases, Department of Movement Disorders, UCL Institute of Neurology, London, UK.; Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK.
Polymenidou M; Institute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland. .
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Źródło :
Nature neuroscience [Nat Neurosci] 2019 Jan; Vol. 22 (1), pp. 65-77. Date of Electronic Publication: 2018 Dec 17.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Brain/*metabolism
DNA-Binding Proteins/*metabolism
Frontotemporal Lobar Degeneration/*metabolism
Protein Aggregates/*physiology
Animals ; Brain/pathology ; Disease Progression ; Frontotemporal Lobar Degeneration/pathology ; HEK293 Cells ; Humans ; Inclusion Bodies/metabolism ; Inclusion Bodies/pathology ; Mass Spectrometry ; Mice ; Neurons/metabolism ; Neurons/pathology ; Phosphorylation
Czasopismo naukowe
Tytuł :
Correction to: Expanding the genetic heterogeneity of intellectual disability.
Autorzy :
Anazi S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Maddirevula S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Salpietro V; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Asi YT; Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
Alsahli S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Alhashem A; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Shamseldin HE; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
AlZahrani F; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Patel N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Ibrahim N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Abdulwahab FM; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Hashem M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Alhashmi N; Department of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman.
Al Murshedi F; Department of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman.
Al Kindy A; Department of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman.
Alshaer A; Pediatric Neurology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Rumayyan A; King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.; Neurology Division, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Al Tala S; Department of Pediatrics and Genetic Unit, Armed Forces Hospital Khamis Mushayt, Riyadh, Saudi Arabia.
Kurdi W; Department of Obstetrics and Gynecology, King Faisal Specialist Hospital, Riyadh, Saudi Arabia.
Alsaman A; Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Alasmari A; Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Banu S; Department of Pediatric Neurology, ICH and SSF Hospital Mirpur, Dhaka, 1216, Bangladesh.
Sultan T; Department of Pediatric Neurology, Institute of Child Health and The Children's Hospital Lahore, 381-D/2, Lahore, Pakistan.
Saleh MM; Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Alkuraya H; Department of Ophthalmology, Specialized Medical Center Hospital, Riyadh, Saudi Arabia.
Salih MA; Division of Pediatric Neurology, Department of Pediatrics, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Aldhalaan H; Pediatric Neurology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Ben-Omran T; Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
Al Musafri F; Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
Ali R; Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
Suleiman J; Division of Neurology, Department of Pediatrics, Tawam Hospital, Al Ain, United Arab Emirates.
Tabarki B; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
El-Hattab AW; Division of Clinical Genetics and Metabolic Disorders, Department of Pediatrics, Tawam Hospital, Al-Ain, United Arab Emirates.
Bupp C; Spectrum Health Genetics, Grand Rapids, MI, USA.
Alfadhel M; Genetics Division, Department of Pediatrics, King Abdullah International Medical Research Centre, King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Al Tassan N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Monies D; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Arold ST; Division of Biological and Environmental Sciences and Engineering (BESE), Computational Bioscience Research Center (CBRC), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Abouelhoda M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Lashley T; Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
Houlden H; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Faqeih E; Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. .; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia. .; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia. .; Spectrum Health Genetics, Grand Rapids, MI, USA. .; Division of Biological and Environmental Sciences and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia. .
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Źródło :
Human genetics [Hum Genet] 2018 Jan; Vol. 137 (1), pp. 105-109.
Typ publikacji :
Journal Article; Published Erratum
Czasopismo naukowe
Tytuł :
Expanding the genetic heterogeneity of intellectual disability.
Autorzy :
Anazi S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Maddirevula S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Salpietro V; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Asi YT; Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
Alsahli S; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Alhashem A; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Shamseldin HE; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
AlZahrani F; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Patel N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Ibrahim N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Abdulwahab FM; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Hashem M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Alhashmi N; Department of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman.
Al Murshedi F; Department of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman.
Al Kindy A; Department of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman.
Alshaer A; Pediatric Neurology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Rumayyan A; King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.; Neurology Division, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Al Tala S; Department of Pediatrics and Genetic Unit, Armed Forces Hospital, Khamis Mushayt, Saudi Arabia.
Kurdi W; Department of Obstetrics and Gynecology, King Faisal Specialist Hospital, Riyadh, Saudi Arabia.
Alsaman A; Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Alasmari A; Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Banu S; Department of Pediatric Neurology, ICH and SSF Hospital Mirpur, Dhaka, 1216, Bangladesh.
Sultan T; Department of Pediatric Neurology, Institute of Child Health and The Children's Hospital Lahore, 381-D/2, Lahore, Pakistan.
Saleh MM; Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Alkuraya H; Department of Ophthalmology, Specialized Medical Center Hospital, Riyadh, Saudi Arabia.
Salih MA; Division of Pediatric Neurology, Department of Pediatrics, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Aldhalaan H; Pediatric Neurology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Ben-Omran T; Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
Al Musafri F; Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
Ali R; Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
Suleiman J; Division of Neurology, Department of Pediatrics, Tawam Hospital, Al Ain, United Arab Emirates.
Tabarki B; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
El-Hattab AW; Division of Clinical Genetics and Metabolic Disorders, Department of Pediatrics, Tawam Hospital, Al-Ain, United Arab Emirates.
Bupp C; Spectrum Health Genetics, Grand Rapids, MI, USA.
Alfadhel M; Genetics Division, Department of Pediatrics, King Abdullah International Medical Research Centre, King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Al Tassan N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Monies D; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Arold ST; Division of Biological and Environmental Sciences and Engineering (BESE), Computational Bioscience Research Center (CBRC), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Abouelhoda M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Lashley T; Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
Houlden H; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Faqeih E; Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. .; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia. .; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia. .; Spectrum Health Genetics, Grand Rapids, MI, USA. .; Division of Biological and Environmental Sciences and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia. .
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Źródło :
Human genetics [Hum Genet] 2017 Nov; Vol. 136 (11-12), pp. 1419-1429. Date of Electronic Publication: 2017 Sep 22.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Genetic Heterogeneity*
Genetic Markers*
Mutation*
Exome/*genetics
Intellectual Disability/*genetics
Female ; Genetic Predisposition to Disease ; High-Throughput Nucleotide Sequencing ; Humans ; Male ; Pedigree ; Protein Conformation
Czasopismo naukowe
Tytuł :
Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar Degeneration.
Autorzy :
Davidson YS; Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Salford Royal Hospital, M6 8HD, Salford, UK.
Robinson AC; Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Salford Royal Hospital, M6 8HD, Salford, UK.
Flood L; Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Salford Royal Hospital, M6 8HD, Salford, UK.
Rollinson S; Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, A V Hill Building, Manchester, M13 9PT, UK.
Benson BC; Institute of Neurology, Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, University College London, 1 Wakefield St, London, WC1N 1PJ, UK.
Asi YT; Institute of Neurology, Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, University College London, 1 Wakefield St, London, WC1N 1PJ, UK.
Richardson A; Cerebral Function Unit, Greater Manchester Neurosciences Centre, Salford Royal Hospital, Stott Lane, M6 8HD, Salford, UK.
Jones M; Cerebral Function Unit, Greater Manchester Neurosciences Centre, Salford Royal Hospital, Stott Lane, M6 8HD, Salford, UK.
Snowden JS; Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Salford Royal Hospital, M6 8HD, Salford, UK.; Cerebral Function Unit, Greater Manchester Neurosciences Centre, Salford Royal Hospital, Stott Lane, M6 8HD, Salford, UK.
Pickering-Brown S; Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, A V Hill Building, Manchester, M13 9PT, UK.
Lashley T; Institute of Neurology, Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, University College London, 1 Wakefield St, London, WC1N 1PJ, UK.
Mann DMA; Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Salford Royal Hospital, M6 8HD, Salford, UK. .
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Źródło :
Acta neuropathologica communications [Acta Neuropathol Commun] 2017 Jun 30; Vol. 5 (1), pp. 54. Date of Electronic Publication: 2017 Jun 30.
Typ publikacji :
Journal Article
MeSH Terms :
Brain/*metabolism
Frontotemporal Lobar Degeneration/*metabolism
Neurites/*metabolism
RNA-Binding Proteins/*metabolism
Aged ; Aged, 80 and over ; Brain/pathology ; C9orf72 Protein/genetics ; Cytoplasm/metabolism ; Cytoplasm/pathology ; DNA-Binding Proteins/metabolism ; Female ; Frontotemporal Lobar Degeneration/genetics ; Frontotemporal Lobar Degeneration/pathology ; Humans ; Inclusion Bodies/metabolism ; Inclusion Bodies/pathology ; Intercellular Signaling Peptides and Proteins/genetics ; Male ; Middle Aged ; Neurites/pathology ; Progranulins ; tau Proteins/genetics ; tau Proteins/metabolism
Czasopismo naukowe
Tytuł :
Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation.
Autorzy :
Kiely AP; Department of Molecular Neuroscience, Queen Square Brain Bank, UCL Institute of Neurology, Queen Square, WC1N 3BG, London, UK. .
Ling H; Department of Molecular Neuroscience, Queen Square Brain Bank, UCL Institute of Neurology, Queen Square, WC1N 3BG, London, UK. .
Asi YT; Department of Molecular Neuroscience, Queen Square Brain Bank, UCL Institute of Neurology, Queen Square, WC1N 3BG, London, UK. .
Kara E; Alzheimer's Disease Research Centre, Harvard medical school & Massachusetts General Hospital, 114 16th Street, Charlestown, MA, 02129, USA. .
Proukakis C; Department of Clinical Neuroscience, UCL Institute of Neurology, London, UK. .
Schapira AH; Department of Clinical Neuroscience, UCL Institute of Neurology, London, UK. .
Morris HR; Department of Clinical Neuroscience, UCL Institute of Neurology, London, UK. .
Roberts HC; Academic Geriatric Medicine, University of Southampton, Southampton, UK. .
Lubbe S; Department of Clinical Neuroscience, UCL Institute of Neurology, London, UK. .
Limousin P; Sobell Department of Motor Neuroscience and Movement Disorders, Unit of Functional Neurosurgery, UCL Institute of Neurology, UCL, London, UK. .
Lewis PA; Department of Molecular Neuroscience and Reta Lila Weston Institute of Neurological Studies, UCL Institute of Neurology, London, UK. .; School of Pharmacy, University of Reading, Whiteknights, Reading, UK. .
Lees AJ; Department of Molecular Neuroscience, Queen Square Brain Bank, UCL Institute of Neurology, Queen Square, WC1N 3BG, London, UK. .; Department of Molecular Neuroscience and Reta Lila Weston Institute of Neurological Studies, UCL Institute of Neurology, London, UK. .
Quinn N; National Hospital for Neurology and Neurosurgery, Queen Square, London, UK. .
Hardy J; Department of Molecular Neuroscience, Queen Square Brain Bank, UCL Institute of Neurology, Queen Square, WC1N 3BG, London, UK. .; Department of Molecular Neuroscience and Reta Lila Weston Institute of Neurological Studies, UCL Institute of Neurology, London, UK. .
Love S; Clinical Neurosciences, University of Bristol, Bristol, UK. .
Revesz T; Department of Molecular Neuroscience, Queen Square Brain Bank, UCL Institute of Neurology, Queen Square, WC1N 3BG, London, UK. .
Houlden H; Department of Molecular Neuroscience and Reta Lila Weston Institute of Neurological Studies, UCL Institute of Neurology, London, UK. .
Holton JL; Department of Molecular Neuroscience, Queen Square Brain Bank, UCL Institute of Neurology, Queen Square, WC1N 3BG, London, UK. .
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Źródło :
Molecular neurodegeneration [Mol Neurodegener] 2015 Aug 27; Vol. 10, pp. 41. Date of Electronic Publication: 2015 Aug 27.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Amino Acid Substitution*
Mutation, Missense*
Point Mutation*
Brain/*pathology
Multiple System Atrophy/*genetics
Parkinson Disease/*genetics
alpha-Synuclein/*genetics
Age of Onset ; Aged ; Antiparkinson Agents/therapeutic use ; Codon/genetics ; Dementia/genetics ; Dementia/pathology ; Disease Progression ; Female ; Gene Duplication ; Humans ; Inclusion Bodies/ultrastructure ; Male ; Middle Aged ; Multiple System Atrophy/pathology ; Parkinson Disease/drug therapy ; Parkinson Disease/pathology ; Parkinson Disease/psychology ; Pedigree ; Protein Conformation ; Protein Processing, Post-Translational ; Symptom Assessment ; Young Adult ; alpha-Synuclein/chemistry
Czasopismo naukowe
Tytuł :
Minimal change multiple system atrophy: an aggressive variant?
Autorzy :
Ling H; Queen Square Brain Bank, Department of Molecular Neuroscience, UCL Institute of Neurology, UK.; Reta Lila Weston Institute of Neurological Studies, UCL Institute of Neurology, London, UK.
Asi YT; Queen Square Brain Bank, Department of Molecular Neuroscience, UCL Institute of Neurology, UK.
Petrovic IN; Reta Lila Weston Institute of Neurological Studies, UCL Institute of Neurology, London, UK.; Institute of Neurology, School of Medicine, Belgrade, Serbia.
Ahmed Z; Queen Square Brain Bank, Department of Molecular Neuroscience, UCL Institute of Neurology, UK.
Prashanth LK; University of Toronto, Toronto, Canada.; Edmond J. Safra Program in Parkinson's Disease, Toronto Western Hospital, Toronto, Canada.
Hazrati LN; University of Toronto, Toronto, Canada.; Edmond J. Safra Program in Parkinson's Disease, Toronto Western Hospital, Toronto, Canada.
Nishizawa M; Department of Neurology, Niigata University, Japan.
Ozawa T; Department of Neurology, Niigata University, Japan.
Lang A; University of Toronto, Toronto, Canada.; Edmond J. Safra Program in Parkinson's Disease, Toronto Western Hospital, Toronto, Canada.
Lees AJ; Queen Square Brain Bank, Department of Molecular Neuroscience, UCL Institute of Neurology, UK.; Reta Lila Weston Institute of Neurological Studies, UCL Institute of Neurology, London, UK.
Revesz T; Queen Square Brain Bank, Department of Molecular Neuroscience, UCL Institute of Neurology, UK.
Holton JL; Queen Square Brain Bank, Department of Molecular Neuroscience, UCL Institute of Neurology, UK.
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Źródło :
Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2015 Jun; Vol. 30 (7), pp. 960-7. Date of Electronic Publication: 2015 Apr 08.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Tissue Banks*
Brain/*pathology
Inclusion Bodies/*pathology
Multiple System Atrophy/*classification
Multiple System Atrophy/*pathology
alpha-Synuclein/*metabolism
Adult ; Age of Onset ; Aged ; Aged, 80 and over ; Brain/metabolism ; Humans ; Inclusion Bodies/metabolism ; Male ; Middle Aged ; Multiple System Atrophy/metabolism
Czasopismo naukowe
Tytuł :
Neuropathological features of multiple system atrophy with cognitive impairment.
Autorzy :
Asi YT; Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Ling H
Ahmed Z
Lees AJ
Revesz T
Holton JL
Pokaż więcej
Źródło :
Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2014 Jun; Vol. 29 (7), pp. 884-8. Date of Electronic Publication: 2014 Apr 18.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Brain/*pathology
Cognition/*physiology
Cognition Disorders/*pathology
Multiple System Atrophy/*pathology
Nerve Degeneration/*pathology
Neurons/*pathology
Aged ; Aged, 80 and over ; Cognition Disorders/etiology ; Female ; Humans ; Male ; Middle Aged ; Multiple System Atrophy/complications ; Nerve Degeneration/complications
Czasopismo naukowe
Tytuł :
Alpha-synuclein mRNA expression in oligodendrocytes in MSA.
Autorzy :
Asi YT; Queen Square Brain Bank, Department of Molecular Neuroscience, UCL Institute of Neurology, London, United Kingdom.
Simpson JE
Heath PR
Wharton SB
Lees AJ
Revesz T
Houlden H
Holton JL
Pokaż więcej
Źródło :
Glia [Glia] 2014 Jun; Vol. 62 (6), pp. 964-70. Date of Electronic Publication: 2014 Mar 03.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression Regulation*
Brain/*metabolism
Multiple System Atrophy/*metabolism
Oligodendroglia/*metabolism
RNA, Messenger/*biosynthesis
alpha-Synuclein/*biosynthesis
Aged ; Aged, 80 and over ; Brain/pathology ; Cohort Studies ; Female ; Humans ; Male ; Middle Aged ; Multiple System Atrophy/pathology ; Oligodendroglia/pathology
Czasopismo naukowe
Tytuł :
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?
Autorzy :
Kiely AP; Queen Square Brain Bank, UCL Institute of Neurology, London, UK. />Asi YT
Kara E
Limousin P
Ling H
Lewis P
Proukakis C
Quinn N
Lees AJ
Hardy J
Revesz T
Houlden H
Holton JL
Pokaż więcej
Źródło :
Acta neuropathologica [Acta Neuropathol] 2013 May; Vol. 125 (5), pp. 753-69. Date of Electronic Publication: 2013 Feb 12.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Multiple System Atrophy/*etiology
Mutation/*genetics
Parkinson Disease/*complications
Parkinson Disease/*genetics
alpha-Synuclein/*genetics
Adult ; Age Factors ; Humans ; Male ; Middle Aged ; Young Adult
Czasopismo naukowe
Tytuł :
Identification and quantification of oligodendrocyte precursor cells in multiple system atrophy, progressive supranuclear palsy and Parkinson's disease.
Autorzy :
Ahmed Z; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Asi YT
Lees AJ
Revesz T
Holton JL
Pokaż więcej
Źródło :
Brain pathology (Zurich, Switzerland) [Brain Pathol] 2013 May; Vol. 23 (3), pp. 263-73. Date of Electronic Publication: 2012 Oct 23.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Multiple System Atrophy/*pathology
Oligodendroglia/*pathology
Parkinson Disease/*pathology
Supranuclear Palsy, Progressive/*pathology
Aged ; Aged, 80 and over ; Axons/pathology ; Cerebellum/metabolism ; Cerebellum/pathology ; Chondroitin Sulfate Proteoglycans/metabolism ; Female ; Fluorescent Antibody Technique, Indirect ; Gliosis/pathology ; Humans ; Image Processing, Computer-Assisted ; Immunohistochemistry ; Inclusion Bodies/pathology ; Male ; Middle Aged ; Myelin Sheath/pathology ; alpha-Synuclein/metabolism ; tau Proteins/metabolism
Czasopismo naukowe
Tytuł :
The neuropathology, pathophysiology and genetics of multiple system atrophy.
Autorzy :
Ahmed Z; Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
Asi YT
Sailer A
Lees AJ
Houlden H
Revesz T
Holton JL
Pokaż więcej
Źródło :
Neuropathology and applied neurobiology [Neuropathol Appl Neurobiol] 2012 Feb; Vol. 38 (1), pp. 4-24.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms :
Multiple System Atrophy/*genetics
Multiple System Atrophy/*pathology
Multiple System Atrophy/*physiopathology
Animals ; Brain/metabolism ; Brain/pathology ; Brain/physiopathology ; Humans ; alpha-Synuclein/genetics ; alpha-Synuclein/metabolism
Czasopismo naukowe
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