Zobrazeno 1 - 10
of 1 812
pro vyhledávání: '"Chinnery, P"'
Autor:
Xin Huang, Chris Fowler, Yihan Li, Qiao-Xin Li, Jiaqi Sun, Yijun Pan, Liang Jin, Keyla A. Perez, Céline Dubois, Yen Y. Lim, Candace Drysdale, Rebecca L. Rumble, Holly R. Chinnery, Christopher C. Rowe, Ralph N. Martins, Paul Maruff, James D. Doecke, Yong Lin, Abdel A. Belaidi, Kevin J. Barnham, Colin L. Masters, Ben J. Gu
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-17 (2024)
Abstract Impaired clearance of amyloid β (Aβ) in late-onset Alzheimer’s disease (AD) affects disease progression. The role of peripheral monocytes in Aβ clearance from the central nervous system (CNS) is unclear. We use a flow cytometry assay to
Externí odkaz:
https://doaj.org/article/3d0335505eb94001ae1c6a1edbac7289
Autor:
Meaghen Quinlan-Davidson, Mahalia Dixon, Gina Chinnery, Lisa D. Hawke, Srividya Iyer, Katherine Moxness, Matthew Prebeg, Lehana Thabane, J. L. Henderson
Publikováno v:
BMC Public Health, Vol 24, Iss 1, Pp 1-13 (2024)
Abstract Background Prior research has showed the importance of providing integrated support services to prevent and reduce youth not in education, employment, or training (NEET) related challenges. There is limited evidence on NEET youth’s perspec
Externí odkaz:
https://doaj.org/article/c92e461ba93d4c13942862e6d9efb566
Autor:
Alexander G. Murley, Catarina Rua, Heather Biggs, Christopher T. Rodgers, Tomasz Matys, Jelle van denAmeele, Rita Horvath, Patrick F. Chinnery
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 5, Pp 1359-1364 (2024)
Abstract Neuroferritinopathy is a disorder of neurodegeneration with brain iron accumulation that has no proven disease‐modifying treatments. Clinical trials require biomarkers of iron deposition. We examined brain iron accumulation in one presympt
Externí odkaz:
https://doaj.org/article/1e728dc0d0f242039b2d5260cacfbd04
Autor:
Patrick F Chinnery, Rita Horvath, Nour Elkhateeb, Katherine Schon, Thiloka E Ratnaike, Angela Lochmüller, Christopher Gilmartin
Publikováno v:
BMJ Neurology Open, Vol 6, Iss 1 (2024)
Background We aimed to determine whether sodium valproate (VPA) should be contraindicated in all mitochondrial diseases, due to known VPA-induced severe hepatotoxicity in some mitochondrial diseases.Methods We systematically reviewed the published li
Externí odkaz:
https://doaj.org/article/fb5ec582cd4348f697749b386c6430fa
Autor:
Benedict D. Michael, Cordelia Dunai, Edward J. Needham, Kukatharmini Tharmaratnam, Robyn Williams, Yun Huang, Sarah A. Boardman, Jordan J. Clark, Parul Sharma, Krishanthi Subramaniam, Greta K. Wood, Ceryce Collie, Richard Digby, Alexander Ren, Emma Norton, Maya Leibowitz, Soraya Ebrahimi, Andrew Fower, Hannah Fox, Esteban Tato, Mark A. Ellul, Geraint Sunderland, Marie Held, Claire Hetherington, Franklyn N. Egbe, Alish Palmos, Kathy Stirrups, Alexander Grundmann, Anne-Cecile Chiollaz, Jean-Charles Sanchez, James P. Stewart, Michael Griffiths, Tom Solomon, Gerome Breen, Alasdair J. Coles, Nathalie Kingston, John R. Bradley, Patrick F. Chinnery, Jonathan Cavanagh, Sarosh R. Irani, Angela Vincent, J. Kenneth Baillie, Peter J. Openshaw, Malcolm G. Semple, ISARIC4C Investigators, COVID-CNS Consortium, Leonie S. Taams, David K. Menon
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract To understand neurological complications of COVID-19 better both acutely and for recovery, we measured markers of brain injury, inflammatory mediators, and autoantibodies in 203 hospitalised participants; 111 with acute sera (1–11 days pos
Externí odkaz:
https://doaj.org/article/b91096b3ed5a4dec92a987b9259afe0a
Publikováno v:
Frontiers in Education, Vol 9 (2024)
COVID-19 laid bare many failings and shortcomings of state systems, institutions and structures which aim to protect citizens against harm. As observed from the outcomes of the pandemic in many parts of the Global South and Global North, the resilien
Externí odkaz:
https://doaj.org/article/a65180da73d34baab369d0599f840dc7
Autor:
Toby Charles Major, Eszter Sara Arany, Katherine Schon, Magdolna Simo, Veronika Karcagi, Jelle van den Ameele, Patrick Yu Wai Man, Patrick F. Chinnery, Catarina Olimpio, Rita Horvath
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
BackgroundLeber Hereditary Optic Neuropathy (LHON) is the most common inherited mitochondrial disease characterized by bilateral, painless, subacute visual loss with a peak age of onset in the second to third decade. Historically, LHON was thought to
Externí odkaz:
https://doaj.org/article/48c871d2ccba431b9451d553f5fb705c
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