Zobrazeno 1 - 10
of 420
pro vyhledávání: '"Thomas T Warner"'
Autor:
Rajasree Nambron, Edina Silajdžić, Eirini Kalliolia, Chris Ottolenghi, Peter Hindmarsh, Nathan R Hill, Seán J Costelloe, Nicholas G Martin, Vincenzo Positano, Hilary C Watt, Chris Frost, Maria Björkqvist, Thomas T Warner
Publikováno v:
PLoS ONE, Vol 11, Iss 1, p e0146480 (2016)
BackgroundHuntington's disease patients have a number of peripheral manifestations suggestive of metabolic and endocrine abnormalities. We, therefore, investigated a number of metabolic factors in a 24-hour study of Huntington's disease gene carriers
Externí odkaz:
https://doaj.org/article/418822ab2bc146d98df51b9f0cc3fa02
Autor:
Laís Orrico Donnabella Bastos, Marilisa Mantovani Guerreiro, Andrew John Lees, Thomas T Warner, Laura Silveira-Moriyama
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0131641 (2015)
ObjectivesTo study the effects of age and cognition on the performance of children aged 3 to 18 years on a culturally adapted version of the 16 item smell identification test from Sniffin' Sticks (SS16).MethodsA series of pilots were conducted on 29
Externí odkaz:
https://doaj.org/article/676fd823d9694c7b8cfc27fb8dedb2d2
Autor:
Eirini Kalliolia, Edina Silajdžić, Rajasree Nambron, Seán J Costelloe, Nicholas G Martin, Nathan R Hill, Chris Frost, Hilary C Watt, Peter Hindmarsh, Maria Björkqvist, Thomas T Warner
Publikováno v:
PLoS ONE, Vol 10, Iss 10, p e0138848 (2015)
Huntington's disease is an inherited neurodegenerative disorder characterised by motor, cognitive and psychiatric disturbances. Patients exhibit other symptoms including sleep and mood disturbances, muscle atrophy and weight loss which may be linked
Externí odkaz:
https://doaj.org/article/625e9d7485994ebdb52003c5ccd1562c
Autor:
Pollyanna A Goh, Sara Caxaria, Catharina Casper, Cecilia Rosales, Thomas T Warner, Pete J Coffey, Amit C Nathwani
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e81622 (2013)
A systematic evaluation of three different methods for generating induced pluripotent stem (iPS) cells was performed using the same set of parental cells in our quest to develop a feeder independent and xeno-free method for somatic cell reprogramming
Externí odkaz:
https://doaj.org/article/4a595ece45d948ddbb6ce4d05341ceb7
Autor:
Patrick W. Cullinane, Riona Fumi, Marte Theilmann Jensen, Edwin Jabbari, Thomas T. Warner, Tamas Revesz, Huw R. Morris, Jonathan D. Rohrer, Zane Jaunmuktane
Publikováno v:
Movement Disorders Clinical Practice. 10:691-694
Autor:
Sasivimol Virameteekul, Tamas Revesz, Zane Jaunmuktane, Thomas T. Warner, Eduardo De Pablo‐Fernández
Publikováno v:
Movement Disorders. 38:444-452
The recent International Parkinson and Movement Disorder Society diagnostic criteria for multiple system atrophy (MDS-MSA) have been developed to improve diagnostic accuracy although their diagnostic properties have not been evaluated.The aims were t
Autor:
Sasivimol Virameteekul, Tamas Revesz, Zane Jaunmuktane, Thomas T. Warner, Eduardo De Pablo‐Fernández
Publikováno v:
Movement Disorders. 38:558-566
Clinical diagnostic accuracy of Parkinson's disease (PD) remains suboptimal. Changes in disease concept may have improved clinical diagnostic accuracy in the past decade. However, current clinical diagnostic criteria have not been validated against n
Autor:
Yang Yang, Yang Shi, Manuel Schweighauser, Xianjun Zhang, Abhay Kotecha, Alexey G. Murzin, Holly J. Garringer, Patrick W. Cullinane, Yuko Saito, Tatiana Foroud, Thomas T. Warner, Kazuko Hasegawa, Ruben Vidal, Shigeo Murayama, Tamas Revesz, Bernardino Ghetti, Masato Hasegawa, Tammaryn Lashley, Sjors H. W. Scheres, Michel Goedert
Publikováno v:
Nature. 610:791-795
Parkinson's disease (PD) is the most common movement disorder, with resting tremor, rigidity, bradykinesia and postural instability being major symptoms
Autor:
Samuel Shribman, Thomas Marjot, Abubakar Sharif, Sunitha Vimalesvaran, Aftab Ala, Graeme Alexander, Anil Dhawan, James Dooley, Godfrey T Gillett, Deirdre Kelly, Alisdair McNeill, Thomas T Warner, Valerie Wheater, William Griffiths, Oliver Bandmann
Publikováno v:
The Lancet Gastroenterology & Hepatology. 7:560-575
Wilson's disease is an autosomal-recessive disorder of copper metabolism with hepatic, neurological, psychiatric, ophthalmological, haematological, renal, and rheumatological manifestations. Making a diagnosis can be challenging given that no single
Autor:
Rebecca R Valentino, William J Scotton, Shanu F Roemer, Tammaryn Lashley, Michael G Heckman, Maryam Shoai, Alejandro Martinez-Carrasco, Nicole Tamvaka, Ronald L Walton, Matthew C Baker, Hannah L Macpherson, Raquel Real, Alexandra I Soto-Beasley, Kin Mok, Tamas Revesz, Thomas T Warner, Zane Jaunmuktane, Bradley F Boeve, Elizabeth A Christopher, Michael DeTure, Ranjan Duara, Neill R Graff-Radford, Keith A Josephs, David S Knopman, Shunsuke Koga, Melissa E Murray, Kelly E Lyons, Rajesh Pahwa, Joseph E Parisi, Ronald C Petersen, Jennifer Whitwell, Lea T Grinberg, Bruce Miller, Athena Schlereth, William W Seeley, Salvatore Spina, Murray Grossman, David J Irwin, Edward B Lee, EunRan Suh, John Q Trojanowski, Vivianna M Van Deerlin, David A Wolk, Theresa R Connors, Patrick M Dooley, Matthew P Frosch, Derek H Oakley, Iban Aldecoa, Mircea Balasa, Ellen Gelpi, Sergi Borrego-Écija, Rosa Maria de Eugenio Huélamo, Jordi Gascon-Bayarri, Raquel Sánchez-Valle, Pilar Sanz-Cartagena, Gerard Piñol-Ripoll, Laura Molina-Porcel, Eileen H Bigio, Margaret E Flanagan, Tamar Gefen, Emily J Rogalski, Sandra Weintraub, Javier Redding-Ochoa, Koping Chang, Juan C Troncoso, Stefan Prokop, Kathy L Newell, Bernardino Ghetti, Matthew Jones, Anna Richardson, Andrew C Robinson, Federico Roncaroli, Julie Snowden, Kieren Allinson, Oliver Green, James B Rowe, Poonam Singh, Thomas G Beach, Geidy E Serrano, Xena E Flowers, James E Goldman, Allison C Heaps, Sandra P Leskinen, Andrew F Teich, Sandra E Black, Julia L Keith, Mario Masellis, Istvan Bodi, Andrew King, Safa-Al Sarraj, Claire Troakes, Glenda M Halliday, John R Hodges, Jillian J Kril, John B Kwok, Olivier Piguet, Marla Gearing, Thomas Arzberger, Sigrun Roeber, Johannes Attems, Christopher M Morris, Alan J Thomas, Bret M. Evers, Charles L White, Naguib Mechawar, Anne A Sieben, Patrick P Cras, Bart B De Vil, Peter Paul P.P. De Deyn, Charles Duyckaerts, Isabelle Le Ber, Danielle Seihean, Sabrina Turbant-Leclere, Ian R MacKenzie, Catriona McLean, Matthew D Cykowski, John F Ervin, Shih-Hsiu J Wang, Caroline Graff, Inger Nennesmo, Rashed M Nagra, James Riehl, Gabor G Kovacs, Giorgio Giaccone, Benedetta Nacmias, Manuela Neumann, Lee-Cyn Ang, Elizabeth C Finger, Cornelis Blauwendraat, Mike A Nalls, Andrew B Singleton, Dan Vitale, Cristina Cunha, Agostinho Carvalho, Zbigniew K Wszolek, Huw R Morris, Rosa Rademakers, John A Hardy, Dennis W Dickson, Jonathan D Rohrer, Owen A Ross
Publikováno v:
medRxiv
BackgroundPick’s disease (PiD) is a rare and predominantly sporadic form of frontotemporal dementia that is classified as a primary tauopathy. PiD is pathologically defined by argyrophilic inclusion Pick bodies and ballooned neurons in the frontal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eb436da4c7362a38f76655e19fddf0a
https://europepmc.org/articles/PMC10168402/
https://europepmc.org/articles/PMC10168402/