Search Results - "Richardson, Anna MT"

Classification and pathology of primary progressive aphasia by Harris, Jennifer M, Gall, Claire, Thompson, Jennifer C, Richardson, Anna M.T, Neary, David, du Plessis, Daniel, Pal, Piyali, Mann, David M.A, Snowden, Julie S, Jones, Matthew

“…OBJECTIVE:We aimed to determine the extent to which patients with progressive language impairment conform to 2011 primary progressive aphasia (PPA)…”
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Examining the language and behavioural profile in FTD and ALS-FTD by Saxon, Jennifer A, Thompson, Jennifer C, Jones, Matthew, Harris, Jennifer M, Richardson, Anna MT, Langheinrich, Tobias, Neary, David, Mann, David MA, Snowden, Julie S

“…BackgroundA proportion of patients with behavioural variant frontotemporal dementia (bvFTD) develop amyotrophic lateral sclerosis (ALS). It is currently…”
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The clinical diagnosis of early-onset dementias: diagnostic accuracy and clinicopathological relationships by Snowden, Julie S., Thompson, Jennifer C., Stopford, Cheryl L., Richardson, Anna M. T., Gerhard, Alex, Neary, David, Mann, David M. A.

“…Accuracy of clinical diagnosis of dementia is increasingly important for therapeutic and scientific investigations. In this study, we examine diagnostic…”
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Working memory, attention, and executive function in Alzheimer’s disease and frontotemporal dementia by Stopford, Cheryl L., Thompson, Jennifer C., Neary, David, Richardson, Anna M.T., Snowden, Julie S.

“…Working memory deficits are a recognised feature of Alzheimer’s disease (AD). They are commonly ascribed to central executive impairment and assumed to relate…”
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Sensitivity and specificity of FTDC criteria for behavioral variant frontotemporal dementia by Harris, Jennifer M, Gall, Claire, Thompson, Jennifer C, Richardson, Anna M.T, Neary, David, du Plessis, Daniel, Pal, Piyali, Mann, David M.A, Snowden, Julie S, Jones, Matthew

“…OBJECTIVE:We aimed to assess sensitivity and specificity of the updated criteria for behavioral variant frontotemporal dementia (bvFTD) based on a large…”
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Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations by Pickering-Brown, Stuart M., Rollinson, Sara, Du Plessis, Daniel, Morrison, Karen E., Varma, Anoop, Richardson, Anna M. T., Neary, David, Snowden, Julie S., Mann, David M. A.

“…Two hundred and twenty-three consecutive patients fulfilling clinical diagnostic criteria for frontotemporal lobar degeneration (FTLD), and 259 patients with…”
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C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts by Costa, Beatrice, Manzoni, Claudia, Bernal-Quiros, Manuel, Kia, Demis A., Aguilar, Miquel, Alvarez, Ignacio, Alvarez, Victoria, Andreassen, Ole, Anfossi, Maria, Bagnoli, Silvia, Benussi, Luisa, Bernardi, Livia, Binetti, Giuliano, Blackburn, Daniel, Boada, Mercè, Borroni, Barbara, Bowns, Lucy, Bråthen, Geir, Bruni, Amalia C., Chiang, Huei-Hsin, Clarimon, Jordi, Colville, Shuna, Conidi, Maria E., Cope, Tom E., Cupidi, Chiara, Di Battista, Maria Elena, Diehl-Schmid, Janine, Diez-Fairen, Monica, Dols-Icardo, Oriol, Durante, Elisabetta, Flisar, Dušan, Galimberti, Daniela, Gallo, Maura, Gallucci, Maurizio, Ghidoni, Roberta, Graff, Caroline, Grafman, Jordan H., Grossman, Murray, Hardy, John, Hernández, Isabel, Holloway, Guy J.T., Huey, Edward D., Illán-Gala, Ignacio, Karydas, Anna, Khoshnood, Behzad, Kramberger, Milica G., Lewis, Patrick A., Lleó, Alberto, Madhan, Gaganjit K., Maver, Aleš, Menendez-Gonzalez, Manuel, Milan, Graziella, Miller, Bruce, Mol, Merel O., Momeni, Parastoo, Moreno-Grau, Sonia, Morris, Chris M., Nacmias, Benedetta, Nilsson, Christer, Novelli, Valeria, Öijerstedt, Linn, Padovani, Alessandro, Pal, Suvankar, Pastor, Pau, Peterlin, Borut, Piaceri, Irene, Pickering-Brown, Stuart, Pijnenburg, Yolande A.L., Puca, Annibale A., Rainero, Innocenzo, Rendina, Antonella, Richardson, Anna M.T., Rogaeva, Ekaterina, Rogelj, Boris, Rollinson, Sara, Rossi, Giacomina, Rossmeier, Carola, Rubino, Elisa, Ruiz, Agustín, Sanchez-Valle, Raquel, Sando, Sigrid B., Santillo, Alexander F., Saxon, Jennifer, Smirne, Nicoletta, Sorbi, Sandro, Tagliavini, Fabrizio, Thompson, Jennifer C., Trojanowski, John Q., Van Deerlin, Vivianna M., Van der Zee, Julie, Van Broeckhoven, Christine, van Rooij, Jeroen, Van Swieten, John C., Veronesi, Arianna, Vitale, Emilia, Waldö, Maria L., Woodward, Cathy, Escott-Price, Valentina, Polke, James M., Ferrari, Raffaele

“…We sought to characterize expansions in relation to genetic ancestry and age at onset (AAO) and to use these measures to discriminate the behavioral from the…”
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A POSITRON EMISSION TOMOGRAPHY STUDY OF [18F]–FLORBETAPIR IN ALZHEIMER'S DISEASE AND FRONTOTEMPORAL DEMENTIA by Kobylecki, Christopher, Langheinrich, Tobias, Hinz, Rainer, Vardy, Emma RLC, Martino, Maria–Elena, Richardson, Anna MT, Snowden, Julie S, Anton–Rodriguez, Jose, Neary, David, Mann, David M, Gerhard, Alex, Herholz, Karl

“…Background Deposits of fibrillar amyloid β (Aβ) protein are important in the pathophysiology of Alzheimer's disease (AD), but not in frontotemporal dementia…”
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Progressive aphasia presenting with deep dyslexia and dysgraphia by Snowden, Julie S., Kindell, Jacqueline, Thompson, Jennifer C., Richardson, Anna M.T., Neary, David

“…Primary progressive aphasia is clinically heterogeneous. We report a patient, alias Don, with a novel form of progressive aphasia, characterised by deep…”
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Glucocerebrosidase mutations in diffuse Lewy body disease by Nishioka, Kenya, Ross, Owen A, Vilariño-Güell, Carles, Cobb, Stephanie A, Kachergus, Jennifer M, Mann, David M.A, Snowden, Julie, Richardson, Anna M.T, Neary, David, Robinson, Christopher A, Rajput, Alex, Papapetropoulos, Spiridon, Mash, Deborah C, Pahwa, Rajesh, Lyons, Kelly E, Wszolek, Zbigniew K, Dickson, Dennis W, Farrer, Matthew J

“…Abstract Clinicogenetic and pathological studies have shown that mutations of the glucocerebrosidase gene ( GBA ) are a risk factor for Parkinson’s disease and…”
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C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts by Costa, Beatrice, Manzoni, Claudia, Bernal-Quiros, Manuel, Kia, Demis A, Aguilar, Miquel, Alvarez, Ignacio, Alvarez, Victoria, Andreassen, Ole, Anfossi, Maria, Bagnoli, Silvia, Benussi, Luisa, Bernardi, Livia, Binetti, Giuliano, Blackburn, Daniel, Boada, Mercè, Borroni, Barbara, Bowns, Lucy, Bruni, Amalia C, Chiang, Huei-Hsin, Clarimon, Jordi, Colville, Shuna, Conidi, Maria E, Cope, Tom E, Cruchaga, Carlos, Cupidi, Chiara, Di Battista, Maria Elena, Diehl-Schmid, Janine, Diez-Fairen, Monica, Durante, Elisabetta, Flisar, Dušan, Frangipane, Francesca, Galimberti, Daniela, Gallo, Maura, Gallucci, Maurizio, Ghidoni, Roberta, Graff, Caroline, Grafman, Jordan H, Hardy, John, Hernández, Isabel, Holloway, Guy JT, Huey, Edward D, Illán-Gala, Ignacio, Karydas, Anna, Khoshnood, Behzad, Kramberger, Milica G, Kristiansen, Mark, Lleó, Alberto, Madhan, Gaganjit K, Maletta, Raffaele, Menendez-Gonzalez, Manuel, Milan, Graziella, Mol, Merel O, Momeni, Parastoo, Moreno-Grau, Sonia, Nacmias, Benedetta, Nilsson, Christer, Novelli, Valeria, Öijerstedt, Linn, Padovani, Alessandro, Pal, Suvankar, Panchbhaya, Yasmin, Pastor, Pau, Peterlin, Borut, Piaceri, Irene, Pickering-Brown, Stuart, Puca, Annibale A, Rainero, Innocenzo, Rendina, Antonella, Richardson, Anna MT, Rogaeva, Ekaterina, Rogelj, Boris, Rossi, Giacomina, Rossmeier, Carola, Rowe, James B, Rubino, Elisa, Ruiz, Agustín, Sanchez-Valle, Raquel, Sando, Sigrid B, Santillo, Alexander F, Saxon, Jennifer, Scarpini, Elio, Serpente, Maria, Smirne, Nicoletta, Sorbi, Sandro, Suh, EunRan, Tagliavini, Fabrizio, Thompson, Jennifer C, Trojanowski, John Q, Van Deerlin, Vivianna M, Van der Zee, Julie, Van Broeckhoven, Christine, van Rooij, Jeroen, Van Swieten, John C, Veronesi, Arianna, Vitale, Emilia, Waldö, Maria L, Woodward, Cathy, Escott-Price, Valentina, Polke, James M, Ferrari, Raffaele

“…OBJECTIVE:We sought to characterise C9orf72 expansions in relation to genetic ancestry and age at onset (AAO), and to use these parameters to discriminate the…”
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Recent origin and spread of a common Welsh MAPT splice mutation causing frontotemporal lobar degeneration by Colombo, Roberto, Tavian, Daniela, Baker, Matthew C., Richardson, Anna M. T., Snowden, Julie S., Neary, David, Mann, David M. A., Pickering-Brown, Stuart M.

“…IVS10+16C>T is the most prevalent mutation in the microtubule-associated protein tau gene ( MAPT ) causing frontotemporal lobar degeneration (FTLD) in…”
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Functional neuroanatomical associations of working memory in early‐onset Alzheimer's disease by Kobylecki, Christopher, Haense, Cathleen, Harris, Jennifer M., Stopford, Cheryl L., Segobin, Shailendra H., Jones, Matthew, Richardson, Anna M.T., Gerhard, Alexander, Anton‐Rodriguez, José, Thompson, Jennifer C., Herholz, Karl, Snowden, Julie S.

“…Objective To characterize metabolic correlates of working memory impairment in clinically defined subtypes of early‐onset Alzheimer's disease. Background…”
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Joseph F Quinn (ed.), Neurology in practice: Dementia by Richardson, Anna MT

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