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Authors: van Rheenen, Wouter | Shatunov, Aleksey | Yang, Jian | de Visser, Marianne | Goris, An | Weber, Markus | Shaw, Christopher E | Smith, Bradley N | Pansarasa, Orietta | Cereda, Cristina | Del Bo, Roberto | Comi, Giacomo P | D'Alfonso, Sandra | Fogh, Isabella | Bertolin, Cinzia | Sorarù, Gianni | Mazzini, Letizia | Pensato, Viviana | Gellera, Cinzia | Tiloca, Cinzia | Ratti, Antonia | Calvo, Andrea | Moglia, Cristina | Brunetti, Maura | van Doormaal, Perry T. C | Arcuti, Simona | Capozzo, Rosa | Zecca, Chiara | Lunetta, Christian | Penco, Silvana | Riva, Nilo | Padovani, Alessandro | Filosto, Massimiliano | Muller, Bernard | Stuit, Robbert Jan | Tazelaar, Gijs H. P | Blair, Ian | Zhang, Katharine | McCann, Emily P | Fifita, Jennifer A | Nicholson, Garth A | Rowe, Dominic B | Pamphlett, Roger | Kiernan, Matthew C | Grosskreutz, Julian | Witte, Otto W | Koppers, Max | Ringer, Thomas | Prell, Tino | Stubendorff, Beatrice | Kurth, Ingo | Hübner, Christian A | Leigh, P. Nigel | Casale, Federico | Chio, Adrian | Beghi, Ettore | Pupillo, Elisabetta | Blokhuis, Anna M | Tortelli, Rosanna | Logroscino, Giancarlo | Powell, John | Ludolph, Albert C | Weishaupt, Jochen H | Robberecht, Wim | Van Damme, Philip | Franke, Lude | Pers, Tune H | Brown, Robert H | Sproviero, William | Glass, Jonathan D | Landers, John E | Hardiman, Orla | Andersen, Peter M | Corcia, Philippe | Vourc'h, Patrick | Silani, Vincenzo | Wray, Naomi R | Visscher, Peter M | de Bakker, Paul I. W | Jones, Ashley R | van Es, Michael A | Pasterkamp, R. Jeroen | Lewis, Cathryn M | Breen, Gerome | Al-Chalabi, Ammar | van den Berg, Leonard H | Veldink, Jan H | Kenna, Kevin P | van Eijk, Kristel R | Dekker, Annelot M | Harschnitz, Oliver | Schellevis, Raymond D | Brands, William J | Medic, Jelena | Menelaou, Androniki | Vajda, Alice | Ticozzi, Nicola | Lin, Kuang | Rogelj, Boris | Vrabec, Katarina | McLaughlin, Russell L | Ravnik-Glavač, Metka | Koritnik, Blaž | Zidar, Janez | Leonardis, Lea | Grošelj, Leja Dolenc | Millecamps, Stéphanie | Salachas, François | Meininger, Vincent | de Carvalho, Mamede | Pinto, Susana | Diekstra, Frank P | Mora, Jesus S | Rojas-García, Ricardo | Polak, Meraida | Chandran, Siddharthan | Colville, Shuna | Swingler, Robert | Morrison, Karen E | Shaw, Pamela J | Hardy, John | Orrell, Richard W | Pulit, Sara L | Pittman, Alan | Sidle, Katie | Fratta, Pietro | Malaspina, Andrea | Topp, Simon | Petri, Susanne | Abdulla, Susanne | Drepper, Carsten | Sendtner, Michael | Meyer, Thomas | van der Spek, Rick A. A | Ophoff, Roel A | Staats, Kim A | Wiedau-Pazos, Martina | Lomen-Hoerth, Catherine | Van Deerlin, Vivianna M | Trojanowski, John Q | Elman, Lauren | McCluskey, Leo | Basak, A. Nazli | Tunca, Ceren | Võsa, Urmo | Hamzeiy, Hamid | Parman, Yesim | Meitinger, Thomas | Lichtner, Peter | Radivojkov-Blagojevic, Milena | Andres, Christian R | Maurel, Cindy | Bensimon, Gilbert | Landwehrmeyer, Bernhard | Brice, Alexis | de Jong, Simone | Payan, Christine A. M | Saker-Delye, Safaa | Dürr, Alexandra | Wood, Nicholas W | Tittmann, Lukas | Lieb, Wolfgang | Franke, Andre | Rietschel, Marcella | Cichon, Sven | Nöthen, Markus M | Robinson, Matthew R | Amouyel, Philippe | Tzourio, Christophe | Dartigues, Jean-François | Uitterlinden, Andre G | Rivadeneira, Fernando | Estrada, Karol | Hofman, Albert | Curtis, Charles | Blauw, Hylke M | van der Kooi, Anneke J
Date: 2016
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/1208872
Description: To elucidate the genetic architecture of amyotrophic lateral sclerosis (ALS) and find associated loci, we assembled a custom imputation reference panel from whole-genome-sequenced patients with ALS an ... More
Reviewed: Reviewed
Date: 2015
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/1047110
Description: Objective: Recognizing depressive symptoms in patients with amyotrophic lateral sclerosis (ALS) remains problematic given the potential overlap with the normal psychological responses to a terminal il ... More
Reviewed: Reviewed
Date: 2015
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/1047496
Description: Background: Patients with amyotrophic lateral sclerosis (ALS) face numerous decisions for symptom management and quality of life. Models of decision making in chronic disease and cancer care are insuf ... More
Reviewed: Reviewed
Date: 2015
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/1219584
Description: Importance- A gap in the literature exists regarding progression in behavioral variant frontotemporal dementia (BVFTD). Guidance is needed concerning markers that will enable clinicians to discriminat ... More
Reviewed: Reviewed
Date: 2014
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/1217724
Description: Amyotrophic lateral sclerosis (ALS) is a multisystem disease that overlaps with frontotemporal dementia (FTD). Although FTD patients exhibit prominent deficits in emotion perception and social cogniti ... More
Reviewed: Reviewed
Date: 2013
Subject Keyword: 110300 Clinical Sciences | Genetics | Risk | SOD1
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/314725
Description: Although anticipation has been previously reported in the copper/zinc superoxide dismutase-1 (SOD1) associated familial amyotrophic lateral sclerosis (FALS), some have argued that this may represent a ... More
Reviewed: Reviewed
Date: 2013
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/314741
Description: Two decades after the discovery that 20% of familial amyotrophic lateral sclerosis (ALS) cases were linked to mutations in the superoxide dismutase-1 (SOD1) gene, a substantial proportion of the remai ... More
Reviewed: Reviewed
Date: 2013
Subject Keyword: 110900 Neurosciences
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/274726
Description: Objective: Expansions of a hexanucleotide repeat in C9ORF72 are a common cause of familial amyotrophic lateral sclerosis (ALS) and a small proportion of sporadic ALS cases. We sought to examine clinic ... More
Reviewed: Reviewed
Date: 2013
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/349493
Description: Purpose: Family carers of patients with amyotrophic lateral sclerosis (ALS) are presumed to have frequent involvement in decision-making for symptom management and quality of life. To better understan ... More
Full Text: Full Text
Reviewed: Reviewed
Date: 2012
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/349544
Description: Background: The aim of this study was to explore clinician perspectives on patient decision-making in multidisciplinary care for amyotrophic lateral sclerosis (ALS), in an attempt to identify factors ... More
Full Text: Full Text
Reviewed: Reviewed
Date: 2012
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/349516
Description: Background: Patients with amyotrophic lateral sclerosis (ALS) are required to make decisions concerning quality of life and symptom management over the course of their disease. Clinicians perceive tha ... More
Full Text: Full Text
Reviewed: Reviewed
Date: 2011
Subject Keyword: 110300 Clinical Sciences
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/146161
Description: Objective: To determine clinically related characteristics in patients with pure lower motor neuron (LMN) syndromes, not fulfilling accepted diagnostic criteria, who were likely to respond to intraven ... More
Full Text: Full Text
Reviewed: Reviewed
Date: 2010
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/117593
Description: Objective: Diffusion tensor imaging (DTI) recently identified structural abnormalities of corticomotoneurons in asymptomatic copper/zinc superoxide-dismutase-1 (SOD-1) gene mutation carriers. The pote ... More
Reviewed: Reviewed
Date: 2010
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/221579
Description: Objective: FUS gene mutations were recently identified in familial amyotrophic lateral sclerosis (ALS). The present studies sought to define the clinical, post-mortem and neurophysiological phenotypes ... More
Reviewed: Reviewed
Date: 2008
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/314286
Description: Familial amyotrophic lateral sclerosis (FALS) is an inherited neurodegenerative disorder of the motor neurons. While 10–15% of cases are caused by mutations in the copper/zinc superoxide-dismutase-1 ( ... More
Reviewed: Reviewed
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