Occurrence of Amyotrophic Lateral Sclerosis in Type 1 Gaucher Disease

by Oliveira, Lais M, Rastin, Tara, Nimmo, Graeme A M, Ross, Jay P, Dion, Patrick A, Zhang, Ming, Nevay, Dayna-Lynn, Arkadir, David, Gotkine, Marc, Barnett, Carolina, Shoesmith, Christen L, Zimran, Ari, Rogaeva, Ekaterina A, Zinman, Lorne, Rouleau, Guy A, Gan-Or, Ziv, Amato, Dominick, Kalia, Lorraine V
Published in Neurology. Genetics

Amyotrophic lateral sclerosis: update for family physicians

by Shoesmith, Christen L, Strong, Michael J
Published in Canadian family physician

A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study

by Bergström, Sofia, Remnestål, Julia, Olofsson, Jennie, Seelaar, Harro, Synofzik, Matthis, Sanchez-Valle, Raquel, Moreno, Fermin, Finger, Elizabeth, Tartaglia, Carmela, Vandenberghe, Rik, Laforce, Robert, Galimberti, Daniela, Borroni, Barbara, Butler, Chris R., Ducharme, Simon, Graff, Caroline, Rowe, James B., Tagliavini, Fabrizio, Le Ber, Isabelle, Levin, Johannes, Otto, Markus, Frisoni, Giovanni, Ghidoni, Roberta, Sorbi, Sandro, Jelic, Vesna, Anderl-Straub, Sarah, Archetti, Silvana, Arighi, Andrea, Balasa, Mircea, Bender, Benjamin, Benussi, Alberto, Benussi, Luisa, Binetti, Giuliano, Borrego-Ecija, Sergi, Bruffaerts, Rose, Cantoni, Valentina, Cash, David, Castelo-Branco, Miguel, Convery, Rhian, Cope, Thomas, Di Fede, Giuseppe, Duro, Diana, Fenoglio, Chiara, Ferrari, Camilla, Ferreira, Catarina B., Fox, Nick, Freedman, Morris, Fumagalli, Giorgio, Gabilondo, Alazne, Gasparotti, Roberto, Gauthier, Serge, Gazzina, Stefano, Giaccone, Giorgio, Gorostidi, Ana, Greaves, Caroline, Guerreiro, Rita, Hoegen, Tobias, Indakoetxea, Begoña, Karnath, Hans-Otto, Langheinrich, Tobias, Leitão, Maria João, Lombardi, Gemma, Loosli, Sandra, Miltenberger, Gabriel, Mitchell, Sara, Moore, Katrina, Nacmias, Benedetta, Nicholas, Jennifer, Ourselin, Sebastien, Padovani, Alessandro, Papma, Janne M., Peakman, Georgia, Pievani, Michela, Pijnenburg, Yolande, Polito, Cristina, Prioni, Sara, Rademakers, Rosa, Rittman, Tim, Rosa-Neto, Pedro, Rossi, Giacomina, Schönecker, Sonja, Semler, Elisa, Shafei, Rachelle, Shoesmith, Christen, Taipa, Ricardo, Tang-Wai, David, Thomas, David L., Thompson, Paul, Thonberg, Håkan, Timberlake, Carolyn, Todd, Emily, Van Damme, Philip, Vandenbulcke, Mathieu, Verdelho, Ana, Villanua, Jorge, Warren, Jason, Wilke, Carlo, Woollacott, Ione, Wlasich, Elisabeth, Zulaica, Miren
Published in Molecular neurodegeneration

Soluble Epoxide Hydrolase Derived Linoleic Acid Oxylipins, Small Vessel Disease Markers, and Neurodegeneration in Stroke

by Yu, Di, Liang, Nuanyi, Zebarth, Julia, Shen, Qing, Ozzoude, Miracle, Goubran, Maged, Rabin, Jennifer S, Ramirez, Joel, Scott, Christopher J M, Gao, Fuqiang, Bartha, Robert, Symons, Sean, Haddad, Seyyed Mohammad Hassan, Berezuk, Courtney, Tan, Brian, Kwan, Donna, Hegele, Robert A, Dilliott, Allison A, Nanayakkara, Nuwan D, Binns, Malcolm A, Beaton, Derek, Arnott, Stephen R, Lawrence-Dewar, Jane M, Hassan, Ayman, Dowlatshahi, Dar, Mandzia, Jennifer, Sahlas, Demetrios, Casaubon, Leanne, Saposnik, Gustavo, Otoki, Yurika, Lanctôt, Krista L, Masellis, Mario, Black, Sandra E, Swartz, Richard H, Taha, Ameer Y, Swardfager, Walter
Published in Journal of the American Heart Association

Phenotypic and molecular analyses of primary lateral sclerosis

by Mitsumoto, Hiroshi, Nagy, Peter L, Gennings, Chris, Murphy, Jennifer, Andrews, Howard, Goetz, Raymond, Floeter, Mary Kay, Hupf, Jonathan, Singleton, Jessica, Barohn, Richard J, Nations, Sharon, Shoesmith, Christen, Kasarskis, Edward, Factor-Litvak, Pam
Published in Neurology. Genetics

Extending the phenotypic spectrum assessed by the CDR plus NACC FTLD in genetic frontotemporal dementia

by Samra, Kiran, Peakman, Georgia, MacDougall, Amy M, Bouzigues, Arabella, Greaves, Caroline V, Convery, Rhian S, van Swieten, John C, Jiskoot, Lize, Seelaar, Harro, Moreno, Fermin, Sanchez-Valle, Raquel, Laforce, Robert, Graff, Caroline, Masellis, Mario, Tartaglia, Maria Carmela, Rowe, James B, Borroni, Barbara, Finger, Elizabeth, Synofzik, Matthis, Galimberti, Daniela, Vandenberghe, Rik, de Mendonça, Alexandre, Butler, Chris R, Gerhard, Alexander, Ducharme, Simon, Ber, Isabelle Le, Tiraboschi, Pietro, Santana, Isabel, Pasquier, Florence, Levin, Johannes, Otto, Markus, Sorbi, Sandro, Rohrer, Jonathan D, Russell, Lucy L
Published in Alzheimer's & dementia : diagnosis, assessment & disease monitoring

Disease-related cortical thinning in presymptomatic granulin mutation carriers

by van Swieten, John, Moreno, Fermín, Masellis, Mario, Graff, Caroline, Galimberti, Daniela, Laforce, Robert, Finger, Elizabeth, Vandenberghe, Rik, Tagliavini, Fabrizio, de Mendonça, Alexandre, Santana, Isabel, Synofzik, Matthis, Ducharme, Simon, Levin, Johannes, Danek, Adrian, Gerhard, Alex, Otto, Markus, Butler, Chris, Frisoni, Giovanni, Sorbi, Sandro, Heller, Carolin, Bocchetta, Martina, Moore, Katrina M, Rohrer, Jonathan D, Sanchez-Valle, Raquel, Rossor, Martin N., Shafei, Rachelle, Greaves, Caroline, Guerreiro, Rita, Bras, Jose, Thomas, David L., Nicholas, Jennifer, Mead, Simon, Meeter, Lieke, Papma, Janne, van Minkelen, Rick, Pijnenburg, Yolande, TaintaMD, Mikel, de Arriba, Maria, Villanua, Jorge, Diaz, Zigor, Olives, Jaume, Lladó, Albert, Balasa, Mircea, Antonell, Anna, Bargallo, Nuria, Premi, Enrico, Cosseddu, Maura, Padovani, Alessandro, Gasparotti, Roberto, Archetti, Silvana, Black, Sandra, Mitchell, Sara, Rogaeva, Ekaterina, Freedman, Morris, Keren, Ron, Tang-Wai, David, Öijerstedt, Linn, Andersson, Christin, Jelic, Vesna, Thonberg, Hakan, Arighi, Andrea, Fenoglio, Chiara, Fumagalli, Giorgio, Cope, Thomas, Timberlake, Carolyn, Shoesmith, Christen, Rademakers, Rosa, Wilke, Carlo, Vandamme, Philip, Vandenbulcke, Mathieu, Maruta, Carolina, Ferreira, Catarina B., Miltenberger, Gabriel, Verdelho, Ana, Afonso, Sónia, Caroppo, Paola, Di Fede, Giuseppe, Giaccone, Giorgio, Prioni, Sara, Redaelli, Veronica, Rossi, Giacomina, Tiraboschi, Pietro, Duro, Diana, Rosario Almeida, Maria, Castelo-Branco, Miguel, João Leitão, Maria, Tabuas-Pereira, Miguel, Santiago, Beatriz, Gauthier, Serge, Rosa-Neto, Pedro, Veldsman, Michele, Flanagan, Toby, Prix, Catharina, Hoegen, Tobias, Wlasich, Elisabeth, Loosli, Sandra, Schonecker, Sonja, Semler, Elisa, Anderl-Straub, Sarah
Published in NeuroImage clinical

Contribution of rare variant associations to neurodegenerative disease presentation

by Dilliott, Allison A., Abdelhady, Abdalla, Sunderland, Kelly M., Farhan, Sali M. K., Abrahao, Agessandro, Binns, Malcolm A., Black, Sandra E., Borrie, Michael, Casaubon, Leanne K., Dowlatshahi, Dar, Finger, Elizabeth, Fischer, Corinne E., Frank, Andrew, Freedman, Morris, Grimes, David, Hassan, Ayman, Jog, Mandar, Kumar, Sanjeev, Kwan, Donna, Lang, Anthony E., Mandzia, Jennifer, Masellis, Mario, McIntyre, Adam D., Pasternak, Stephen H., Pollock, Bruce G., Rajji, Tarek K., Rogaeva, Ekaterina, Sahlas, Demetrios J., Saposnik, Gustavo, Sato, Christine, Seitz, Dallas, Shoesmith, Christen, Steeves, Thomas D. L., Swartz, Richard H., Tan, Brian, Tang-Wai, David F., Tartaglia, Maria C., Turnbull, John, Zinman, Lorne, Hegele, Robert A.
Published in Npj genomic medicine

Genetic forms of primary progressive aphasia within the GENetic Frontotemporal dementia Initiative (GENFI) cohort: comparison with sporadic primary progressive aphasia

by Samra, Kiran, MacDougall, Amy M, Bouzigues, Arabella, Bocchetta, Martina, Cash, David M, Greaves, Caroline V, Convery, Rhian S, Hardy, Chris, van Swieten, John C, Seelaar, Harro, Jiskoot, Lize C, Moreno, Fermin, Sanchez-Valle, Raquel, Laforce, Robert, Graff, Caroline, Masellis, Mario, Tartaglia, Maria Carmela, Rowe, James B, Borroni, Barbara, Finger, Elizabeth, Synofzik, Matthis, Galimberti, Daniela, Vandenberghe, Rik, de Mendonça, Alexandre, Butler, Chris R, Gerhard, Alexander, Ducharme, Simon, Le Ber, Isabelle, Santana, Isabel, Pasquier, Florence, Levin, Johannes, Otto, Markus, Sorbi, Sandro, Warren, Jason D, Rohrer, Jonathan D, Russell, Lucy L
Published in Brain communications

Structural MRI predicts clinical progression in presymptomatic genetic frontotemporal dementia: findings from the GENetic Frontotemporal dementia Initiative cohort

by Bocchetta, Martina, Todd, Emily G, Bouzigues, Arabella, Cash, David M, Nicholas, Jennifer M, Convery, Rhian S, Russell, Lucy L, Thomas, David L, Malone, Ian B, Iglesias, Juan Eugenio, van Swieten, John C, Jiskoot, Lize C, Seelaar, Harro, Borroni, Barbara, Galimberti, Daniela, Sanchez-Valle, Raquel, Laforce, Robert, Moreno, Fermin, Synofzik, Matthis, Graff, Caroline, Masellis, Mario, Tartaglia, Maria Carmela, Rowe, James B, Vandenberghe, Rik, Finger, Elizabeth, Tagliavini, Fabrizio, de Mendonça, Alexandre, Santana, Isabel, Butler, Chris R, Ducharme, Simon, Gerhard, Alexander, Danek, Adrian, Levin, Johannes, Otto, Markus, Sorbi, Sandro, Le Ber, Isabelle, Pasquier, Florence, Rohrer, Jonathan D
Published in Brain communications

Analysis of brain atrophy and local gene expression in genetic frontotemporal dementia

by Altmann, Andre, Cash, David M, Bocchetta, Martina, Heller, Carolin, Reynolds, Regina, Moore, Katrina, Convery, Rhian S, Thomas, David L, van Swieten, John C, Moreno, Fermin, Sanchez-Valle, Raquel, Borroni, Barbara, Laforce, Jr, Robert, Masellis, Mario, Tartaglia, Maria Carmela, Graff, Caroline, Galimberti, Daniela, Rowe, James B, Finger, Elizabeth, Synofzik, Matthis, Vandenberghe, Rik, de Mendonça, Alexandre, Tagliavini, Fabrizio, Santana, Isabel, Ducharme, Simon, Butler, Chris R, Gerhard, Alex, Levin, Johannes, Danek, Adrian, Frisoni, Giovanni, Ghidoni, Roberta, Sorbi, Sandro, Otto, Markus, Ryten, Mina, Rohrer, Jonathan D
Published in Brain communications

Targeted copy number variant identification across the neurodegenerative disease spectrum

by Dilliott, Allison A., Zhang, Kristina K., Wang, Jian, Abrahao, Agessandro, Binns, Malcolm A., Black, Sandra E., Borrie, Michael, Dowlatshahi, Dar, Finger, Elizabeth, Fischer, Corinne E., Frank, Andrew, Freedman, Morris, Grimes, David, Hassan, Ayman, Jog, Mandar, Kumar, Sanjeev, Lang, Anthony E., Mandzia, Jennifer, Masellis, Mario, Pasternak, Stephen H., Pollock, Bruce G., Rajji, Tarek K., Rogaeva, Ekaterina, Sahlas, Demetrios J., Saposnik, Gustavo, Sato, Christine, Seitz, Dallas, Shoesmith, Christen, Steeves, Thomas D. L., Swartz, Richard H., Tan, Brian, Tang‐Wai, David F., Tartaglia, Maria C., Turnbull, John, Zinman, Lorne, Hegele, Robert A.
Published in Molecular genetics & genomic medicine

Hierarchical spectral clustering reveals brain size and shape changes in asymptomatic carriers of C9orf72

by Bruffaerts, Rose, Gors, Dorothy, Bárcenas Gallardo, Alicia, Vandenbulcke, Mathieu, Van Damme, Philip, Suetens, Paul, van Swieten, John C, Borroni, Barbara, Sanchez-Valle, Raquel, Moreno, Fermin, Laforce, Robert, Graff, Caroline, Synofzik, Matthis, Galimberti, Daniela, Rowe, James B, Masellis, Mario, Tartaglia, Maria Carmela, Finger, Elizabeth, de Mendonça, Alexandre, Tagliavini, Fabrizio, Butler, Chris R, Santana, Isabel, Gerhard, Alexander, Ducharme, Simon, Levin, Johannes, Danek, Adrian, Otto, Markus, Rohrer, Jonathan D, Dupont, Patrick, Claes, Peter, Vandenberghe, Rik
Published in Brain communications

The Transitions to Long-term In Home Ventilator Engagement Study (Transitions to LIVE): study protocol for a pragmatic randomized controlled trial

by Amin, Reshma, Gershon, Andrea, Buchanan, Francine, Pizzuti, Regina, Qazi, Adam, Patel, Nishali, Pinto, Ruxandra, Moretti, Myla E, Ambreen, Munazzah, Rose, Louise
Published in Current controlled trials in cardiovascular medicine