Rezultati - Catherine Lomen‐Hoerth
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Extensive FUS‐Immunoreactive Pathology in Juvenile Amyotrophic Lateral Sclerosis with Basophilic Inclusions od Eric J. Huang, Jiasheng Zhang, Felix Geser, John Q. Trojanowski, Jonathan B. Strober, Dennis W. Dickson, Robert H. Brown, Barbara E. Shapiro, Catherine Lomen‐Hoerth
Izdano 2010Artigo -
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Serious Bacterial Infections Acquired During Treatment of Patients Given a Diagnosis of Chronic Lyme Disease — United States od Natalie S. Marzec, Christina A. Nelson, Paul Waldron, Brian G. Blackburn, Syed Hosain, Tara L. Greenhow, Gary M. Green, Catherine Lomen‐Hoerth, Marjorie Golden, Paul S. Mead
Izdano 2017Artigo -
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Behaviour, physiology and experience of pathological laughing and crying in amyotrophic lateral sclerosis od Nicholas Olney, Madeleine S. Goodkind, Catherine Lomen‐Hoerth, Patrick Kenneth Whalen, Craig Williamson, Daniel C. Holley, Alice Verstaen, Lisa M. Brown, Bruce L. Miller, John Kornak, Robert W. Levenson, Howard J. Rosen
Izdano 2011Artigo -
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Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia od Loes M. Olde Loohuis, Serghei Mangul, Anil P. S. Ori, Guillaume Jospin, David Koslicki, Harry Taegyun Yang, Timothy Wu, Marco P. Boks, Catherine Lomen‐Hoerth, Martina Wiedau‐Pazos, Rita M. Cantor, Willem M. de Vos, René S. Kahn, Eleazar Eskin, Roel A. Ophoff
Izdano 2018Artigo -
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Deciphering amyotrophic lateral sclerosis: What phenotype, neuropathology and genetics are telling us about pathogenesis od John Ravits, Stanley H. Appel, Robert H. Baloh, Richard J. Barohn, Benjamin Rix Brooks, Lauren Elman, Mary Kay Floeter, Christopher E. Henderson, Catherine Lomen‐Hoerth, Jeffrey D. Macklis, Leo McCluskey, Hiroshi Mitsumoto, Serge Przedborski, Jeffrey D. Rothstein, John Q. Trojanowski, Leonard H. van den Berg, Steven P. Ringel
Izdano 2013Artigo -
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Revised Airlie House consensus guidelines for design and implementation of ALS clinical trials od Leonard H. van den Berg, Eric J. Sorenson, Gary Gronseth, Eric A. Macklin, Jinsy Andrews, Robert H. Baloh, Michael Benatar, James Berry, Adriano Chió, Philippe Corcia, Angela Genge, Amelie K. Gubitz, Catherine Lomen‐Hoerth, Christopher McDermott, Erik P. Pioro, Jeffrey Rosenfeld, Vincenzo Silani, Martin R. Turner, Markus Weber, Benjamin Rix Brooks, Robert G. Miller, Hiroshi Mitsumoto
Izdano 2019Artigo -
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Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III od Petra Kaufmann, John L.P. Thompson, Gilberto Levy, Richard Buchsbaum, Jeremy M. Shefner, Lisa S. Krivickas, Jonathan Katz, Yvonne D. Rollins, Richard J. Barohn, Carlayne E. Jackson, Ezgi Tiryaki, Catherine Lomen‐Hoerth, Carmel Armon, Rup Tandan, Stacy A. Rudnicki, Kourosh Rezania, Robert Sufit, Alan Pestronk, Steven Novella, Terry Heiman‐Patterson, Edward J. Kasarskis, Erik P. Pioro, Jacqueline Montes, Rachel Arbing, Darleen Vecchio, Alexandra I. Barsdorf, Hiroshi Mitsumoto, Bruce Levin
Izdano 2009Artigo -
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Whole-Genome Analysis of Sporadic Amyotrophic Lateral Sclerosis od Travis Dunckley, Matthew J. Huentelman, David W. Craig, John V. Pearson, Szabolcs Szelinger, Keta Joshipura, Rebecca F. Halperin, Chelsea Stamper, Kendall R. Jensen, David Letizia, Sharon Hesterlee, Alan Pestronk, Todd Levine, Tulio E. Bertorini, Michael C. Graves, Tahseen Mozaffar, Carlayne E. Jackson, Peter Bosch, April McVey, Arthur Dick, Richard J. Barohn, Catherine Lomen‐Hoerth, Jeffrey Rosenfeld, Daniel T. O’Connor, Kuixing Zhang, Richard Crook, Henrik Ryberg, Michael Hutton, Jonathan Katz, Ericka P. Simpson, Hiroshi Mitsumoto, Robert Bowser, Robert G. Miller, Stanley H. Appel, Dietrich A. Stephan
Izdano 2007Artigo -
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Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype od Nicola J. Rutherford, Michael G. Heckman, Mariely DeJesus‐Hernandez, Matt Baker, Alexandra I. Soto‐Ortolaza, Sruti Rayaprolu, Heather Stewart, Elizabeth Finger, Kathryn Volkening, William W. Seeley, Kimmo J. Hatanpaa, Catherine Lomen‐Hoerth, Andrew Kertesz, Eileen H. Bigio, Carol F. Lippa, David S. Knopman, Hans A. Kretzschmar, Manuela Neumann, Richard J. Caselli, Charles L. White, Ian R. Mackenzie, Ronald Petersen, Michael J. Strong, Bruce L. Miller, Bradley F. Boeve, Ryan J. Uitti, Khrista Boylan, Zbigniew K. Wszołek, Neill R. Graff‐Radford, Dennis W. Dickson, Owen A. Ross, Rosa Rademakers
Izdano 2012Artigo -
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TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson’s disease od Sruti Rayaprolu, Bianca Mullen, Matt Baker, Timothy Lynch, Elizabeth Finger, William W. Seeley, Kimmo J. Hatanpaa, Catherine Lomen‐Hoerth, Andrew Kertesz, Eileen H. Bigio, Carol F. Lippa, Keith A. Josephs, David S. Knopman, Charles L. White, Richard J. Caselli, Ian R. Mackenzie, Bruce L. Miller, Magdalena Boczarska‐Jedynak, Grzegorz Opala, Anna Krygowska‐Wajs, Maria Barcikowska, Steven G. Younkin, Ronald Petersen, Nilüfer Ertekin‐Taner, Ryan J. Uitti, James F. Meschia, Khrista Boylan, Bradley F. Boeve, Neill R. Graff‐Radford, Zbigniew K. Wszołek, Dennis W. Dickson, Rosa Rademakers, Owen A. Ross
Izdano 2013Artigo -
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Ataxin-2 repeat-length variation and neurodegeneration od Owen A. Ross, Nicola J. Rutherford, Matthew Baker, Alexandra I. Soto‐Ortolaza, Minerva M. Carrasquillo, M. DeJesus-Hernandez, Joy Adamson, M. Li, Kathryn Volkening, Elizabeth Finger, William W. Seeley, Kimmo J. Hatanpaa, Catherine Lomen‐Hoerth, Andrew Kertesz, Eileen H. Bigio, Carol F. Lippa, Bryan K. Woodruff, David S. Knopman, Charles L. White, Jay A. van Gerpen, James F. Meschia, Ian R. Mackenzie, Khrista Boylan, Bradley F. Boeve, Bruce L. Miller, Michael J. Strong, Ryan J. Uitti, Steven G. Younkin, N. R. Graff-Radford, Ronald Petersen, Zbigniew K. Wszołek, Dennis W. Dickson, Rosa Rademakers
Izdano 2011Artigo -
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Cognitive-behavioral screening reveals prevalent impairment in a large multicenter ALS cohort od Jennifer Murphy, Pam Factor‐Litvak, Raymond R. Goetz, Catherine Lomen‐Hoerth, Péter L. Nagy, Jonathan Hupf, Jessica Singleton, Susan Woolley, Howard Andrews, Daragh Heitzman, Richard Bedlack, Jonathan Katz, Richard J. Barohn, Eric J. Sorenson, Björn Oskarsson, J. Americo M. Fernandes Filho, Edward J. Kasarskis, Tahseen Mozaffar, Yvonne D. Rollins, Sharon Nations, Andrea Swenson, Boguslawa A. Koczon-Jaremko, Hiroshi Mitsumoto, Jennifer Murphy, Pam Factor‐Litvak, Raymond R. Goetz, Cathy Lomen-Hoerth, Péter L. Nagy, Jon Hupf, Jess Singleton, Susan Woolley, Howard Andrews, Daragh Heitzman, Richard Bedlack, Jonathan Katz, Richard J. Barohn, Eric J. Sorenson, Björn Oskarsson, J. Americo M. Fernandes Filho, Edward J. Kasarskis, Tahseen Mozaffar, Yvonne D. Rollins, Sharon Nations, Andrea Swenson, Boguslawa A. Koczon-Jaremko, Hiroshi Mitsumoto, Christa Campanella, David Merle, Tejal Shah, Meredith Pasmantier Kim, Yei-Won Lee, Georgia Christodoulou, Kate Dalton, J. S. Kidd, Erin H. Gilbert, Mary Kilty, Wendy Rodriguez, Shari Hand, Michelle Washington, Brent Spears, Brandie Burson, Karen Grace, Candace Lee Boyette, Robert G. Miller, Dallas Forshew, Joni Beemsterboer, Will Harris, Shelley McCoy, Thaïs Zayas-Bazan, Chow Saephanh, April McVey, Mazen M. Dimachkie, Mamatha Pasnoor, Yunxia Wang, Lowell Tilzer, Maureen Walsh, Laura Herbelin, Christian Pearson, Joe Sibinski, Kristy A. Anderson, Sherry Klingerman, Delana Weis, Nanette C. Joyce, Steffany Lim, Michelle Cregan, Kathie Vanderpool, Deborah R. Taylor, Samantha Thomas, Jason H. King, Robert D. Wells, Y-Nhy Duong, Dennis Robins, Claudia Villerme, Yvonne D. Rollins, Steven P. Ringel, Dianna Quan, Elizabeth Whitethorn, Annabel K. Wang, Veronica Martin, Brian Minton
Izdano 2016Artigo -
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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis od Wouter van Rheenen, Aleksey Shatunov, Annelot M. Dekker, Russell L. McLaughlin, Frank P. Diekstra, Sara L. Pulit, Rick A. A. van der Spek, Urmo Võsa, Simone de Jong, Matthew R. Robinson, Jian Yang, Isabella Fogh, Perry Tc van Doormaal, Gijs Tazelaar, Max Koppers, Anna M. Blokhuis, William Sproviero, Ashley Jones, Kevin P. Kenna, Kristel R. van Eijk, Oliver Harschnitz, Raymond D. Schellevis, William J. Brands, Jelena Medic, Androniki Menelaou, Alice Vajda, Nicola Ticozzi, Kuang Lin, Boris Rogelj, Katarina Vrabec, Metka Ravnik‐Glavač, Blaž Koritnik, Janez Zidar, Lea Leonardis, Leja Dolenc Grošelj, Stéphanie Millecamps, François Salachas, Vincent Meininger, Mamede de Carvalho, Susana Pinto, Jesús S. Mora, Ricardo Rojas-García, Meraida Polak, Siddharthan Chandran, Shuna Colville, Robert Swingler, Karen Morrison, Pamela J. Shaw, John Hardy, Richard W. Orrell, Alan Pittman, Katie Sidle, Pietro Fratta, Andrea Malaspina, Simon Topp, Susanne Petri, Susanne Abdulla, Carsten Drepper, Michael Sendtner, Thomas Meyer, Roel A. Ophoff, Kim A. Staats, Martina Wiedau‐Pazos, Catherine Lomen‐Hoerth, Vivianna M. Van Deerlin, John Q. Trojanowski, Lauren Elman, Leo McCluskey, A. Nazlı Başak, Ceren Tunca, Hamid Hamzeiy, Yeşim Parman, Thomas Meitinger, Peter Lichtner, Milena Radivojkov‐Blagojevic, Christian Andrés, Cindy Maurel, Gilbert Bensimon, G. Bernhard Landwehrmeyer, Alexis Brice, Christine Payan, Safaa Saker-Delye, Alexandra Dürr, Nicholas Wood, Lukas Tittmann, Wolfgang Lieb, André Franke, Marcella Rietschel, Sven Cichon, Markus M. Nöthen, Philippe Amouyel, Christophe Tzourio, Jean‐François Dartigues, André G. Uitterlinden, Fernando Rivadeneira, Karol Estrada, Albert Hofman, Charles Curtis, Hylke M. Blauw, Anneke J. van der Kooi
Izdano 2016Artigo -
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Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS od Tess D. Pottinger, Joshua E. Motelow, Gundula Povysil, Cristiane Araújo Martins Moreno, Zhong Ren, Hemali Phatnani, Matthew B. Harms, Justin Kwan, Dhruv Sareen, Han‐I Wang, James R. Broach, Zachary Simmons, Ximena Arcila-Londono, Steve Parrott, Edward B. Lee, Steve Parrott, Vivianna M. Van Deerlin, Ernest Fraenkel, Lyle W. Ostrow, Frank Baas, Noah Zaitlen, James Berry, Andrea Malaspina, Pietro Fratta, Gregory A. Cox, Leslie M. Thompson, Steven Finkbeiner, Efthimios Dardiotis, Timothy M. Miller, Siddharthan Chandran, Steve Parrott, Suvankar Pal, Eran Hornstein, Daniel J. MacGowan, Terry Heiman‐Patterson, Molly Hammell, Nikolaos A. Patsopoulos, Josh Dubnau, Avindra Nath, Timothy J. Aitman, Javier Santoyo‐López, Nicola Williams, Jonathan Berg, Ruth McGowan, Zosia Miedzybrodzka, Mary Porteous, Edward S. Tobias, Hiroshi Mitsumoto, Pam Factor‐Litvak, Regina M. Santella, Howard Andrews, Daragh Heitzman, Richard Bedlack, Jonathan Katz, Robert G. Miller, Steve Parrott, Dallas Forshew, Richard J. Barohn, Eric J. Sorenson, Björn Oskarsson, Edward J. Kasarskis, Steve Parrott, Catherine Lomen-Hoerth, Jennifer Murphy, Yvonne D. Rollins, Tahseen Mozaffar, J. Americo Fernandes, Andrea Swenson, Sharon Nations, Jeremy M. Shefner, Jinsy Andrews, Agnes Koczon-Jaremko, Péter L. Nagy, Pam Factor‐Litvak, Rejina Santella, Howard Andrews, Raymond R. Goetz, Chris Gennings, Jennifer Murphy, Mary Kay Floeter, Richard J. Barohn, Sharon Nations, Christen Shoesmith, Edward J. Kasarskis, Matthew Harms, Stanley H. Appel, Robert H. Baloh, Richard Bedlack, Siddharthan Chandran, Laura A. Foster, Stephen A. Goutman, Ericka Greene, Chafic Karam, David Lacomis, George Manousakis, Jonathan Mill, Suvankar Pals, Dhruv Sareen, Alex Sherman, Zachary Simmons
Izdano 2024Artigo -
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Genetic correlation between amyotrophic lateral sclerosis and schizophrenia od Russell L. McLaughlin, Dick Schijven, Wouter van Rheenen, Kristel R. van Eijk, Margaret O’Brien, René S. Kahn, Roel A. Ophoff, An Goris, Daniel G. Bradley, Ammar Al‐Chalabi, Leonard H. van den Berg, Jurjen J. Luykx, Orla Hardiman, Jan H. Veldink, Aleksey Shatunov, Annelot M. Dekker, Frank P. Diekstra, Sara L. Pulit, Rick A. A. van der Spek, Perry T.C. van Doormaal, William Sproviero, Ashley Jones, Garth A. Nicholson, Dominic B. Rowe, Roger Pamphlett, Matthew C. Kiernan, Denis C. Bauer, Tim Kahlke, Kelly L. Williams, Filip Eftimov, Isabella Fogh, Nicola Ticozzi, Kuang Lin, Stéphanie Millecamps, François Salachas, Vincent Meininger, Mamede de Carvalho, Susana Pinto, Jesús S. Mora, Ricardo Rojas-García, Meraida Polak, Siddharthan Chandran, Shuna Colville, Robert Swingler, Karen Morrison, Pamela J. Shaw, John Hardy, Richard W. Orrell, Alan Pittman, Katie Sidle, Pietro Fratta, Andrea Malaspina, Susanne Petri, Susanna Abdulla, Carsten Drepper, Michael Sendtner, Thomas Meyer, Martina Wiedau‐Pazos, Catherine Lomen‐Hoerth, Vivianna M. Van Deerlin, John Q. Trojanowski, Lauren Elman, Leo McCluskey, Nazlı Başak, Thomas Meitinger, Peter Lichtner, Milena Blagojevic-Radivojkov, Christian Andrés, Cindy Maurel, Gilbert Bensimon, G. Bernhard Landwehrmeyer, Alexis Brice, Christine Payan, Safa Saker-Delye, Alexandra Dürr, Nicholas Wood, Lukas Tittmann, Wolfgang Lieb, André Franke, Marcella Rietschel, Sven Cichon, Markus M. Nöuthen, Philippe Amouyel, Christophe Tzourio, Jean François Dartigues, André G. Uitterlinden, Fernando Rivadeneira, Karol Estrada, Albert Hofman, Charles Curtis, Anneke J. van der Kooi, Marianne de Visser, Markus Weber, Christopher E. Shaw, Bradley Smith, Orietta Pansarasa, Cristina Cereda, Roberto Del Bo, Giacomo P. Comi, Sandra D’Alfonso
Izdano 2017Artigo
Iskalna orodja:
Sorodne teme
Medicine
Disease
Amyotrophic lateral sclerosis
Biology
Gene
Genetics
Internal medicine
Pathology
Neuroscience
Psychology
Dementia
Psychiatry
Frontotemporal dementia
Bioinformatics
Neurodegeneration
Phenotype
Allele
C9orf72
Cell biology
Clinical trial
Cognition
Computational biology
Computer science
Degenerative disease
Frontotemporal lobar degeneration
Gene expression
Genetic association
Genome-wide association study
Genotype
Medical education