检索结果 - Catherine Lomen‐Hoerth

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  1. 1
    Cognitive and behavioral challenges in caring for patients with frontotemporal dementia and amyotrophic lateral sclerosis

    Cognitive and behavioral challenges in caring for patients with frontotemporal dementia and amyotrophic lateral sclerosis 由 Jennifer Merrilees, Jennifer Klapper, Jennifer Murphy, Catherine Lomen‐Hoerth, Bruce L. Miller

    出版 2010
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  2. 2
    Professional identity formation in disorienting times

    Professional identity formation in disorienting times 由 Geoffrey V. Stetson, Irina V. Kryzhanovskaya, Catherine Lomen‐Hoerth, Karen E. Hauer

    出版 2020
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  3. 3
    Tissue-specific alternative splicing generates two isoforms of the trkA receptor

    Tissue-specific alternative splicing generates two isoforms of the trkA receptor 由 Philip Barker, Catherine Lomen‐Hoerth, Erin Gensch, Susan O. Meakin, David J. Glass, Eric M. Shooter

    出版 1993
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  4. 4
    Quantifying disease progression in amyotrophic lateral sclerosis

    Quantifying disease progression in amyotrophic lateral sclerosis 由 Neil G. Simon, Martin R. Turner, Steve Vucic, Ammar Al‐Chalabi, Jeremy M. Shefner, Catherine Lomen‐Hoerth, Matthew C. Kiernan

    出版 2014
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    Revisão
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  5. 5
    Comprehensive cell type decomposition of circulating cell-free DNA with CelFiE

    Comprehensive cell type decomposition of circulating cell-free DNA with CelFiE 由 Christa Caggiano, Barbara Celona, Fleur C. Garton, Joel Mefford, Brian L. Black, Robert D. Henderson, Catherine Lomen‐Hoerth, Andrew Dahl, Noah Zaitlen

    出版 2021
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  6. 6
    Extensive FUS‐Immunoreactive Pathology in Juvenile Amyotrophic Lateral Sclerosis with Basophilic Inclusions

    Extensive FUS‐Immunoreactive Pathology in Juvenile Amyotrophic Lateral Sclerosis with Basophilic Inclusions 由 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

    出版 2010
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  7. 7
    Serious Bacterial Infections Acquired During Treatment of Patients Given a Diagnosis of Chronic Lyme Disease — United States

    Serious Bacterial Infections Acquired During Treatment of Patients Given a Diagnosis of Chronic Lyme Disease — United States 由 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

    出版 2017
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  8. 8
    Behaviour, physiology and experience of pathological laughing and crying in amyotrophic lateral sclerosis

    Behaviour, physiology and experience of pathological laughing and crying in amyotrophic lateral sclerosis 由 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

    出版 2011
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  9. 9
    Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia

    Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia 由 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

    出版 2018
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  10. 10
    Deciphering amyotrophic lateral sclerosis: What phenotype, neuropathology and genetics are telling us about pathogenesis

    Deciphering amyotrophic lateral sclerosis: What phenotype, neuropathology and genetics are telling us about pathogenesis 由 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

    出版 2013
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  11. 11
    Revised Airlie House consensus guidelines for design and implementation of ALS clinical trials

    Revised Airlie House consensus guidelines for design and implementation of ALS clinical trials 由 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

    出版 2019
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  12. 12
    Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III

    Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III 由 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

    出版 2009
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  13. 13
    Whole-Genome Analysis of Sporadic Amyotrophic Lateral Sclerosis

    Whole-Genome Analysis of Sporadic Amyotrophic Lateral Sclerosis 由 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

    出版 2007
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  14. 14
    Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype

    Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype 由 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

    出版 2012
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  15. 15
    TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson’s disease

    TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson’s disease 由 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

    出版 2013
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  16. 16
    Ataxin-2 repeat-length variation and neurodegeneration

    Ataxin-2 repeat-length variation and neurodegeneration 由 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

    出版 2011
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  17. 17
    Cognitive-behavioral screening reveals prevalent impairment in a large multicenter ALS cohort

    Cognitive-behavioral screening reveals prevalent impairment in a large multicenter ALS cohort 由 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

    出版 2016
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  18. 18
    Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

    Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis 由 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

    出版 2016
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  19. 19
    Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS

    Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS 由 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

    出版 2024
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  20. 20
    Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

    Genetic correlation between amyotrophic lateral sclerosis and schizophrenia 由 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

    出版 2017
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