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There are 24684 results for: content related to: Angiogenin, a piece of the complex puzzle of neurodegeneration

  1. You have full text access to this OnlineOpen article
    C9ORF72 Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease

    Annals of Human Genetics

    Volume 77, Issue 5, September 2013, Pages: 351–363, Karen Nuytemans, Güney Bademci, Martin M. Kohli, Gary W. Beecham, Liyong Wang, Juan I. Young, Fatta Nahab, Eden R. Martin, John R. Gilbert, Michael Benatar, Jonathan L. Haines, William K. Scott, Stephan Züchner, Margaret A. Pericak-Vance and Jeffery M. Vance

    Article first published online : 12 JUL 2013, DOI: 10.1111/ahg.12033

  2. Genetic heterogeneity of amyotrophic lateral sclerosis: Implications for clinical practice and research

    Muscle & Nerve

    Volume 49, Issue 6, June 2014, Pages: 786–803, Xiaowei W. Su, James R. Broach, James R. Connor, Glenn S. Gerhard and Zachary Simmons

    Article first published online : 8 APR 2014, DOI: 10.1002/mus.24198

  3. Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis

    Annals of Neurology

    Volume 74, Issue 2, August 2013, Pages: 180–187, Sorana Ciura, Serena Lattante, Isabelle Le Ber, Morwena Latouche, Hervé Tostivint, Alexis Brice and Edor Kabashi

    Article first published online : 24 SEP 2013, DOI: 10.1002/ana.23946

  4. You have full text access to this OnlineOpen article
    Lack of unique neuropathology in amyotrophic lateral sclerosis associated with p.K54E angiogenin (ANG) mutation

    Neuropathology and Applied Neurobiology

    Volume 39, Issue 5, August 2013, Pages: 562–571, J. Kirby, J. R. Highley, L. Cox, E. F. Goodall, C. Hewitt, J. A. Hartley, H. C. Hollinger, M. Fox, P. G. Ince, C. J. McDermott and P. J. Shaw

    Article first published online : 9 JUL 2013, DOI: 10.1111/nan.12007

  5. You have full text access to this OnlineOpen article
    A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats

    Human Mutation

    Volume 34, Issue 2, February 2013, Pages: 363–373, Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Mathieu Vandenbulcke, Kristel Sleegers, Anne Sieben, Veerle Bäumer, Githa Maes, Ellen Corsmit, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Robert Perneczky, Janine Diehl-Schmid, Alexandre de Mendonça, Gabriel Miltenberger-Miltenyi, Sónia Pereira, José Pimentel, Benedetta Nacmias, Silvia Bagnoli, Sandro Sorbi, Caroline Graff, Huei-Hsin Chiang, Marie Westerlund, Raquel Sanchez-Valle, Albert Llado, Ellen Gelpi, Isabel Santana, Maria Rosário Almeida, Beatriz Santiago, Giovanni Frisoni, Orazio Zanetti, Cristian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Ludger Schöls, Michael T. Heneka, Frank Jessen, Radoslav Matej, Eva Parobkova, Gabor G. Kovacs, Thomas Ströbel, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Adrian Danek, Thomas Arzberger, Gian Maria Fabrizi, Silvia Testi, Eric Salmon, Patrick Santens, Jean-Jacques Martin, Patrick Cras, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Christine Van Broeckhoven, Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Stéphanie Philtjens, Kristel Sleegers, Veerle Bäumer, Githa Maes, Ellen Corsmit, Marc Cruts, Christine Van Broeckhoven, Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Stéphanie Philtjens, Jessie Theuns, Kristel Sleegers, Veerle Bäumer, Githa Maes, Marc Cruts, Christine Van Broeckhoven, Sebastiaan Engelborghs, Peter P. De Deyn, Patrick Cras, Sebastiaan Engelborghs, Peter P. De Deyn, Mathieu Vandenbulcke, Mathieu Vandenbulcke, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Robert Perneczky, Janine Diehl-Schmid, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Ludger Schöls, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Ludger Schöls, Michael T. Heneka, Frank Jessen, Alfredo Ramirez, Delia Kurzwelly, Carmen Sachtleben, Wolfgang Mairer, Alexandre de Mendonça, Gabriel Miltenberger-Miltenyi, Sónia Pereira, Clara Firmo, José Pimentel, Raquel Sanchez-Valle, Albert Llado, Anna Antonell, Jose Molinuevo , Ellen Gelpi, Caroline Graff, Huei-Hsin Chiang, Marie Westerlund, Caroline Graff, Anne Kinhult Ståhlbom, Håkan Thonberg, Inger Nennesmo, Anne Börjesson-Hanson, Benedetta Nacmias, Silvia Bagnoli, Sandro Sorbi, Valentina Bessi, Irene Piaceri, Isabel Santana, Beatriz Santiago, Isabel Santana, Maria Helena Ribeiro, Maria Rosário Almeida, Catarina Oliveira, João Massano, Carolina Garret, Paula Pires, Giovanni Frisoni, Orazio Zanetti, Cristian Bonvicini, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Ivailo Tournev, Gabor G. Kovacs, Thomas Ströbel, Michael T. Heneka, Frank Jessen, Alfredo Ramirez, Delia Kurzwelly, Carmen Sachtleben, Wolfgang Mairer;, Frank Jessen, Radoslav Matej, Eva Parobkova, Adrian Danel, Thomas Arzberger, Gian Maria Fabrizi, Silvia Testi, Sergio Ferrari, Tiziana Cavallaro, Eric Salmon, Patrick Santens, Patrick Cras and on behalf of the European Early-Onset Dementia (EOD) Consortium

    Article first published online : 4 JAN 2013, DOI: 10.1002/humu.22244

  6. You have full text access to this OnlineOpen article
    A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia

    Neuropathology and Applied Neurobiology

    Volume 40, Issue 4, June 2014, Pages: 502–513, Tammaryn Lashley, Jonathan D. Rohrer, Colin Mahoney, Elizabeth Gordon, Jon Beck, Simon Mead, Jason Warren, Martin Rossor and Tamas Revesz

    Article first published online : 22 APR 2014, DOI: 10.1111/nan.12100

  7. Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: A population-based case–control cohort study of familial and sporadic amyotrophic lateral sclerosis

    Annals of Neurology

    Volume 74, Issue 5, November 2013, Pages: 699–708, Susan Byrne, Mark Heverin, Marwa Elamin, Peter Bede, Catherine Lynch, Kevin Kenna, Russell MacLaughlin, Cathal Walsh, Ammar Al Chalabi and Orla Hardiman

    Article first published online : 10 SEP 2013, DOI: 10.1002/ana.23969

  8. Frontotemporal lobar degeneration with TDP-43 proteinopathy and chromosome 9p repeat expansion in C9ORF72: clinicopathologic correlation

    Neuropathology

    Volume 33, Issue 2, April 2013, Pages: 122–133, Eileen H. Bigio, Sandra Weintraub, Rosa Rademakers, Matt Baker, Saman S. Ahmadian, Alfred Rademaker, Bing Bing Weitner, Qinwen Mao, Kyung-Hwa Lee, Manjari Mishra, Rakhee A. Ganti and M-Marsel Mesulam

    Article first published online : 18 JUN 2012, DOI: 10.1111/j.1440-1789.2012.01332.x

  9. Clinical and genetic heterogeneity of amyotrophic lateral sclerosis

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 408–416, M Sabatelli, A Conte and M Zollino

    Article first published online : 12 MAR 2013, DOI: 10.1111/cge.12117

  10. Angiogenin variation and Parkinson disease

    Annals of Neurology

    Volume 71, Issue 5, May 2012, Pages: 725–727, Sruti Rayaprolu, Alexandra Soto-Ortolaza, Rosa Rademakers, Ryan J. Uitti, Zbigniew K. Wszolek and Owen A. Ross

    Article first published online : 20 APR 2012, DOI: 10.1002/ana.23586

  11. Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease

    Movement Disorders

    Volume 29, Issue 6, May 2014, Pages: 827–830, Karen Nuytemans, Vanessa Inchausti, Gary W. Beecham, Liyong Wang, Dennis W. Dickson, John Q. Trojanowski, Virginia M.-Y. Lee, Deborah C. Mash, Matthew P. Frosch, Tatiana M. Foroud, Lawrence S. Honig, Thomas J. Montine, Ted M. Dawson, Eden R. Martin, William K. Scott and Jeffery M. Vance

    Article first published online : 26 FEB 2014, DOI: 10.1002/mds.25838

  12. Molecular Genetics of Frontotemporal Dementia

    Standard Article

    eLS

    Raffaele Ferrari, Avinash Thumma and Parastoo Momeni

    Published Online : 15 MAY 2013, DOI: 10.1002/9780470015902.a0024457

  13. 2012 Annual Meeting Sunday, October 7, 2012 Poster Session Abstracts

    Annals of Neurology

    Volume 72, Issue S16, 2012, Pages: S1–S120,

    Article first published online : 28 DEC 2012, DOI: 10.1002/ana.23769

  14. C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia

    Movement Disorders

    Volume 27, Issue 14, December 2012, Pages: 1835–1836, Brent L. Fogel, Mochtar Pribadi, Sarah Pi, Susan L. Perlman, Daniel H. Geschwind and Giovanni Coppola

    Article first published online : 18 OCT 2012, DOI: 10.1002/mds.25245

  15. Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 279–283, SG Lindquist, M Duno, M Batbayli, A Puschmann, H Braendgaard, S Mardosiene, K Svenstrup, LH Pinborg, K Vestergaard, LE Hjermind, J Stokholm, BB Andersen, P Johannsen and JE Nielsen

    Article first published online : 4 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01903.x

  16. Analysis of the C9orf72 Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide

    Human Mutation

    Volume 34, Issue 1, January 2013, Pages: 79–82, Alberto García-Redondo, Oriol Dols-Icardo, Ricard Rojas-García, Jesús Esteban-Pérez, Pilar Cordero-Vázquez, José Luis Muñoz-Blanco, Irene Catalina, Miguel González-Muñoz, Luis Varona, Esther Sarasola, Monica Povedano, Teresa Sevilla, Antonio Guerrero, Julio Pardo, Adolfo López de Munain, Celedonio Márquez-Infante, Francisco Javier Rodríguez de Rivera, Pau Pastor, Ivonne Jericó, Amaya Álvarez de Arcaya, Jesús S. Mora, Jordi Clarimón, The C9ORF72 Spanish Study Group, Juan Francisco Gonzalo-Martínez, Alexandra Juárez-Rufián, Gabriela Atencia, Rosario Jiménez-Bautista, Yolanda Morán, Javier Mascías, María Hernández-Barral, Solange Kapetanovic, María García-Barcina, Carmen Alcalá, Álvaro Vela, Concepción Ramírez-Ramos, Lucía Galán, Jordi Pérez-Tur, Beatriz Quintáns, M Jesús Sobrido, Roberto Fernández-Torrón, Juan José Poza, Ana Gorostidi, Carmen Paradas, Pablo Villoslada, Pilar Larrodé, José Luis Capablo, Jordi Pascual-Calvet, Miguel Goñi, Yolanda Morgado, Miriam Guitart, Sira Moreno-Laguna, Almudena Rueda, Carlos Martín-Estefanía, Carlos Cemillán, Rafael Blesa and Alberto Lleó

    Article first published online : 11 OCT 2012, DOI: 10.1002/humu.22211

  17. Mouse models of frontotemporal dementia

    Annals of Neurology

    Volume 72, Issue 6, December 2012, Pages: 837–849, Erik D. Roberson

    Article first published online : 31 DEC 2012, DOI: 10.1002/ana.23722

  18. Clinical variability and additional mutations in amyotrophic lateral sclerosis patients with p.N352S mutations in TARDBP

    Neuropathology and Applied Neurobiology

    Volume 40, Issue 3, April 2014, Pages: 356–358, M. van Blitterswijk, R. Rademakers and L. H. van den Berg

    Article first published online : 13 MAR 2014, DOI: 10.1111/nan.12099

  19. You have free access to this content
    Amyotrophic lateral sclerosis: Problems and prospects

    Annals of Neurology

    Volume 74, Issue 3, September 2013, Pages: 309–316, Jemeen Sreedharan and Robert H. Brown Jr

    Article first published online : 9 OCT 2013, DOI: 10.1002/ana.24012

  20. C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: A genome-wide meta-analysis

    Annals of Neurology

    Volume 76, Issue 1, July 2014, Pages: 120–133, Frank P. Diekstra, Vivianna M. Van Deerlin, John C. van Swieten, Ammar Al-Chalabi, Albert C. Ludolph, Jochen H. Weishaupt, Orla Hardiman, John E. Landers, Robert H. Brown Jr, Michael A. van Es, R. Jeroen Pasterkamp, Max Koppers, Peter M. Andersen, Karol Estrada, Fernando Rivadeneira, Albert Hofman, André G. Uitterlinden, Philip van Damme, Judith Melki, Vincent Meininger, Aleksey Shatunov, Christopher E. Shaw, P. Nigel Leigh, Pamela J. Shaw, Karen E. Morrison, Isabella Fogh, Adriano Chiò, Bryan J. Traynor, David Czell, Markus Weber, Peter Heutink, Paul I. W. de Bakker, Vincenzo Silani, Wim Robberecht, Leonard H. van den Berg and Jan H. Veldink

    Article first published online : 27 JUN 2014, DOI: 10.1002/ana.24198