HuGE Literature Finder
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| The Frequency of Genetic Mutations Associated With Behavioral Variant Frontotemporal Dementia in Chinese Han Patients. Frontiers in aging neuroscience 2021 13 699836. Liu Li, Cui Bo, Chu Min, Cui Yue, Jing Donglai, Li Dan, Xie Kexin, Kong Yu, Xia Tianxinyu, Wang Chaodong, Wu Liyo |
| [C9orf72-associated frontotemporal dementia in the Russian population]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2020 120 (9): 98-106. Shpilyukova Yu A, Fedotova E Yu, Berdnikovich E S, Konovalov R N, Zakharova M N, Grishina D A, Yakhno N N, Illarioshkin S |
| Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia. Journal of neurology 2017 Jun 264 (6): 1091-1098. Marjanovic Ivan V, Selak-Djokic Biljana, Peric Stojan, Jankovic Milena, Arsenijevic Vladimir, Basta Ivana, Lavrnic Dragana, Stefanova Elka, Stevic Zori |
| GBA-associated parkinsonism and dementia: beyond a-synucleinopathies? European journal of neurology : the official journal of the European Federation of Neurological Societies 2015 Nov . Pilotto A, Schulte C, Hauser A K, Biskup S, Munz M, Brockmann K, Schaeffer E, Synofzik M, Maetzler W, Suenkel U, Srulijes K, Gasser T, Berg |
| Screening for C9orf72 Expansion Mutation in Serbian Patients with Early-Onset Dementia. Dementia and geriatric cognitive disorders 2015 Sep 40 (5-6): 358-365. Mandic-Stojmenovic Gorana, Stefanova Elka, Dobricic Valerija, Novakovic Ivana, Stojkovic Tanja, Jesic Aleksandar, Kostic Vladim |
| C9ORF72 repeat expansion is not a significant cause of late onset cerebellar ataxia syndrome. Journal of the neurological sciences 2014 Dec 347 (1-2): 322-4. Hsiao Cheng-Tsung, Tsai Pei-Chien, Liao Yi-Chu, Lee Yi-Chung, Soong Bing-W |
| Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion. Brain : a journal of neurology 2014 Nov 137 (Pt 11): 3047-60. Lee Suzee E, Khazenzon Anna M, Trujillo Andrew J, Guo Christine C, Yokoyama Jennifer S, Sha Sharon J, Takada Leonel T, Karydas Anna M, Block Nikolas R, Coppola Giovanni, Pribadi Mochtar, Geschwind Daniel H, Rademakers Rosa, Fong Jamie C, Weiner Michael W, Boxer Adam L, Kramer Joel H, Rosen Howard J, Miller Bruce L, Seeley William |
| Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers. Neurobiology of aging 2014 Oct 35 (10): 2421.e13-7. van Blitterswijk Marka, Mullen Bianca, Heckman Michael G, Baker Matthew C, DeJesus-Hernandez Mariely, Brown Patricia H, Murray Melissa E, Hsiung Ging-Yuek R, Stewart Heather, Karydas Anna M, Finger Elizabeth, Kertesz Andrew, Bigio Eileen H, Weintraub Sandra, Mesulam Marsel, Hatanpaa Kimmo J, White Charles L, Neumann Manuela, Strong Michael J, Beach Thomas G, Wszolek Zbigniew K, Lippa Carol, Caselli Richard, Petrucelli Leonard, Josephs Keith A, Parisi Joseph E, Knopman David S, Petersen Ronald C, Mackenzie Ian R, Seeley William W, Grinberg Lea T, Miller Bruce L, Boylan Kevin B, Graff-Radford Neill R, Boeve Bradley F, Dickson Dennis W, Rademakers Ro |
| C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome. Journal of neurology 2014 Oct 261 (10): 1917-21. Kosti? Vladimir S, Dobri?i? Valerija, Stankovi? Iva, Rali? Vesna, Stefanova El |
| Frontotemporal dementia associated with the C9ORF72 mutation: a unique clinical profile. JAMA neurology 2014 Mar 71 (3): 331-9. Devenney Emma, Hornberger Michael, Irish Muireann, Mioshi Eneida, Burrell James, Tan Rachel, Kiernan Matthew C, Hodges John |
| Lack of c9orf72 repeat expansion in taiwanese patients with mixed neurodegenerative disorders. Frontiers in neurology 2014 5 59. Lin Chin-Hsien, Chen Ta-Fu, Chiu Ming-Jang, Lin Han-I, Wu Ruey-Me |
| Identification of C9orf72 repeat expansions in patients with amyotrophic lateral sclerosis and frontotemporal dementia in mainland China. Neurobiology of aging 2013 Oct . Jiao B, Tang B, Liu X, Yan X, Zhou L, Yang Y, Wang J, Xia K, Shen L |
| Progressive amnestic dementia, hippocampal sclerosis, and mutation in C9ORF72. Acta neuropathologica 2013 Oct 126 (4): 545-54. Murray Melissa E, Bieniek Kevin F, Banks Greenberg M, DeJesus-Hernandez Mariely, Rutherford Nicola J, van Blitterswijk Marka, Niemantsverdriet Ellis, Ash Peter E, Gendron Tania F, Kouri Naomi, Baker Matt, Goodman Ira J, Petrucelli Leonard, Rademakers Rosa, Dickson Dennis |
| Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation. Biological psychiatry 2013 Sep 74 (5): 384-91. Galimberti Daniela, Fenoglio Chiara, Serpente Maria, Villa Chiara, Bonsi Rossana, Arighi Andrea, Fumagalli Giorgio G, Del Bo Roberto, Bruni Amalia C, Anfossi Maria, Clodomiro Alessandra, Cupidi Chiara, Nacmias Benedetta, Sorbi Sandro, Piaceri Irene, Bagnoli Silvia, Bessi Valentina, Marcone Alessandra, Cerami Chiara, Cappa Stefano F, Filippi Massimo, Agosta Federica, Magnani Giuseppe, Comi Giancarlo, Franceschi Massimo, Rainero Innocenzo, Giordana Maria Teresa, Rubino Elisa, Ferrero Patrizia, Rogaeva Ekaterina, Xi Zhengrui, Confaloni Annamaria, Piscopo Paola, Bruno Giuseppe, Talarico Giuseppina, Cagnin Annachiara, Clerici Francesca, Dell'Osso Bernardo, Comi Giacomo P, Altamura A Carlo, Mariani Claudio, Scarpini El |
| Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease. Clinical genetics 2013 Mar 83 (3): 279-83. Lindquist S G, Duno M, Batbayli M, Puschmann A, Braendgaard H, Mardosiene S, Svenstrup K, Pinborg L H, Vestergaard K, Hjermind L E, Stokholm J, Andersen B B, Johannsen P, Nielsen J |
| C9orf72 repeat expansions are a rare genetic cause of parkinsonism. Brain : a journal of neurology 2013 Feb 136 (Pt 2): 385-91. Lesage Suzanne, Le Ber Isabelle, Condroyer Christel, Broussolle Emmanuel, Gabelle Audrey, Thobois Stéphane, Pasquier Florence, Mondon Karl, Dion Patrick A, Rochefort Daniel, Rouleau Guy A, Dürr Alexandra, Brice Alexis, |
| C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing. Journal of Alzheimer's disease : JAD 2012 Dec . Le Ber I, Camuzat A, Guillot-Noel L, Hannequin D, Lacomblez L, Golfier V, Puel M, Martinaud O, Deramecourt V, Rivaud-Pechoux S, Millecamps S, Vercelletto M, Couratier P, Sellal F, Pasquier F, Salachas F, Thomas-Antérion C, Didic M, Pariente J, Seilhean D, Ruberg M, Wargon I, Blanc F, Camu W, Michel BF, Berger E, Sauvée M, Thauvin-Robinet C, Mondon K, Tournier-Lasserve E, Goizet C, Fleury M, Viennet G, Verpillat P, Meininger V, Duyckaerts C, Dubois B, Brice A |
| CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis. Neurobiology of aging 2012 Aug 33 (8): 1852.e1-3. Groen Ewout J N, van Rheenen Wouter, Koppers Max, van Doormaal Perry T C, Vlam Lotte, Diekstra Frank P, Dooijes Dennis, Pasterkamp R Jeroen, van den Berg Leonard H, Veldink Jan |
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- Page last updated:Jun 28, 2022
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