HuGE Literature Finder
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Records 1-40
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Prevalence of amyloid-? pathology in distinct variants of primary progressive aphasia.
Annals of neurology 2018 Sep . Bergeron David, Gorno-Tempini Maria L, Rabinovici Gil D, Santos-Santos Miguel A, Seeley William, Miller Bruce L, Pijnenburg Yolande, Keulen M Antoinette, Groot Colin, van Berckel Bart N M, van der Flier Wiesje M, Scheltens Philip, Rohrer Jonathan D, Warren Jason D, Schott Jonathan M, Fox Nick C, Sanchez-Valle Raquel, Grau-Rivera Oriol, Gelpi Ellen, Seelaar Harro, Papma Janne M, van Swieten John C, Hodges John R, Leyton Cristian E, Piguet Olivier, Rogalsky Emily J, Mesulam Marsel M, Koric Lejla, Nora Kristensen, Pariente Jérémie, Dickerson Bradford, Mackenzie Ian R, Hsiung Ging-Yuek R, Belliard Serge, Irwin David J, Wolk David A, Grossman Murray, Jones Matthew, Harris Jennifer, Mann David, Snowden Julie S, Chrem-Mendez Patricio, Calandri Ismael L, Amengual Alejandra A, Miguet-Alfonsi Carole, Magnin Eloi, Magnani Giuseppe, Santangelo Roberto, Deramecourt Vincent, Pasquier Florence, Mattsson Niklas, Nilsson Christer, Hansson Oskar, Keith Julia, Masellis Mario, Black Sandra E, Matías-Guiu Jordi A, Cabrera-Martin María-Nieves, Paquet Claire, Dumuirger Julien, Teichmann Marc, Sarazin Marie, Bottlaender Michel, Dubois Bruno, Rowe Christopher C, Villemagne Victor L, Vandenberghe Rik, Granadillo Elias, Teng Edmond, Mendez Mario, Meyer Philipp T, Frings Lars, Lleó Alberto, Blesa Rafael, Fortea Juan, Seo Sang Won, Diehl-Schmid Janine, Grimmer Timo, Frederiksen Kristian Steen, Sánchez-Juan Pascual, Chételat Gaël, Jansen Willemijn, Bouchard Rémi W, Robert Laforce, Visser Pieter Jelle, Ossenkoppele R |
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Genetics of dementia in a Finnish cohort.
European journal of human genetics : EJHG 2018 Feb . Pasanen Petra, Myllykangas Liisa, Pöyhönen Minna, Kiviharju Anna, Siitonen Maija, Hardy John, Bras Jose, Paetau Anders, Tienari Pentti J, Guerreiro Rita, Verkkoniemi-Ahola Au |
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Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia.
Journal of Alzheimer's disease : JAD 2018 61 (3): 1179-1187. Maletta Raffaele, Smirne Nicoletta, Bernardi Livia, Anfossi Maria, Gallo Maura, Conidi Maria Elena, Colao Rosanna, Puccio Gianfranco, Curcio Sabrina A M, Laganà Valentina, Frangipane Francesca, Cupidi Chiara, Mirabelli Maria, Vasso Franca, Torchia Giusi, Muraca Maria G, Di Lorenzo Raffaele, Rose Giuseppina, Montesanto Alberto, Passarino Giuseppe, Bruni Amalia |
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TMEM106B and ApoE polymorphisms in CHMP2B-mediated frontotemporal dementia (FTD-3).
Neurobiology of aging 2017 Jul . Rostgaard Nina, Roos Peter, Budtz-Jørgensen Esben, Johannsen Peter, Waldemar Gunhild, Nørremølle Anne, Lindquist Suzanne G, Gydesen Susanne, Brown Jeremy M, Collinge John, Isaacs Adrian M, , Nielsen Troels T, Nielsen Jørgen |
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Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia.
Brain : a journal of neurology 2017 Apr . Mishra Aniket, Ferrari Raffaele, Heutink Peter, Hardy John, Pijnenburg Yolande, Posthuma Danielle, |
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Updated meta-analysis of the role of APOE ?2/?3/?4 alleles in frontotemporal lobar degeneration.
Oncotarget 2017 Apr . Su Wen-Hua, Shi Zhi-Hong, Liu Shu-Ling, Wang Xiao-Dan, Liu Shuai, Ji Yo |
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Interaction with the MAPT H1H1 Genotype Increases Dementia Risk in APOE ?4 Carriers in a Population of Southern India.
Dementia and geriatric cognitive disorders 2016 Oct 42 (5-6): 255-264. Jairani P S, Aswathy P M, Gopala Srinivas, Verghese Joe, Mathuranath P |
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Neuropathologic differences by race from the National Alzheimer's Coordinating Center.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2016 Apr . Graff-Radford Neill R, Besser Lilah M, Crook Julie E, Kukull Walter A, Dickson Dennis |
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Associations between APOE polymorphisms and seven diseases with cognitive impairment including Alzheimer's disease, frontotemporal dementia, and dementia with Lewy bodies in southeast China.
Psychiatric genetics 2016 Mar . Chen Ke-Liang, Sun Yi-Min, Zhou Yan, Zhao Qian-Hua, Ding Ding, Guo Qi-H |
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Association of Frontotemporal Dementia GWAS Loci with Late-Onset Alzheimer's Disease in a Northern Han Chinese Population.
Journal of Alzheimer's disease : JAD 2016 Feb . Tan Chen-Chen, Wan Yu, Tan Meng-Shan, Zhang Wei, Wang Zi-Xuan, Sun Fu-Rong, Miao Dan, Tan Lan, Yu Jin-T |
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The Role of APOE in the Occurrence of Frontotemporal Dementia in Amyotrophic Lateral Sclerosis.
JAMA neurology 2016 Feb . Chiò Adriano, Brunetti Maura, Barberis Marco, Iazzolino Barbara, Montuschi Anna, Ilardi Antonio, Cammarosano Stefania, Canosa Antonio, Moglia Cristina, Calvo Andr |
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MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOE?4 Noncarriers: Results from the Dementia Genetics Spanish Consortium.
Journal of Alzheimer's disease : JAD 2015 Sep . Pastor Pau, Moreno Fermín, Clarimón Jordi, Ruiz Agustín, Combarros Onofre, Calero Miguel, López de Munain Adolfo, Bullido Maria J, de Pancorbo Marian M, Carro Eva, Antonell Anna, Coto Eliecer, Ortega-Cubero Sara, Hernandez Isabel, Tárraga Lluís, Boada Mercè, Lleó Alberto, Dols-Icardo Oriol, Kulisevsky Jaime, Vázquez-Higuera José Luis, Infante Jon, Rábano Alberto, Fernández-Blázquez Miguel Ángel, Valentí Meritxell, Indakoetxea Begoña, Barandiarán Myriam, Gorostidi Ana, Frank-García Ana, Sastre Isabel, Lorenzo Elena, Pastor María A, Elcoroaristizabal Xabier, Lennarz Martina, Maier Wolfang, Rámirez Alfredo, Serrano-Ríos Manuel, Lee Suzee E, Sánchez-Juan Pascu |
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Differential clinicopathologic and genetic features of late-onset amnestic dementias.
Acta neuropathologica 2014 Sep 128 (3): 411-21. Murray Melissa E, Cannon Ashley, Graff-Radford Neill R, Liesinger Amanda M, Rutherford Nicola J, Ross Owen A, Duara Ranjan, Carrasquillo Minerva M, Rademakers Rosa, Dickson Dennis |
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Cerebrospinal fluid tau levels predict prognosis in non-inherited frontotemporal dementia.
Neuro-degenerative diseases 2014 13 (4): 224-9. Borroni Barbara, Benussi Alberto, Cosseddu Maura, Archetti Silvana, Padovani Alessand |
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Genetic modifiers in carriers of repeat expansions in the C9ORF72 gene.
Molecular neurodegeneration 2014 9 38. van Blitterswijk Marka, Mullen Bianca, Wojtas Aleksandra, Heckman Michael G, Diehl Nancy N, 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 |
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TMEM106B and APOE polymorphisms interact to confer risk for late-onset Alzheimer's disease in Han Chinese.
Journal of neural transmission (Vienna, Austria : 1996) 2014 121 (3): 283-7. Lu Rui-Chun, Wang Hao, Tan Meng-Shan, Yu Jin-Tai, Tan L |
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Apolipoprotein E polymorphisms in frontotemporal lobar degeneration: a meta-analysis.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2013 Nov 9 (6): 706-13. Rubino Elisa, Vacca Alessandro, Govone Flora, De Martino Paola, Pinessi Lorenzo, Rainero Innocen |
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TOMM40 polymorphisms in Italian Alzheimer's disease and frontotemporal dementia patients.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2013 Jun 34 (6): 995-8. Bagnoli Silvia, Piaceri Irene, Tedde Andrea, Bessi Valentina, Bracco Laura, Sorbi Sandro, Nacmias Benedet |
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Apolipoprotein ? ?4 frequency is increased among Chinese patients with frontotemporal dementia and Alzheimer's disease.
Dementia and geriatric cognitive disorders 2013 36 (3-4): 163-70. Ji Yong, Liu Mengyuan, Huo Ya Ruth, Liu Shuling, Shi Zhihong, Liu Shuai, Wisniewski Thomas, Wang Jinhu |
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Disease state fingerprint in frontotemporal degeneration with reference to Alzheimer's disease and mild cognitive impairment.
Journal of Alzheimer's disease : JAD 2013 35 (4): 727-39. Muñoz-Ruiz Miguel Ángel, Hartikainen Päivi, Hall Anette, Mattila Jussi, Koikkalainen Juha, Herukka Sanna-Kaisa, Julkunen Valtteri, Vanninen Ritva, Liu Yawu, Lötjönen Jyrki, Soininen Hilk |
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Investigation of c9orf72 in 4 neurodegenerative disorders.
Archives of neurology 2012 Dec 69 (12): 1583-90. Xi Zhengrui, Zinman Lorne, Grinberg Yakov, Moreno Danielle, Sato Christine, Bilbao Juan M, Ghani Mahdi, Hernández Isabel, Ruiz Agustín, Boada Mercè, Morón Francisco J, Lang Anthony E, Marras Connie, Bruni Amalia, Colao Rosanna, Maletta Raffaele G, Puccio Gianfranco, Rainero Innocenzo, Pinessi Lorenzo, Galimberti Daniela, Morrison Karen E, Moorby Catriona, Stockton Joanne D, Masellis Mario, Black Sandra E, Hazrati Lili-Naz, Liang Yan, van Haersma de With Jan, Fornazzari Luis, Villagra Roque, Rojas-Garcia Ricardo, Clarimón Jordi, Mayeux Richard, Robertson Janice, St George-Hyslop Peter, Rogaeva Ekateri |
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Definite behavioral variant of frontotemporal dementia with C9ORF72 expansions despite positive Alzheimer's disease cerebrospinal fluid biomarkers.
Journal of Alzheimer's disease : JAD 2012 32 (1): 19-22. Wallon David, Rovelet-Lecrux Anne, Deramecourt Vincent, Pariente Jeremie, Auriacombe Sophie, Le Ber Isabelle, Schraen Suzanna, Pasquier Florence, Campion Dominique, Hannequin Didi |
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Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration.
Journal of Alzheimer's disease : JAD 2012 31 (3): 537-42. Villa Chiara, Ghezzi Laura, Fenoglio Chiara, Clerici Francesca, Marcone Alessandra, Benussi Luisa, Ghidoni Roberta, Gallone Salvatore, Serpente Maria, Cantoni Claudia, Ridolfi Elisa, Bonsi Rossana, Cerami Chiara, Cappa Stefano, Binetti Giuliano, Franceschi Massimo, Rainero Innocenzo, Mariani Claudio, Bresolin Nereo, Scarpini Elio, Galimberti Danie |
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TOMM40, APOE, and APOC1 in primary progressive aphasia and frontotemporal dementia.
Journal of Alzheimer's disease : JAD 2012 31 (4): 731-40. Seripa Davide, Bizzarro Alessandra, Pilotto Andrea, Palmieri Orazio, Panza Francesco, D'Onofrio Grazia, Gravina Carolina, Archetti Silvana, Daniele Antonio, Borroni Barbara, Padovani Alessandro, Masullo Car |
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Synaptic changes in frontotemporal lobar degeneration: correlation with MAPT haplotype and APOE genotype.
Neuropathology and applied neurobiology 2011 Jun 37 (4): 366-80. Connelly S J, Mukaetova-Ladinska E B, Abdul-All Z, Alves da Silva J, Brayne C, Honer W G, Mann D M |
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Clinical features and APOE genotype of pathologically proven early-onset Alzheimer disease.
Neurology 2011 May 76 (20): 1720-5. Balasa M, Gelpi E, Antonell A, Rey M J, Sánchez-Valle R, Molinuevo J L, Lladó A, |
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The APOE gene locus in frontotemporal dementia and primary progressive aphasia.
Archives of neurology 2011 May 68 (5): 622-8. Seripa Davide, Bizzarro Alessandra, Panza Francesco, Acciarri Adele, Pellegrini Fabio, Pilotto Alberto, Masullo Car |
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Genetic background predicts poor prognosis in frontotemporal lobar degeneration.
Neuro-degenerative diseases 2011 8 (5): 289-95. Borroni B, Grassi M, Archetti S, Papetti A, Del Bo R, Bonvicini C, Comi G P, Gennarelli M, Bellelli G, Di Luca M, Padovani |
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Establishing short-term prognosis in Frontotemporal Lobar Degeneration spectrum: role of genetic background and clinical phenotype.
Neurobiology of aging 2010 Feb 31 (2): 270-9. Borroni Barbara, Grassi Mario, Agosti Chiara, Premi Enrico, Archetti Silvana, Alberici Antonella, Bellelli Giuseppe, Caimi Luigi, Di Luca Monica, Padovani Alessand |
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[Frontotemporal dementia in association with a family history of dementia and ApoE polymorphism].
Der Nervenarzt 2010 Jan 81 (1): 75-8. Zintl M, Petkov M, Schmitz G, Hajak G, Klünemann H |
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BuChE K variant is decreased in Alzheimer's disease not in fronto-temporal dementia.
Journal of neural transmission (Vienna, Austria : 1996) 2010 Jan . Bizzarro A, Guglielmi V, Lomastro R, Valenza A, Lauria A, Marra C, Silveri MC, Tiziano FD, Brahe C, Masullo C |
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Increased levels of soluble LR11 in cerebrospinal fluid of patients with Alzheimer disease.
Dementia and geriatric cognitive disorders 2010 30 (1): 28-32. Ikeuchi Takeshi, Hirayama Satoshi, Miida Takashi, Fukamachi Isamu, Tokutake Takayoshi, Ebinuma Hiroyuki, Takubo Kohei, Kaneko Hiroyuki, Kasuga Kensaku, Kakita Akiyoshi, Takahashi Hitoshi, Bujo Hideaki, Saito Yasushi, Nishizawa Masato |
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A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.
Brain : a journal of neurology 2008 Mar 131 (Pt 3): 706-20. Beck Jonathan, Rohrer Jonathan D, Campbell Tracy, Isaacs Adrian, Morrison Karen E, Goodall Emily F, Warrington Elizabeth K, Stevens John, Revesz Tamas, Holton Janice, Al-Sarraj Safa, King Andrew, Scahill Rachael, Warren Jason D, Fox Nick C, Rossor Martin N, Collinge John, Mead Sim |
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Association study to evaluate the serotonin transporter and apolipoprotein E genes in frontotemporal lobar degeneration in Italy.
Journal of human genetics 2008 53 (11-12): 1029-33. Albani Diego, Prato Francesca, Fenoglio Chiara, Batelli Sara, Dusi Sabrina, De Mauro Stefania, Polito Letizia, Lovati Carlo, Galimberti Daniela, Mariani Claudio, Scarpini Elio, Forloni Gianlui |
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Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
The Lancet. Neurology 2007 Oct 6 (10): 857-68. Rademakers Rosa, Baker Matt, Gass Jennifer, Adamson Jennifer, Huey Edward D, Momeni Parastoo, Spina Salvatore, Coppola Giovanni, Karydas Anna M, Stewart Heather, Johnson Nancy, Hsiung Ging-Yuek, Kelley Brendan, Kuntz Karen, Steinbart Ellen, Wood Elisabeth McCarty, Yu Chang-En, Josephs Keith, Sorenson Eric, Womack Kyle B, Weintraub Sandra, Pickering-Brown Stuart M, Schofield Peter R, Brooks William S, Van Deerlin Vivianna M, Snowden Julie, Clark Christopher M, Kertesz Andrew, Boylan Kevin, Ghetti Bernardino, Neary David, Schellenberg Gerard D, Beach Thomas G, Mesulam Marsel, Mann David, Grafman Jordan, Mackenzie Ian R, Feldman Howard, Bird Thomas, Petersen Ron, Knopman David, Boeve Bradley, Geschwind Dan H, Miller Bruce, Wszolek Zbigniew, Lippa Carol, Bigio Eileen H, Dickson Dennis, Graff-Radford Neill, Hutton Mi |
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The apolipoprotein E epsilon4 allele selectively increases the risk of frontotemporal lobar degeneration in males.
Journal of neurology, neurosurgery, and psychiatry 2006 Feb 77 (2): 154-8. Srinivasan R, Davidson Y, Gibbons L, Payton A, Richardson A M T, Varma A, Julien C, Stopford C, Thompson J, Horan M A, Pendleton N, Pickering-Brown S M, Neary D, Snowden J S, Mann D M |
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Functional correlates of Apolipoprotein E genotype in Frontotemporal Lobar Degeneration.
BMC neurology 2006 6 (): 31. Borroni Barbara, Perani Daniela, Archetti Silvana, Agosti Chiara, Paghera Barbara, Bellelli Giuseppe, Di Luca Monica, Padovani Alessand |
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Differences in tau and apolipoprotein E polymorphism frequencies in sporadic frontotemporal lobar degeneration syndromes.
Archives of neurology 2002 Apr 59 (4): 611-5. Short Rodney A, Graff-Radford Neill R, Adamson Jennifer, Baker Matt, Hutton Mi |
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Hippocampal sclerosis in the elderly: genetic and pathologic findings, some mimicking Alzheimer disease clinically.
Alzheimer disease and associated disorders 0 25 (4): 364-8. Pao Winnie C, Dickson Dennis W, Crook Julia E, Finch NiCole A, Rademakers Rosa, Graff-Radford Neill |
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Prion protein codon 129 polymorphism modifies age at onset of frontotemporal dementia with the C.709-1G>A progranulin mutation.
Alzheimer disease and associated disorders 0 25 (1): 93-5. Moreno Fermín, Alzualde Ainhoa, Camblor Pablo Martínez, Barandiaran Myriam, Van Deerlin Vivianna M, Gabilondo Alazne, Martí Massó José F, López de Munain Adolfo, Indakoetxea Bego |
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- Page last updated:May 9, 2019
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