Human Genome Epidemiology Literature Finder
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Records 1 - 29 (of 29 Records) |
| Query Trace: Frontotemporal Lobar Degeneration and APOE[original query] |
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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 |
| 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 |
| 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 |
| CSF biomarkers in frontotemporal lobar degeneration: relations with clinical characteristics, apolipoprotein E genotype, and neuroimaging. Journal of neurology, neurosurgery, and psychiatry 2006 1 77 (2): 246-8. Pijnenburg Y A L, Schoonenboom S N M, Barkhof F, Knol D L, Mulder C, Van Kamp G J, Van Swieten J C, Scheltens |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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, |
| 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 |
| 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 |
| Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels. Archives of neurology 2011 1 68 (5): 581-6. Cruchaga Carlos, Graff Caroline, Chiang Huei-Hsin, Wang Jun, Hinrichs Anthony L, Spiegel Noah, Bertelsen Sarah, Mayo Kevin, Norton Joanne B, Morris John C, Goate Alis |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Updated meta-analysis of the role of APOE e2/e3/e4 alleles in frontotemporal lobar degeneration. Oncotarget 2017 Apr . Su Wen-Hua, Shi Zhi-Hong, Liu Shu-Ling, Wang Xiao-Dan, Liu Shuai, Ji Yo |
| 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, Rogalski Emily J, Mesulam Marsel M, Koric Lejla, Nora Kristensen, Pariente Jeéreémie, 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, Dumurgier 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, Laforce Robert Jr, Visser Pieter Jelle, Ossenkoppele R |
| Argyrophilic Grain Pathology in Frontotemporal Lobar Degeneration: Demographic, Clinical, Neuropathological, and Genetic Features. Journal of Alzheimer's disease : JAD 2018 5 63 (3): 1109-1117. Gil María José, Manzano María Sagrario, Cuadrado María Luz, Fernández Cristina, Góméz Elena, Matesanz Carmen, Calero Miguel, Rábano Alber |
| Cognitive decline in amyotrophic lateral sclerosis: Neuropathological substrate and genetic determinants. Brain pathology (Zurich, Switzerland) 2021 Feb e12942. Borrego-Écija Sergi, Turon-Sans Janina, Ximelis Teresa, Aldecoa Iban, Molina-Porcel Laura, Povedano Mónica, Rubio Miguel Angel, Gámez Josep, Cano Antonio, Paré-Curell Martí, Bajo Lorena, Sotoca Javier, Clarimón Jordi, Balasa Mircea, Antonell Anna, Lladó Albert, Sánchez-Valle Raquel, Rojas-García Ricard, Gelpi Ell |
| The molecular spectrum of amyloid-beta (A?) in neurodegenerative diseases beyond Alzheimer's disease. Brain pathology (Zurich, Switzerland) 2023 8 e13210. Shojiro Ichimata, Koji Yoshida, Jun Li, Ekaterina Rogaeva, Anthony E Lang, Gabor G Kova |
| Alzheimer's disease pathology: pathways between chronic vascular risk factors and blood-brain barrier dysfunction in a cohort of patients with different types of dementia. Frontiers in aging neuroscience 2023 5 15 1088140. Jinghuan Gan, Xia Yang, Guili Zhang, Xudong Li, Shuai Liu, Wei Zhang, Yong |
| CSF neurogranin levels as a biomarker in Alzheimer's disease and frontotemporal lobar degeneration: a cross-sectional analysis. Alzheimer's research & therapy 2024 9 16 (1): 199. Vanesa Jurasova, Ross Andel, Alzbeta Katonova, Katerina Veverova, Terezie Zuntychova, Hana Horakova, Martin Vyhnalek, Tereza Kolarova, Vaclav Matoska, Kaj Blennow, Jakub Ho |
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