Human Genome Epidemiology Literature Finder
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Records 1 - 25 (of 25 Records) |
| Query Trace: Aphasia and APOE[original query] |
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| The Apolipoprotein E genotype in patients affected by syndromes with focal cortical atrophy. Neuroscience letters 2001 May 303 (2): 87-90. Masullo C, Daniele A, Fazio V M, Seripa D, Gravina C, Filippini V, Grossi D, Fragassi N, Nichelli P, Leone M, Gainotti |
| 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 |
| Association between apolipoprotein E4 and rehabilitation outcome in hospitalized ischemic stroke patients. Archives of physical medicine and rehabilitation 2003 Jul 84 (7): 973-6. Treger Iuly, Froom Paul, Ring Haim, Friedman Gide |
| 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 |
| Cognitive phenotypes in Alzheimer's disease and genetic risk. Cortex; a journal devoted to the study of the nervous system and behavior 2007 Oct 43 (7): 835-45. Snowden Julie S, Stopford Cheryl L, Julien Camille L, Thompson Jennifer C, Davidson Yvonne, Gibbons Linda, Pritchard Antonia, Lendon Corinne L, Richardson Anna M, Varma Anoop, Neary David, Mann Dav |
| 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 |
| APOE epsilon 2/epsilon 4 genotype a risk factor for primary progressive aphasia in women. Archives of neurology 2009 Jul 66 (7): 910-2. Daniele Antonio, Matera Maria G, Seripa Davide, Acciarri Adele, Bizzarro Alessandra, Pilotto Alberto, Masullo Car |
| Clinical syndromes associated with posterior atrophy: early age at onset AD spectrum. Neurology 2009 Nov 73 (19): 1571-8. Migliaccio R, Agosta F, Rascovsky K, Karydas A, Bonasera S, Rabinovici G D, Miller B L, Gorno-Tempini 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, |
| 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 |
| FOXP2, APOE, and PRNP: new modulators in primary progressive aphasia. Journal of Alzheimer's disease : JAD 2012 28 (4): 941-50. Premi Enrico, Pilotto Andrea, Alberici Antonella, Papetti Alice, Archetti Silvana, Seripa Davide, Daniele Antonio, Masullo Carlo, Garibotto Valentina, Paghera Barbara, Caobelli Federico, Padovani Alessandro, Borroni Barba |
| 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 |
| Fibromyalgia, mood disorders, and intense creative energy: A1AT polymorphisms are not always silent. Neurotoxicology 2012 Dec 33 (6): 1454-72. Schmechel Donald E, Edwards Christopher |
| APOE e4 influences ß-amyloid deposition in primary progressive aphasia and speech apraxia. Alzheimer's & dementia : the journal of the Alzheimer's Association 2014 Nov 10 (6): 630-6. Josephs Keith A, Duffy Joseph R, Strand Edythe A, Machulda Mary M, Senjem Matthew L, Lowe Val J, Jack Clifford R, Whitwell Jennifer |
| Aphasic variant of Alzheimer disease: Clinical, anatomic, and genetic features. Neurology 2016 Sep 87 (13): 1337-43. Rogalski Emily, Sridhar Jaiashre, Rader Benjamin, Martersteck Adam, Chen Kewei, Cobia Derin, Thompson Cynthia K, Weintraub Sandra, Bigio Eileen H, Mesulam M-Mars |
| Tau PET patterns mirror clinical and neuroanatomical variability in Alzheimer's disease. Brain : a journal of neurology 2016 Mar . Ossenkoppele Rik, Schonhaut Daniel R, Schöll Michael, Lockhart Samuel N, Ayakta Nagehan, Baker Suzanne L, O'Neil James P, Janabi Mustafa, Lazaris Andreas, Cantwell Averill, Vogel Jacob, Santos Miguel, Miller Zachary A, Bettcher Brianne M, Vossel Keith A, Kramer Joel H, Gorno-Tempini Maria L, Miller Bruce L, Jagust William J, Rabinovici Gil |
| 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, |
| 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 |
| APOE is a correlate of phenotypic heterogeneity in Alzheimer disease in a national cohort. Neurology 2019 11 94 (6): e607-e612. Weintraub Sandra, Teylan Merilee, Rader Benjamin, Chan Kwun C G, Bollenbeck Mark, Kukull Walter A, Coventry Christina, Rogalski Emily, Bigio Eileen, Mesulam M-Mars |
| Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia. Neurobiology of aging 2020 9 99 99.e15-99.e22. Rosas Irene, Martínez Carmen, Coto Eliecer, Clarimón Jordi, Lleó Alberto, Illán-Gala Ignacio, Dols-Icardo Oriol, Borroni Barbara, Almeida Maria Rosário, van der Zee Julie, Van Broeckhoven Christine, , Bruni Amalia C, Anfossi Maria, Bernardi Livia, Maletta Raffaele, Serpente María, Galimberti Daniela, Scarpini Elio, Rossi Giacomina, Caroppo Paola, Benussi Luisa, Ghidoni Roberta, Binetti Giuliano, Nacmias Benedetta, Sorbi Sandro, Piaceri Irene, Bagnoli Silvia, Antonell Anna, Sánchez-Valle Raquel, De la Casa-Fages Beatriz, Grandas Francisco, Diez-Fairen Mónica, Pastor Pau, Ferrari Raffaele, , Queimaliños-Perez Daniel, Pérez-Oliveira Sergio, Álvarez Victoria, Menéndez-González Manu |
| Pathobiological Subtypes of Alzheimer Disease. Dementia and geriatric cognitive disorders 2021 1 49 (4): 321-333. Jellinger Kurt |
| Loss of speech and functional impairment in Alzheimer's disease-related primary progressive aphasia: predictive factors of decline. Neurobiology of aging 2022 6 117 59-70. Mazzeo Salvatore, Polito Cristina, Lassi Michael, Bagnoli Silvia, Mattei Marta, Padiglioni Sonia, Berti Valentina, Lombardi Gemma, Giacomucci Giulia, De Cristofaro Maria Teresa, Passeri Alessandro, Ferrari Camilla, Nacmias Benedetta, Mazzoni Alberto, Sorbi Sandro, Bessi Valenti |
| Missing apolipoprotein E ?4 allele associated with nonamnestic Alzheimer's disease in a Tunisian population. Journal of genetics 2022 101 . Fray Saloua, Achouri-Rassas Afef, Belal Samir, Messaoud Tai |
| APOE ?4 influences within and between network functional connectivity in posterior cortical atrophy and logopenic progressive aphasia. Alzheimer's & dementia : the journal of the Alzheimer's Association 2023 3 . Singh Neha Atulkumar, Martin Peter R, Graff-Radford Jonathan, Machulda Mary M, Carrasquillo Minerva M, Ertekin-Taner Nilufer, Josephs Keith A, Whitwell Jennifer |
| Pure LATE-NC: Frequency, clinical impact, and the importance of considering APOE genotype when assessing this and other subtypes of non-Alzheimer's pathologies. Acta neuropathologica 2024 11 148 (1): 66. Yuriko Katsumata, Xian Wu, Khine Zin Aung, David W Fardo, Davis C Woodworth, S Ahmad Sajjadi, Sandra O Tomé, Dietmar Rudolf Thal, Juan C Troncoso, Koping Chang, Charles Mock, Peter T Nels |
- Page last reviewed:Feb 1, 2024
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