HuGE Literature Finder
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| Investigating a Genetic Link Between Alzheimer's Disease and CADASIL-Related Cerebral Small Vessel Disease. Molecular neurobiology 2022 Sep . Dunn Paul J, Lea Rodney A, Maksemous Neven, Smith Robert A, Sutherland Heidi G, Haupt Larisa M, Griffiths Lyn |
| Amyloid Precursor Protein A713T Mutation in Calabrian Patients with Alzheimer's Disease: A Population Genomics Approach to Estimate Inheritance from a Common Ancestor. Biomedicines 2022 1 10 (1): . Abondio Paolo, Sarno Stefania, Giuliani Cristina, Laganà Valentina, Maletta Raffaele, Bernardi Livia, Bruno Francesco, Colao Rosanna, Puccio Gianfranco, Frangipane Francesca, Borroni Barbara, Van Broeckhoven Christine, Luiselli Donata, Bruni Amal |
| Amyloid Precursor Protein Variant, E665D, Associated With Unique Clinical and Biomarker Phenotype. American journal of Alzheimer's disease and other dementias 2021 1 36 1533317520981225. Abbatemarco Justin R, Jones Stephen E, Larvie Mykol, Bekris Lynn M, Khrestian Maria E, Krishnan Kamini, Leverenz James |
| Amyloid PET pattern with dementia and amyloid angiopathy in Taiwan familial AD with D678H APP mutation. Journal of the neurological sciences 2019 2 398 107-116. Huang Chu-Yun, Hsiao Ing-Tsung, Lin Kun-Ju, Huang Kuo-Lun, Fung Hon-Chung, Liu Chi-Hung, Chang Ting-Yu, Weng Yi-Ching, Hsu Wen-Chun, Yen Tzu-Chen, Huang Chin-Cha |
| Cerebral amyloid angiopathy-related inflammation: a case report presenting with a rare variant in SORL1 gene. BMC neurology 2019 5 19 (1): 97. Du Yanjiao, Liu Chao, Ma Congmin, Xu Xiaohui, Zhou Xufeng, Zhou Haitao, Huang Ch |
| Patterns and severity of vascular amyloid in Alzheimer's disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer's disease. Acta neuropathologica 2018 May . Mann David M A, Davidson Yvonne S, Robinson Andrew C, Allen Nancy, Hashimoto Tadafumi, Richardson Anna, Jones Matthew, Snowden Julie S, Pendleton Neil, Potier Marie-Claude, Laquerrière Annie, Prasher Vee, Iwatsubo Takeshi, Strydom And |
| Rare Genetic Variant in SORL1 May Increase Penetrance of Alzheimer's Disease in a Family with Several Generations of APOE-?4 Homozygosity. Journal of Alzheimer's disease : JAD 2017 56 (1): 63-74. Louwersheimer Eva, Cohn-Hokke Petra E, Pijnenburg Yolande A L, Weiss Marjan M, Sistermans Erik A, Rozemuller Annemieke J, Hulsman Marc, van Swieten John C, van Duijn Cock M, Barkhof Frederik, Koene Teddy, Scheltens Philip, Van der Flier Wiesje M, Holstege Hen |
| Genetic determinants of white matter hyperintensities and amyloid angiopathy in familial Alzheimer's disease. Neurobiology of aging 2015 Sep . Ryan Natalie S, Biessels Geert-Jan, Kim Lois, Nicholas Jennifer M, Barber Philip A, Walsh Phoebe, Gami Priya, Morris Huw R, Bastos-Leite António J, Schott Jonathan M, Beck Jon, Mead Simon, Chavez-Gutierrez Lucia, de Strooper Bart, Rossor Martin N, Revesz Tamas, Lashley Tammaryn, Fox Nick |
| Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy. European journal of human genetics : EJHG 2015 Apr . Nicolas Gaël, Wallon David, Goupil Claudia, Richard Anne-Claire, Pottier Cyril, Dorval Véronique, Sarov-Rivière Mariana, Riant Florence, Hervé Dominique, Amouyel Philippe, Guerchet Maelenn, Ndamba-Bandzouzi Bebene, Mbelesso Pascal, Dartigues Jean-François, Lambert Jean-Charles, Preux Pierre-Marie, Frebourg Thierry, Campion Dominique, Hannequin Didier, Tournier-Lasserve Elisabeth, Hébert Sébastien S, Rovelet-Lecrux An |
| APP mutations in the Aß coding region are associated with abundant cerebral deposition of Aß38. Acta neuropathologica 2012 Dec 124 (6): 809-21. Moro Maria Luisa, Giaccone Giorgio, Lombardi Raffaella, Indaco Antonio, Uggetti Andrea, Morbin Michela, Saccucci Stefania, Di Fede Giuseppe, Catania Marcella, Walsh Dominic M, Demarchi Andrea, Rozemuller Annemieke, Bogdanovic Nenad, Bugiani Orso, Ghetti Bernardino, Tagliavini Fabriz |
| No evidence of APP point mutation and locus duplication in individuals with cerebral amyloid angiopathy. European journal of neurology : the official journal of the European Federation of Neurological Societies 2011 Oct 18 (10): 1279-81. Domingues-Montanari S, Parés M, Hernández-Guillamon M, Fernández-Cadenas I, Mendioroz M, Ortega G, Boada M, Masjuan J, Huertas N, Alvarez-Sabín J, Delgado P, Montaner J, |
| Screening for familial APP mutations in sporadic cerebral amyloid angiopathy. PloS one 2010 5 (11): e13949. Biffi Alessandro, Plourde Anna, Shen Yiping, Onofrio Robert, Smith Eric E, Frosch Matthew, Prada Claudia M, Gusella James, Greenberg Steven M, Rosand Jonath |
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