HuGE Literature Finder
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Genetic Spectrum and Clinical Heterogeneity of Chinese Frontotemporal Dementia Patients: Data from PUMCH Dementia Cohort. Journal of Alzheimer's disease : JAD 2022 Aug . Dong Liling, Wang Jie, Liu Caiyan, Li Jie, Mao Chenhui, Huang Xinying, Chu Shanshan, Peng Bin, Cui Liying, Gao Ji |
Neurocognitive patterns across genetic levels in behavioral variant frontotemporal dementia: a multiple single cases study. BMC neurology 2022 12 22 (1): 454. Santamaría-García Hernando, Ogonowsky Natalia, Baez Sandra, Palacio Nicole, Reyes Pablo, Schulte Michael, López Andrea, Matallana Diana, Ibanez Agust |
Profiling morphologic MRI features of motor neuron disease caused by TARDBP mutations. Frontiers in neurology 2022 8 13 931006. Spinelli Edoardo Gioele, Ghirelli Alma, Riva Nilo, Canu Elisa, Castelnovo Veronica, Domi Teuta, Pozzi Laura, Carrera Paola, Silani Vincenzo, Chiò Adriano, Filippi Massimo, Agosta Federi |
Structural MRI Signatures in Genetic Presentations of the Frontotemporal Dementia/Motor Neuron Disease Spectrum. Neurology 2021 9 97 (16): e1594-e1607. Spinelli Edoardo Gioele, Ghirelli Alma, Basaia Silvia, Cividini Camilla, Riva Nilo, Canu Elisa, Castelnovo Veronica, Domi Teuta, Magnani Giuseppe, Caso Francesca, Caroppo Paola, Prioni Sara, Rossi Giacomina, Tremolizzo Lucio, Appollonio Ildebrando, Silani Vincenzo, Carrera Paola, Filippi Massimo, Agosta Federi |
Mixed TDP-43 proteinopathy and tauopathy in frontotemporal lobar degeneration: nine case series. Journal of neurology 2018 10 265 (12): 2960-2971. Kim Eun-Joo, Brown Jesse A, Deng Jersey, Hwang Ji-Hye L, Spina Salvatore, Miller Zachary A, DeMay Mary G, Valcour Victor, Karydas Anna, Ramos Eliana Marisa, Coppola Giovanni, Miller Bruce L, Rosen Howard J, Seeley William W, Grinberg Lea |
Value of 18fluorodeoxyglucose-positron-emission tomography in amyotrophic lateral sclerosis: a prospective study. JAMA neurology 2014 May 71 (5): 553-61. Van Laere Koen, Vanhee Annelies, Verschueren Jolien, De Coster Liesbeth, Driesen An, Dupont Patrick, Robberecht Wim, Van Damme Phil |
Genetic overlap between apparently sporadic motor neuron diseases. PloS one 2012 7 (11): 11. van Blitterswijk M, Vlam L, van Es MA, van der Pol WL, Hennekam EA, Dooijes D, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH |
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