Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Atrophy and SOD1[original query] |
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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 |
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 |
Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants. Neurologic clinics 2015 Nov 33 (4): 855-76. Saberi Shahram, Stauffer Jennifer E, Schulte Derek J, Ravits Jo |
Noncoding repeat expansions for ALS in Japan are associated with the ATXN8OS gene. Neurology. Genetics 2018 8 4 (4): e252. Hirano Makito, Samukawa Makoto, Isono Chiharu, Saigoh Kazumasa, Nakamura Yusaku, Kusunoki Susu |
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 |
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