Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Muscular Atrophy and C9orf72[original query] |
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Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases. Neurology 2012 Jul . van Rheenen W, van Blitterswijk M, Huisman MH, Vlam L, van Doormaal PT, Seelen M, Medic J, Dooijes D, de Visser M, van der Kooi AJ, Raaphorst J, Schelhaas HJ, van der Pol WL, Veldink JH, van den Berg LH |
Analysis of the C9orf72 gene in spinal muscular atrophy patients. Amyotrophic lateral sclerosis & frontotemporal degeneration 2014 Dec 15 (7-8): 563-8. Alías Laura, Bernal Sara, Barceló Maria J, Martínez-Hernández Rebeca, Martínez Elisabeth, Baiget Montserrat, Tizzano Eduardo |
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 |
C9orf72 hexanucleotide repeat expansion found in suspected spinobulbar muscular atrophy (SBMA). Neurologia i neurochirurgia polska 2022 6 56 (3): 276-280. Radziwonik Wiktoria, Elert-Dobkowska Ewelina, Tomczuk Filip, Wozniak Aleksandra, Sobanska Anna, Stepniak Iwona, Koziorowski Dariusz, Zaremba Jacek, Su?ek An |
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- Page last updated:May 20, 2024
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