Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Sclerosis and CBS[original query] |
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Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease. Clinical genetics 2013 Mar 83 (3): 279-83. Lindquist S G, Duno M, Batbayli M, Puschmann A, Braendgaard H, Mardosiene S, Svenstrup K, Pinborg L H, Vestergaard K, Hjermind L E, Stokholm J, Andersen B B, Johannsen P, Nielsen J |
Genetic variants of homocysteine metabolism and multiple sclerosis: a case-control study. Neuroscience letters 2014 Mar 562 75-8. Ineichen Benjamin V, Keskitalo Salla, Farkas Melinda, Bain Nadja, Kallweit Ulf, Weller Michael, Klotz Luisa, Linnebank Micha |
Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriers. Alzheimer's & dementia (Amsterdam, Netherlands) 2015 Dec 1 (4): 481-6. Caroppo Paola, Camuzat Agnès, De Septenville Anne, Couratier Philippe, Lacomblez Lucette, Auriacombe Sophie, Flabeau Olivier, Jornéa Ludmila, Blanc Frederic, Sellal François, Cretin Benjamin, Meininger Vincent, Fleury Marie-Céline, Couarch Philippe, Dubois Bruno, Brice Alexis, Le Ber Isabel |
TARDBP mutations in a cohort of Italian patients with Parkinson's disease and atypical parkinsonisms. Frontiers in aging neuroscience 2022 10 14 1020948. Tiloca Cinzia, Goldwurm Stefano, Calcagno Narghes, Verde Federico, Peverelli Silvia, Calini Daniela, Zecchinelli Anna Lena, Sangalli Davide, Ratti Antonia, Pezzoli Gianni, Silani Vincenzo, Ticozzi Nico |
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- Page last updated:Apr 22, 2024
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