Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: Atrophy and HD[original query] |
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Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases? Psychiatric genetics 2001 Dec 11 (4): 201-5. Savi? D, Topisirovi? I, Keckarevi? M, Keckarevi? D, Major T, Culjkovi? B, Stojkovi? O, Rakocevi?-Stojanovi? V, Mladenovi? J, Todorovi? S, Apostolski S, Romac |
Caudate nucleus atrophy in Huntington's disease and its relationship with clinical and genetic parameters. Functional neurology 0 20 (3): 127-30. Roth Jan, Klempìi Jirí, Jech Robert, Zidovská Jana, Uhrová Tereza, Doubek Pavel, Ulmanová Olga, Brozová Hana, Volfová Markéta, Serranová Tereza, Ruzicka Evz |
Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene. Neurologia i neurochirurgia polska 0 42 (3): 203-9. Su?ek-Piatkowska Anna, Krysa Wioletta, Zdzienicka Elzbieta, Szirkowiec Walentyna, Hoffman-Zacharska Dorota, Rajkiewicz Marta, Fidzia?ska Elzbieta, Kowalska Grazyna, Zaremba Jac |
Screening for FXTAS in 95 Spanish patients negative for Huntington disease. Genetic testing 2008 Mar 12 (1): 135-8. Rodriguez-Revenga Laia, Santos M Mònica, Sánchez Aurora, Pujol Montserrat, Gómez-Anson Beatriz, Badenas Celia, Jiménez Dolores, Madrigal Irene, Milà Montserr |
Relationship between CAG repeat length and brain volume in premanifest and early Huntington's disease. Journal of neurology 2009 Feb 256 (2): 203-12. Henley Susie M D, Wild Edward J, Hobbs Nicola Z, Scahill Rachael I, Ridgway Gerard R, Macmanus David G, Barker Roger A, Fox Nick C, Tabrizi Sarah |
Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data. The Lancet. Neurology 2012 Jan 11 (1): 42-53. Tabrizi Sarah J, Reilmann Ralf, Roos Raymund A C, Durr Alexandra, Leavitt Blair, Owen Gail, Jones Rebecca, Johnson Hans, Craufurd David, Hicks Stephen L, Kennard Christopher, Landwehrmeyer Bernhard, Stout Julie C, Borowsky Beth, Scahill Rachael I, Frost Chris, Langbehn Douglas R, |
Globus pallidus degeneration and clinicopathological features of Huntington disease. Annals of neurology 2016 Jun . Singh-Bains Malvindar K, Tippett Lynette J, Hogg Virginia M, Synek Beth J, Roxburgh Richard H, Waldvogel Henry J, Faull Richard L |
Two different phenomena in basic motor speech performance in premanifest Huntington disease. Neurology 2016 Mar . Skodda Sabine, Grönheit Wenke, Lukas Carsten, Bellenberg Barbara, von Hein Sarah M, Hoffmann Rainer, Saft Carst |
Multiple system atrophy and CAG repeat length: A genetic screening of polyglutamine disease genes in Italian patients. Neuroscience letters 2018 5 678 37-42. Mongelli Alessia, Sarro Lidia, Rizzo Elena, Nanetti Lorenzo, Meucci Nicoletta, Pezzoli Gianni, Goldwurm Stefano, Taroni Franco, Mariotti Caterina, Gellera Cinz |
Spinocerebellar ataxia with axonal neuropathy type 1 revisited. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2019 6 67 139-144. Scott Patrick, Al Kindi Adila, Al Fahdi Amira, Al Yarubi Naeema, Bruwer Zandre, Al Adawi Samir, Nandhagopal Ramachandir |
Clinical, radiological, and genetic characteristics in patients with Huntington's disease in a Taiwanese cohort. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2020 Jul . Chen Szu-Ju, Lee Bo-Chin, Lee Ni-Chung, Chien Yin-Hsiu, Hwu Wuh-Liang, Lin Chin-Hsi |
Mutant huntingtin and neurofilament light have distinct longitudinal dynamics in Huntington's disease. Science translational medicine 2020 Dec 12 (574): . Rodrigues Filipe B, Byrne Lauren M, Tortelli Rosanna, Johnson Eileanoir B, Wijeratne Peter A, Arridge Marzena, De Vita Enrico, Ghazaleh Naghmeh, Houghton Richard, Furby Hannah, Alexander Daniel C, Tabrizi Sarah J, Schobel Scott, Scahill Rachael I, Heslegrave Amanda, Zetterberg Henrik, Wild Edward |
Mild Cognitive Impairment as an Early Landmark in Huntington's Disease. Frontiers in neurology 2021 12 678652. Zhang Ying, Zhou Junyi, Gehl Carissa R, Long Jeffrey D, Johnson Hans, Magnotta Vincent A, Sewell Daniel, Shannon Kathleen, Paulsen Jane |
Intermediate and Expanded HTT Alleles and the Risk for ?-Synucleinopathies. Movement disorders : official journal of the Movement Disorder Society 2022 7 37 (9): 1841-1849. Pérez-Oliveira Sergio, Álvarez Ignacio, Rosas Irene, Menendez-González Manuel, Blázquez-Estrada Marta, Aguilar Miquel, Corte Daniela, Buongiorno Mariateresa, Molina-Porcel Laura, Aldecoa Iban, Martí María J, Sánchez-Juan Pascual, Infante Jon, González-Aramburu Isabel, García-González Pablo, Rosende-Roca Maitée, Boada Mercè, Ruiz Agustín, Periñán María Teresa, Macías-García Daniel, Muñoz-Delgado Laura, Gómez-Garre Pilar, Mir Pablo, Clarimón Jordi, Lleo Alberto, Alcolea Daniel, De la Casa-Fages Beatriz, Duarte Israel, Álvarez Victoria, Pastor P |
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 |
Language disorders in patients with striatal lesions: Deciphering the role of the striatum in language performance. Cortex; a journal devoted to the study of the nervous system and behavior 2023 6 166 91-106. Lorna Le Stanc, Katia Youssov, Maria Giavazzi, Agnès Sliwinski, Anne-Catherine Bachoud-Lévi, Charlotte Jacquem |
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