Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: Chorea and HD[original query] |
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Prevalence of Huntington disease in New South Wales in 1996. The Medical journal of Australia 2000 Aug 173 (4): 187-90. McCusker E A, Casse R F, Graham S J, Williams D B, Lazarus |
Trinucleotide repeat analysis of Huntington's disease gene in Singapore. Annals of the Academy of Medicine, Singapore 2001 Mar 30 (2): 122-7. Law H Y, Ng I S, Yoon C S, Zhao Y, Wong M |
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 |
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype. Journal of human genetics 2006 51 (8): 645-51. Costa Maria do Carmo, Teixeira-Castro Andreia, Constante Marco, Magalhães Marina, Magalhães Paula, Cerqueira Joana, Vale José, Passão Vitorina, Barbosa Célia, Robalo Conceição, Coutinho Paula, Barros José, Santos Manuela M, Sequeiros Jorge, Maciel Patríc |
The association of CAG repeat length with clinical progression in Huntington disease. Neurology 2006 Apr 66 (7): 1016-20. Rosenblatt A, Liang K-Y, Zhou H, Abbott M H, Gourley L M, Margolis R L, Brandt J, Ross C |
Chinese patients with Huntington's disease initially presenting with spinocerebellar ataxia. Clinical genetics 2012 Jul 9999 (999A): 999A. Dong Y, Sun YM, Liu ZJ, Ni W, Shi SS, Wu ZY |
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies. Neurology 2014 Jan 82 (4): 292-9. Hensman Moss Davina J, Poulter Mark, Beck Jon, Hehir Jason, Polke James M, Campbell Tracy, Adamson Garry, Mudanohwo Ese, McColgan Peter, Haworth Andrea, Wild Edward J, Sweeney Mary G, Houlden Henry, Mead Simon, Tabrizi Sarah |
C9ORF72 hexanucleotide repeat expansions are a frequent cause of Huntington disease phenocopies in the Greek population. Neurobiology of aging 2015 Jan 36 (1): 547.e13-6. Koutsis Georgios, Karadima Georgia, Kartanou Chrisoula, Kladi Athina, Panas Mari |
C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome. Journal of neurology 2014 Oct 261 (10): 1917-21. Kosti? Vladimir S, Dobri?i? Valerija, Stankovi? Iva, Rali? Vesna, Stefanova El |
Factors influencing the clinical expression of intermediate CAG repeat length mutations of the Huntington's disease gene. Journal of neurology 2015 Feb 262 (2): 277-84. Panegyres Peter K, Shu Chen-Chun, Chen Huei-Yang, Paulsen Jane |
Clinical manifestations of intermediate allele carriers in Huntington disease. Neurology 2016 Jul . Cubo Esther, Ramos-Arroyo María A, Martinez-Horta Saul, Martínez-Descalls Asunción, Calvo Sara, Gil-Polo Cecilia, |
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 |
Molecular Imaging in Huntington's Disease. International review of neurobiology 2018 11 142 289-333. Wilson Heather, Politis Mari |
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 |
Differential Transcriptome Profiling Unveils Novel Deregulated Gene Signatures Involved in Pathogenesis of Alzheimer's Disease. Biomedicines 2022 3 10 (3): . Singh Himanshu Narayan, Swarup Vishnu, Dubey Navneet Kumar, Jha Niraj Kumar, Singh Anjani Kumar, Lo Wen-Cheng, Kumar Sanj |
Genetic screening for Huntington disease phenocopies in Sweden: A tertiary center case series focused on short tandem repeat (STR) disorders. Journal of the neurological sciences 2023 6 451 120707. Martin Paucar, José Laffita-Mesa, Valter Niemelä, Helena Malmgren, Inger Nennesmo, Kristina Lagerstedt-Robinson, Magnus Nordenskjöld, Per Svenningss |
A mother and her daughter carrying a pathogenic expansion of the HTT gene with a phenotype encompassing motor neuron disease and Huntington's disease. Clinical genetics 2023 12 . Antonio Canosa, Sara Cabras, Francesca Di Pede, Umberto Manera, Rosario Vasta, Cristina Moglia, Andrea Calvo, Salvatore Gallone, Adriano Ch |
Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis. Journal of the Chinese Medical Association : JCMA 2023 1 86 (1): 47-51. Jih Kang-Yang, Lai Kuan-Lin, Lin Kon-Ping, Liao Yi-Chu, Lee Yi-Chu |
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- Page last updated:Apr 16, 2024
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