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7. Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion. Koutsis G; Karadima G; Pandraud A; Sweeney MG; Paudel R; Houlden H; Wood NW; Panas M J Neurol; 2012 Sep; 259(9):1874-8. PubMed ID: 22297462 [TBL] [Abstract][Full Text] [Related]
8. Genetic screening for Huntington disease phenocopies in Sweden: A tertiary center case series focused on short tandem repeat (STR) disorders. Paucar M; Laffita-Mesa J; Niemelä V; Malmgren H; Nennesmo I; Lagerstedt-Robinson K; Nordenskjöld M; Svenningsson P J Neurol Sci; 2023 Aug; 451():120707. PubMed ID: 37379724 [TBL] [Abstract][Full Text] [Related]
9. Differential diagnosis of Huntington's disease: what the clinician should know. Cardoso F Neurodegener Dis Manag; 2014; 4(1):67-72. PubMed ID: 24640980 [TBL] [Abstract][Full Text] [Related]
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11. Hereditary chorea - what else to consider when the Huntington's disease genetics test is negative? Malek N; Newman EJ Acta Neurol Scand; 2017 Jan; 135(1):25-33. PubMed ID: 27150574 [TBL] [Abstract][Full Text] [Related]
12. Huntington's disease and Huntington's disease-like syndromes: an overview. Gövert F; Schneider SA Curr Opin Neurol; 2013 Aug; 26(4):420-7. PubMed ID: 23812307 [TBL] [Abstract][Full Text] [Related]
13. Absence of Acanthocytosis in Huntington's Disease-like 2: A Prospective Comparison with Huntington's Disease. Anderson DG; Carmona S; Naidoo K; Coetzer TL; Carr J; Rudnicki DD; Walker RH; Margolis RL; Krause A Tremor Other Hyperkinet Mov (N Y); 2017; 7():512. PubMed ID: 29226019 [TBL] [Abstract][Full Text] [Related]
14. 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. Sułek-Piatkowska A; Krysa W; Zdzienicka E; Szirkowiec W; Hoffman-Zacharska D; Rajkiewicz M; Fidziańska E; Kowalska G; Zaremba J Neurol Neurochir Pol; 2008; 42(3):203-9. PubMed ID: 18651325 [TBL] [Abstract][Full Text] [Related]
15. Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes. Stevanin G; Fujigasaki H; Lebre AS; Camuzat A; Jeannequin C; Dode C; Takahashi J; San C; Bellance R; Brice A; Durr A Brain; 2003 Jul; 126(Pt 7):1599-603. PubMed ID: 12805114 [TBL] [Abstract][Full Text] [Related]
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19. Huntington's disease-like 2 with an expansion mutation of the Junctophilin-3 gene; first reported case from Botswana. Ocampo C; Daimari R; Oyekunle AA J Clin Neurosci; 2018 Jan; 47():126-127. PubMed ID: 29066237 [TBL] [Abstract][Full Text] [Related]
20. Comparison of the Huntington's Disease like 2 and Huntington's Disease Clinical Phenotypes. Anderson DG; Ferreira-Correia A; Rodrigues FB; Aziz NA; Carr J; Wild EJ; Margolis RL; Krause A Mov Disord Clin Pract; 2019 Apr; 6(4):302-311. PubMed ID: 31061838 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]