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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1927 1
1974 2
1980 3
1982 2
1983 2
1984 3
1987 2
1990 1
1992 1
1993 4
1994 14
1995 17
1996 16
1997 13
1998 10
1999 21
2000 9
2001 13
2002 17
2003 15
2004 13
2005 9
2006 6
2007 14
2008 11
2009 7
2010 9
2011 8
2012 9
2013 6
2014 6
2015 6
2016 12
2017 9
2018 10
2019 3
2020 10
2021 13
2022 13
2023 4
2024 0

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Similar articles for PMID: 12805114

322 results

Results by year

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Page 1
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.
Costa MDC, Teixeira-Castro A, Constante M, Magalhães M, Magalhães P, Cerqueira J, Vale J, Passão V, Barbosa C, Robalo C, Coutinho P, Barros J, Santos MM, Sequeiros J, Maciel P. Costa MDC, et al. J Hum Genet. 2006;51(8):645-651. doi: 10.1007/s10038-006-0001-9. Epub 2006 Jul 21. J Hum Genet. 2006. PMID: 16858508 Free PMC article.
Huntington's disease-like 2 in Brazil--report of 4 patients.
Rodrigues GG, Walker RH, Brice A, Cazeneuve C, Russaouen O, Teive HA, Munhoz RP, Becker N, Raskin S, Werneck LC, Junior WM, Tumas V. Rodrigues GG, et al. Mov Disord. 2008 Nov 15;23(15):2244-7. doi: 10.1002/mds.22223. Mov Disord. 2008. PMID: 18816802
Huntington's Disease-like 2 (HDL2) in North America and Japan.
Margolis RL, Holmes SE, Rosenblatt A, Gourley L, O'Hearn E, Ross CA, Seltzer WK, Walker RH, Ashizawa T, Rasmussen A, Hayden M, Almqvist EW, Harris J, Fahn S, MacDonald ME, Mysore J, Shimohata T, Tsuji S, Potter N, Nakaso K, Adachi Y, Nakashima K, Bird T, Krause A, Greenstein P. Margolis RL, et al. Ann Neurol. 2004 Nov;56(5):670-4. doi: 10.1002/ana.20248. Ann Neurol. 2004. PMID: 15468075
322 results