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Results by year

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

Year Number of Results
1913 1
1914 1
1961 1
1972 1
1973 1
1974 1
1975 3
1976 3
1980 2
1981 2
1982 4
1984 3
1985 1
1986 2
1987 2
1988 1
1989 1
1990 3
1992 2
1993 5
1994 3
1995 3
1996 5
1997 4
1998 1
1999 6
2000 7
2001 8
2002 6
2003 5
2004 10
2005 8
2006 8
2007 5
2008 5
2009 4
2010 2
2011 6
2012 4
2013 10
2014 8
2015 11
2016 18
2017 16
2018 18
2019 22
2020 21
2021 24
2022 30
2023 7
2024 2

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Similar articles for PMID: 24787759

289 results

Results by year

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Page 1
Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.
Le Ber I, Moreira MC, Rivaud-Péchoux S, Chamayou C, Ochsner F, Kuntzer T, Tardieu M, Saïd G, Habert MO, Demarquay G, Tannier C, Beis JM, Brice A, Koenig M, Dürr A. Le Ber I, et al. Brain. 2003 Dec;126(Pt 12):2761-72. doi: 10.1093/brain/awg283. Epub 2003 Sep 23. Brain. 2003. PMID: 14506070 Free article.
Inherited ataxia with slow saccades.
Chakor RT, Bharote H. Chakor RT, et al. J Postgrad Med. 2012 Oct-Dec;58(4):318-25. doi: 10.4103/0022-3859.105471. J Postgrad Med. 2012. PMID: 23298936
[Clinical picture of spinocerebellar ataxia type I (SCA1)].
Milewska D, Piłkowska E, Jakubowska T, Rakowicz M, Niewiadomska M, Niedzielska K, Walinowska E, Wochnik-Dyjas D, Rejnowski G, Zdzienicka E, Mierzewska H, Hoffman-Zacharska D, Zaremba J. Milewska D, et al. Neurol Neurochir Pol. 2001 Nov-Dec;35(6):993-1011. Neurol Neurochir Pol. 2001. PMID: 11987714 Polish.
A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34.
Ozaki K, Doi H, Mitsui J, Sato N, Iikuni Y, Majima T, Yamane K, Irioka T, Ishiura H, Doi K, Morishita S, Higashi M, Sekiguchi T, Koyama K, Ueda N, Miura Y, Miyatake S, Matsumoto N, Yokota T, Tanaka F, Tsuji S, Mizusawa H, Ishikawa K. Ozaki K, et al. JAMA Neurol. 2015 Jul;72(7):797-805. doi: 10.1001/jamaneurol.2015.0610. JAMA Neurol. 2015. PMID: 26010696
289 results