Similar articles for PMID: 14981189

Year	Number of Results
1993	1
1994	2
1995	6
1996	1
1998	1
1999	2
2000	6
2001	5
2002	5
2003	6
2004	11
2005	6
2006	5
2007	4
2008	4
2009	1
2010	5
2011	5
2012	2
2013	1
2014	3
2015	2
2016	2
2017	2
2019	1
2020	2
2024	0

1

Japanese SCA families with an unusual phenotype linked to a locus overlapping with SCA15 locus.

Hara K, Fukushima T, Suzuki T, Shimohata T, Oyake M, Ishiguro H, Hirota K, Miyashita A, Kuwano R, Kurisaki H, Yomono H, Goto J, Kanazawa I, Tsuji S. Hara K, et al. Neurology. 2004 Feb 24;62(4):648-51. doi: 10.1212/01.wnl.0000110190.08412.25. Neurology. 2004. PMID: 14981189

2

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.

Chung MY, Lu YC, Cheng NC, Soong BW. Chung MY, et al. Brain. 2003 Jun;126(Pt 6):1293-9. doi: 10.1093/brain/awg130. Brain. 2003. PMID: 12764052

3

Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus.

Dudding TE, Friend K, Schofield PW, Lee S, Wilkinson IA, Richards RI. Dudding TE, et al. Neurology. 2004 Dec 28;63(12):2288-92. doi: 10.1212/01.wnl.0000147299.80872.d1. Neurology. 2004. PMID: 15623688

4

A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1.

Miyoshi Y, Yamada T, Tanimura M, Taniwaki T, Arakawa K, Ohyagi Y, Furuya H, Yamamoto K, Sakai K, Sasazuki T, Kira J. Miyoshi Y, et al. Neurology. 2001 Jul 10;57(1):96-100. doi: 10.1212/wnl.57.1.96. Neurology. 2001. PMID: 11445634

5

The contactin 4 gene locus at 3p26 is a candidate gene of SCA16.

Miura S, Shibata H, Furuya H, Ohyagi Y, Osoegawa M, Miyoshi Y, Matsunaga H, Shibata A, Matsumoto N, Iwaki A, Taniwaki T, Kikuchi H, Kira J, Fukumaki Y. Miura S, et al. Neurology. 2006 Oct 10;67(7):1236-41. doi: 10.1212/01.wnl.0000238510.84932.82. Neurology. 2006. PMID: 17030759

6

Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families.

Hara K, Shiga A, Nozaki H, Mitsui J, Takahashi Y, Ishiguro H, Yomono H, Kurisaki H, Goto J, Ikeuchi T, Tsuji S, Nishizawa M, Onodera O. Hara K, et al. Neurology. 2008 Aug 19;71(8):547-51. doi: 10.1212/01.wnl.0000311277.71046.a0. Epub 2008 Jun 25. Neurology. 2008. PMID: 18579805

7

Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.

Hirano R, Takashima H, Okubo R, Tajima K, Okamoto Y, Ishida S, Tsuruta K, Arisato T, Arata H, Nakagawa M, Osame M, Arimura K. Hirano R, et al. Neurogenetics. 2004 Dec;5(4):215-21. doi: 10.1007/s10048-004-0194-z. Epub 2004 Sep 29. Neurogenetics. 2004. PMID: 15455264

8

Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred.

Bürk K, Zühlke C, König IR, Ziegler A, Schwinger E, Globas C, Dichgans J, Hellenbroich Y. Bürk K, et al. Neurology. 2004 Jan 27;62(2):327-9. doi: 10.1212/01.wnl.0000103293.63340.c1. Neurology. 2004. PMID: 14745083 Review.

9

Spinocerebellar ataxia type 15.

Gardner RJ, Knight MA, Hara K, Tsuji S, Forrest SM, Storey E. Gardner RJ, et al. Cerebellum. 2005;4(1):47-50. doi: 10.1080/14734220410019029. Cerebellum. 2005. PMID: 15895559 Review.

10

A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.

Brkanac Z, Bylenok L, Fernandez M, Matsushita M, Lipe H, Wolff J, Nochlin D, Raskind WH, Bird TD. Brkanac Z, et al. Arch Neurol. 2002 Aug;59(8):1291-5. doi: 10.1001/archneur.59.8.1291. Arch Neurol. 2002. PMID: 12164726

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

87 results

Results by year