PubMed (OMIM) for id: 383962

Year	Number of Results
1960	1
1962	1
1968	2
1970	1
1971	1
1972	1
1975	1
1976	4
1978	1
1979	3
1980	1
1981	6
1982	1
1983	3
1984	3
1985	1
1986	1
1987	3
1988	4
1989	6
1990	6
1991	2
1992	2
1993	2
1994	3
1995	2
1996	3
1997	11
1998	4
1999	10
2000	6
2001	7
2002	7
2003	1
2004	1
2024	0

1

Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotype.

Giacchetti M, Monticelli A, De Biase I, Pianese L, Turano M, Filla A, De Michele G, Cocozza S. Giacchetti M, et al. J Med Genet. 2004 Apr;41(4):293-5. doi: 10.1136/jmg.2003.015289. J Med Genet. 2004. PMID: 15060107 Free PMC article. No abstract available.

2

Cardiac aspects of Friedreich's ataxia.

BOYER SH 4th, CHISHOLM AW, McKUSICK VA. BOYER SH 4th, et al. Circulation. 1962 Mar;25:493-505. doi: 10.1161/01.cir.25.3.493. Circulation. 1962. PMID: 13872187 No abstract available.

3

Friedreich's ataxia: a neurocardiac disease.

HARTMAN JM, BOOTH RW. HARTMAN JM, et al. Am Heart J. 1960 Nov;60:716-20. doi: 10.1016/0002-8703(60)90354-9. Am Heart J. 1960. PMID: 13711956 No abstract available.

4

DNA triplet repeats mediate heterochromatin-protein-1-sensitive variegated gene silencing.

Saveliev A, Everett C, Sharpe T, Webster Z, Festenstein R. Saveliev A, et al. Nature. 2003 Apr 24;422(6934):909-13. doi: 10.1038/nature01596. Nature. 2003. PMID: 12712207

5

A cellular model for Friedreich Ataxia reveals small-molecule glutathione peroxidase mimetics as novel treatment strategy.

Jauslin ML, Wirth T, Meier T, Schoumacher F. Jauslin ML, et al. Hum Mol Genet. 2002 Nov 15;11(24):3055-63. doi: 10.1093/hmg/11.24.3055. Hum Mol Genet. 2002. PMID: 12417527

6

Up-regulation of c-Jun N-terminal kinase pathway in Friedreich's ataxia cells.

Pianese L, Busino L, De Biase I, De Cristofaro T, Lo Casale MS, Giuliano P, Monticelli A, Turano M, Criscuolo C, Filla A, Varrone S, Cocozza S. Pianese L, et al. Hum Mol Genet. 2002 Nov 1;11(23):2989-96. doi: 10.1093/hmg/11.23.2989. Hum Mol Genet. 2002. PMID: 12393810

7

Friedreich ataxia: effects of genetic understanding on clinical evaluation and therapy.

Lynch DR, Farmer JM, Balcer LJ, Wilson RB. Lynch DR, et al. Arch Neurol. 2002 May;59(5):743-7. doi: 10.1001/archneur.59.5.743. Arch Neurol. 2002. PMID: 12020255 Review.

8

Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.

Silveira I, Miranda C, Guimarães L, Moreira MC, Alonso I, Mendonça P, Ferro A, Pinto-Basto J, Coelho J, Ferreirinha F, Poirier J, Parreira E, Vale J, Januário C, Barbot C, Tuna A, Barros J, Koide R, Tsuji S, Holmes SE, Margolis RL, Jardim L, Pandolfo M, Coutinho P, Sequeiros J. Silveira I, et al. Arch Neurol. 2002 Apr;59(4):623-9. doi: 10.1001/archneur.59.4.623. Arch Neurol. 2002. PMID: 11939898

9

Frataxin knockin mouse.

Miranda CJ, Santos MM, Ohshima K, Smith J, Li L, Bunting M, Cossée M, Koenig M, Sequeiros J, Kaplan J, Pandolfo M. Miranda CJ, et al. FEBS Lett. 2002 Feb 13;512(1-3):291-7. doi: 10.1016/s0014-5793(02)02251-2. FEBS Lett. 2002. PMID: 11852098 Free article.

10

Intrafamilial phenotypic variability in Friedreich ataxia associated with a G130V mutation in the FRDA gene.

McCabe DJ, Wood NW, Ryan F, Hanna MG, Connolly S, Moore DP, Redmond J, Barton DE, Murphy RP. McCabe DJ, et al. Arch Neurol. 2002 Feb;59(2):296-300. doi: 10.1001/archneur.59.2.296. Arch Neurol. 2002. PMID: 11843702

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

111 results

Results by year