Muscle coenzyme Q10 deficiencies in ataxia with oc... [Neurology. 2007] - PubMed

Save items

loading

Related citations in PubMed

Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients. [Neurogenetics. 2011]
Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.
Castellotti B, Mariotti C, Rimoldi M, Fancellu R, Plumari M, Caimi S, Uziel G, Nardocci N, Moroni I, Zorzi G, et al. Neurogenetics. 2011 Aug; 12(3):193-201. Epub 2011 Apr 5.
Early-onset ataxia with oculomotor apraxia with a novel APTX mutation. [Pediatr Neurol. 2005]
Early-onset ataxia with oculomotor apraxia with a novel APTX mutation.
Ito A, Yamagata T, Mori M, Momoi MY. Pediatr Neurol. 2005 Jul; 33(1):53-6.
Novel mutations in the senataxin DNA/RNA helicase domain in ataxia with oculomotor apraxia 2. [Neurology. 2006]
Novel mutations in the senataxin DNA/RNA helicase domain in ataxia with oculomotor apraxia 2.
Fogel BL, Perlman S. Neurology. 2006 Dec 12; 67(11):2083-4.
Review [Autosomal recessive cerebellar ataxias with oculomotor apraxia]. [Rev Neurol (Paris). 2006]
Review [Autosomal recessive cerebellar ataxias with oculomotor apraxia].
Le Ber I, Rivaud-Péchoux S, Brice A, Dürr A. Rev Neurol (Paris). 2006 Feb; 162(2):177-84.
Review Short-patch single-strand break repair in ataxia oculomotor apraxia-1. [Biochem Soc Trans. 2009]
Review Short-patch single-strand break repair in ataxia oculomotor apraxia-1.
Reynolds JJ, El-Khamisy SF, Caldecott KW. Biochem Soc Trans. 2009 Jun; 37(Pt 3):577-81.

See reviews... See all...

Cited by 7 PubMed Central articles

Review Primary and secondary CoQ(10) deficiencies in humans. [Biofactors. 2011]
Review Primary and secondary CoQ(10) deficiencies in humans.
Quinzii CM, Hirano M. Biofactors. 2011 Sep; 37(5):361-5. Epub 2011 Oct 11.
Aprataxin localizes to mitochondria and preserves mitochondrial function. [Proc Natl Acad Sci U S A. 2011]
Aprataxin localizes to mitochondria and preserves mitochondrial function.
Sykora P, Croteau DL, Bohr VA, Wilson DM 3rd. Proc Natl Acad Sci U S A. 2011 May 3; 108(18):7437-42. Epub 2011 Apr 18.
Review Coenzyme Q and mitochondrial disease. [Dev Disabil Res Rev. 2010]
Review Coenzyme Q and mitochondrial disease.
Quinzii CM, Hirano M. Dev Disabil Res Rev. 2010 Jun; 16(2):183-8.

See all...

Related information

Related Citations
Calculated set of PubMed citations closely related to the selected article(s) retrieved using a word weight algorithm. Related articles are displayed in ranked order from most to least relevant, with the “linked from” citation displayed first.
Compound (MeSH Keyword)
PubChem chemical compound records that are classified under the same Medical Subject Headings (MeSH) controlled vocabulary as the current articles.
Gene (OMIM)
Gene records associated with Online Mendelian Inheritance in Man (OMIM) records that cite the current articles in their reference lists.
Nucleotide (Weighted)
Nucleotide records associated with the current articles through the Gene database. These are the related sequences on the Gene record that are added manually by NCBI.
OMIM (calculated)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as references in the light bulb links within or in the citations at the end of the OMIM record. The references available through the light bulb link are collected using the PubMed related articles algorithm to identify records with similar terminology to the OMIM record.
OMIM (cited)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as reference cited at the end of the OMIM record.
Protein (Weighted)
Protein records associated with the current articles through related Gene database records. These are the related sequences on the Gene record that are added manually by NCBI.
Substance (MeSH Keyword)
PubChem chemical substance (submitted) records that are classified under the same Medical Subject Headings (MeSH) controlled vocabulary as the current articles.
Cited in PMC
Full-text articles in the PubMed Central Database that cite the current articles.

Recent activity

Clear Turn Off Turn On

Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1.
Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1.
Neurology. 2007 Jan 23 ;68(4):295-7.

PubMed
Combined aspirin-oral anticoagulant therapy compared with oral anticoagulant the...
Combined aspirin-oral anticoagulant therapy compared with oral anticoagulant therapy alone among patients at risk for cardiovascular disease: a meta-analysis of randomized trials.
Arch Intern Med. 2007 Jan 22 ;167(2):117-24.

PubMed
Boundaries as distance regulators in personal relationships.
Boundaries as distance regulators in personal relationships.
Fam Process. 1991 Dec ;30(4):393-406.

PubMed
The predominant cAMP-stimulated 3 x 5 kb StAR mRNA contains specific sequence el...
The predominant cAMP-stimulated 3 x 5 kb StAR mRNA contains specific sequence elements in the extended 3'UTR that confer high basal instability.
J Mol Endocrinol. 2007 Feb ;38(1-2):159-79.

PubMed
Cdc37 has distinct roles in protein kinase quality control that protect nascent ...
Cdc37 has distinct roles in protein kinase quality control that protect nascent chains from degradation and promote posttranslational maturation.
J Cell Biol. 2007 Jan 29 ;176(3):319-28. Epub 2007 Jan 22 .

PubMed

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

PubMed

Result Filters

Display Settings:

Send to:

Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1.

Source

Abstract

MeSH Terms, Substances

MeSH Terms

Substances

LinkOut - more resources

Full Text Sources

Medical

Supplemental Content

Save items

Related citations in PubMed

Cited by 7 PubMed Central articles

Related information

Recent activity

Simple NCBI Directory

Getting Started

Resources

Popular

Featured

NCBI Information