Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

2013
2025

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

Year Number of Results
2013 1
2019 1
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Search Results

2 results

Results by year

Filters applied: . Clear all
Page 1
Mitochondrial depletion syndromes in children and adults.
Finsterer J, Ahting U. Finsterer J, et al. Can J Neurol Sci. 2013 Sep;40(5):635-44. doi: 10.1017/s0317167100014852. Can J Neurol Sci. 2013. PMID: 23968935 Review.
To highlight differences between early-onset and adult mitochondrial depletion syndromes (MDS) concerning etiology and genetic background, pathogenesis, phenotype, clinical presentation and their outcome. ...The outcome appears to be more favorable in adult t …
To highlight differences between early-onset and adult mitochondrial depletion syndromes (MDS) concerning etiology and …
Genetic neuromuscular disorders: living the era of a therapeutic revolution. Part 2: diseases of motor neuron and skeletal muscle.
Vita G, Vita GL, Musumeci O, Rodolico C, Messina S. Vita G, et al. Neurol Sci. 2019 Apr;40(4):671-681. doi: 10.1007/s10072-019-03764-z. Epub 2019 Feb 25. Neurol Sci. 2019. PMID: 30805745 Review.
Positive evidences are discussed about lamotrigine and ranolazine in non-dystrophic myotonias, chaperons in Pompe disease, and nucleosides in mitochondrial DNA depletion induced by thymidine kinase 2 deficiency....
Positive evidences are discussed about lamotrigine and ranolazine in non-dystrophic myotonias, chaperons in Pompe disease, and nucleosides i …