Search Page
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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2022 | 2 |
2023 | 2 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
A review of major causative genes in congenital myopathies.
J Hum Genet. 2023 Mar;68(3):215-225. doi: 10.1038/s10038-022-01045-w. Epub 2022 Jun 7.
J Hum Genet. 2023.
PMID: 35668205
Review.
Centronuclear Myopathy Caused by Defective Membrane Remodelling of Dynamin 2 and BIN1 Variants.
Fujise K, Noguchi S, Takeda T.
Fujise K, et al.
Int J Mol Sci. 2022 Jun 3;23(11):6274. doi: 10.3390/ijms23116274.
Int J Mol Sci. 2022.
PMID: 35682949
Free PMC article.
Review.
Item in Clipboard
Characteristics of the muscle involvement along the disease progression in a large cohort of oculopharyngodistal myopathy compared to oculopharyngeal muscular dystrophy.
Eura N, Noguchi S, Ogasawara M, Kumutpongpanich T, Hayashi S, Nishino I; OPDM/OPMD Image Study Group.
Eura N, et al.
J Neurol. 2023 Dec;270(12):5988-5998. doi: 10.1007/s00415-023-11906-9. Epub 2023 Aug 27.
J Neurol. 2023.
PMID: 37634163
Item in Clipboard
Cite
Cite