Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1990 1
1991 1
1992 1
2002 1
2020 0
Text availability
Article attribute
Article type
Publication date

Search Results

4 results
Results by year
Filters applied: . Clear all
Page 1
Aggregation of actin and cofilin in identical twins with juvenile-onset dystonia.
Gearing M, Juncos JL, Procaccio V, Gutekunst CA, Marino-Rodriguez EM, Gyure KA, Ono S, Santoianni R, Krawiecki NS, Wallace DC, Wainer BH. Gearing M, et al. Ann Neurol. 2002 Oct;52(4):465-76. doi: 10.1002/ana.10319. Ann Neurol. 2002. PMID: 12325076 Free PMC article.
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.
Newman NJ, Lott MT, Wallace DC. Newman NJ, et al. Am J Ophthalmol. 1991 Jun 15;111(6):750-62. doi: 10.1016/s0002-9394(14)76784-4. Am J Ophthalmol. 1991. PMID: 2039048
Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation.
Stone EM, Newman NJ, Miller NR, Johns DR, Lott MT, Wallace DC. Stone EM, et al. J Clin Neuroophthalmol. 1992 Mar;12(1):10-4. J Clin Neuroophthalmol. 1992. PMID: 1532593
Mitochondria and Leber's hereditary optic neuropathy.
Newman NJ, Wallace DC. Newman NJ, et al. Am J Ophthalmol. 1990 Jun 15;109(6):726-30. doi: 10.1016/s0002-9394(14)72445-6. Am J Ophthalmol. 1990. PMID: 2346203 No abstract available.