These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
196 related items for PubMed ID: 15623735
1. Leber hereditary optic neuropathy with chorea and dementia resembling Huntington disease. Morimoto N, Nagano I, Deguchi K, Murakami T, Fushimi S, Shoji M, Abe K. Neurology; 2004 Dec 28; 63(12):2451-2. PubMed ID: 15623735 [No Abstract] [Full Text] [Related]
2. Acute Bilateral Leber Hereditary Optic Neuropathy. Khetan V, Zanolli M, Levin AV. J Pediatr Ophthalmol Strabismus; 2015 Dec 28; 52(4):256. PubMed ID: 26214724 [No Abstract] [Full Text] [Related]
9. Leber Hereditary Optic Neuropathy: Visual Recovery in a Patient With the Rare m.3890G>A Point Mutation. Murray JJ, Nolan KW, McClelland C, Lee MS. J Neuroophthalmol; 2017 Jun 28; 37(2):166-171. PubMed ID: 27798429 [Abstract] [Full Text] [Related]
10. Leber hereditary optic neuropathy and multiple sclerosis: the mitochondrial connection. Manjunath V, Bhatti MT. Can J Ophthalmol; 2015 Feb 28; 50(1):e14-7. PubMed ID: 25677293 [No Abstract] [Full Text] [Related]
11. Leber hereditary optic neuropathy due to a new ND1 mutation. Soldath P, Wegener M, Sander B, Rosenberg T, Duno M, Wibrand F, Vissing J. Ophthalmic Genet; 2017 Feb 28; 38(5):480-485. PubMed ID: 28139165 [Abstract] [Full Text] [Related]
12. Huntington's disease-like 2 can present as chorea-acanthocytosis. Saiki S, Sakai K, Saiki M, Hirose G. Neurology; 2004 Sep 14; 63(5):939-40; author reply 939-40. PubMed ID: 15365163 [No Abstract] [Full Text] [Related]
13. Posterior reversible encephalopathy syndrome in a leber hereditary optic neuropathy patient with mitochondrial DNA 11778G>A point mutation. Da Y, Zhang X, Li F, Yang X, Zhang X, Jia J. J Neuroophthalmol; 2013 Sep 14; 33(3):276-8. PubMed ID: 23782927 [Abstract] [Full Text] [Related]
14. A Case of Atypical Leber Hereditary Optic Neuropathy With Slow, Symmetrical Progression Over Three Years. Chun BY, Kim DW, Son BJ. J Neuroophthalmol; 2018 Sep 14; 38(3):421-422. PubMed ID: 30106804 [No Abstract] [Full Text] [Related]
15. m.3635G>A mutation as a cause of Leber hereditary optic neuropathy. Kodroń A, Krawczyński MR, Tońska K, Bartnik E. J Clin Pathol; 2014 Jul 14; 67(7):639-41. PubMed ID: 24747208 [Abstract] [Full Text] [Related]