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Journal Abstract Search
151 related items for PubMed ID: 2018507
1. Mutation detection in Leber's hereditary optic neuropathy by PCR with allele-specific priming. Nørby S, Lestienne P, Nelson I, Rosenberg T. Biochem Biophys Res Commun; 1991 Mar 15; 175(2):631-6. PubMed ID: 2018507 [Abstract] [Full Text] [Related]
3. [Mitochondrial DNA mutation in Leber's hereditary optic neuropathy in China]. Zhang LS, Huang Y, Li FY. Zhonghua Yi Xue Za Zhi; 1994 Jun 15; 74(6):349-51, 390. PubMed ID: 7994643 [Abstract] [Full Text] [Related]
4. Mutation-specific PCR: a rapid and inexpensive diagnostic method, as exemplified by mitochondrial DNA analysis in Leber's hereditary optic neuropathy. Nørby S. DNA Cell Biol; 1993 Jun 15; 12(6):549-52. PubMed ID: 8101084 [Abstract] [Full Text] [Related]
5. Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy. Stone EM, Coppinger JM, Kardon RH, Donelson J. Arch Ophthalmol; 1990 Oct 15; 108(10):1417-20. PubMed ID: 1977373 [Abstract] [Full Text] [Related]
6. [Molecular genetic analysis for Leber's hereditary optic neuropathy (LHON)]. Tanno Y, Yoneda M, Tanaka K, Tsuji S. Nihon Rinsho; 1993 Sep 15; 51(9):2396-402. PubMed ID: 8411719 [Abstract] [Full Text] [Related]
7. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Kellar-Wood H, Robertson N, Govan GG, Compston DA, Harding AE. Ann Neurol; 1994 Jul 15; 36(1):109-12. PubMed ID: 8024249 [Abstract] [Full Text] [Related]
8. Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy. Johns DR, Berman J. Biochem Biophys Res Commun; 1991 Feb 14; 174(3):1324-30. PubMed ID: 1900003 [Abstract] [Full Text] [Related]
9. [Leber's optic neuropathy: new diagnostic prospects]. Pagot V, Malecaze F, Rötig A, Simorre V, Maillard P, Mathis A, Munnich A. J Fr Ophtalmol; 1992 Feb 14; 15(1):19-23. PubMed ID: 1602101 [Abstract] [Full Text] [Related]
10. [DNA diagnosis of Leber's hereditary optic neuropathy]. Mashima Y, Oguchi Y, Uemura Y, Kudoh J, Sakai K, Shimizu N. Nippon Ganka Gakkai Zasshi; 1990 Jul 14; 94(7):683-7. PubMed ID: 2220506 [Abstract] [Full Text] [Related]
12. High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy. Mashima Y, Hiida Y, Oguchi Y, Kudoh J, Shimizu N. Hum Genet; 1993 Aug 14; 92(1):101-2. PubMed ID: 8103501 [Abstract] [Full Text] [Related]
14. A new mitochondrial DNA mutation in the tRNA leucine 1 gene (C3275A) in a patient with Leber's hereditary optic neuropathy. Garcia-Lozano JR, Aguilera I, Bautista J, Nuñez-Roldan A. Hum Mutat; 2000 Jan 14; 15(1):120-1. PubMed ID: 10612844 [No Abstract] [Full Text] [Related]
15. Analysis of mitochondrial DNA in Leber's hereditary optic neuropathy. Poulton J, Deadman ME, Bronte-Stewart J, Foulds WS, Gardiner RM. J Med Genet; 1991 Nov 14; 28(11):765-70. PubMed ID: 1770533 [Abstract] [Full Text] [Related]