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Journal Abstract Search

665 related items for PubMed ID: 18841565

  • 21. [Leber's hereditary optic atrophy. A hereditary disease caused by mitochondrial DNA mutation].
    Nørby S, Rosenberg T.
    Ugeskr Laeger; 1990 Oct 22; 152(43):3149-52. PubMed ID: 2238193
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  • 22. [Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].
    Yang JH, Tong Y, Li BH, Chen YK.
    Zhonghua Yan Ke Za Zhi; 2005 Mar 22; 41(3):243-5. PubMed ID: 15840367
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  • 23. [Mutation analysis in a family of Leber hereditary optic neuropathy].
    She CY, Gu H, Xu J, Ma K, Liu NP.
    Zhonghua Yan Ke Za Zhi; 2011 Dec 22; 47(12):1080-3. PubMed ID: 22336116
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  • 24. Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
    Leo-Kottler B, Christ-Adler M, Baumann B, Zrenner E, Wissinger B.
    Ger J Ophthalmol; 1996 Jul 22; 5(4):233-40. PubMed ID: 8854108
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  • 25. Vision improvement in a Taiwanese (Han Chinese) family with Leber's hereditary optic neuropathy.
    Lin HZ, Pang CY, Chen SP, Tsai RK.
    Kaohsiung J Med Sci; 2012 Dec 22; 28(12):679-82. PubMed ID: 23217361
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  • 27. [Leber's optic neuropathy: a case report].
    Pato-Pato A, Cimas-Hernando I, Lorenzo-González JR.
    Rev Neurol; 2012 Dec 22; 42(1):22-4. PubMed ID: 16402322
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  • 30. Leber's hereditary optic neuropathy associated with multiple sclerosis: Harding's syndrome.
    Parry-Jones AR, Mitchell JD, Gunarwardena WJ, Shaunak S.
    Pract Neurol; 2008 Apr 22; 8(2):118-21. PubMed ID: 18344382
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  • 33. [Sudden blindness: consider Leber's hereditary optic neuropathy].
    Schieving JH, de Vries BB, Hol F, Stroink H.
    Ned Tijdschr Geneeskd; 2008 Oct 25; 152(43):2313-6. PubMed ID: 19024058
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  • 34. Stargardt's type maculopathy in a patient with 11778 Leber's optic neuropathy.
    Yen MY, Wei YH, Liu JH.
    J Neuroophthalmol; 1996 Jun 25; 16(2):120-3. PubMed ID: 8797169
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  • 35. 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 25; 67(7):639-41. PubMed ID: 24747208
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  • 36. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families.
    Martin-Kleiner I, Gabrilovac J, Bradvica M, Vidović T, Cerovski B, Fumić K, Boranić M.
    Coll Antropol; 2006 Mar 25; 30(1):171-4. PubMed ID: 16617593
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  • 37. Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.
    Brown MD, Allen JC, Van Stavern GP, Newman NJ, Wallace DC.
    Am J Med Genet; 2001 Dec 15; 104(4):331-8. PubMed ID: 11754070
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  • 38. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
    Mao YJ, Qu J, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb 15; 25(1):45-9. PubMed ID: 18247303
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  • 39. Influence of mutation type on clinical expression of Leber hereditary optic neuropathy.
    Spruijt L, Kolbach DN, de Coo RF, Plomp AS, Bauer NJ, Smeets HJ, de Die-Smulders CE.
    Am J Ophthalmol; 2006 Apr 15; 141(4):676-82. PubMed ID: 16564802
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  • 40. [Clinical examination of Leber hereditary optic neuropathy in patients with the same gene mutation].
    Chelstowska J, Mroczek K, Niebudek D, Małecka-Idzikowska A, Bartnik E, Hanna Nizankowska M, Sasiadek M.
    Przegl Lek; 2002 Apr 15; 59(10):777-9. PubMed ID: 12632910
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