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Title: HETEROPLASMY IN LEBER HEREDITARY OPTIC NEUROPATHY
Author(s): SMITH, KH
Source: ARCHIVES OF OPHTHALMOLOGY Volume: 111 Issue: 11 Pages: 1486-1490 Published: NOV 1993
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1. Title: Hereditary optic atrophies
Author(s): Poloschek CM, Lagreze WA
Source: OPHTHALMOLOGE   Volume: 106   Issue: 9   Pages: 845-856   Published: SEP 2009
2. Title: Inherited mitochondrial optic neuropathies
Author(s): Yu-Wai-Man P, Griffiths PG, Hudson G, et al.
Source: JOURNAL OF MEDICAL GENETICS   Volume: 46   Issue: 3   Pages: 145-158   Published: MAR 2009
3. Title: Mitochondrial DNA Haplogroups M7b1 ' 2 and M8a Affect Clinical Expression of Leber Hereditary Optic Neuropathy in Chinese Families with the m.11778G -> A Mutation
Author(s): Ji YL, Zhang AM, Jia XY, et al.
Source: AMERICAN JOURNAL OF HUMAN GENETICS   Volume: 83   Issue: 6   Pages: 760-768   Published: DEC 12 2008
4. Title: Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background
Author(s): Hudson G, Carelli V, Spruijt L, et al.
Source: AMERICAN JOURNAL OF HUMAN GENETICS   Volume: 81   Issue: 2   Pages: 228-233   Published: AUG 2007
5. Title: Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy
Author(s): Phasukkijwatana N, Chuenkongkaew WL, Suphavilai R, et al.
Source: JOURNAL OF HUMAN GENETICS   Volume: 51   Issue: 12   Pages: 1110-1117   Published: 2006
6. Title: Mitochondrial abnormalities in patients with LHON-like optic neuropathies
Author(s): Abu-Amero KK, Bosley TM
Source: INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE   Volume: 47   Issue: 10   Pages: 4211-4220   Published: OCT 2006
7. Title: Leber's hereditary optic neuropathy: A multifactorial disease
Author(s): Yen MY, Wang AG, Wei YH
Source: PROGRESS IN RETINAL AND EYE RESEARCH   Volume: 25   Issue: 4   Pages: 381-396   Published: JUL 2006
8. Title: The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees
Author(s): Phasukkijwatana N, Chuenkongkaew WL, Suphavilai R, et al.
Source: JOURNAL OF HUMAN GENETICS   Volume: 51   Issue: 4   Pages: 298-304   Published: 2006
9. Title: De novo COX2 mutation in a LHON family of Caucasian origin: implication for the role of mtDNA polymorphism in human pathology
Author(s): Zhadanov SI, Atamanov VV, Zhadanov NI, et al.
Source: JOURNAL OF HUMAN GENETICS   Volume: 51   Issue: 3   Pages: 161-170   Published: 2006
10. Title: Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study
Author(s): Quiros PA, Torres RJ, Salomao S, et al.
Source: BRITISH JOURNAL OF OPHTHALMOLOGY   Volume: 90   Issue: 2   Pages: 150-153   Published: FEB 2006