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5 in total

1. Microphotometric analysis of NADH-tetrazolium reductase deficiency in fibroblasts of patients with Leber hereditary optic neuropathy.

Authors: S Malik; H Sudoyo; S Marzuki
Journal: J Inherit Metab Dis Date: 2000-11 Impact factor: 4.982

2. Leber's hereditary optic neuropathy with 14484 mutation in Central Java, Indonesia.

Authors: Tomoki Nishioka; Mamoru Tasaki; Augustinus Soemantri; Marbaniati Dyat; J C Susanto; Moedrik Tamam; Bambang Sudarmanto; Takafumi Ishida
Journal: J Hum Genet Date: 2003-06-24 Impact factor: 3.172

3. Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy.

Authors: H Y Handoko; P J Wirapati; H A Sudoyo; M Sitepu; S Marzuki
Journal: J Med Genet Date: 1998-08 Impact factor: 6.318

4. The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees.

Authors: Nopasak Phasukkijwatana; Wanicha L Chuenkongkaew; Rungnapa Suphavilai; Bhoom Suktitipat; Sarinee Pingsuthiwong; Ngamkae Ruangvaravate; La-Ongsri Atchaneeyasakul; Sukhuma Warrasak; Anuchit Poonyathalang; Thanyachai Sura; Patcharee Lertrit
Journal: J Hum Genet Date: 2006-02-14 Impact factor: 3.172

5. Mutation in mitochondrial complex I ND6 subunit is associated with defective response to hypoxia in human glioma cells.

Authors: Carrie DeHaan; Bahram Habibi-Nazhad; Elizabeth Yan; Nicole Salloum; Matthew Parliament; Joan Allalunis-Turner
Journal: Mol Cancer Date: 2004-07-12 Impact factor: 27.401

5 in total