PubMed期刊
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作者:Phasukkijwatana Nopasak , Lertrit Patcharee ...
来源:[J].Current Eye Research, 2011, Vol.36 (9), pp.775-81PubMed
摘要:To compare the concentrations of epitheliotrophic factors in autologous serum eye drops (ASE) prepared from sera of chronic Stevens-Johnson syndrome (SJS) patients with dry eyes to those prepared from non-autoimmune dry eye controls and to study the stability of the epitheli...
作者:Phasukkijwatana Nopasak , Kunhapan Bussaraporn ...
来源:[J].Human Genetics, 2010, Vol.128 (1), pp.39-49PubMed
摘要:Leber hereditary optic neuropathy (LHON) is the most common mitochondrially inherited disease causing blindness, preferentially in young adult males. Most of the patients carry the G11778A mitochondrial DNA (mtDNA) mutation. However, the marked incomplete penetrance and the gende...
作者:Phasukkijwatana Nopasak , Chuenkongkaew Wanicha L ...
来源:[J].Journal of Human Genetics(IF 2.365), 2006, Vol.51 (4), pp.298-304PubMed
摘要:Leber hereditary optic neuropathy (LHON) is characterized by acute or subacute bilateral visual loss, and affects mostly young males. The most common mitochondrial DNA mutation responsible for LHON worldwide is G11778A. Despite different genetic backgrounds, which are believed to...
作者:Phasukkijwatana Nopasak , Chuenkongkaew Wanicha L ...
来源:[J].Journal of Human Genetics(IF 2.365), 2006, Vol.51 (12), pp.1110-7PubMed
摘要:Leber hereditary optic neuropathy (LHON) is characterized by the acute or subacute bilateral painless loss of central vision, predominantly in young males. G11778A is the most common mitochondrial DNA mutation responsible for the disease. Thirty-seven percent of our LHON pedigree...
作者:Phasukkijwatana Nopasak , Joyjinda Yutthana ...
来源:[J].Investigative Ophthalmology & Visual Science, 2011, Vol.52 (7), pp.4742-8PubMed
摘要:To investigate the role of mitochondrial DNA (mt DNA) background on the expression of Leber hereditary optic neuropathy (LHON) in Southeast Asian carriers of the G11778A mutation.;;Complete mtDNA sequences were analyzed from 53 unrelated Southeast Asian G11778A LHON pedigrees in ...
作者:Phasukkijwatana Nopasak , Lertrit Patcharee
来源:[J].Journal of Neuro-Ophthalmology(IF 1.628), 2005, Vol.25 (3), pp.173-5PubMed
摘要:The proportion of mutant mtDNA in blood has been found to correlate with the frequency of visual loss in cases with mtDNA mutations associated with Leber hereditary optic neuropathy (LHON), especially in men. We sought to determine this correlation in a Thai population of LHON.;;...
作者:Phasukkijwatana Nopasak , Iafe Nicholas , Sarraf David
来源:[J].Retinal cases & brief reports, 2017, Vol.11 Suppl 1, pp.S68-S72PubMed
摘要:To describe the quantitative optical coherence tomography angiography analysis of the superficial and deep retinal capillary plexus in a case of A29 birdshot chorioretinopathy (BCR) complicated by retinal neovascularization.;;Multimodal retinal imaging, including optical coherenc...
作者:Phasukkijwatana Nopasak , Novais Eduardo ...
来源:[J].American journal of ophthalmology, 2016, Vol.169, pp.235-48PubMed
摘要:The range of subretinal hyperreflective material (SHRM) seen in macular disease includes type 2 macular neovascularization, fibrosis, exudation, vitelliform material, and hemorrhage. The prognostic significance of SHRM has been evaluated retrospectively in clinical trials, b...
作者:Phasukkijwatana Nopasak , Vaclavik Veronika ...
来源:[J].Retinal cases & brief reports, 2017, Vol.11 Suppl 1, pp.S113-S120PubMed
摘要:To describe the multimodal imaging findings, including optical coherence tomography angiography analysis, and spectrum of etiologies associated with Amalric triangular choroidal infarction.;;This study is a multicenter, retrospective, observational case series review of the clini...
作者:... Xu David , Phasukkijwatana Nopasak , Sarraf David
来源:[J].Retinal cases & brief reports, 2017, Vol.11 Suppl 1, pp.S121-S123PubMed
摘要:To report novel en face imaging findings of multiple evanescent white dot syndrome.;;A 25-year-old woman presented with photopsia and vision loss affecting the left eye. Ophthalmic examination, color fundus photography, fluorescein angiography, spectral domain optical coherence t...

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