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Proportion of 11778 mutant mitochondrial DNA and clinical expression in a thai population with leber hereditary optic neuropathy.
Chuenkongkaew WL, Suphavilai R, Vaeusorn L, Phasukkijwatana N, Lertrit P, Suktitipat B. Chuenkongkaew WL, et al. Among authors: suphavilai r. J Neuroophthalmol. 2005 Sep;25(3):173-5. doi: 10.1097/01.wno.0000176631.87234.49. J Neuroophthalmol. 2005. PMID: 16148621
Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
Tharaphan P, Chuenkongkaew WL, Luangtrakool K, Sanpachudayan T, Suktitipat B, Suphavilai R, Srisawat C, Sura T, Lertrit P. Tharaphan P, et al. Among authors: suphavilai r. J Neuroophthalmol. 2006 Dec;26(4):264-7. doi: 10.1097/01.wno.0000249318.88991.c4. J Neuroophthalmol. 2006. PMID: 17204919
Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy.
Phasukkijwatana N, Chuenkongkaew WL, Suphavilai R, Luangtrakool K, Kunhapan B, Lertrit P. Phasukkijwatana N, et al. Among authors: suphavilai r. J Hum Genet. 2006;51(12):1110-1117. doi: 10.1007/s10038-006-0073-6. Epub 2006 Oct 28. J Hum Genet. 2006. PMID: 17072496
The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees.
Phasukkijwatana N, Chuenkongkaew WL, Suphavilai R, Suktitipat B, Pingsuthiwong S, Ruangvaravate N, Atchaneeyasakul LO, Warrasak S, Poonyathalang A, Sura T, Lertrit P. Phasukkijwatana N, et al. Among authors: suphavilai r. J Hum Genet. 2006;51(4):298-304. doi: 10.1007/s10038-006-0361-1. Epub 2006 Feb 14. J Hum Genet. 2006. PMID: 16477364
Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation.
Chuenkongkaew W, Lertrit P, Suphavilai R. Chuenkongkaew W, et al. Among authors: suphavilai r. Southeast Asian J Trop Med Public Health. 2004 Mar;35(1):167-8. Southeast Asian J Trop Med Public Health. 2004. PMID: 15272763
Leber's hereditary optic neuropathy in Thailand.
Chuenkongkaew WL, Lertrit P, Poonyathalang A, Sura T, Ruangvaravate N, Atchaneeyasakul L, Suphavilai R. Chuenkongkaew WL, et al. Among authors: suphavilai r. Jpn J Ophthalmol. 2001 Nov-Dec;45(6):665-8. doi: 10.1016/s0021-5155(01)00423-3. Jpn J Ophthalmol. 2001. PMID: 11754915
An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy.
Chuenkongkaew WL, Lertrit P, Limwongse C, Nilanont Y, Boonyapisit K, Sangruchi T, Chirapapaisan N, Suphavilai R. Chuenkongkaew WL, et al. Among authors: suphavilai r. Eur J Neurol. 2005 May;12(5):388-91. doi: 10.1111/j.1468-1331.2004.01060.x. Eur J Neurol. 2005. PMID: 15804271
Serum levels of zinc and copper in normal subjects.
Lekhakul S, Siddhikol C, Suphavilai R, Skulchan V, Kritalugsana S, Prinksulaka P. Lekhakul S, et al. Among authors: suphavilai r. J Med Assoc Thai. 1987 Oct;70(10):583-6. J Med Assoc Thai. 1987. PMID: 3320254 Review. No abstract available.
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