Chuenkongkaew WL - Search Results

1

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. Jpn J Ophthalmol. 2001 Nov-Dec;45(6):665-8. doi: 10.1016/s0021-5155(01)00423-3. Jpn J Ophthalmol. 2001. PMID: 11754915

2

Orbital pseudotumor: clinical features and outcomes.

Chirapapaisan N, Chuenkongkaew W, Pornpanich K, Vangveeravong S. Chirapapaisan N, et al. Asian Pac J Allergy Immunol. 2007 Dec;25(4):215-8. Asian Pac J Allergy Immunol. 2007. PMID: 18402294

3

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. Southeast Asian J Trop Med Public Health. 2004 Mar;35(1):167-8. Southeast Asian J Trop Med Public Health. 2004. PMID: 15272763

4

A prospective randomized trial of megadose methylprednisolone and high dose dexamethasone for traumatic optic neuropathy.

Chuenkongkaew W, Chirapapaisan N. Chuenkongkaew W, et al. J Med Assoc Thai. 2002 May;85(5):597-603. J Med Assoc Thai. 2002. PMID: 12188391 Clinical Trial.

5

Optic neuritis: characteristics and visual outcome.

Chuenkongkaew W, Chirapapaisan N. Chuenkongkaew W, et al. J Med Assoc Thai. 2003 Mar;86(3):238-43. J Med Assoc Thai. 2003. PMID: 12757063

6

Diagnostic value of visual evoked potentials for clinical diagnosis of multiple sclerosis.

Chirapapaisan N, Laotaweerungsawat S, Chuenkongkaew W, Samsen P, Ruangvaravate N, Thuangtong A, Chanvarapha N. Chirapapaisan N, et al. Doc Ophthalmol. 2015 Feb;130(1):25-30. doi: 10.1007/s10633-014-9466-6. Epub 2014 Oct 21. Doc Ophthalmol. 2015. PMID: 25330954

7

Diurnal changes in retinal nerve fiber layer thickness with obstructive sleep apnea/hypopnea syndrome.

Chirapapaisan N, Likitgorn T, Pleumchitchom M, Sakiyalak D, Banhiran W, Saiman M, Chuenkongkaew W. Chirapapaisan N, et al. Int J Ophthalmol. 2016 Jul 18;9(7):979-83. doi: 10.18240/ijo.2016.07.07. eCollection 2016. Int J Ophthalmol. 2016. PMID: 27500104 Free PMC article.

8

Profiling the mitochondrial proteome of Leber's Hereditary Optic Neuropathy (LHON) in Thailand: down-regulation of bioenergetics and mitochondrial protein quality control pathways in fibroblasts with the 11778G>A mutation.

Tun AW, Chaiyarit S, Kaewsutthi S, Katanyoo W, Chuenkongkaew W, Kuwano M, Tomonaga T, Peerapittayamongkol C, Thongboonkerd V, Lertrit P. Tun AW, et al. PLoS One. 2014 Sep 12;9(9):e106779. doi: 10.1371/journal.pone.0106779. eCollection 2014. PLoS One. 2014. PMID: 25215595 Free PMC article.

9

Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy.

Kaewsutthi S, Phasukkijwatana N, Joyjinda Y, Chuenkongkaew W, Kunhapan B, Tun AW, Suktitipat B, Lertrit P. Kaewsutthi S, et al. Invest Ophthalmol Vis Sci. 2011 Jul 1;52(7):4742-8. doi: 10.1167/iovs.10-5816. Invest Ophthalmol Vis Sci. 2011. PMID: 21398275

10

Identification of the variants in PARL, the nuclear modifier gene, responsible for the expression of LHON patients in Thailand.

Istikharah R, Tun AW, Kaewsutthi S, Aryal P, Kunhapan B, Katanyoo W, Chuenkongkaew W, Lertrit P. Istikharah R, et al. Exp Eye Res. 2013 Nov;116:55-7. doi: 10.1016/j.exer.2013.08.007. Epub 2013 Aug 22. Exp Eye Res. 2013. PMID: 23973714 Review.

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