A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation

by Wanicha Chuenkongkaew, Patcharee Lertrit, Rungnapa Suphavilai
Published 2018

Stability of epitheliotrophic factors in autologous serum eye drops from chronic Stevens-Johnson syndrome dry eye compared to non-autoimmune dry eye

by Nopasak Phasukkijwatana, Patcharee Lertrit, Sompong Liammongkolkul, Pinnita Prabhasawat
Published 2018

An unusual electrophysiologic finding in acute stage of Leber's hereditary optic neuropathy

by Wanicha L. Chuenkongkaew, Patthanee Samsen, Patcharee Lertrit, Nualanong Thanasombatsakul
Published 2018

Polyglutamined expanded androgen receptor interacts with chaperonin CCT

by Suttikarn Pongtepaditep, Thawornchai Limjindaporn, Patcharee Lertrit, Chatchawan Srisawat, Chanin Limwongse
Published 2018

Oculopharyngodistal myopathy in a Thai family

by Rawiphan Witoonpanich, Sriphan Phankhian, Thanyachai Sura, Patcharee Lertrit, Suchart Phudhichareonrat
Published 2018

Seizures in myoclonic epilepsy with ragged-red fibers detected by DNA analysis : A case report

by Oraporn Sitburana, Suchart Phudhichareonrat, Rungnapa Supavilai, Rawiphan Witoonpanich, Patcharee Lertrit
Published 2018

Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy

by Herawati Sudoyo, Helena Suryadi, Patcharee Lertrit, Patcharin Pramoonjago, Diana Lyrawati, Sangkot Marzuki
Published 2018

Leber's Hereditary Optic Neuropathy (LHON) withmitochondrial ND4 gene mutation (11778) in a Thai patient

by Patcharee Lertrit, Yanee Trongpanich, Charoensri Mungkornkarn, Ngamkae Ruangvaravate, Arisav Imsumran, Neelobol Neungton
Published 2018

Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy

by Nopasak Phasukkijwatana, Wanicha L. Chuenkongkaew, Rungnapa Suphavilai, Komon Luangtrakool, Bussaraporn Kunhapan, Patcharee Lertrit
Published 2018

Mitochondrial DNA history of Sri Lankan ethnic people: Their relations within the island and with the Indian subcontinental populations

by Lanka Ranaweera, Supannee Kaewsutthi, Aung Win Tun, Hathaichanoke Boonyarit, Samerchai Poolsuwan, Patcharee Lertrit
Published 2018

Leber's hereditary optic neuropathy in Thailand

by Wanicha L. Chuenkongkaew, Patcharee Lertrit, Anuchit Poonyathalang, Thanyachai Sura, L. Atchaneeyasakul, Rungnapa Suphavilai
Published 2018

Proportion of 11778 mutant mitochondrial DNA and clinical expression in a Thai population with Leber hereditary optic neuropathy

by Wanicha L. Chuenkongkaew, Rungnapa Suphavilai, Lookjan Vaeusorn, Nopasak Phasukkijwatana, Patcharee Lertrit, Bhoom Suktitipat
Published 2018

Characterization of 2-deoxy-D-glucose uptake in fibroblast cultures derived from patients with A3243G mitochondrial DNA mutation

by Komon Luangtrakool, Farrah Yasmin Tate, Rachael Shepherd, Sarah Campbell, Carolyn M. Sue, Patcharee Lertrit
Published 2018

Genetic history of Southeast Asian populations as revealed by ancient and modern human mitochondrial DNA analysis

by Patcharee Lertrit, Samerchai Poolsuwan, Rachanie Thosarat, Thitima Sanpachudayan, Hathaichanoke Boonyarit, Chatchai Chinpaisal, Bhoom Suktitipat
Published 2018

Clinical expression and mitochondrial deoxyribonucleic acid study in twins with 14484 Leber’s hereditary optic neuropathy: A case report

by Wanicha Leetiratanai Chuenkongkaew, Buakhwan Chinkulkitnivat, Patcharee Lertrit, Niphon Chirapapaisan, Supannee Kaewsutthi, Bhoom Suktitipat, Chalermchai Mitrpant
Published 2022

Experience of ApoE study in Thai elderly

by Vorapun Senanarong, Kamoltip Harnphadungkit, Patcharee Lertrit, Chalermchai Mitrpant, Suthipol Udompunthurak, Chanin Limwong, Naraporn Prayoonwiwat, Niphon Poungvarin
Published 2018

Mitochondrial haplogroup background may influence Southeast Asian G11778A leber hereditary optic neuropathy

by Supannee Kaewsutthi, Nopasak Phasukkijwatana, Yutthana Joyjinda, Wanicha Chuenkongkaew, Bussaraporn Kunhapan, Aung Win Tun, Bhoom Suktitipat, Patcharee Lertrit
Published 2018

A unique 3.5-kb deletion of the mitochondrial genome in Thai patients with Kearns-Sayre syndrome

by Patcharee Lertrit, Arisa Imsumran, Pongkiat Karnkirawattana, Voraphan Devahasdin, Tumtip Sangruchi, La Ongsri Atchaneeyasakul, Charoensri Mungkornkarn, Neelobol Neungton
Published 2018

Association of Mitochondrial DNA Polymorphisms With Pediatric-Onset Cyclic Vomiting Syndrome

by Kirana Veenin, Duangrurdee Wattanasirichaigoon, Bhoom Suktitipat, Saisuda Noojarern, Patcharee Lertrit, Thipwimol Tim-Aroon, Supannee Kaewsutthi, Suporn Treepongkaruna
Published 2022

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

by Rochmy Istikharah, Aung Win Tun, Supannee Kaewsutthi, Pratibha Aryal, Bussaraporn Kunhapan, Wanphen Katanyoo, Wanicha Chuenkongkaew, Patcharee Lertrit
Published 2018