Sensitivity and frequencies of dystrophin gene mutations in Thai DMD/BMD patients as detected by multiplex PCR

بواسطة Thanyachai Sura, Jakris Eu-ahsunthornwattana, Sarinee Pingsuthiwong, Manisa Busabaratana
منشور في 2018

A genetic association study between growth differentiation factor 5 (GDF 5) polymorphism and knee osteoarthritis in Thai population

بواسطة Tulyapruek Tawonsawatruk, Theeraroj Changthong, Sarinee Pingsuthiwong, Objoon Trachoo, Thanyachai Sura, Wiwat Wajanavisit
منشور في 2018

Novel COL1A1 gene mutation (R1026X) of type I osteogenesis imperfecta: A first case report

بواسطة Sathit Niramitmahapanya, Thitinun Anusornvongchai, Sarinee Pingsuthiwong, Veerasak Sarinnapakorn, Chaicharn Deerochanawong, Thongkum Sunthornthepvarakul
منشور في 2018

Prevalence of the C677T methylenetetrahydrofolate reductase mutation in Thai patients with deep vein thrombosis

بواسطة Pantep Angchaisuksiri, Sarinee Pingsuthiwong, Thanyachai Sura, Katcharin Aryuchai, Manisa Busabaratana, Vichai Atichartakarn
منشور في 2018

A genetic association study between growth differentiation factor 5 (GDF 5) polymorphism and knee osteoarthritis in Thai population

بواسطة Tulyapruek Tawonsawatruk, Theeraroj Changthong, Sarinee Pingsuthiwong, Objoon Trachoo, Thanyachai Sura, Wiwat Wajanavisit
منشور في 2017

Prevalence of the G1691A mutation in the factor V gene (Factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population

بواسطة Pantep Angchaisuksiri, Sarinee Pingsuthiwong, Katcharin Aryuchai, Manisa Busabaratana, Thanyachai Sura, Vichai Atichartakarn, Piyamitr Sritara
منشور في 2018

Congestive heart failure with rhabdomyolysis and acute renal failure in a manifesting female carrier of duchenne muscular dystrophy with duplication of dystrophin gene

بواسطة Atchara Tunteeratum, Rawiphan Witoonpanich, Suchart Phudhichareonrat, Jakris Eu-Ahsunthornwattana, Sarinee Pingsuthiwong, Kanoknan Srichan, Thanyachai Sura
منشور في 2018

The unique characteristics of Thai Leber hereditary optic neuropathy: Analysis of 30 G11778A pedigrees

بواسطة Nopasak Phasukkijwatana, Wanicha L. Chuenkongkaew, Rungnapa Suphavilai, Bhoom Suktitipat, Sarinee Pingsuthiwong, Ngamkae Ruangvaravate, La Ongsri Atchaneeyasakul, Sukhuma Warrasak, Anuchit Poonyathalang, Thanyachai Sura, Patcharee Lertrit
منشور في 2018

A novel H572R mutation in the transforming growth factor-β-induced gene in a Thai family with lattice corneal dystrophy type I

بواسطة La Ongsri Atchaneeyasakul, Binoy Appukuttan, Sarinee Pingsuthiwong, Pa Thai Yenchitsomanus, Adisak Trinavarat, Chatchawan Srisawat, Trevor J. McFarland, J. Timothy Stout, Patcharee Wichyanuwat, Wanna Thongnoppakhun
منشور في 2018