การวินิจฉัยและการรักษากลุ่มอาการมาร์แฟน

by โอบจุฬ ตราชู, Objoon Trachoo
Published 2022

โรคหัวใจที่ถ่ายทอดทางพันธุกรรม

by โอบจุฬ ตราชู, Objoon Trachoo
Published 2022

Chromosome 20p inverted duplication deletion identified in a Thai female adult with mental retardation, obesity, chronic kidney disease and characteristic facial features

by Objoon Trachoo, Montira Assanatham, Natini Jinawath, Arkom Nongnuch
Published 2018

Impact of slc47a1 (Rs2289669 g>a) variant on metformin associated lactic acidosis patients

by Pechngam Chaivanit, Somchai Yongsiri, Pakaphan Dinchuthai, Objoon Trachoo
Published 2019

Building Up a Standrad Physical Measurement Database in Healthy Medical Students and Postgraduate Medical Trainees: A Tool for Clinical Evaluation of Adult Dysmorphology

by Pat Tanprom, Objoon Trachoo, ภัทร์ ตันพรหม, โอบจุฬ ตราชู
Published 2022

Hypertrophic Cardiomyopathy: From Genes to Bedside

by Objoon Trachoo, Tarinee Tangcharoen, โอบจุฬ ตราชู, ธารินี ตั้งเจริญ
Published 2022

A novel mutation in thyroid peroxidase gene causing congenital goitrous hypothyroidism in a German-Thai patient

by Chutintorn Sriphrapradang, Yotsapon Thewjitcharoen, Suwannee Chanprasertyothin, Soontaree Nakasatien, Thep Himathongkam, Objoon Trachoo
Published 2018

Haemoglobin Hope in a northern Thai family: First identification of homozygous haemoglobin Hope associated with haemoglobin H disease

by Thanyachai Sura, Manisa Busabaratana, Supak Youngcharoen, Raewadee Wisedpanichkij, Vip Viprakasit, Objoon Trachoo
Published 2018

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

by Tulyapruek Tawonsawatruk, Theeraroj Changthong, Sarinee Pingsuthiwong, Objoon Trachoo, Thanyachai Sura, Wiwat Wajanavisit
Published 2018

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

by Tulyapruek Tawonsawatruk, Theeraroj Changthong, Sarinee Pingsuthiwong, Objoon Trachoo, Thanyachai Sura, Wiwat Wajanavisit
Published 2017

Noonan syndrome, metabolic syndrome and stroke-in-the-young: Coincidence, causal or contribution?

by Jakris Eu-Ahsunthornwattana, Objoon Trachoo, Donniphat Dejsuphong, Atchara Tunteeratum, Kanoknan Srichan, Thanyachai Sura
Published 2018

Novel PANK2 mutation discovered among South East Asian children living in Thailand affected with pantothenate kinase associated neurodegeneration

by Kullasate Sakpichaisakul, Vitchayaporn E. Saengow, Papit Suwanpratheep, Kanokpan Rongnoparat, Bhakbhoom Panthan, Objoon Trachoo
Published 2020

Fine-needle aspiration cytology of parathyroid carcinoma mimic Hürthle cell thyroid neoplasm

by Chutintorn Sriphrapradang, Pattana Sornmayura, Niramol Chanplakorn, Objoon Trachoo, Pattarana Sae-Chew, Rangsima Aroonroch
Published 2018

Amelioration of osteogenesis in iPSC-derived mesenchymal stem cells from osteogenesis imperfecta patients by endoplasmic reticulum stress inhibitor

by Thitinat Duangchan, Tulyapruek Tawonsawatruk, Chanika Angsanuntsukh, Objoon Trachoo, Suradej Hongeng, Narisorn Kitiyanant, Aungkura Supokawej
Published 2022

Association of estrogen receptor-alpha single-nucleotide polymorphism (codon 594 G-->A) and Thai patients affected by knee osteoarthritis.

by Tulyapruek Tawonsawatruk, Objoon Trachoo, Thanaphot Channoom, Thanyachai Sura, Jakris Eu-ahsunthornwattana, Patarawan Woratanarat, Wiwat Wajanavisit
Published 2018

First successful trial of preimplantation genetic diagnosis for pantothenate kinase-associated neurodegeneration

by Objoon Trachoo, Chonthicha Satirapod, Bhakbhoom Panthan, Matchuporn Sukprasert, Angkana Charoenyingwattana, Wasun Chantratita, Wicharn Choktanasiri, Suradej Hongeng
Published 2018

Screening of Fabry disease in patients with end-stage renal disease of unknown etiology: The first Thailand study

by Objoon Trachoo, Paisan Jittorntam, Sarunpong Pibalyart, Saowanee Kajanachumphol, Norasak Suvachittanont, Suthep Patputthipong, Piyatida Chuengsaman, Arkom Nongnuch
Published 2018

Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: Longitudinal clinical course, molecular characterization, and developmen...

by Thanyachai Sura, Objoon Trachoo, Vip Viprakasit, Prin Vathesatogkit, Atchara Tunteeratum, Manisa Busabaratana, Raewadee Wisedpanichkij, Parttraporn Isarangkura
Published 2018

Etiologies of Dilated Cardiomyopathy in Patients Manifested With Congestive Heart Failure in Ramathibodi Hospital

by Sasima Srisukh, Objoon Trachoo, Tarinee Tangcharoen, ศศิมา ศรีศุข, โอบจุฬ ตราชู, ธารินี ตั้งเจริญ
Published 2022

Molecular characterization of hereditary persistence of fetal hemoglobin in the Karen People of Thailand

by Objoon Trachoo, Thanyachai Sura, Anavaj Sakuntabhai, Pratap Singhasivanon, Srivicha Krudsood, Waraphon Phimpraphi, Somporn Krasaesub, Suporn Chanjarunee, Sornchai Looareesuwan
Published 2018