5'UTR Repeat Polymorphisms of the BMPR2 gene in Children with Pulmonary Hypertension associated with Congenital Heart Disease

بواسطة Alisa Limsuwan, Lulin Choubtum, Duangrurdee Wattanasirichaigoon
منشور في 2018

Gonadotropin-releasing hormone testing in premature thelarche

بواسطة Lulin Choubtum, Pat Mahachoklertwattana, Arporn Sriphrapradang, Chawalit Preeyasombat
منشور في 2018

The role of prostacyclin (PGI<inf>2</inf>) and thromboxane A<inf>2</inf>(TXA<inf>2</inf>) in pathogenesis of dengue hemorrhagic fever (DHF)

بواسطة Chawalit Preeyasombat, Suporn Treepongkaruna, Arporn Sriphrapradang, Lulin Choubtum
منشور في 2018

Topical 100% serum eye drops for treating corneal epithelial defect after ocular surgery

بواسطة Kaevalin Lekhanont, Passara Jongkhajornpong, Lulin Choubtum, Varintorn Chuckpaiwong
منشور في 2018

Insulin-Like Growth Factor-I (IGF-I) Screening for the Diagnosis of Growth Hormone (GH) Deficiency

بواسطة Arporn Sriphrapradang, Lulin Choubtum, Pat Mahachoklertwattana, Chawalit Preeyasombat
منشور في 2018

Accuracy of glucose meters in measuring low blood glucose levels

بواسطة Lulin Choubtum, Pat Mahachoklertwattana, Umaporn Udomsubpayakul, Chawalit Preeyasombat
منشور في 2018

Erratum: Topical 100% serum eye drops for treating corneal epithelial defect after ocular surgery (BioMed Research International)

بواسطة Kaevalin Lekhanont, Passara Jongkhajornpong, Lulin Choubtum, Varintorn Chuckpaiwong
منشور في 2018

Short-term cyproheptadine therapy in underweight children: Effects on growth and serum insulin-like growth factor-I

بواسطة Pat Mahachoklertwattana, Santhira Wanasuwankul, Preamrudee Poomthavorn, Lulin Choubtum, Arporn Sriphrapradang
منشور في 2018

Novel missense mutations of SAR1B gene in an infant with chylomicron retention disease

بواسطة Suporn Treepongkaruna, Nalinee Chongviriyaphan, Umaporn Suthutvoravut, Dussadee Charoenpipop, Lulin Choubtum, Duangrurdee Wattanasirichaigoon
منشور في 2018

Bone mineral density in children and young adults with β-thalassemia trait

بواسطة Pat Mahachoklertwattana, Ampaiwan Chuansumrit, Lulin Choubtum, Arporn Sriphrapradang, Rojana Sirisriro, Rajata Rajatanavin
منشور في 2018

Thyroid function in healthy thai neonates

بواسطة Pat Mahachoklertwattana, Arporn Sriphrapradang, Sarayut Supapannachart, Aroonwan Pongsuwan, Lulin Choubtum, Rajata Rajatanavin
منشور في 2018

A serum- and feeder-free technique of culturing human corneal epithelial stem cells on amniotic membrane

بواسطة Kaevalin Lekhanont, Lulin Choubtum, Roy S. Chuck, Tarinee Sa-ngiampornpanit, Varintorn Chuckpaiwong, Anun Vongthongsri
منشور في 2018

Association between bone mineral density and erythropoiesis in Thai children and adolescents with thalassemia syndromes

بواسطة Pat Mahachoklertwattana, Pensri Pootrakul, Ampaiwan Chuansumrit, Lulin Choubtum, Arporn Sriphrapradang, Rojana Sirisriro, Rajata Rajatanavin
منشور في 2018

Four novel and three recurrent mutations of the BTK gene and pathogenic effects of putative splice mutations

بواسطة Duangrurdee Wattanasirichaigoon, Suwat Benjaponpitak, Chonnamet Techasaensiri, Wasu Kamchaisatian, Pakit Vichyanond, Sucheela Janwityanujit, Lulin Choubtum, Sayomporn Sirinavin
منشور في 2018

Bone histomorphometry in children and adolescents with β-thalassemia disease: Iron-associated focal osteomalacia

بواسطة Pat Mahachoklertwattana, Vorachai Sirikulchayanonta, Ampaiwan Chuansumrit, Patcharee Karnsombat, Lulin Choubtum, Arporn Sriphrapradang, Somnuek Domrongkitchaiporn, Rojana Sirisriro, Rajata Rajatanavin
منشور في 2018

Glucocerebrosidase mutations in Thai patients with Parkinson's disease

بواسطة Teeratorn Pulkes, Lulin Choubtum, Sermsiri Chitphuk, Ammarin Thakkinstian, Sunsanee Pongpakdee, Kongkiat Kulkantrakorn, Suchat Hanchaiphiboolkul, Somsak Tiamkao, Pairoj Boonkongchuen
منشور في 2018

Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: A Thai multicentre study

بواسطة Lulin Choubtum, Pirada Witoonpanich, Suchat Hanchaiphiboolkul, Roongroj Bhidayasiri, Onanong Jitkritsadakul, Sunsanee Pongpakdee, Suppachok Wetchaphanphesat, Pairoj Boonkongchuen, Teeratorn Pulkes
منشور في 2018

Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study

بواسطة Lulin Choubtum, Pirada Witoonpanich, Suchat Hanchaiphiboolkul, Roongroj Bhidayasiri, Onanong Jitkritsadakul, Sunsanee Pongpakdee, Suppachok Wetchaphanphesat, Pairoj Boonkongchuen, Teeratorn Pulkes
منشور في 2017

Skewed X chromosome inactivation in girls and female adolescents with autoimmune thyroid disease

بواسطة Suttikarn Santiwatana, Pat Mahachoklertwattana, Chanin Limwongse, Patcharin Khlairit, Sarunyu Pongratanakul, Ekkapong Roothumnong, Kanjana Prangphan, Lulin Choubtum, Duantida Songdej, Preamrudee Poomthavorn
منشور في 2019