Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Lulin Choubtum"'
Autor:
Lulin Choubtum1,2, Pirada Witoonpanich1, Suchat Hanchaiphiboolkul3, Roongroj Bhidayasiri4, Onanong Jitkritsadakul4, Sunsanee Pongpakdee5, Suppachok Wetchaphanphesat6, Pairoj Boonkongchuen1, Teeratorn Pulkes1 teeratorn.pul@mahidol.ac.th
Publikováno v:
BMC Neurology. 12/1/2015, Vol. 15 Issue 1, p1-6. 6p. 1 Chart, 1 Graph.
Autor:
Sunsanee Pongpakdee, Pirada Witoonpanich, Lulin Choubtum, Suchat Hanchaiphiboolkul, Teeratorn Pulkes, Kongkiat Kulkantrakorn, Somsak Tiamkao
Publikováno v:
Parkinsonism & Related Disorders. 28:146-149
Introduction Spinocerebellar ataxia type 17 (SCA17) is an inherited cerebellar degeneration associated with trinucleotide repeat expansions in the TATA-binding protein gene (TBP). Low-range expansions of TBP have recently been described in associatio
Autor:
Kawinthra Khwanraj, Lulin Choubtum, Aruchalean Taweewongsounton, Somsak Tanrattanakorn, Teeratorn Pulkes, Permphan Dharmasaroja
Publikováno v:
Journal of Neurology Research. 6:12-17
Autor:
Preamrudee Poomthavorn, Kanjana Prangphan, Duantida Songdej, Lulin Choubtum, Patcharin Khlairit, Pat Mahachoklertwattana, Suttikarn Santiwatana, Ekkapong Roothumnong, Chanin Limwongse, Sarunyu Pongratanakul
Publikováno v:
Clinical endocrinology. 89(6)
Objective Skewed X chromosome inactivation (XCI) was associated with female predominance in adult autoimmune thyroid disease (ATD). In normal females, skewed XCI is increased with age. Whether early-onset skewed XCI is associated with childhood ATD r
Autor:
Sermsiri Chitphuk, Ammarin Thakkinstian, Suchat Hanchaiphiboolkul, Teeratorn Pulkes, Pairoj Boonkongchuen, Kongkiat Kulkantrakorn, Somsak Tiamkao, Sunsanee Pongpakdee, Lulin Choubtum
Publikováno v:
Parkinsonism & Related Disorders. 20:986-991
GBA mutations are an important risk factor in developing Parkinson's disease (PD) worldwide. The study aimed to determine the frequency and clinical characteristics of GBA mutations in a Thai PD cohort of 480 patients and 395 control subjects.Direct
Publikováno v:
Heart, Lung and Circulation. 22:204-210
The mutations of bone morphogenetic protein receptor type 2 ( BMPR2 ) in patients with idiopathic pulmonary hypertension has been well defined. We investigated the occurrence of BMPR2 mutation and genetic polymorphisms in children with pulmonary hype
Publikováno v:
BioMed Research International, Vol 2013 (2013)
BioMed Research International
BioMed Research International
The purpose of this study was to investigate the efficacy and safety of topical 100% serum eye drops for corneal epithelial defect after ocular surgery. A total of 181 patients who received topical 100% serum therapy for the treatment of corneal epit
Autor:
Lulin Choubtum, Pirada Witoonpanich, Suchat Hanchaiphiboolkul, Roongroj Bhidayasiri, Onanong Jitkritsadakul, Sunsanee Pongpakdee, Suppachok Wetchaphanphesat, Pairoj Boonkongchuen, Teeratorn Pulkes
Primer sets and annealing temperatures for KCND3 sequencing. (DOCX 17 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::112763190792f61ec2649799320d2ce6
Autor:
Pat Mahachoklertwattana, Arporn Sriphrapradang, Rajata Rajatanavin, Rojana Sirisriro, Ampaiwan Chuansumrit, Lulin Choubtum
Publikováno v:
Clinical Endocrinology. 58:273-279
Summary objective Thalassaemia/haemoglobinopathy is a hereditary disease causing increased erythropoiesis and expansion of the bone marrow cavity. As a consequence, there is a reduction in trabecular bone tissue resulting in osteopenia/osteoporosis.
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2014 (2014)
BioMed Research International, Vol 2014 (2014)
The authors would like to make the following changes. (1) In the original Table 1, operations part, there were some erroneous calculations of the percentage of each operation. They are corrected as shown in the current version of Table 1. (2) In the