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Clinical Biochemistry|July 19, 2011
Combination of multiplex PCR and DHPLC-based strategy for CYP2D6 genotyping scheme in ThaisPayiarat Suwannasri, Wanna Thongnoppakhun, Pornpen Pramyothin, et al.
Pharmacogenomics and Personalized Medicine|October 1, 2019
Influence of <i>CYP2D6, CYP3A5, ABCB1, APOE</i> polymorphisms and nongenetic factors on donepezil treatment in patients with Alzheimer's disease and vascular dementiaThitipon Yaowaluk, Vorapun Senanarong, Chanin Limwongse, et al.
World Journal of Gastroenterology|March 24, 2005
A Thai family with hereditary pancreatitis and increased cancer risk due to a mutation in PRSS1 geneTheeraphong Pho-Iam, Wanna Thongnoppakhun, Pa-Thai Yenchitsomanus, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|August 11, 2020
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) in a Thai Patient: The Classic Clinical Manifestations, Funduscopic Feature, and Brain Imaging Findings with a Novel Mutation in the <i>SACS</i> GeneJindapa Srikajon, Yuvadee Pitakpatapee, Chanin Limwongse, et al.
American Journal of Medical Genetics. Part A|September 27, 2006
A newly recognized polyosteolysis/hyperostosis syndromePiranit N Kantaputra, Chanin Limwongse, Ajchara Koolvisoot, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutationPiranit Nik Kantaputra, Ans van den Ouweland, Tumtip Sangruchi, et al.
Neuromuscular Disorders : NMD|September 23, 2020
Genotype and age at diagnosis in Thai boys with Duchenne muscular dystrophy (DMD)Pattareeya Yamputchong, Theeraphong Pho-Iam, Chanin Limwongse, et al.
Eneurologicalsci|August 17, 2019
Case series: Childhood Charcot-Marie-Tooth: Predominance of axonal subtypeApirada Thongsing, Theeraphong Pho-Iam, Chanin Limwongse, et al.
Haematologica|April 22, 2006
Mutations of AML1 in non-M0 acute myeloid leukemia: six novel mutations and a high incidence of cooperative events in a South-east Asian populationChirayu U Auewarakul, Amporn Leecharendkeat, Wanna Thongnoppakhun, et al.
Neuropediatrics|October 21, 2021
Sleep Disorder: An Overlooked Manifestation of Glucose Transporter Type-1 Deficiency SyndromeKingthong Anurat, Chaiyos Khongkhatithum, Thipwimol Tim-Aroon, et al.
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