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Plos One|July 20, 2022
Correlation between clinical presentations, radiological findings and high risk histopathological features of primary enucleated eyes with advanced retinoblastoma at Queen Sirikit National Institute of Child Health: 5 years resultSupawan Surukrattanaskul, Bungornrat Keyurapan, Nutsuchar Wangtiraumnuay
Case Reports in Oncology|May 1, 2023
Digital Gangrene and Antiphospholipid Syndrome in a Retinoblastoma Patient with Chromosome 13q Deletion: A Case ReportNutsuchar Wangtiraumnuay, Supawan Surakrattanaskul, Chonthida Wangkittikul
Idcases|September 22, 2023
Periocular ecthyma gangrenosum with <i>Pseudomonas septicemia</i> in an infant: A case reportSupawan Surukrattanaskul, Rosana Pittayapongpat, Nutsuchar Wangtiraumnuay
Clinical Optometry|August 11, 2021
Prevalence of Prescription Glasses in the First-Grade Thai Students (7-8 Years Old)Nutsuchar Wangtiraumnuay, Sumalin Trichaiyaporn, Sirin Lueangaram, et al.
European Journal of Ophthalmology|September 9, 2017
Novel ABCA4 mutation leads to loss of a conserved C-terminal motif: implications for predicting pathogenicity based on genetic testingNutsuchar Wangtiraumnuay, Jenina Capasso, Mai Tsukikawa, et al.
Strabismus|January 6, 2021
Outcomes of pediatric accommodative esotropia with botulinum toxin A treatment in ThailandNutsuchar Wangtiraumnuay, Supawan Surukrattanaskul, Thamolwan Surakiatchanukul, et al.
Journal of Pediatric Ophthalmology and Strabismus|July 20, 2019
Evaluation of a Free Public Smartphone Application to Detect Leukocoria in High-Risk Children Aged 1 to 6 YearsAldo Vagge, Nutsuchar Wangtiraumnuay, Marco Pellegrini, et al.
Journal of Human Genetics|August 19, 2021
Cryptophthalmos, dental anomalies, oral vestibule defect, and a novel FREM2 mutationPiranit Nik Kantaputra, Nutsuchar Wangtiraumnuay, Chumpol Ngamphiw, et al.
Ophthalmic Genetics|April 21, 2018
Ophthalmic manifestations of Heimler syndrome due to PEX6 mutationsNutsuchar Wangtiraumnuay, Waleed Abed Alnabi, Mai Tsukikawa, et al.
Molecular Vision|January 15, 2024
Protein modeling and in silico analysis to assess pathogenicity of <i>ABCA4</i> variants in patients with inherited retinal diseaseSenem Cevik, Nutsuchar Wangtiraumnuay, Kristof Van Schelvergem, et al.
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