Wangtiraumnuay N - Search Results

1

Outcomes of pediatric accommodative esotropia with botulinum toxin A treatment in Thailand.

Wangtiraumnuay N, Surukrattanaskul S, Surakiatchanukul T, Masaya-Anon P, Hiriotappa J. Wangtiraumnuay N, et al. Strabismus. 2021 Mar;29(1):26-33. doi: 10.1080/09273972.2020.1871379. Epub 2021 Jan 6. Strabismus. 2021. PMID: 33404269

2

Prevalence of Prescription Glasses in the First-Grade Thai Students (7-8 Years Old).

Wangtiraumnuay N, Trichaiyaporn S, Lueangaram S, Surukrattanaskul S, Wongkittirux K. Wangtiraumnuay N, et al. Clin Optom (Auckl). 2021 Aug 3;13:235-242. doi: 10.2147/OPTO.S323999. eCollection 2021. Clin Optom (Auckl). 2021. PMID: 34377043 Free PMC article.

3

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 result.

Surukrattanaskul S, Keyurapan B, Wangtiraumnuay N. Surukrattanaskul S, et al. Among authors: wangtiraumnuay n. PLoS One. 2022 Jul 20;17(7):e0270362. doi: 10.1371/journal.pone.0270362. eCollection 2022. PLoS One. 2022. PMID: 35857757 Free PMC article.

4

The Global Retinoblastoma Outcome Study: a prospective, cluster-based analysis of 4064 patients from 149 countries.

Global Retinoblastoma Study Group. Global Retinoblastoma Study Group. Lancet Glob Health. 2022 Aug;10(8):e1128-e1140. doi: 10.1016/S2214-109X(22)00250-9. Lancet Glob Health. 2022. PMID: 35839812 Free PMC article.

5

Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations.

Wangtiraumnuay N, Alnabi WA, Tsukikawa M, Thau A, Capasso J, Sharony R, Inglehearn CF, Levin AV. Wangtiraumnuay N, et al. Ophthalmic Genet. 2018 Jun;39(3):384-390. doi: 10.1080/13816810.2018.1432063. Ophthalmic Genet. 2018. PMID: 29676688

6

Ophthalmic manifestations associated with RARB mutations.

Wangtiraumnuay N, Kopinsky S, Iyer P, Capasso J, Whitehead R, Schneider A, Levin AV. Wangtiraumnuay N, et al. Clin Dysmorphol. 2019 Jan;28(1):46-49. doi: 10.1097/MCD.0000000000000246. Clin Dysmorphol. 2019. PMID: 30281527 No abstract available.

7

Cryptophthalmos, dental anomalies, oral vestibule defect, and a novel FREM2 mutation.

Kantaputra PN, Wangtiraumnuay N, Ngamphiw C, Olsen B, Intachai W, Tucker AS, Tongsima S. Kantaputra PN, et al. Among authors: wangtiraumnuay n. J Hum Genet. 2022 Feb;67(2):115-118. doi: 10.1038/s10038-021-00972-4. Epub 2021 Aug 19. J Hum Genet. 2022. PMID: 34408272

8

Optical Coherence Tomography in Knobloch Syndrome.

Thau A, Tsukikawa M, Wangtiraumnuay N, Capasso J, Affel E, Alnabi WA, Adam M, Alsulaiman SM, Spirn M, Levin AV. Thau A, et al. Among authors: wangtiraumnuay n. Ophthalmic Surg Lasers Imaging Retina. 2019 Aug 1;50(8):e203-e210. doi: 10.3928/23258160-20190806-13. Ophthalmic Surg Lasers Imaging Retina. 2019. PMID: 31415705

9

Novel ABCA4 mutation leads to loss of a conserved C-terminal motif: implications for predicting pathogenicity based on genetic testing.

Wangtiraumnuay N, Capasso J, Tsukikawa M, Levin A, Biswas-Fiss E. Wangtiraumnuay N, et al. Eur J Ophthalmol. 2018 Jan;28(1):123-126. doi: 10.5301/ejo.5001019. Epub 2018 Feb 19. Eur J Ophthalmol. 2018. PMID: 28885670 Free article.

10

Evaluation of a Free Public Smartphone Application to Detect Leukocoria in High-Risk Children Aged 1 to 6 Years.

Vagge A, Wangtiraumnuay N, Pellegrini M, Scotto R, Iester M, Traverso CE. Vagge A, et al. Among authors: wangtiraumnuay n. J Pediatr Ophthalmol Strabismus. 2019 Jul 1;56(4):229-232. doi: 10.3928/01913913-20190516-01. J Pediatr Ophthalmol Strabismus. 2019. PMID: 31322712

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