Publications by authors named "Tim Phetthong"

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Disseminated Histoplasmosis and Campylobacter jejuni Bacteremia Coinfection Revealing Autosomal Dominant NFKB1 Deficiency-Related Common Variable Immunodeficiency.
Shodok Promsanjan, Chawisa Panaphorn, Tim Phetthong, Dhitiwat Changpradub, Panitan Pradubpongsa

Med Mycol J· November 2025

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A rare cause of echogenic kidneys with oligohydramnios in the fetus: report of two different cases.
Tim Phetthong, Krit Achaloetvaranon, Sanpon Diawtipsukon

BMC Pregnancy Childbirth· October 2024

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A novel AP1S2 variant causing leaky splicing in X-linked intellectual disability: Further delineation and intrafamilial variability.
Saisuda Noojarern, Thipwimol Tim-Aroon, Kingthong Anurat, Tim Phetthong, Arthaporn Khongkraparn

Am J Med Genet A· September 2024

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Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients.
Tim Phetthong, Thipwimol Tim-Aroon, Arthaporn Khongkraparn, Saisuda Noojarern, Chulaluck Kuptanon

Orphanet J Rare Dis· December 2021

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Compound Heterozygote of Point Mutation and Chromosomal Microdeletion Involving Coinciding with Variant in Syndromic Intellectual Disability.
Tim Phetthong, Arthaporn Khongkrapan, Natini Jinawath, Go-Hun Seo, Duangrurdee Wattanasirichaigoon

Genes (Basel)· October 2021

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Genotype-Phenotype Correlation of G6PD Mutations among Central Thai Children with G6PD Deficiency.
Boonchai Boonyawat, Tim Phetthong, Nithipun Suksumek, Chanchai Traivaree

Anemia· February 2021

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Kabuki syndrome with midgut malrotation and hyperinsulinemic hypoglycemia: A rare co-occurrence from Thailand.
Tim Phetthong, Thipwimol Tim-Aroon, Arthaporn Khongkrapan, Preamrudee Poomthavorn, Duangrurdee Wattanasirichaigoon

Am J Med Genet A· August 2020

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