Parith Wongkittichote

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 13

Top Topics

Tandem Mass Spectrometry

Ultra High Performance Liquid Chromatography

Acute Kidney Injury

Top Venues

Clinical chemistry

Journal of inherited metabolic disease

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Parith Wongkittichote, Cassandra Pantano, Miao He, Xinying Hong, Matthew M Demczko
Clinical, biochemical and molecular characterization of a new case with FDX2 -related mitochondrial disorder: Potential biomarkers and treatment options. JIMD reports 65 (2) (2024)
Parith Wongkittichote, Se Hyun Cho, Artis Miller, Kaitlyn King, Zackary M Herbst, Zhimei Ren, Michael H Gelb, Xinying Hong
Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry Analysis of Urinary Oligosaccharides and Glycoamino Acids for the Diagnosis of Mucopolysaccharidosis and Glycoproteinosis. Clinical chemistry (2024)
Parith Wongkittichote, Se Hyun Cho, Artis Miller, Kaitlyn King, Zackary M Herbst, Zhimei Ren, Michael H Gelb, Xinying Hong
Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry Analysis of Urinary Oligosaccharides and Glycoamino Acids for the Diagnosis of Mucopolysaccharidosis and Glycoproteinosis. Clinical chemistry 70 (6) (2024)
Parith Wongkittichote, Cassandra Pantano, Miao He, Xinying Hong, Matthew M Demczko
Clinical, biochemical and molecular characterization of a new case with FDX2 -related mitochondrial disorder: Potential biomarkers and treatment options. JIMD reports 65 (2) (2024)
Parith Wongkittichote, Sanmati R Cuddapah, Stephen R Master, Dorothy K Grange, Dennis Dietzen, Stephen M Roper, Rebecca D Ganetzky
Biochemical characterization of patients with dihydrolipoamide dehydrogenase deficiency. JIMD reports 64 (5) (2023)
Parith Wongkittichote, Edward B Cook, Francis Jeshira Reynoso Santos, Rebecca C Ahrens-Nicklas, Xinying Hong, Rebecca D Ganetzky
Low Arginine Suggesting the Diagnosis of Mitochondrial Cardiomyopathy. The journal of applied laboratory medicine (2023)
Parith Wongkittichote, Andrew Edmondson, Xinying Hong
Thymine Hyperexcretion in a Patient with Abnormal Newborn Screen for Glutaric Aciduria Type I. Clinical chemistry 69 (4) (2023)
Parith Wongkittichote, Rebecca D Ganetzky, Matthew M Demczko, Xinying Hong, Miao He, Stephen R Master
Low Plasma Citrulline Guiding the Diagnosis of a Mitochondrial Disorder. Clinical chemistry 69 (6) (2023)
Suneeta Madan-Khetarpal, Maio He, Parith Wongkittichote, Steven F Dobrowolski
Congenital Disorder of Glycosylation in a Child with Macrosomia. Clinical chemistry 69 (12) (2023)
Parith Wongkittichote, Jamie S Kondis, Lindsay M Peglar, Jennifer M Strahle, Michelle Miller-Thomas, Katherine B Abell
Pathogenic variant in NFIA associated with subdural hematomas mimicking nonaccidental trauma. American journal of medical genetics. Part A 188 (5) (2022)
Ibrahim Elsharkawi, Parith Wongkittichote, Earnest James Paul Daniel, Rodrigo Tzovenos Starosta, Keisuke Ueda, Bobby G Ng, Hudson H Freeze, Miao He, Marwan S Shinawi
DDOST-CDG: Clinical and molecular characterization of a third patient with a milder and a predominantly movement disorder phenotype. Journal of inherited metabolic disease (2022)
Parith Wongkittichote, Daniel J Wegner, Marwan S Shinawi
Novel exon-skipping variant disrupting the basic domain of HCFC1 causes intellectual disability without metabolic abnormalities in both male and female patients. Journal of human genetics 66 (7) (2021)
Parith Wongkittichote, James R Watson, Jennifer M Leonard, Elizabeth R Toolan, Patricia I Dickson, Dorothy K Grange
Fatal COVID-19 infection in a patient with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: A case report. JIMD reports 56 (1) (2020)