1. A 3-Year-Old Girl with Acute Liver Failure and Status Epilepticus. (3rd November 2022) Authors: Wongkittichote, Parith; Dietzen, Dennis J; Grange, Dorothy K; Roper, Stephen M Journal: Clinical chemistry Issue: Volume 68:Number 11(2022) Page Start: 1471 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. DDOST‐CDG: Clinical and molecular characterization of a third patient with a milder and a predominantly movement disorder phenotype. Issue 1 (17th October 2022) Authors: Elsharkawi, Ibrahim; Wongkittichote, Parith; Daniel, Earnest James Paul; Starosta, Rodrigo Tzovenos; Ueda, Keisuke; Ng, Bobby G.; Freeze, Hudson H.; He, Miao; Shinawi, Marwan Journal: Journal of inherited metabolic disease Issue: Volume 46:Issue 1(2023) Page Start: 92 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Expanding allelic and phenotypic spectrum of ZC4H2‐related disorder: A novel hypomorphic variant and high prevalence of tethered cord. Issue 2 (31st October 2022) Authors: Wongkittichote, Parith; Choi, Tae‐Ik; Kim, Oc‐Hee; Riley, Kacie; Koeberl, Dwight; Narayanan, Vinodh; Ramsey, Keri; Balak, Chris; Schwartz, Charles E.; Cueto‐Gonzalez, Anna Maria; Casadesus, Francina Munell; Kim, Cheol‐Hee; Shinawi, Marwan S. Journal: Clinical genetics Issue: Volume 103:Issue 2(2023) Page Start: 167 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Fatal COVID‐19 infection in a patient with long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: A case report. Issue 1 (10th September 2020) Authors: Wongkittichote, Parith; Watson, James R.; Leonard, Jennifer M.; Toolan, Elizabeth R.; Dickson, Patricia I.; Grange, Dorothy K. Journal: JIMD reports Issue: Volume 56:Issue 1(2020) Page Start: 40 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Overexpression of the peroxin Pex34p suppresses impaired acetate utilization in yeast lacking the mitochondrial aspartate/glutamate carrier Agc1p. Issue 8 (11th November 2019) Authors: Chalermwat, Chalongchai; Thosapornvichai, Thitipa; Wongkittichote, Parith; Phillips, John D; Cox, James E; Jensen, Amornrat N; Wattanasirichaigoon, Duangrurdee; Jensen, Laran T Journal: FEMS yeast research Issue: Volume 19:Issue 8(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Pathogenic variant in NFIA associated with subdural hematomas mimicking nonaccidental trauma. Issue 5 (10th January 2022) Authors: Wongkittichote, Parith; Kondis, Jamie S.; Peglar, Lindsay M.; Strahle, Jennifer M.; Miller‐Thomas, Michelle; Abell, Katherine B. Journal: American journal of medical genetics Issue: Volume 188:Issue 5(2022) Page Start: 1538 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Prediction of the functional effect of novel SLC25A13 variants using a S. cerevisiae model of AGC2 deficiency. Issue 5 (3rd October 2012) Authors: Wongkittichote, Parith; Tungpradabkul, Sumalee; Wattanasirichaigoon, Duangrurdee; Jensen, Laran T. Journal: Journal of inherited metabolic disease Issue: Volume 36:Issue 5(2013) Page Start: 821 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Thymine Hyperexcretion in a Patient with Abnormal Newborn Screen for Glutaric Aciduria Type I. (24th January 2023) Authors: Wongkittichote, Parith; Edmondson, Andrew; Hong, Xinying Journal: Clinical chemistry Issue: Volume 69:Number 4(2023) Page Start: 431 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗