Kononets V, Zharmakhanova G, Balmagambetova S, Syrlybayeva L, Berdesheva G, Zhussupova Z
Front Pediatr. 2025; 13:1463294.
PMID: 40051910
PMC: 11882580.
DOI: 10.3389/fped.2025.1463294.
Nguyen K, Dien T, Can T, Thao B, Do T, Dang T
Int J Mol Sci. 2025; 26(4).
PMID: 40004108
PMC: 11855759.
DOI: 10.3390/ijms26041644.
Kido J, Makris G, Santra S, Haberle J
J Inherit Metab Dis. 2024; 47(6):1144-1156.
PMID: 38503330
PMC: 11586594.
DOI: 10.1002/jimd.12722.
Gupta N, Endrakanti M, Bhat M, Rao N, Kaur R, Kabra M
Indian J Pediatr. 2023; 91(7):675-681.
PMID: 37420116
DOI: 10.1007/s12098-023-04651-4.
Men S, Liu S, Zheng Q, Yang S, Mao H, Wang Z
Mol Genet Genomic Med. 2023; 11(6):e2152.
PMID: 36787440
PMC: 10265071.
DOI: 10.1002/mgg3.2152.
Establishment and Validation of Reference Values for Amino Acids and Acylcarnitines in Dried Blood Spots for Omani Newborns Using Tandem Mass Spectrometry.
Al-Riyami S, Al-Manei M, Al-Fahdi A, Al-Thihli K
Oman Med J. 2022; 37(5):e426.
PMID: 36188883
PMC: 9464332.
DOI: 10.5001/omj.2022.88.
Dandy-Walker malformation in methylmalonic acidemia: a rare case report.
Liu J, Liu Z, Yan H, Li Y
BMC Pediatr. 2021; 21(1):398.
PMID: 34511063
PMC: 8436548.
DOI: 10.1186/s12887-021-02874-y.
Effects of Reducing L-Carnitine Supplementation on Carnitine Kinetics and Cardiac Function in Hemodialysis Patients: A Multicenter, Single-Blind, Placebo-Controlled, Randomized Clinical Trial.
Sugiyama M, Hazama T, Nakano K, Urae K, Moriyama T, Ariyoshi T
Nutrients. 2021; 13(6).
PMID: 34073024
PMC: 8230272.
DOI: 10.3390/nu13061900.
Early Detection and Diagnosis of Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency Missed by Newborn Screening Using Tandem Mass Spectrometry.
Shigetomi H, Tanaka T, Nagao M, Tsutsumi H
Int J Neonatal Screen. 2020; 4(1):5.
PMID: 33072931
PMC: 7548893.
DOI: 10.3390/ijns4010005.
Anesthetic management of a patient with methylmalonic acidemia: a case report.
Uemura Y, Kakuta N, Tanaka K, Tsutsumi Y
JA Clin Rep. 2020; 4(1):71.
PMID: 32025901
PMC: 6966740.
DOI: 10.1186/s40981-018-0209-7.
A 7-Year Report of Spectrum of Inborn Errors of Metabolism on Full-Term and Premature Infants in a Chinese Neonatal Intensive Care Unit.
Zhang W, Yang Y, Peng W, Chang J, Mei Y, Yan L
Front Genet. 2020; 10:1302.
PMID: 31998365
PMC: 6967400.
DOI: 10.3389/fgene.2019.01302.
Genetic Analysis of Peroxisomal Genes Required for Longevity in a Yeast Model of Citrin Deficiency.
Chalermwat C, Thosapornvichai T, Jensen L, Wattanasirichaigoon D
Diseases. 2020; 8(1).
PMID: 31936501
PMC: 7151034.
DOI: 10.3390/diseases8010002.
Expanded newborn screening for inborn errors of metabolism by tandem mass spectrometry in newborns from Xinxiang city in China.
Ma S, Guo Q, Zhang Z, He Z, Yue A, Song Z
J Clin Lab Anal. 2020; 34(5):e23159.
PMID: 31916308
PMC: 7246475.
DOI: 10.1002/jcla.23159.
Serum C14:1/C12:1 ratio is a useful marker for differentiating affected patients with very long-chain acyl-CoA dehydrogenase deficiency from heterozygous carriers.
Yamada K, Osawa Y, Kobayashi H, Hasegawa Y, Fukuda S, Yamaguchi S
Mol Genet Metab Rep. 2019; 21:100535.
PMID: 31844625
PMC: 6895747.
DOI: 10.1016/j.ymgmr.2019.100535.
Expanded Newborn Screening for Inborn Errors of Metabolism by Tandem Mass Spectrometry in Suzhou, China: Disease Spectrum, Prevalence, Genetic Characteristics in a Chinese Population.
Wang T, Ma J, Zhang Q, Gao A, Wang Q, Li H
Front Genet. 2019; 10:1052.
PMID: 31737040
PMC: 6828960.
DOI: 10.3389/fgene.2019.01052.
A Japanese case of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency who presented with severe metabolic acidosis and fatty liver without hypoglycemia.
Lee T, Takami Y, Yamada K, Kobayashi H, Hasegawa Y, Sasai H
JIMD Rep. 2019; 48(1):19-25.
PMID: 31392109
PMC: 6606983.
DOI: 10.1002/jmd2.12051.
Systematic literature review and meta-analysis on the epidemiology of methylmalonic acidemia (MMA) with a focus on MMA caused by methylmalonyl-CoA mutase (mut) deficiency.
Almasi T, Guey L, Lukacs C, Csetneki K, Voko Z, Zelei T
Orphanet J Rare Dis. 2019; 14(1):84.
PMID: 31023387
PMC: 6485056.
DOI: 10.1186/s13023-019-1063-z.
Systematic literature review and meta-analysis on the epidemiology of propionic acidemia.
Almasi T, Guey L, Lukacs C, Csetneki K, Voko Z, Zelei T
Orphanet J Rare Dis. 2019; 14(1):40.
PMID: 30760309
PMC: 6375193.
DOI: 10.1186/s13023-018-0987-z.
Age-Specific Cut-off Values of Amino Acids and Acylcarnitines for Diagnosis of Inborn Errors of Metabolism Using Liquid Chromatography Tandem Mass Spectrometry.
Sarker S, Islam M, Biswas A, Sarower Bhuyan G, Sultana R, Sultana N
Biomed Res Int. 2019; 2019:3460902.
PMID: 30723736
PMC: 6339774.
DOI: 10.1155/2019/3460902.
[Medium-chain acyl-CoA dehydrogenase deficiency: neonatal screening and follow-uP].
Tong F, Jiang P, Yang R, Huang X, Zhou X, Hong F
Zhongguo Dang Dai Er Ke Za Zhi. 2019; 21(1):52-57.
PMID: 30675864
PMC: 7390178.