These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
121 related articles for article (PubMed ID: 37702680)
1. Association Analysis of Gene Sequencing by NeoSeq Combined with Tandem Mass Spectrum and Four Neonatal Diseases. Xue S; Zhu J; Zhang H; Han L; Yang R; Dai P; Ding G Clin Lab; 2023 Sep; 69(9):. PubMed ID: 37702680 [TBL] [Abstract][Full Text] [Related]
2. A comprehensive multiplex PCR based exome-sequencing assay for rapid bloodspot confirmation of inborn errors of metabolism. Wang W; Yang J; Xue J; Mu W; Zhang X; Wu W; Xu M; Gong Y; Liu Y; Zhang Y; Xie X; Gu W; Bai J; Cram DS BMC Med Genet; 2019 Jan; 20(1):3. PubMed ID: 30612563 [TBL] [Abstract][Full Text] [Related]
3. NeoSeq: a new method of genomic sequencing for newborn screening. Wang H; Yang Y; Zhou L; Wang Y; Long W; Yu B Orphanet J Rare Dis; 2021 Nov; 16(1):481. PubMed ID: 34794485 [TBL] [Abstract][Full Text] [Related]
4. Abnormal biochemical indicators of neonatal inherited metabolic disease in carriers. Guo F; Zhou L; Zhang F; Yu B; Yang Y; Liu Z Orphanet J Rare Dis; 2024 Apr; 19(1):145. PubMed ID: 38575986 [TBL] [Abstract][Full Text] [Related]
5. An Economic Evaluation of Neonatal Screening for Inborn Errors of Metabolism Using Tandem Mass Spectrometry in Thailand. Thiboonboon K; Leelahavarong P; Wattanasirichaigoon D; Vatanavicharn N; Wasant P; Shotelersuk V; Pangkanon S; Kuptanon C; Chaisomchit S; Teerawattananon Y PLoS One; 2015; 10(8):e0134782. PubMed ID: 26258410 [TBL] [Abstract][Full Text] [Related]
6. Incidence and genetic variants of inborn errors of metabolism identified through newborn screening: A 7-year study in eastern coastal areas of China. Men S; Liu S; Zheng Q; Yang S; Mao H; Wang Z; Gu Y; Tang X; Wang L Mol Genet Genomic Med; 2023 Jun; 11(6):e2152. PubMed ID: 36787440 [TBL] [Abstract][Full Text] [Related]
7. Incidence of newborn screening disorders among 56632 infants in Central Saudi Arabia. A 6-year study. Mohamed S; Elsheikh W; Al-Aqeel AI; Alhashem AM; Alodaib A; Alahaideb L; Almashary M; Alharbi F; AlMalawi H; Ammari A; Almohaimeed S Saudi Med J; 2020 Jul; 41(7):703-708. PubMed ID: 32601637 [TBL] [Abstract][Full Text] [Related]
8. Spectrum analysis of inborn errors of metabolism for expanded newborn screening in a northwestern Chinese population. Zhang R; Qiang R; Song C; Ma X; Zhang Y; Li F; Wang R; Yu W; Feng M; Yang L; Wang X; Cai N Sci Rep; 2021 Jan; 11(1):2699. PubMed ID: 33514801 [TBL] [Abstract][Full Text] [Related]
9. Prevalence and mutation analysis of short/branched chain acyl-CoA dehydrogenase deficiency (SBCADD) detected on newborn screening in Wisconsin. Van Calcar SC; Baker MW; Williams P; Jones SA; Xiong B; Thao MC; Lee S; Yang MK; Rice GM; Rhead W; Vockley J; Hoffman G; Durkin MS Mol Genet Metab; 2013; 110(1-2):111-5. PubMed ID: 23712021 [TBL] [Abstract][Full Text] [Related]
10. Newborn screening for inborn errors of metabolism in a northern Chinese population. Liu G; Liu X; Lin Y J Pediatr Endocrinol Metab; 2023 Mar; 36(3):278-282. PubMed ID: 36662638 [TBL] [Abstract][Full Text] [Related]
11. [Newborn screening in France: news and perspectives]. Gernez E; Roland E; Dhaenens CM; Renom G; Mention K Ann Biol Clin (Paris); 2024 Apr; 82(1):24-31. PubMed ID: 38638016 [TBL] [Abstract][Full Text] [Related]
12. [Screening of newborns for inborn errors of metabolism by tandem mass spectrometry]. Simonsen H Ugeskr Laeger; 2002 Nov; 164(48):5607-12. PubMed ID: 12523003 [TBL] [Abstract][Full Text] [Related]
13. Inborn errors of metabolism detectable by tandem mass spectrometry in Beijing. Yang N; Gong LF; Zhao JQ; Yang HH; Ma ZJ; Liu W; Wan ZH; Kong YY J Pediatr Endocrinol Metab; 2020 May; 33(5):639-645. PubMed ID: 32304307 [TBL] [Abstract][Full Text] [Related]
14. The status of neonatal screening in China, 2013. Zhong K; Wang W; He F; Wang Z J Med Screen; 2016 Jun; 23(2):59-61. PubMed ID: 26238341 [TBL] [Abstract][Full Text] [Related]
15. Nationwide survey of extended newborn screening by tandem mass spectrometry in Taiwan. Niu DM; Chien YH; Chiang CC; Ho HC; Hwu WL; Kao SM; Chiang SH; Kao CH; Liu TT; Chiang H; Hsiao KJ J Inherit Metab Dis; 2010 Oct; 33(Suppl 2):S295-305. PubMed ID: 20567911 [TBL] [Abstract][Full Text] [Related]
16. Screening for neonatal inherited metabolic disorders by tandem mass spectrometry in Guangzhou. Tang C; Tan M; Xie T; Tang F; Liu S; Wei Q; Liu J; Huang Y Zhejiang Da Xue Xue Bao Yi Xue Ban; 2021 Aug; 50(4):463-471. PubMed ID: 34704419 [TBL] [Abstract][Full Text] [Related]
17. Selective screening for inborn errors of metabolism by tandem mass spectrometry at Sohag University Hospital, Egypt. Magdy RM; Abd-Elkhalek HS; Bakheet MA; Mohamed MM Arch Pediatr; 2022 Jan; 29(1):36-43. PubMed ID: 34848132 [TBL] [Abstract][Full Text] [Related]
18. Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening. Shibata N; Hasegawa Y; Yamada K; Kobayashi H; Purevsuren J; Yang Y; Dung VC; Khanh NN; Verma IC; Bijarnia-Mahay S; Lee DH; Niu DM; Hoffmann GF; Shigematsu Y; Fukao T; Fukuda S; Taketani T; Yamaguchi S Mol Genet Metab Rep; 2018 Sep; 16():5-10. PubMed ID: 29946514 [TBL] [Abstract][Full Text] [Related]
19. Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening. Lin Y; Wang W; Lin C; Zheng Z; Fu Q; Peng W; Chen D Orphanet J Rare Dis; 2021 Aug; 16(1):339. PubMed ID: 34344405 [TBL] [Abstract][Full Text] [Related]
20. Biochemical, molecular, and clinical features of patients with glutaric acidemia type 1 identified through large-scale newborn screening in Zhejiang Province, China. Lin Y; Zhu X; Zhang C; Yin X; Miao H; Hu Z; Yang J; Wu B; Huang X Clin Chim Acta; 2022 May; 530():113-118. PubMed ID: 35367405 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]