Xu F - Search Results

1

Prenatal Diagnosis of Glutaric Acidemia I Based on Amniotic Fluid Samples in 42 Families Using Genetic and Biochemical Approaches.

Xiao B, Qiu W, Ye J, Zhang H, Zhu H, Wang L, Liang L, Xu F, Chen T, Xu Y, Yu Y, Gu X, Han L. Xiao B, et al. Among authors: xu f, xu y. Front Genet. 2020 May 20;11:496. doi: 10.3389/fgene.2020.00496. eCollection 2020. Front Genet. 2020. PMID: 32508882 Free PMC article.

2

Value of amniotic fluid homocysteine assay in prenatal diagnosis of combined methylmalonic acidemia and homocystinuria, cobalamin C type.

Chen T, Liang L, Zhang H, Ye J, Qiu W, Xiao B, Zhu H, Wang L, Xu F, Gong Z, Gu X, Han L. Chen T, et al. Among authors: xu f. Orphanet J Rare Dis. 2021 Mar 10;16(1):125. doi: 10.1186/s13023-021-01762-z. Orphanet J Rare Dis. 2021. PMID: 33691766 Free PMC article.

3

Evaluation of the Clinical, Biochemical, Neurological, and Genetic Presentations of Glutaric Aciduria Type 1 in Patients From China.

E H, Liang L, Zhang H, Qiu W, Ye J, Xu F, Gong Z, Gu X, Han L. E H, et al. Among authors: xu f. Front Genet. 2021 Jul 7;12:702374. doi: 10.3389/fgene.2021.702374. eCollection 2021. Front Genet. 2021. PMID: 34306040 Free PMC article.

4

Prenatal Diagnosis of Isovaleric Acidemia From Amniotic Fluid Using Genetic and Biochemical Approaches.

Ding S, Liang L, Qiu W, Zhang H, Xiao B, Dong L, Ji W, Xu F, Gong Z, Gu X, Wang L, Han L. Ding S, et al. Among authors: xu f. Front Genet. 2022 Jun 30;13:898860. doi: 10.3389/fgene.2022.898860. eCollection 2022. Front Genet. 2022. PMID: 35846131 Free PMC article.

5

[Analysis of 12 cases with methylmalonicacidemia cblA type].

E H, Han L, Ye J, Qiu W, Zhang H, Liang L, Wang Y, Wang J, Ji W, Chen T, Xu F, Gu X. E H, et al. Among authors: xu f. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Feb 10;37(2):101-105. doi: 10.3760/cma.j.issn.1003-9406.2020.02.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32034731 Chinese.

6

Clinical characteristics and genotype analysis of five infants with cblX type of methylmalonic acidemia.

Wang F, Liang L, Ling S, Yu Y, Chen T, Xu F, Gong Z, Han L. Wang F, et al. Among authors: xu f. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2022 Jun 25;51(3):298-305. doi: 10.3724/zdxbyxb-2022-0194. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2022. PMID: 36207831 Free PMC article. English.

7

A pilot study of expanded newborn screening for 573 genes related to severe inherited disorders in China: results from 1,127 newborns.

Luo X, Sun Y, Xu F, Guo J, Li L, Lin Z, Ye J, Gu X, Yu Y. Luo X, et al. Among authors: xu f. Ann Transl Med. 2020 Sep;8(17):1058. doi: 10.21037/atm-20-1147. Ann Transl Med. 2020. PMID: 33145277 Free PMC article.

8

Clinical, biochemical, and genotype-phenotype correlations of 118 patients with Niemann-Pick disease Types A/B.

Hu J, Maegawa GHB, Zhan X, Gao X, Wang Y, Xu F, Qiu W, Han L, Gu X, Zhang H. Hu J, et al. Among authors: xu f. Hum Mutat. 2021 May;42(5):614-625. doi: 10.1002/humu.24192. Epub 2021 Mar 19. Hum Mutat. 2021. PMID: 33675270

9

Gene expression profiles in the brain of phenylketonuria mouse model reversed by the low phenylalanine diet therapy.

Hong S, Zhu T, Zheng S, Zhan X, Xu F, Gu X, Liang L. Hong S, et al. Among authors: xu f. Metab Brain Dis. 2021 Dec;36(8):2405-2414. doi: 10.1007/s11011-021-00818-0. Epub 2021 Sep 15. Metab Brain Dis. 2021. PMID: 34524592

10

Glycolysis-Based Genes Are Potential Biomarkers in Thyroid Cancer.

Xu F, Xu H, Li Z, Huang Y, Huang X, Li Y, Zheng X, Chen Y, Lin L. Xu F, et al. Among authors: xu h. Front Oncol. 2021 Apr 26;11:534838. doi: 10.3389/fonc.2021.534838. eCollection 2021. Front Oncol. 2021. PMID: 33981593 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

15,276 results

Search Page

Filters