Xuefan Gu
Overview
Explore the profile of Xuefan Gu including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
155
Citations
1339
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Qiu W, Wang R, Liang L, Sun Y, Zhou R, Wang X, et al.
Infect Drug Resist
. 2024 Dec;
17:5675-5684.
PMID: 39720618
Introduction: Growth hormone (GH) is crucial for immune system development and regulation, potentially benefiting COVID-19 outcomes. However, there are limited studies on the role of GH treatment in COVID-19 in...
2.
Li H, Huo L, Zhang R, Gu X, Chen G, Yuan Y, et al.
Ecotoxicol Environ Saf
. 2024 Dec;
290:117564.
PMID: 39700769
Soil is the place where human beings, plants, and animals depend on for their survival and the link between the various ecological layers. Groundwater is an important component of water...
3.
Luo X, Hou L, Zhong Y, Zhao S, Chen X, Dong Q, et al.
Clin Endocrinol (Oxf)
. 2024 Nov;
102(2):136-146.
PMID: 39513569
Objective: Children born small for gestational age (SGA) are at increased risk of health issues. This study evaluated the efficacy, safety and optimal dose of PEGylated-recombinant human growth hormone (PEG-rhGH)...
4.
Hao L, Ling S, Ding S, Qiu W, Zhang H, Zhang K, et al.
Pediatr Res
. 2024 Sep;
PMID: 39306609
Background: Methylmalonic acidemia (MMA) is the most common organic acidemia in China, with cblC (cblC-MMA) and mut (mut-MMA) being the predominant subtypes. The present study aimed to investigate the prognostic...
5.
Ling S, Wu S, Shuai R, Yu Y, Qiu W, Wei H, et al.
Hum Genomics
. 2024 Jul;
18(1):84.
PMID: 39075538
Background: Isolated methylmalonic acidemia, an autosomal recessive disorder of propionate metabolism, is usually caused by mutations in the methylmalonyl-CoA mutase gene (mut-type). Because no universal consensus was made on whether...
6.
Long-Read Sequencing Solves Complex Structure of CYP21A2 in a Large 21-Hydroxylase Deficiency Cohort
Wang R, Luo X, Sun Y, Liang L, Mao A, Lu D, et al.
J Clin Endocrinol Metab
. 2024 Jul;
110(2):406-416.
PMID: 39049755
Context: Genetic testing for 21-hydroxylase deficiency (21-OHD) is always challenging. The current approaches of short-read sequencing and multiplex ligation-dependent probe amplification (MLPA) are insufficient for the detection of chimeric genes...
7.
Chang S, Zhan X, Liu Y, Song H, Gong Z, Han L, et al.
JAMA Netw Open
. 2024 May;
7(5):e2410754.
PMID: 38739391
Importance: Newborn screening (NBS) for lysosomal storage disorders (LSDs) is becoming an increasing concern in public health. However, the birth prevalence of these disorders is rarely reported in the Chinese...
8.
Zhang Y, Qiu W, Zhang H, Chen T, Xu F, Gu X, et al.
Zhejiang Da Xue Xue Bao Yi Xue Ban
. 2024 Apr;
53(2):207-212.
PMID: 38650450
Objectives: To investigate the clinical characteristic and genetic variants of children with carnitine palmitoyltransferase 2 (CPT2) deficiency. Methods: The clinical and genetic data of 6 children with CPT2 deficiency were...
9.
Du Y, Jiang P, Yang J, Zhao M, Wu L, Hui Y, et al.
Clin Lab
. 2024 Apr;
70(4).
PMID: 38623669
Background: We aimed to evaluate the diagnostic capabilities of Chinese laboratories for inherited metabolic disorders (IMDs) using gas chromatography-mass spectrometry (GC-MS) on urine samples. Meanwhile, based on the result of...
10.
Su H, Zhang H, Wu J, Huang L, Zhang M, Xu W, et al.
Adv Sci (Weinh)
. 2024 Feb;
11(15):e2305701.
PMID: 38348590
Phenylketonuria (PKU) is the most common inherited metabolic disease in humans. Clinical screening of newborn heel blood samples for PKU is costly and time-consuming because it requires multiple procedures, like...