Wen-Juan Qiu
Overview
Explore the profile of Wen-Juan Qiu including associated specialties, affiliations and a list of published articles.
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Articles
54
Citations
219
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0
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Recent Articles
1.
Wu S, E H, Yu Y, Ling S, Liang L, Qiu W, et al.
World J Pediatr
. 2023 Dec;
20(8):848-858.
PMID: 38070096
Background: The aim of this study was to characterize the variable phenotypes and outcomes associated with the methylmalonic aciduria and homocystinuria type C protein gene (MMACHC) c.482G > A mutation...
2.
Bao P, Ye J, Han L, Qiu W, Zhang H, Yu Y, et al.
World J Pediatr
. 2018 Nov;
15(1):66-71.
PMID: 30443829
Background: This study aimed to explore the value of applying a new pterin marker (isoxanthopterin) to the traditional urine pterin analysis to reduce the rate of mis-diagnosis of 6-pyruvoyltetrahydropterin synthase...
3.
Wang Y, Ye J, Qiu W, Han L, Gao X, Liang L, et al.
Acta Pharmacol Sin
. 2018 Jun;
40(2):279-287.
PMID: 29872134
Mucolipidosis II α/β, mucolipidosis III α/β, and mucolipidosis III γ are autosomal recessive disorders belonging to the family of lysosomal storage disorders caused by deficiency of the UDP-N-acetylglucosamine, a lysosomal...
4.
Ye J, Qiu W, Han L, Zhang H, Gu X
Chin Med J (Engl)
. 2015 Nov;
128(21):2979-80.
PMID: 26521805
No abstract available.
5.
Chu S, Ye J, Zhang H, Han L, Qiu W, Gao X, et al.
World J Pediatr
. 2015 Oct;
11(4):366-73.
PMID: 26454440
Background: X-linked adrenoleukodystrophy (X-ALD) is a fatal neurodegenerative disease caused by mutations in the adenosine triphosphate-binding cassette D1 (ABCD1) gene. This study aimed to retrospectively investigate the clinical characteristics of...
6.
Han L, Huang Z, Han F, Ye J, Qiu W, Zhang H, et al.
World J Pediatr
. 2015 Oct;
11(4):358-65.
PMID: 26454439
Background: This study aims to study MUT gene mutation spectrum in Chinese patients with isolated methylmalonic academia (MMA) and their clinical features for the potential genotype-phenotype correlation. Methods: Forty-three patients...
7.
Zhang W, Wu W, Gu J, Sun Y, Ye X, Qiu W, et al.
J Crit Care
. 2015 Feb;
30(3):606-12.
PMID: 25708120
Purpose: This study was designed to identify the incidence and independent perioperative risk factors associated with postoperative delirium of patients who underwent coronary artery bypass grafting (CABG) in a large...
8.
Hypertrophic cardiomyopathy in pompe disease is not limited to the classic infantile-onset phenotype
Lee D, Qiu W, Lee J, Chien Y, Hwu W
JIMD Rep
. 2014 Sep;
17:71-5.
PMID: 25213570
Pompe disease is a genetic disorder caused by a deficiency of acid α-glucosidase (GAA). Patients with classic infantile-onset Pompe disease usually present with hypertrophic cardiomyopathy and die before 1 year...
9.
Lu D, Ye J, Han L, Qiu W, Zhang H, Zhou J, et al.
World J Pediatr
. 2014 Aug;
10(3):219-26.
PMID: 25124972
Background: This study aimed to investigate the mutation spectrum of the QDPR gene, to determine the effect of mutations on dihydropteridine reductase (DHPR) structure/function, to discuss the potential genotypephenotype correlation,...
10.
Zhang R, Li Y, Qiu W, Ye J, Han L, Zhang H, et al.
World J Pediatr
. 2014 May;
10(2):119-25.
PMID: 24801231
Background: Very long chain acyl-CoA dehydrogenase deficiency (VLCADD) is an inherited metabolic disease caused by deleterious mutations in the ACADVL gene that encodes very long chain acyl-CoA dehydrogenase (VLCAD), and...