Duoling Li
Overview
Explore the profile of Duoling Li 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
15
Citations
131
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Zhao Y, Yu X, Li D, He J, Li Y, Zhang B, et al.
Orphanet J Rare Dis
. 2024 Jul;
19(1):267.
PMID: 39010129
Background: Late-onset Pompe disease (LOPD) is mainly characterized by progressive limb-girdle muscle weakness and respiratory impairment, whereas stroke and cerebrovascular abnormalities have been insufficiently studied in LOPD. This study aimed...
2.
Zhang N, Liu F, Zhao Y, Sun X, Wen B, Lu J, et al.
J Pathol
. 2024 Feb;
263(1):8-21.
PMID: 38332735
Pompe disease is a lysosomal storage disorder that preferentially affects muscles, and it is caused by GAA mutation coding acid alpha-glucosidase in lysosome and glycophagy deficiency. While the initial pathology...
3.
Wen B, Tang S, Lv X, Li D, Xu J, Olsen R, et al.
Hum Mol Genet
. 2021 Oct;
31(7):1115-1129.
PMID: 34718578
To observe a long-term prognosis in late-onset multiple acyl-coenzyme-A dehydrogenation deficiency (MADD) patients and to determine whether riboflavin should be administrated in the long-term and high-dosage manner, we studied the...
4.
Hou Y, Shao K, Yan Y, Dai T, Li W, Zhao Y, et al.
J Neurol
. 2021 May;
269(1):280-293.
PMID: 34021410
Objective: To characterize the clinical and pathological features of anti-HMGCR myopathy. Methods: The presence of anti-HMGCR antibody in the serum of 227 patients with idiopathic inflammatory myopathy (IIM) and 100...
5.
Zhang T, Yan C, Liu Y, Cao L, Ji K, Li D, et al.
Neuropsychiatr Dis Treat
. 2021 May;
17:1451-1458.
PMID: 34012265
Purpose: Leukodystrophies are frequently regarded as childhood disorders, but they can occur at any age, and the clinical and imaging patterns of the adult-onset form are usually different from the...
6.
Li B, Li D, Huang W, Che Y
Transl Pediatr
. 2021 Jan;
9(6):795-801.
PMID: 33457301
Background: Acute respiratory distress syndrome (ARDS) is a common pediatric disease, with an increasing mortality rate in recent years. This study aims to explore the effects of lung recruitment on...
7.
Lin Y, Xu X, Wang W, Liu F, Zhao D, Li D, et al.
Mitochondrion
. 2020 Dec;
57:1-8.
PMID: 33279600
Background: Mitochondrial disorders are a group of heterogeneous diseases characterized by biochemical disturbances in oxidative phosphorylation (OXPHOS). Mutations in mitochondrial transfer RNA (mt-tRNA) genes are the most frequently in mitochondrial...
8.
Xu J, Li D, Lv J, Xu X, Wen B, Lin P, et al.
Ann Neurol
. 2018 Sep;
84(5):659-673.
PMID: 30232818
Objective: Riboflavin-responsive multiple acyl-coenzyme A dehydrogenation deficiency (RR-MADD) is an inherited fatty acid metabolism disorder mainly caused by genetic defects in electron transfer flavoprotein-ubiquinone oxidoreductase (ETF:QO). The variant ETF:QO protein...
9.
Wen B, Li D, Li W, Zhao Y, Yan C
Neurol Sci
. 2015 Apr;
36(6):853-9.
PMID: 25827849
We report a case with late onset riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency (MADD) characterized by decreased acyl-carnitine profile in serum which is consistent with primary systemic carnitine deficiency (CDSP) while...
10.
Shan J, Chen B, Lin P, Li D, Luo Y, Ji K, et al.
Neuromolecular Med
. 2014 Oct;
16(4):782-6.
PMID: 25283883
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant late-onset neuromuscular degenerative disease characterized by ptosis, dysphagia, and proximal muscle weakness. The genetic basis has been identified as an abnormal (GCN)...