Chuan-Qiang Pu
Overview
Explore the profile of Chuan-Qiang Pu including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
23
Citations
95
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0
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Recent Articles
1.
Zhang Y, Pu C, Ban R, Liu H, Shi Q, Lu X
Chin Med J (Engl)
. 2018 Dec;
131(24):2986-2988.
PMID: 30539912
No abstract available.
2.
Ban R, Guo J, Pu C, Shi Q, Liu H, Zhang Y
Chin Med J (Engl)
. 2018 Oct;
131(20):2519-2520.
PMID: 30334547
No abstract available.
3.
Ban R, Guo J, Pu C, Shi Q, Liu H, Zhang Y
Chin Med J (Engl)
. 2018 Jun;
131(13):1569-1574.
PMID: 29941710
Background: Myoclonic epilepsy with ragged red fibers (MERRF) syndrome is characterized by myoclonus, generalized epilepsy, cerebellar ataxia, and ragged red fibers (RRFs) in the muscle. T-to-C transition at nucleotide position...
4.
Liu H, Pu C, Shi Q, Zhang Y, Ban R
Chin Med J (Engl)
. 2018 Feb;
131(4):448-453.
PMID: 29451150
Background: Pompe disease is a rare lysosomal glycogen storage disorder linked to the acid alpha-glucosidase gene (GAA). A wide clinical and genetic variability exists between patients from different ethnic populations,...
5.
Zhang Y, Dai Y, Han J, Chen Z, Ling L, Pu C, et al.
Chin Med J (Engl)
. 2017 Sep;
130(19):2279-2282.
PMID: 28937031
Background: Congenital myasthenic syndromes (CMSs) are a group of clinically and genetically heterogeneous disorders caused by impaired neuromuscular transmission. The defect of AGRN was one of the causes of CMS...
6.
Wang H, Wang J, Wang Y, Fan J, Mo G, Gong F, et al.
Acta Neurol Belg
. 2016 Oct;
117(1):259-267.
PMID: 27709505
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an autosomal recessive disorder associated with mitochondrial alterations. MNGIE is characterized by severe gastrointestinal dysmotility, cachexia, ophthalmoplegia, ptosis, peripheral neuropathy, and leukoencephalopathy. The condition is...
7.
Chen T, Lu X, Wang H, Ban R, Liu H, Shi Q, et al.
Chin Med J (Engl)
. 2016 Jul;
129(15):1805-10.
PMID: 27453229
Background: Myopathies with rimmed vacuoles are a heterogeneous group of muscle disorders with progressive muscle weakness and varied clinical manifestations but similar features in muscle biopsies. Here, we describe a...
8.
Yin X, Han G, Jiang X, Shi Q, Pu C
Chin Med J (Engl)
. 2016 Apr;
129(9):1047-52.
PMID: 27098789
Background: Dermatomyositis (DM) and polymyositis (PM) are common inflammatory myopathies whose immunopathogenic mechanisms remain poorly understood. The NOD-like receptor family, pyrin domain containing 3 (NLRP3) inflammasome is a type of...
9.
Shi Q, Tian C, Liu J, Pu C
Nan Fang Yi Ke Da Xue Xue Bao
. 2015 Apr;
35(4):602-5.
PMID: 25907954
Objective: To investigate effect of CD4(+) CD25(+) Foxp3(+) Tregs in the treatment of autoimmune myositis (EAM) in mice and explore the possible mechanisms. Methods: Mouse models of EAM were divided...
10.
Cong L, Pu C, Shi Q, Wang Q, Lu X
Int J Clin Exp Pathol
. 2014 Aug;
7(7):4143-9.
PMID: 25120794
This study is to investigate the expression of complement membrane attack complex (C5b-9) in the skeletal muscle of patients with necrotizing myopathy (NM), and to investigate the relationship between C5b-9...