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1.
HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy.
Proc Natl Acad Sci U S A
; 117(10): 5472-5477, 2020 03 10.
Article
in English
| MEDLINE | ID: mdl-32086392
2.
D-dimers (DD) in CVST.
Int J Neurosci
; 127(6): 524-530, 2017 Jun.
Article
in English
| MEDLINE | ID: mdl-27426719
3.
Incidence and risk factors of pleural effusions in patients with POEMS syndrome.
Hematol Oncol
; 33(2): 80-4, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-24519469
4.
The characteristics of ascites in patients with POEMS syndrome.
Ann Hematol
; 92(12): 1661-4, 2013 Dec.
Article
in English
| MEDLINE | ID: mdl-23811954
5.
[The determination of medical reference values for tumor markers in cerebrospinal fluid].
Zhonghua Yi Xue Za Zhi
; 89(5): 355-6, 2009 Feb 10.
Article
in Zh
| MEDLINE | ID: mdl-19563718
6.
[MyoD mRNA expression in skeletal muscle of patients with myotonic dystrophy].
Zhonghua Yi Xue Za Zhi
; 89(7): 466-8, 2009 Feb 24.
Article
in Zh
| MEDLINE | ID: mdl-19567095
7.
Identification of Seven Novel Mutations in the Acid Alpha-glucosidase Gene in Five Chinese Patients with Late-onset Pompe Disease.
Chin Med J (Engl)
; 131(4): 448-453, 2018 Feb 20.
Article
in English
| MEDLINE | ID: mdl-29451150
8.
A Novel Mutation of Mitochondrial T14709C Causes Myoclonic Epilepsy with Ragged Red Fibers Syndrome in a Chinese Patient.
Chin Med J (Engl)
; 131(13): 1569-1574, 2018 Jul 05.
Article
in English
| MEDLINE | ID: mdl-29941710
9.
[Investigating the diagnostic value of MHC-I expression in polymyositis].
Zhonghua Yi Xue Za Zhi
; 87(11): 754-6, 2007 Mar 20.
Article
in Zh
| MEDLINE | ID: mdl-17565844
10.
A Novel AGRN Mutation Leads to Congenital Myasthenic Syndrome Only Affecting Limb-girdle Muscle.
Chin Med J (Engl)
; 130(19): 2279-2282, 2017 Oct 05.
Article
in English
| MEDLINE | ID: mdl-28937031
11.
A novel thymidine phosphorylase mutation in a Chinese MNGIE patient.
Acta Neurol Belg
; 117(1): 259-267, 2017 Mar.
Article
in English
| MEDLINE | ID: mdl-27709505
12.
Increased Expression of the NOD-like Receptor Family, Pyrin Domain Containing 3 Inflammasome in Dermatomyositis and Polymyositis is a Potential Contributor to Their Pathogenesis.
Chin Med J (Engl)
; 129(9): 1047-52, 2016 May 05.
Article
in English
| MEDLINE | ID: mdl-27098789
13.
Oculopharyngeal Weakness, Hypophrenia, Deafness, and Impaired Vision: A Novel Autosomal Dominant Myopathy with Rimmed Vacuoles.
Chin Med J (Engl)
; 129(15): 1805-10, 2016 Aug 05.
Article
in English
| MEDLINE | ID: mdl-27453229
14.
[Regulatory T cells in the treatment of autoimmune myositis in mice: efficacy and mechanism].
Nan Fang Yi Ke Da Xue Xue Bao
; 35(4): 602-5, 2015 Apr.
Article
in Zh
| MEDLINE | ID: mdl-25907954
15.
Complement membrane attack complex is related with immune-mediated necrotizing myopathy.
Int J Clin Exp Pathol
; 7(7): 4143-9, 2014.
Article
in English
| MEDLINE | ID: mdl-25120794
16.
Clinical and pathological features of patients with nemaline myopathy.
Mol Med Rep
; 10(1): 175-82, 2014 Jul.
Article
in English
| MEDLINE | ID: mdl-24788569
17.
Reply to "Mitochondrial tRNA Glutamic Acid Variant 14709T>C Manifesting as Myoclonic Epilepsy with Ragged Red Fibers".
Chin Med J (Engl)
; 131(20): 2519-2520, 2018 Oct 20.
Article
in English
| MEDLINE | ID: mdl-30334547
18.
Clinical, Pathological, and Genetic Features of Two Chinese Cases with Filamin C Myopathy.
Chin Med J (Engl)
; 131(24): 2986-2988, 2018 Dec 20.
Article
in English
| MEDLINE | ID: mdl-30539912
19.
Chinese specific characteristics of sporadic Creutzfeldt-Jakob disease: a retrospective analysis of 57 cases.
PLoS One
; 8(3): e58442, 2013.
Article
in English
| MEDLINE | ID: mdl-23516482
20.
Dural enhancement detected by magnetic resonance imaging reflecting the underlying causes of cerebral venous sinus thrombosis.
Chin Med J (Engl)
; 125(8): 1513-6, 2012 Apr.
Article
in English
| MEDLINE | ID: mdl-22613663