Search details
1.
Postoperative cognitive dysfunction in heart transplantation recipients.
Clin Transplant
; 38(5): e15337, 2024 May.
Article
in English
| MEDLINE | ID: mdl-38762786
2.
Simultaneous T1, T2, and T2* Mapping of Carotid Plaque: The SIMPLE* Technique.
Radiology
; 307(3): e222061, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36853181
3.
Integrated head and neck imaging of symptomatic patients with stroke using simultaneous non-contrast cardiovascular magnetic resonance angiography and intraplaque hemorrhage imaging as compared with digital subtraction angiography.
J Cardiovasc Magn Reson
; 24(1): 19, 2022 03 21.
Article
in English
| MEDLINE | ID: mdl-35307027
4.
Brujavanoids A-U, structurally diverse apotirucallane-type triterpenoids from Brucea javanica and their anti-inflammatory effects.
Bioorg Chem
; 127: 106012, 2022 10.
Article
in English
| MEDLINE | ID: mdl-35830756
5.
Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients.
Clin Genet
; 99(3): 384-395, 2021 03.
Article
in English
| MEDLINE | ID: mdl-33200426
6.
A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients.
Clin Genet
; 97(5): 789-790, 2020 05.
Article
in English
| MEDLINE | ID: mdl-31909476
7.
Congenital muscular dystrophies in China.
Clin Genet
; 96(3): 207-215, 2019 09.
Article
in English
| MEDLINE | ID: mdl-31066047
8.
FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies.
J Hum Genet
; 61(12): 1013-1020, 2016 Dec.
Article
in English
| MEDLINE | ID: mdl-27439679
9.
Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutation.
J Hum Genet
; 61(8): 753-9, 2016 Aug.
Article
in English
| MEDLINE | ID: mdl-27193224
10.
GABA in the anterior cingulate cortex mediates the association of white matter hyperintensities with executive function: a magnetic resonance spectroscopy study.
Aging (Albany NY)
; 16(5): 4282-4298, 2024 Mar 01.
Article
in English
| MEDLINE | ID: mdl-38441529
11.
Anti-inflammatory lanostane triterpenoids with rearranged spirobi[indene] scaffold and their biogenetically related analogues from Euphorbia maculata.
Phytochemistry
; 211: 113682, 2023 Jul.
Article
in English
| MEDLINE | ID: mdl-37084863
12.
HyperCKemia: An early sign of childhood-onset neutral lipid storage disease with myopathy.
Neuromuscul Disord
; 33(9): 81-89, 2023 09.
Article
in English
| MEDLINE | ID: mdl-37620213
13.
Uniparental disomy for chromosome 1 with POMGNT1 splice-site variant causes muscle-eye-brain disease.
Front Genet
; 14: 1170089, 2023.
Article
in English
| MEDLINE | ID: mdl-37342771
14.
Decreased GABA levels of the anterior and posterior cingulate cortex are associated with executive dysfunction in mild cognitive impairment.
Front Neurosci
; 17: 1220122, 2023.
Article
in English
| MEDLINE | ID: mdl-37638325
15.
Metabolic profiling integrated with pharmacokinetics to reveal the material basis of Xiaokeyinshui extract combination in the treatment of type 2 diabetes in rats.
J Pharm Biomed Anal
; 225: 115224, 2023 Feb 20.
Article
in English
| MEDLINE | ID: mdl-36603394
16.
An integrative non-invasive malignant brain tumors classification and Ki-67 labeling index prediction pipeline with radiomics approach.
Eur J Radiol
; 158: 110639, 2023 Jan.
Article
in English
| MEDLINE | ID: mdl-36463703
17.
Seizures and EEG characteristics in a cohort of pediatric patients with dystroglycanopathies.
Seizure
; 101: 39-47, 2022 Oct.
Article
in English
| MEDLINE | ID: mdl-35863218
18.
Recessive mutations in proximal I-band of TTN gene cause severe congenital multi-minicore disease without cardiac involvement.
Neuromuscul Disord
; 29(5): 350-357, 2019 05.
Article
in English
| MEDLINE | ID: mdl-31053406
19.
Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy.
Sci Rep
; 8(1): 14989, 2018 10 09.
Article
in English
| MEDLINE | ID: mdl-30301903
20.
Genetic and Clinical Advances of Congenital Muscular Dystrophy.
Chin Med J (Engl)
; 130(21): 2624-2631, 2017 Nov 05.
Article
in English
| MEDLINE | ID: mdl-29067961