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Year | Number of Results |
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2022 | 3 |
2023 | 4 |
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qian gui sheng[Author]
(80 results)?
A case of West syndrome and global developmental delay in a child with a heterozygous mutation in the TBL1XR1 gene: A case report.
Medicine (Baltimore). 2023 May 12;102(19):e33744. doi: 10.1097/MD.0000000000033744.
Medicine (Baltimore). 2023.
PMID: 37171308
Free PMC article.
Retroperitoneal leiomyoma located in the broad ligament: A case report.
Zhang XS, Lin SZ, Liu YJ, Zhou L, Chen QD, Wang WQ, Li JY.
Zhang XS, et al. Among authors: chen qd.
World J Clin Cases. 2022 Nov 16;10(32):12022-12027. doi: 10.12998/wjcc.v10.i32.12022.
World J Clin Cases. 2022.
PMID: 36405292
Free PMC article.
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Children with infectious pneumonia caused by Ralstonia insidiosa: A case report.
Lin SZ, Qian MJ, Wang YW, Chen QD, Wang WQ, Li JY, Yang RT, Wang XY, Mu CY, Jiang K.
Lin SZ, et al. Among authors: chen qd.
World J Clin Cases. 2023 Mar 26;11(9):2002-2008. doi: 10.12998/wjcc.v11.i9.2002.
World J Clin Cases. 2023.
PMID: 36998962
Free PMC article.
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Eosinophilic granuloma of the clavicle in an 11-year-old Chinese girl: A case report.
Chen QD, Lin SZ, Zhou J, Chen XX, Yang RT, Wang X, Li JY, Feng XC, Liu YS, Jiang K, Feng JH.
Chen QD, et al.
Medicine (Baltimore). 2023 Jun 30;102(26):e34139. doi: 10.1097/MD.0000000000034139.
Medicine (Baltimore). 2023.
PMID: 37390234
Free PMC article.
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VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report.
Wu XH, Lin SZ, Zhou YQ, Wang WQ, Li JY, Chen QD.
Wu XH, et al. Among authors: chen qd.
World J Clin Cases. 2022 Aug 26;10(24):8749-8754. doi: 10.12998/wjcc.v10.i24.8749.
World J Clin Cases. 2022.
PMID: 36157797
Free PMC article.
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Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report.
Lin SZ, Ma QJ, Pang QM, Chen QD, Wang WQ, Li JY, Zhang SL.
Lin SZ, et al. Among authors: chen qd.
World J Clin Cases. 2022 Nov 6;10(31):11486-11492. doi: 10.12998/wjcc.v10.i31.11486.
World J Clin Cases. 2022.
PMID: 36387827
Free PMC article.
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Retinitis pigmentosa with or without skeletal abnormalities due to homozygous mutations in the CWC27 gene: A case report.
Qi YF, Ma X, Lin SZ, Wang WQ, Li JY, Chen QD, Liu L.
Qi YF, et al. Among authors: chen qd.
Medicine (Baltimore). 2023 Dec 22;102(51):e36357. doi: 10.1097/MD.0000000000036357.
Medicine (Baltimore). 2023.
PMID: 38134094
Free PMC article.
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