Dai YL - Search Results

1

Hereditary Thrombotic Thrombocytopenic Purpura in a Chinese Boy With a Novel Compound Heterozygous Mutation of the ADAMTS13 Gene.

Dai YL, Tang X, Chen HB, Peng QY, Guo X, Gao J. Dai YL, et al. Front Pediatr. 2020 Sep 10;8:554. doi: 10.3389/fped.2020.00554. eCollection 2020. Front Pediatr. 2020. PMID: 33014938 Free PMC article.

2

Co-occurrence of TCF3-PBX1 gene fusion, and chromosomal aberration in a pediatric pre-B cell acute lymphoblastic leukemia with clitoris swelling: A case report and literature review.

He GQ, Guo X, Jiang MY, Xu RR, Dai YL, Luo L, Gao J. He GQ, et al. Among authors: dai yl. Medicine (Baltimore). 2021 Feb 26;100(8):e24802. doi: 10.1097/MD.0000000000024802. Medicine (Baltimore). 2021. PMID: 33663097 Free PMC article.

3

Obesity as a Prognostic Factor of Central Nervous System Relapse in Children with Acute Lymphoblastic Leukemia: A Single-Centre Study and Literature Review.

He GQ, Dai YL, Jiang MY, Gao J, Guo X. He GQ, et al. Among authors: dai yl. Evid Based Complement Alternat Med. 2022 Mar 21;2022:7783823. doi: 10.1155/2022/7783823. eCollection 2022. Evid Based Complement Alternat Med. 2022. PMID: 35356245 Free PMC article.

4

Anti-Hu antibody associated paraneoplastic neurological syndrome in a child with ganglioneuroblastoma: A rare case report and literature review.

Dai YL, Xiao L, Pan Z, He GQ, Gao J, Guo X, Huang Z. Dai YL, et al. Medicine (Baltimore). 2024 May 10;103(19):e38148. doi: 10.1097/MD.0000000000038148. Medicine (Baltimore). 2024. PMID: 38728479 Free PMC article. Review.

5

Case Report: A rare infection of multidrug-resistant Aeromonas caviae in a pediatric case with acute lymphoblastic leukemia and review of the literature.

Dai Y, Gao J, Jiang M. Dai Y, et al. Front Pediatr. 2024 May 13;12:1233600. doi: 10.3389/fped.2024.1233600. eCollection 2024. Front Pediatr. 2024. PMID: 38803640 Free PMC article.

6

Rare cases of a second recurrence of nephroblastoma with MLLT1 gene mutation: case report and literature review.

Dai Y, Chen X, He G, Gao J, Guo X. Dai Y, et al. Front Oncol. 2024 Dec 2;14:1487544. doi: 10.3389/fonc.2024.1487544. eCollection 2024. Front Oncol. 2024. PMID: 39687897 Free PMC article.

7

[A case of type 2A juvenile hereditary hemochromatosis].

Fan JL, Zhou BY, Dai YL. Fan JL, et al. Among authors: dai yl. Zhonghua Xin Xue Guan Bing Za Zhi. 2025 Jan 24;53(1):61-63. doi: 10.3760/cma.j.cn112148-20241124-00729. Zhonghua Xin Xue Guan Bing Za Zhi. 2025. PMID: 39806903 Chinese.

8

The diagnosis and management of mucopolysaccharidosis type II.

Mao SJ, Chen QQ, Dai YL, Dong GP, Zou CC. Mao SJ, et al. Among authors: dai yl. Ital J Pediatr. 2024 Oct 8;50(1):207. doi: 10.1186/s13052-024-01769-9. Ital J Pediatr. 2024. PMID: 39380047 Free PMC article. Review.

9

The influence of genotype makeup on the effectiveness of growth hormone therapy in children with Prader-Willi syndrome.

Zhou Q, Chao YQ, Dai YL, Gao Y, Shen Z, Dong GP, Zou CC. Zhou Q, et al. Among authors: dai yl. BMC Pediatr. 2024 Oct 1;24(1):627. doi: 10.1186/s12887-024-05109-y. BMC Pediatr. 2024. PMID: 39354420 Free PMC article.

10

The diagnostic value of neutrophil to lymphocyte ratio, albumin to fibrinogen ratio, and lymphocyte to monocyte ratio in Parkinson's disease: a retrospective study.

Li YM, Xu XH, Ren LN, Xu XF, Dai YL, Yang RR, Jin CQ. Li YM, et al. Among authors: dai yl. Front Neurol. 2024 Sep 2;15:1450221. doi: 10.3389/fneur.2024.1450221. eCollection 2024. Front Neurol. 2024. PMID: 39286804 Free PMC article.

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