Huang TL - Search Results

1

A splice mutation in RASGRP2 gene in the patient with recurrent epistaxis and nasal vascular malformation.

Shi ZY, Lei QL, Duan SQ, Zhou Y, Cui TT, Lin YB, Yang CH, Song CY, Fang CL, Tian X, Zhang XW, Huang TL. Shi ZY, et al. Among authors: huang tl. Platelets. 2024 Dec;35(1):2425664. doi: 10.1080/09537104.2024.2425664. Epub 2024 Nov 8. Platelets. 2024. PMID: 39512176 Free article.

2

A de novo ANK1 mutation associated to hereditary spherocytosis: a case report.

Huang TL, Sang BH, Lei QL, Song CY, Lin YB, Lv Y, Yang CH, Li N, Yang YH, Zhang XW, Tian X. Huang TL, et al. BMC Pediatr. 2019 Feb 18;19(1):62. doi: 10.1186/s12887-019-1436-4. BMC Pediatr. 2019. PMID: 30777044 Free PMC article.

3

Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province.

Huang TL, Zhang TY, Song CY, Lin YB, Sang BH, Lei QL, Lv Y, Yang CH, Li N, Tian X, Yang YH, Zhang XW. Huang TL, et al. Front Pediatr. 2020 Apr 15;8:159. doi: 10.3389/fped.2020.00159. eCollection 2020. Front Pediatr. 2020. PMID: 32351918 Free PMC article.

4

Treatment of Severe Refractory Thrombocytopenia in Brucellosis with Eltrombopag: A Case Report.

Zhang XW, Ren P, Huang TL. Zhang XW, et al. Among authors: huang tl. Pediatr Infect Dis J. 2022 Aug 1;41(8):e332-e335. doi: 10.1097/INF.0000000000003555. Epub 2022 Jul 13. Pediatr Infect Dis J. 2022. PMID: 35421043

5

The long-term efficacy of eltrombopag in children with immune thrombocytopenia.

Yang L, Sang BH, Yang CH, Xiao ZG, Fang CL, Lv Y, Li N, Yang Q, Chai SM, Tian X, Zhang XW, Huang TL. Yang L, et al. Among authors: huang tl. Ann Hematol. 2024 Aug;103(8):2721-2727. doi: 10.1007/s00277-024-05857-y. Epub 2024 Jun 25. Ann Hematol. 2024. PMID: 38916741

6

A Novel HLA-DPA1 Allele, HLA-DPA1*01:204, Was Identified by Next-Generation Sequencing.

He XJ, Wang KX, Zhang P, Huang TL, Zhang XW. He XJ, et al. Among authors: huang tl. HLA. 2024 Oct;104(4):e15710. doi: 10.1111/tan.15710. HLA. 2024. PMID: 39415629

7

A Novel HLA-C Allele, HLA-C*12:419, Was Identified by Next-Generation Sequencing in a Chinese Individual.

Huang TL, Zhang TY, Xiang L, Jiang HC, Zhang XW. Huang TL, et al. HLA. 2024 Dec;104(6):e15785. doi: 10.1111/tan.15785. HLA. 2024. PMID: 39616525

8

Clinical and whole-exome sequencing findings in two siblings from Hani ethnic minority with congenital glycosylation disorders.

Zhang Z, Huang TL, Ma J, He WJ, Gu H. Zhang Z, et al. Among authors: huang tl. BMC Med Genet. 2019 Nov 14;20(1):181. doi: 10.1186/s12881-019-0902-z. BMC Med Genet. 2019. PMID: 31727010 Free PMC article.

9

Langerhans Cell Histiocytosis in a Pediatric Patient with Simultaneous Gastrointestinal and Skin Involvement: A Case Report and Literature Review.

Fang J, Chen J, Deng C, Li J, Huang T, Li Y, Xie Y, Wang M. Fang J, et al. Fetal Pediatr Pathol. 2023 Jun;42(3):483-487. doi: 10.1080/15513815.2022.2142488. Epub 2022 Nov 4. Fetal Pediatr Pathol. 2023. PMID: 36331524 Review.

10

Semaphorin 4D is a potential biomarker in pediatric leukemia and promotes leukemogenesis by activating PI3K/AKT and ERK signaling pathways.

Jiang H, Tang J, Qiu L, Zhang Z, Shi S, Xue L, Kui L, Huang T, Nan W, Zhou B, Zhao C, Yu M, Sun Q. Jiang H, et al. Oncol Rep. 2021 Apr;45(4):1. doi: 10.3892/or.2021.7952. Epub 2021 Mar 2. Oncol Rep. 2021. PMID: 33649851 Free PMC article.

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