Ti-long Huang

Kunming, China

Last Updated: 09/26/2026

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Found 11 publications

Identification of a Novel Compound Heterozygous SEC23B in a Chinese Child with Congenital Dyserythropoietic Anemia Type II.

Identification of a Novel Compound Heterozygous SEC23B in a Chinese Child with Congenital Dyserythropoietic Anemia Type II.

Journal: Hemoglobin

Published: August 04, 2026

Nonsense Variant in the β-Spectrin Gene Causing Hereditary Spherocytosis Identified by Whole-Exome Sequencing in a Child.

Nonsense Variant in the β-Spectrin Gene Causing Hereditary Spherocytosis Identified by Whole-Exome Sequencing in a Child.

Journal: Hemoglobin

Published: December 21, 2025

Long-term efficacy and safety of hetrombopag in paediatric patients with immune thrombocytopenia.

Long-term efficacy and safety of hetrombopag in paediatric patients with immune thrombocytopenia.

Journal: British journal of haematology

Published: March 23, 2025

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

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

Journal: Platelets

Published: November 08, 2024

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

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

Journal: HLA

Published: November 01, 2024

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

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

Journal: HLA

Published: September 06, 2024

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

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

Journal: Annals of hematology

Published: April 05, 2024

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

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

Journal: The Pediatric infectious disease journal

Published: April 14, 2022

Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province.

Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province.

Journal: Frontiers in pediatrics

Published: January 12, 2020

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

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

Journal: BMC medical genetics

Published: February 10, 2019

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

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

Journal: BMC pediatrics

Published: July 04, 2018

Showing 1-11 of 11

Last Updated: 09/26/2026