Variable Genotype-Phenotype Correlations in Patients With a Rare Nondeletional α-thalassemia; Hb Pak Num Po (HBA1-Reference-Cited by-同舟云学术

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Variable Genotype-Phenotype Correlations in Patients With a Rare Nondeletional α-thalassemia; Hb Pak Num Po (HBA1

Published:2014-04 Issue:3 Volume:36 Page:e185-e189
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:

Author:

Sanpakit Kleebsabai,Viprakasit Vip

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference9 articles.

1. Inherited haemoglobin disorders: an increasing global health problem.;Weatherall;Bull World Health Organ,2001

2. Thalassaemia.;Higgs;Lancet,2012

3. The molecular basis of alpha-thalassemia.;Higgs;Cold Spring Harb Perspect Med,2013

4. Alpha-thalassemia syndromes: from clinical and molecular diagnosis to bedside management.;Viprakasit;EHA Educational Book,2013

5. Hb H disease: clinical course and disease modifiers.;Fucharoen;Hematology Am Soc Hematol Educ Program,2009

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment;Thalassemia Reports;2022-11-22

2. Impact of splenectomy on outcomes of hematopoietic stem cell transplantation in pediatric patients with transfusion‐dependent thalassemia;Pediatric Blood & Cancer;2020-06-22

3. Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart’s disease: A hematological, molecular, and diagnostic aspects;International Journal of Laboratory Hematology;2020-05-02

4. Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses;Hemoglobin;2015-11-16

5. α−thalassaemia: a genotype-phenotype correlation and management;ISBT Science Series;2015-04

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