Diagnosis, monitoring, and management of pyruvate kinase deficiency in children-Reference-Cited by-同舟云学术

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Diagnosis, monitoring, and management of pyruvate kinase deficiency in children

Published:2022-04-22 Issue:8 Volume:69 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Johnson Shaniqua¹²,Grace Rachael F.³⁴,Despotovic Jenny M.¹²^ORCID

Affiliation:

1. Department of Pediatrics, Division of Hematology/Oncology Baylor College of Medicine Houston Texas USA

2. Texas Children's Cancer and Hematology Centers Texas Children's Hospital Houston Texas USA

3. Dana‐Farber/Boston Children's Cancer and Blood Disorders Center Boston Massachusetts USA

4. Harvard Medical School Boston Massachusetts USA

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.29696

Reference54 articles.

1. Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: Tabulation of mutant enzymes

2. Estimating the prevalence of pyruvate kinase deficiency from the gene frequency in the general white population

3. Regulatory properties of human erythrocyte hexokinase during cell ageing

4. Red cell pyruvate kinase deficiency: from genetics to clinical manifestations

5. The human liver-type pyruvate kinase (PKL) gene is on chromosome 1 at band q21

Cited by 2 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. Current Status of Molecular Diagnosis of Hereditary Hemolytic Anemia in Korea;Journal of Korean Medical Science;2024

2. Anemia and Associated Risk Factors in Pediatric Patients;Pediatric Health, Medicine and Therapeutics;2023-09

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