Haemophagocytic lymphohistiocytosis in Malaysian children
Author:
Affiliation:
1. Paediatric Haematology‐Oncology Unit, University of Malaya Medical Centre, Kuala Lumpur, Malaysia
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1440-1754.2005.00564.x
Reference25 articles.
1. Modern management of children with haemophagocytic lymphohistiocytosis
2. Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)
3. Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis
4. Pathogenesis of haemophagocytic lymphohistiocytosis
5. HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS
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1. A Young Boy With Hemophagocytic Lymphohistiocytosis Presenting With Vaccine-Related Granulomatous Dermatitis: A Case Report and Literature Review;The American Journal of Dermatopathology;2021-09-21
2. The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India;Frontiers in Immunology;2021-03-05
3. Systematic Review of Primary Immunodeficiency Diseases in Malaysia: 1979–2020;Frontiers in Immunology;2020-08-26
4. Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review;Pediatric Allergy and Immunology;2020-08-24
5. Hemophagocytic lymphohistiocytosis presenting with annular erythema multiforme‑like eruptions in a patient with angioimmunoblastic T cell lymphoma: A case report;Experimental and Therapeutic Medicine;2018-07-06
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